Catalysis as an Enabling Science for Sustainable Polymers
Open accessAbstract
The replacement of current petroleum-based plastics with sustainable alternatives is a crucial but formidable challenge for the modern society. Catalysis presents an enabling tool to facilitate the development of sustainable polymers. This review provides a system-level analysis of sustainable polymers and outlines key criteria with respect to the feedstocks the polymers are derived from, the manner in which the polymers are generated, and the end-of-use options. Specifically, we define sustainable polymers as a class of materials that are derived from renewable feedstocks and exhibit closed-loop life cycles. Among potential candidates, aliphatic polyesters and polycarbonates are promising materials due to their renewable resources and excellent biodegradability. The development of renewable monomers, the versatile synthetic routes to convert these monomers to polyesters and polycarbonate, and the different end-of-use options for these polymers are critically reviewed, with a focus on recent advances in catalytic transformations that lower the technological barriers for developing more sustainable replacements for petroleum-based plastics.
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Written from the paper’s full text.
TL;DR
This review argues that catalysis is an enabling science for sustainable polymers, defined as renewable-feedstock-derived materials with closed-loop life cycles, and focuses on aliphatic polyesters and polycarbonates. It surveys catalytic routes from renewable feedstocks to monomers, polymerization methods, and end-of-use recycling or biodegradation, while noting incomplete sustainability metrics and economic/infrastructure barriers.
Key findings
- Sustainable polymers are defined as materials derived from renewable feedstocks that exhibit closed-loop life cycles; aliphatic polyesters and polycarbonates are highlighted because they can be made from renewable monomers, synthesized by versatile routes, and are biodegradable or chemically recyclable.
- Global plastics production grew from 1.65 million tons in 1950 to 311 million tons in 2014 and is expected to grow 3–4% per year; more than 300 million metric tons of plastic waste is generated annually, with 4.8–12.7 million metric tons entering the ocean.
- Bio-derived plastics remain a small share: in 2014 only 1.7 megatons of more than 300 megatons of polymers produced globally were bio-derived, mainly PLA, biopolyethylene, and bioPET; in the United States in 2014, over 75% of plastic waste was landfilled, and plastics recycling rates are <10%.
- Catalytic advances cited include MnCo2O4-supported Ru giving 99% FDCA yield from base-free air oxidation of HMF, zeolite-catalyzed one-step conversion of lactic acid to lactide at ~79% selectivity at full conversion, and TBD-catalyzed PLA alcoholysis reaching quantitative conversion in 2 min at room temperature with 1.5 equivalents of alcohol per ester bond.
Methods
- This is a review and system-level analysis, not an experimental study; it considers feedstocks, monomer production, polymerization, use, and end-of-use options, focusing on polyesters and polycarbonates as representative sustainable materials.
- It synthesizes literature on catalytic transformations from renewable feedstocks to monomers, monomers to polyesters and polycarbonates, and chemical or biological recycling/degradation, comparing routes by atom efficiency, green catalytic systems, and mild polymerization conditions.
- It includes tabulated thermodynamic parameters for ring-opening polymerization of cyclic esters and comparison tables of polymerization methods for polyesters and polycarbonates.
Limitations
- Stated: there is no universally recognized standard system or set of metrics for quantifying sustainability; life-cycle assessment results vary with modeling assumptions and feedstock choice, are often limited to cradle-to-gate, and switching from petroleum polymers to renewable-resource polymers does not necessarily reduce environmental impacts.
- Stated: many biofeedstocks and biorefinery processes are costly or energy-intensive; sustainable polymers must meet cost and performance benchmarks; the existing plastics economic ecosystem is entrenched, and recovery/reuse infrastructure is underdeveloped.
- Evident: as a review, it reports no new experimental data; its scope excludes biomedical biodegradation of aliphatic polyesters and polycarbonates and focuses on selected polymer classes, so quantitative comparisons depend on cited studies and their assumptions.
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Claims the paper makes
0 of 431 cited sources checked · 0 supported · 0 flagged
- Premisecitation
The rate and time scale of CO2 sequestration for petroleum feedstocks (millions of years) is much slower than the use and release (1-10 year time frame).
“This is in contrast to the carbon cycle for petroleum feedstocks, in which the rate and time scale of CO2 sequestration (millions of years) is much slower than the use and release (1-10 year time frame).”
Quote in the paperNot a substantial claim - Premisereasoning
LCA results are not available before production, much less during design, due to inadequate data.
“That means, LCA results are not available before the production of a product, much less so during the design of a product as a result of inadequate data on environmental impacts.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Bio-derived and biodegradable polymers are emerging as attractive alternatives to conventional petroleum-based polymers.
“Such bio-derived and biodegradable polymers are therefore emerging * DGp° = standard free energy of polymerization as attractive alternatives to conventional petroleum-based polymers.”
Quote in the paperNot a substantial claim - Interpretationreasoning
For energetic efficiency, plastic materials should optimally be derived from polymerization reactions that are not strongly exergonic.
“In order for this process to be energetically efficient, plastic materials should optimally be derived from polymerization reactions that are not strongly exergonic to ensure that, once generated, the materials can be catalytically depolymerized or chemically recycled with minimal energy inputs”
Quote in the paperSubstantial claim - Premisereasoning
Biodegradation requires engineering of polymer composition/formulation or degradation pathway to break down to CO2 and H2O in a reasonable time frame.
“This requires engineering of either the polymer composition/formulation or its degradation pathway so that it can be broken down by microorganisms to primarily CO2 and H2O in a reasonable time frame.”
Quote in the paperNot a substantial claim
- Premisecitation
Quantitative metrics of environmental sustainability are not nearly as well advanced or universally accepted as metrics of economic sustainability.
“Third, quantitative metrics of environmental sustainability [7][8][9][10] are not nearly as well advanced or universally accepted as metrics of economic sustainability.”
Quote in the paperNot a substantial claim - Premisereasoning
The economic incentives and infrastructure for recovery and re-use are not nearly as well developed as those for production of plastics.
“This is a systems-level challenge, as the economic incentives and infrastructure for recovery and re-use are not nearly as well developed as those for production of plastics.”
Quote in the paperNot a substantial claim - Premisecitation
In the United States in 2014, over 75% of plastics wastes were landfilled, with the remainder recycled or incinerated.
“In the United States in 2014, over 75% of plastics wastes were landfilled, 39 with the remainder being either recycled (primarily HDPE and PET) or incinerated.”
Quote in the paperNot a substantial claim - Premisecitation
The majority of recent reviews on sustainable polymers focus on renewable resources for feedstocks and monomers.
“The majority focus on the use of renewable resources for feedstocks and monomers for plastics, particularly biomass-derived monomers and processes for the generation of polymers derived from these monomers.”
Quote in the paperSubstantial claim - Premisereasoning
The scope of LCA is often limited to cradle-to-gate due to lack of complete understanding and inadequate data on environmental fate and impact.
“Although LCA ideally should take into account all stages of the product life cycle, i.e. cradle-to-cradle, the scope of LCA is often limited to cradle-to-gate due to the lack of a complete understanding and inadequate data on the environmental fate and impact of a polymer.”
Quote in the paperNot a substantial claim - Premisecitation
Isomerizing alkoxycarbonylation of methyl oleate catalyzed by a palladium catalyst bearing phosphorus ligands can convert the internal double bond deep in the hydrocarbon chain to a terminal ester group with high yield and selectivity.
“In one example, they showed that isomerizing alkoxycarbonylation of methyl oleate catalyzed by a palladium catalyst bearing phosphorus ligands can convert the internal double bond deep in the hydrocarbon chain to a terminal ester group with high yield and selectivity.100”
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- Interpretationreasoning
Degradability or recyclability is the key to build a circular economy that increases resource utilization and reduces waste generation.
“and the latter is the key to build a circular economy that increases resource utilization and reduces waste generation.”
Quote in the paperSubstantial claim - Premisecitation
Algae has turned up as a cheaper alternative to oilseed crops due to its non-food nature, fast production and recycle rate, and low use of production inputs.
“Oilseed crops such as soybean, rapeseed, and oil palm are the major supply of oils at present, but algae has turned up as a cheaper alternative due to its non-food nature, fast production and recycle rate, and low use of production inputs.82”
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- Premisecitation
Carbohydrates are the most exploited and abundant bio-feedstock for producing building blocks for these polymers.
“Carbohydrates are the most exploited and abundant bio-feedstock for producing building blocks for these polymers.”
Quote in the paperNot a substantial claim - Interpretationcitation
Switching from petroleum polymers to those derived from renewable resources does not necessarily reduce environmental impacts.
“Therefore, one important message from this study is that switching from petroleum polymers to those derived from renewable resources does not necessarily reduce environmental impacts.”
Quote in the paperSubstantial claim - Premisecitation
A variety of long-chain α,ω-diacids can be produced through oxidative cleavage of the alkene group of fatty acids.
“A variety of long-chain a,w-diacids can be produced through oxidative cleavage of the alkene group of fatty acids.33”
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- Interpretationreasoning
Fatty-acid-derived α,ω-difunctional monomers provide access to long-chain aliphatic polyesters with unique properties that bridge the gap between semicrystalline polyolefins and traditional polycondensates.
“These fatty-acid-derived α,ω-difunctional monomers provide access to a class of long-chain aliphatic polyesters with unique properties that bridge the gap between semicrystalline polyolefins and the traditional polycondensates.”
Quote in the paperSubstantial claim - Premisecitation
FDCA is a useful bio-based feedstock for the production of aromatic polyesters.
“Furan-2,5-dicarboxylic acid (FDCA) is a useful bio-based feedstock for the production of aromatic polyesters.103”
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- Interpretationcitation
Plastics derived from renewable feedstocks are not necessarily sustainable.
“However, it should be noted that plastics derived from renewable feedstocks are not necessarily sustainable.”
Quote in the paperSubstantial claim - Premisecitation
The most well-established approach to FDCA is based on a dehydration process to convert C6 sugars to hydroxymethylfurfural (HMF), which is then oxidized to FDCA.
“The most well-established approach is based on a dehydration process to convert C6 sugars to hydroxymethylfurfural (HMF), which is then oxidized to FDCA.106”
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- Premisenone given
Due to the oxygen-rich character of polyesters and polycarbonates, they can be readily sourced from a wide variety of renewable feedstocks.
“Due to the oxygen-rich character of polyesters and polycarbonates, they can be readily sourced from a wide variety of renewable feedstocks.”
Quote in the paperNot a substantial claim - Premisecitation
PLA's physical properties allow it to replace petroleum-based plastics in some types of packaging and fiber applications.
“Its physical properties allow it to replace petroleum-based plastics in some types of packaging and fiber applications.”
Quote in the paperNot a substantial claim - Premisereasoning
Due to relatively high costs and limited material properties, renewable plastics currently make up only a small share of the global plastics market.
“Due to the relatively high costs and limited material properties, renewable plastics currently make up only a small share of the global plastics market.”
Quote in the paperNot a substantial claim - Premisenone given
Currently, most renewable monomers are produced from sugar- or starch-rich crops such as corn and sugar cane.
“Currently, most of the renewable monomers are produced from sugar-or starch-rich crops such as corn and sugar cane.”
Quote in the paperNot a substantial claim - Premisecitation
A MnCo2O4 supported Ru catalyst affords excellent yield of FDCA (99%) from base-free air-oxidation of HMF in water.
“For example, a MnCo2O4 supported Ru catalyst was found to afford excellent yield of FDCA (99%) from base-free air-oxidation of HMF in water.110”
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- Premisecitation
Terpenes and CO2 are useful feedstocks for polyesters and polycarbonates.
“In addition to these two major classes of biomass, terpenes and CO2 are also useful feedstocks for polyesters and polycarbonates.16,83”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
1,4-diacids, including succinic, fumaric, and itaconic acids, are some of the most successful platform chemicals obtained from carbohydrate biorefinery.
“1,4-diacids, including succinic, fumaric, and itaconic acids, are some of the most successful platform chemicals obtained from carbohydrate biorefinery.91”
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- Interpretationreasoning
One disadvantage of oxidative cleavage of fatty acids is that only about half of the fatty acid chain is utilized in the α,ω-difunctional product and the rest is lost as a coupling product of less value.
“One disadvantage of this transformation is that only part (about half) of the fatty acid chain is utilized in the α,ω-difunctional product and the rest is lost as a coupling product of less value.”
Quote in the paperNot a substantial claim - Premisecitation
The conversion of renewable feedstocks to monomers typically involves a mechanical/physical pretreatment followed by multiple biological, chemical, or thermochemical processes.
“The conversion typically involves a mechanical/physical pretreatment (milling, extraction, steam reforming), followed by multiple biological, chemical, or thermochemical processes.77”
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- Interpretationnone given
None of the renewable routes to adipic acid are economically feasible yet.
“However, none of these routes are economically feasible yet.”
Quote in the paperNot a substantial claim - Premisenone given
The monomers of many polyesters and polycarbonates can be derived from biomass or waste gases via biological or chemical transformations.
“First, the monomers of many polyesters and polycarbonates can be derived from biomass or waste gases via biological or chemical transformations.”
Quote in the paperNot a substantial claim - Premisecitation
Vanadyl phosphate catalysts can convert fructose to FDCA in 97% selectivity at 84% conversion.
“Vanadyl phosphate catalysts can convert fructose to FDCA in 97% selectivity at 84% conversion; 112”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [112] source
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- Interpretationreasoning
Given the multiple-step nature of the synthesis from not readily available platform chemicals, substituted CL monomers are not ideal candidates for sustainable polymers.
“Given the multiple-step nature of the synthesis from not readily available platform chemicals, these monomers are not ideal candidates for sustainable polymers.”
Quote in the paperNot a substantial claim - Interpretationcitation
ROP of macrolactones with ring sizes of 19 and 23 generates long-chain polyesters with higher and more predictable molecular weights than the ones prepared from the polycondensation of fatty acids.
“ROP of these macrolactones generates long-chain polyesters with higher and more predicable molecular weights than the ones prepared from the polycondensation of fatty acids.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [181] source
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- Premisecitation
Au/TiO2 catalysts with addition of small amount of Pt can convert succinic acid to γ-BL with 97% selectivity at 97% conversion.
“Au/TiO2 catalysts with addition of small amount of Pt can convert succinic acid to g-BL with 97% selectivity at 97% conversion.173”
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- Interpretationnone given
The overall yields of the routes to four-membered lactones from renewable feedstocks are below 10%.
“However, the overall yields of all these routes are below 10%.”
Quote in the paperNot a substantial claim - Premisecitation
These rigid diols have proven particularly useful for the synthesis of polyester and polycarbonates with high glass transition temperatures.
“These rigid diols have proven particularly useful for the synthesis of polyester and polycarbonates with high glass transition temperatures.88,154”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
The reaction of furoic acid with molten Cs2CO3 under a CO2 flow or 8 bar CO2 can give FDCA in 70-89% yield within 12 h.
“The reaction of furoic acid with molten Cs2CO3 under a CO2 flow or 8 bar CO2 can give FDCA 2-in 70-89% yield within 12 h.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [116] source
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- Premisecitation
1,3-propanediol (PDO) has been industrially produced on a large scale (over 50,000 tons annually) by aerobic fermentation of glucose from corn syrup by a genetically modified strain of E. coli, developed by DuPont Tate & Lyle BioProducts.
“It has been industrially produced on a large scale (over 50,000 tons annually) by aerobic fermentation of glucose from corn syrup by a genetically modified strain of E. coli, developed by DuPont Tate & Lyle BioProducts. 137”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [137] DuPont Tate & Lyle BioProducts. http://www.duponttateandlyle.com/susterra(accessed May 2, 2017).
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- Premisecitation
Lactic acid is a versatile precursor to a variety of monomers, including lactide, propylene glycol, propylene oxide, and acrylic acid.
“Lactic acid is a versatile precursor to a variety of monomers, including lactide, propylene glycol, propylene oxide, and acrylic acid.33”
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- Premisecitation
Dimethyl carbonate (DMC) can be produced by dehydrative condensation of CO2 and alcohols in yields of 40-60% based on acetal.
“Dimethyl carbonate (DMC) can be produced by this method in yields of 40-60% based on acetal.185”
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- Premisecitation
Co(acac)3 in a silica sol-gel system gives 99% selectivity to FDCA from fructose at 72% conversion.
“Co(acac)3 in a silica sol-gel system gives 99% selectivity to FDCA from fructose at 72% conversion.113”
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- Premisecitation
Zhang found that the coupling of 3-chloro-1-propanol with CO2 in the presence of 1.1 equiv. of Cs2CO3 proceeded efficiently under mild conditions (40 °C, 1 atm CO2) to provide trimethylene carbonate in 95% yield.
“Zhang found that the coupling of 3-chloro-1-propanol with CO2 in the presence of 1.1 equiv. of Cs2CO3 proceeded efficiently under mild conditions (40 °C, 1 atm CO2) to provide trimethylene carbonate in 95% yield.200”
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- Premisecitation
A leading technology for the synthesis of BDO from renewable resources is through reduction of bio-based succinic acid.
“A leading technology for the synthesis of BDO from renewable resources is through reduction of bio-based succinic acid.142”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [142] bioamber. https://www.bio-amber.com/bioamber/en/products(accessed May 2, 2017).
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- Premisecitation
Although the step-growth method has been known since the discovery of synthetic polymers in early 20th century, it is still the most frequently used method for the synthesis of polyesters and polycarbonates in industry.
“Although the step-growth method has been known since the discovery of synthetic polymers in early 20 th century, 212 it is still the most frequently used method for the synthesis of polyesters and polycarbonates in industry.”
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- Premisenone given
Catalytic polycondensations for step-growth synthesis are typically conducted at very high temperature (>200 °C) and high vacuum to reach high conversion.
“These catalytic polycondensations are typically conducted at very high temperature (>200 °C) and high vacuum to reach high conversion.”
Quote in the paperNot a substantial claim - Premisecitation
Aliphatic polyesters with high glass transition temperatures (Tg > 60 °C) can be prepared by using a rigid diol such as isosorbide.
“For example, aliphatic polyesters with high glass transition temperatures (Tg > 60 °C) can be prepared by using a rigid diol such as isosorbide.214”
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- Premisecitation
The two-stage procedure has enabled the synthesis of polyesters and polycarbonates with molecular weights over 50 kDa.
“This two-stage procedure has enabled the synthesis of polyesters and polycarbonates with molecular weights over 50 kDa.215,223”
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Metal salts such as titanium alkoxides, tin alkoxides, zinc or magnesium carboxylates are commonly used catalysts for the step-growth synthesis of polyesters and polycarbonates.
“Metal salts such as titanium alkoxides, tin alkoxides, zinc or magnesium carboxylates are commonly used catalysts for the step-growth synthesis of polyesters and polycarbonates.[224][225][226][227]228,229”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
SGP of plant oils derived diols and diacids with > 20 methylene sequences generates polyesters with structures and thermal properties reminiscent of PE.
“For example, SGP of plant oils derived diols and diacids with > 20 methylene sequences generates polyesters with structures and thermal properties reminiscent of PE. 213”
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- Premisecitation
The crystallinity and biodegradation rate of poly(alkylene carbonates) can be adjusted by employing diols with different chain lengths.
“The crystallinity and biodegradation rate of poly(alkylene carbonates) can be adjusted by employing diols with different chain lengths.215,216”
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Methyl 9,10-epoxystearate (MES) derived from oleic acid has been used to prepare polyesters with extremely low Tg (-44 °C).
“Methyl 9,10-epoxystearate (MES) derived from oleic acid has been used to prepare polyesters with extremely low Tg (-44 °C).207”
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- Premisecitation
The use of multifunctional monomers such as glycerol and citric acid enables a facile synthesis of biodegradable thermosets.
“Moreover, the use of multifunctional monomers such as glycerol and citric acid enables a facile synthesis of biodegradable thermosets.217”
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- Premisecitation
Ti(OiPr)4 can mediate the polycondensation of bio-derived diesters (succinate, adipate, sebacate) with 1,4-butanediol under high temperature (up to 240 °C) and in vacuo to generate aliphatic polyesters with Mn > 20 kDa.
“For example, Ti(O i Pr)4 can mediate the polycondensation of several bio-derived diesters (succinate, adipate, sebacate) with 1,4-butanediol under high temperature (up to 240 °C) and in vacuo to generate aliphatic polyesters with Mn > 20 kDa.225,230,231”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationreasoning
Given that many diols and diacids can be readily obtained from biomass, SGP provides a straightforward route to renewable polyesters and polycarbonates.
“Given that many diols and diacids can be readily obtained from biomass (Section 2.1 and 2.2), SGP provides a straightforward route to renewable polyesters and polycarbonates.”
Quote in the paperSubstantial claim - Premisenone given
Organic carbonates such as dimethyl carbonate are currently employed as a safer and greener substitute for phosgene.
“Organic carbonates such as dimethyl carbonate (DMC) are currently employed as a safer and greener substitute for phosgene.”
Quote in the paperNot a substantial claim - Premisecitation
Melt condensation of ω-hydroxyl fatty acids catalyzed by Ti(OiPr)4 via a two-stage polymerization generates polyesters with molecular weights ranging from 50 to 110 kDa.
“Melt condensation of ω-hydroxyl fatty acids, e.g.OH(CH2)13COOH, catalyzed by Ti(O i Pr)4 via a two-stage polymerization (200 °C under N2 then 220 °C under 0.1 mmHg) generate polyesters with molecular weights ranging from 50 to 110 kDa.232”
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- Premisecitation
Kobayashi developed a unique catalytic system using a surfactant-like acid, DBSA, to mediate the emulsion polycondensation of aliphatic carboxylic acids and alcohols in water.
“Kobayashi developed a unique catalytic system [250][251][252] using a surfactant-like acid, such as dodecylbenzenesulfonic acid (DBSA), to mediate the emulsion polycondensation of aliphatic carboxylic acids and alcohols in water.”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Several studies have demonstrated the potential of using CO2 as a renewable and safe carbonyl reagent for the synthesis of polycarbonates.
“Recently, several studies have demonstrated the potential of using CO2 as a renewable and safe carbonyl reagent for the synthesis of polycarbonates (Scheme 5).”
Quote in the paperNot a substantial claim - Premisecitation
This was the first time that a high-molecular-weight linear polyester was produced from itaconic acid without isomerization or cross-linking of the vinylic double bond.
“This was the first time that a high-molecular-weight linear polyester was produced from itaconic acid without isomerization or cross-linking of the vinylic double bond.”
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- Premisecitation
A few studies using Bi(OTf)3 to polymerize plant oil- and suberin-derived long-chain fatty acids generated highly crystalline polyesters with high melting and degradation temperatures as attractive alternatives to petroleum-based polyolefins.
“A few studies using Bi(OTf)3 to polymerize plant oil-237 and suberin-derived 238 long-chain fatty acids generated highly crystalline polyesters with high melting and degradation temperatures as attractive alternatives to petroleum-based polyolefins.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
This mild and environmentally benign system has been successfully applied to several fatty-acid type monomers.
“This mild and environmentally benign system has been successfully applied to several fatty-acid type monomers.253,254”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisereasoning
Because of their strong Lewis acidity, metal triflates can catalyze polycondensation reactions at much milder temperatures (<100 °C).
“Because of their strong Lewis acidity, they can catalyze polycondensation reactions at much milder temperatures (<100 °C).”
Quote in the paperSubstantial claim - Premisereasoning
Metal triflates have become a class of popular polycondensation catalysts.
“Metal triflates have become a class of popular polycondensation catalysts for this reason.”
Quote in the paperNot a substantial claim - Premisecitation
Meier used Sn(Oct)2 to polymerize dimethyl itaconate and long chain diols in the presence of 0.5 wt% 4-methoxyphenol as a radical inhibitor to make linear unsaturated polyesters with Mn up to 11500 Da.
“Meier recently used Sn(Oct)2 to polymerize dimethyl itaconate and long chain diols in the presence of 0.5 wt% of 4-methoxyphenol as a radical inhibitor to make linear unsaturated polyesters with Mn up to 11500 Da. 233”
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- Premisecitation
The high costs and long reaction times of enzyme catalysts largely limit their utility in large-scale manufacture.
“However, the high costs and long reaction times of enzyme catalysts largely limit their utility in large-scale manufacture.257,260”
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Takasu found that scandium triflate selectively esterifies primary hydroxyl groups over secondary or tertiary alcohol.
“Takasu found that scandium triflate (Sc(OTf)3) selectively esterifies primary hydroxyl groups over the secondary or tertiary alcohol.241”
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- Premisecitation
Kadokawa reported a PR3/CBr4/base system to facilitate the direct polycondensation of CO2 with alkane diols at room temperature and ambient pressure.
“Kadokawa reported a PR3/CBr4/base system (Scheme 5a) to facilitate the direct polycondensation of CO2 with alkane diols at room temperature and ambient pressure.261,262”
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Sc(OTf)3 catalyzes a chemoselective polycondensation of tartaric acid or malic acid with polyols such as glycerol and sorbitol under mild conditions to afford linear polyesters (Mn between 4 and 26 kDa) with negligible branching or crosslinking.
“They developed a chemoselective polycondensation of tartaric acid or malic acid with polyols such as glycerol and sorbitol under mild conditions (60 °C, 0.3-3.0mmHg, 0.5 mol% Sc(OTf)3) to afford linear polyesters (Mn between 4 and 26 kDa) with negligible branching or crosslinking.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [241] source
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- Premisecitation
Step-growth polymerization mediated by mild and selective enzyme catalysis provides a metal-free and eco-friendly route to polyesters and polycarbonates.
“SGP mediated by mild and selective enzyme catalysis also provides a metal-free and eco-friendly route to polyesters and polycarbonates.[255][256][257][258][259]”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
Several classes of organocatalysts have been used to catalyze the step-growth polymerization of diols with diacids or carbonates, including strong Brønsted acids and organic bases.
“Several classes of organocatalysts have been used to catalyze the SGP of diols with diacids or carbonates, including strong Brønsted acids such as H2SO4, triflic acid, p-toluenesulfonic acid (PTSA), bis(trifluoromethanesulfonyl)-imide (Tf2NH), 243,244 and organic bases such as TBD, 221,245-247 MTBD, 248 1-n-butyl-3-methylimidazol-2-carboxylate.249”
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Using Bi(OTf)3 as the catalyst, the polycondensation of sebacic acid and various α,ω-alkanediols can be performed at 80 °C under vacuum for 48 h to afford polyesters with Mn up to 30 kDa.
“Using Bi(OTf)3 as the catalyst, the polycondensation of sebacic acid and various a,w-alkanediols can be performed at 80 °C under vacuum for 48 h to afford polyesters with Mn up to 30 kDa. 235,236”
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ROP has been the method of choice for the synthesis of tailor-made drug delivery systems where complex architectures and precise molecular weights are essential to their performance.
“For this reason, ROP has been the method of choice for the synthesis of tailor-made drug delivery systems where complex architectures and precise molecular weights are essential to their performance.269,270”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Because the thermodynamic driving force for ROP is highly dependent on the ring size and substitution pattern of the monomer, only a limited set of cyclic esters and carbonates can be polymerized under practical conditions.
“Because the thermodynamic driving force for ROP is highly dependent on the ring size and substitution pattern of the monomer, 273 only a limited set of cyclic esters and carbonates can be polymerized under practical conditions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [273] Duda A., 2009
Not checked in the free run.
- Premisecitation
A class of strained 8-membered cyclic carbonates derived from diethanolamine were prepared and polymerized to well-defined N-substituted polycarbonates.
“Recently a class of strained 8-memebered cyclic carbonates derived from diethanolamine were prepared and polymerized to well-defined N-substituted polycarbonates.283,284”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
The first catalytic approach for the polycondensation between CO2 and diols was reported by Tomishige in 2016 using CeO2 as the catalyst and 2-cyanopyridine as the dehydrating agent.
“The first catalytic approach for the polycondensation between CO2 and diols was reported by Tomishige in 2016 using CeO2 as the catalyst and 2-cyanopyridine as the dehydrating agent (Scheme 5b).263”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [263] source
Not checked in the free run.
- Premisecitation
As opposed to step-growth polymerizations, ROP allows for a fine degree of control over several important macromolecular parameters including molecular weight, polydispersity, end-group fidelity, regio- and stereoselectivity, and architecture.
“As opposed to step-growth polymerizations, ROP allows for a fine degree of control over several important macromolecular parameters including molecular weight, polydispersity, end-group fidelity, regio-and stereoselectivity, and architecture (block, cyclic, star, etc). 267,268”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisereasoning
Ring-opening polymerization of cyclic esters and carbonates is an efficient method for the synthesis of aliphatic polyester and polycarbonates.
“Ring-opening polymerization of cyclic esters and carbonates is an efficient method for the synthesis of aliphatic polyester and polycarbonates.”
Quote in the paperSubstantial claim - Premisecitation
Feng and Gnanou improved the reaction efficiency of the diol/alkyl dihalide/CO2 polycarbonate synthesis by using Cs2CO3 as the base and 10 bar CO2.
“This method was recently revisited by Feng and Gnanou, who improved the reaction efficiency by using Cs2CO3 as the base and 10 bar CO2 (Scheme 5d).265”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [265] source
Not checked in the free run.
- Premisecitation
At low temperatures (e.g. -40 °C), the ROP of γ-butyrolactone mediated by La[N(SiMe3)2]3 or tert-Bu-P4 can proceed to high conversions (60-90%).
“However, Chen recently found that at low temperatures (e.g.-40 °C), the ROP of γ-BL mediated by La[N(SiMe3)2]3 or tert-Bu-P4 can proceed to high conversions (60 ~ 90%).278”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [278] source
Not checked in the free run.
- Premisecitation
ROP of a few macrolactones (ring size = 14, 16) has been successfully applied to prepare long-chain polyesters with similar structures but higher and more predictable molecular weights than those obtained from the polycondensation of fatty acids.
“ROP of a few macrolactones (ring size = 14, 16) have been successfully applied to prepare longchain polyesters with similar structures but higher and more predictable molecular weights than the ones obtained from the polycondensation of fatty acids.[279][280][281]”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Characterizations of the resulting polymers suggested an alternating incorporation of diols and dihalides into the polycarbonates.
“Characterizations of the resulting polymers suggested an alternating incorporation of diols and dihalides into the polycarbonates.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [264] source
Not checked in the free run.
- Premisecitation
In Du's case, alternating ether and carbonate linkages were observed in the polymer.
“In this case, alternating ether and carbonate linkages were observed in the polymer.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [266] source
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- Premisecitation
Kadokawa's polymerization also generated quantitative wastes including CHBr3, R3P=O, and protonated bases.
“The polymerization also generated quantitative wastes including CHBr3, R3P=O, protonated bases.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisereasoning
For small- and medium-size rings (ring size < 8), ring-opening is driven by enthalpy as a result of release of ring strain.
“For small-and medium-size rings (ring size < 8), ring-opening is driven by enthalpy as a result of release of ring strain.”
Quote in the paperNot a substantial claim - Premisecitation
The use of alkyl dihalides as a third condensation component has been more successful than the direct coupling of CO2 and diols to generate polycarbonates with higher molecular weights.
“In comparison to the direct coupling of CO2 and diols, the use of alkyl dihalides as a third condensation component has been more successful to generate polycarbonates with higher molecular weights.[264][265][266]”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisereasoning
Because of the strong nucleophilic and/or basic character of the anionic initiator/chain ends, transesterification and epimerization are commonly observed for anionic ROPs.
“Because of the strong nucleophilic and/or basic character of the anionic initiator/chain ends, transesterification and epimerization are commonly observed for these anionic ROPs.”
Quote in the paperNot a substantial claim - Premisenone given
The relative rates of chain transfer and propagation steps are mainly controlled by the catalytic processes.
“The relative rates of these steps are mainly controlled by the catalytic processes.”
Quote in the paperSubstantial claim - Premisecitation
Common to all chain-growth polymerizations, chain transfer can compete with chain propagation to undermine the control on the structure and molecular weight distribution of the resulting polymers.
“Common to all chain-growth polymerizations, chain transfer can compete with chain propagation to undermine the control on the structure and molecular weight distribution of the resulting polymers.273”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [273] Duda A., 2009
Not checked in the free run.
- Premisereasoning
As the monomer and alkoxide chain end are both covalently bound to the metal center, the catalyst can exert a great level of control on the rate and selectivity of the polymerization.
“As the monomer and alkoxide chain end are both covalently bound to the metal center, the catalyst can exert a great level of control on the rate and selectivity of the polymerization.”
Quote in the paperNot a substantial claim - Premisecitation
Strong acids and acylating agents can polymerize cyclic esters and carbonates through a cationic pathway.
“Strong acids and acylating agents can polymerize cyclic esters and carbonates through a cationic pathway.273”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [273] Duda A., 2009
Not checked in the free run.
- Interpretationreasoning
The development of selective catalysts that favor chain propagation over any chain transfer and termination events is critical for the synthesis of polyesters and polycarbonates of well-defined structures and architectures.
“Therefore, the development of selective catalysts that favor the chain propagation over any chain transfer and termination events is critical for the synthesis of polyesters and polycarbonates of well-defined structures and architectures.”
Quote in the paperSubstantial claim - Premisecitation
Alkali metal complexes such as butyllithium and potassium methoxide can mediate anionic ROPs via a nucleophilic or enolate-type initiating mechanism.
“Alkali metal complexes such as butyllithium 285 and potassium methoxide 286 can mediate anionic ROPs via a nucleophilic or enolate-type initiating mechanism.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
A variety of initiator/catalyst systems have been developed for ROP of cyclic esters and carbonates.
“A variety of initiator/catalyst systems have been developed for ROP of cyclic esters and carbonates.268,270”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
A zinc catalyst with a bdiiminate amido ligand exhibits excellent reactivity and selectivity for the ROP of a variety of lactones and cyclic carbonates.
“For example, a zinc catalyst with bdiiminate amido ligand ((BDI i Pr)Zn[N(SiMe3)2] exhibits excellent reactivity and selectivity for the ROP of a variety of lactones and cyclic carbonates.296”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [296] source
Not checked in the free run.
- Premisecitation
The synthesis of high molecular weight polymers is rather difficult with cationic catalysts due to the strong tendency of intramolecular transesterification (cyclization) and proton transfer reactions of the cationic propagating species.
“The synthesis of high molecular weight polymers is rather difficult with these catalysts due to the strong tendency of intramolecular transesterification (cyclization) and proton transfer reactions of the cationic propagating species.288”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [288] source
Not checked in the free run.
- Premisecitation
Byers developed a chemoselective copolymerization of LA and epoxides using a redox-switchable iron catalyst.
“In the similar vein, Byers developed a chemoselective copolymerization of LA and epoxides using a redox-switchable iron catalyst (Scheme 8B).320”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [320] source
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- Premisecitation
This zinc catalyst showed exceptionally high regioselectivity (<1% regio-defects) for the ROP of methyl-substituted cyclic carbonates.
“In addition, this catalyst showed exceptionally high regioselectivity (< 1% regio-defects) for the ROP of methyl-substituted cyclic carbonates.298”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [298] source
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- Premisecitation
The use of switchable metal catalysts to strategically modulate the rate and monomer selectivity of ROP is emerging.
“Recently, the use of switchable metal catalysts to strategically modulate the rate and monomer selectivity of ROP is emerging.267”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [267] source
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- Premisecitation
Studies of the resulting polymers have showed a strong correlation between the thermal and mechanical properties of PLAs and their stereosequences.
“Studies of the resulting polymers have showed a strong correlation between the thermal and mechanical properties of PLAs and their stereosequences.300”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [300] source
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- Premisecitation
This distinct substrate selectivity allowed the one-pot copolymerization of the two monomers by in situ switching of the redox state of the catalyst to synthesize poly[(LA-minor-CL)-block-(CL-minor-LA)].
“This distinct substrate selectivity allowed the one-pot copolymerization of the two monomers by in situ switching of the redox state of the catalyst to synthesize poly[(LA-minor-CL)-block-(CL-minor-LA)].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [319] source
Not checked in the free run.
- Premisecitation
Diaconescu reported several redox-switchable group 4 metal complexes supported by a ferrocenyl-based ligand.
“Diaconescu reported several redox-switchable group 4 metal complexes supported by ferrocenyl-based ligand (Scheme 8A).319”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [319] source
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- Premisereasoning
This innovative catalytic strategy has enabled the facile one-pot synthesis of block copolymers of polyesters and polycarbonates.
“This innovative catalytic strategy has enabled the facile one-pot synthesis of block copolymers of polyesters and polycarbonates.”
Quote in the paperSubstantial claim - Premisecitation
Other metal catalysts such as zirconium complexes with bispyrrolidine-salan ligand and zinc complexes with chiral or achiral auxiliary ligands have also been used to generate iso-enriched stereoblock PLAs from rac-LA.
“Other metal catalysts such as zirconium complexes with bispyrrolidine-salan ligand 312 and zinc complexes with chiral or achiral auxiliary ligands [313][314][315][316] (Figure 7) have also been used to generate iso-enriched stereoblock PLAs from rac-LA.”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Syndiotactic PHAs have been synthesized by stereospecific ROP of racemic β-lactones by several rare-earth metal catalysts.
“Syndiotactic poly(3-hydroxyalkanoate)s (PHAs) have been synthesized by stereospecific ROP of racemic b-lactones by several rare-earth metal catalysts.318”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [318] source
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- Premisecitation
Similar copolymerization of LA and epoxides were obtained using a redox-switchable zirconium complex.
“Similar copolymerization of LA and epoxides were obtained using a redox-switchable zirconium complex.321”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [321] source
Not checked in the free run.
- Premisecitation
With only 20 ppm of this zinc catalyst, poly(trimethylene carbonate) with Mn as high as 237 kDa and Ð = 1.68 can be synthesized in quantitative yield within 2 h.
“With only 20 ppm of this catalyst, poly(trimethylene carbonate) with Mn as high as 237 kDa and Ð = 1.68 can be synthesized in quantitative yield within 2 h.297”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [297] source
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- Premisereasoning
This allowed the formation of clean diblock copolymers.
“This allowed the formation of clean diblock copolymers.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [320] source
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- Premisecitation
This approach was extended to a monomer mixture of epoxide, lactone, anhydride, and CO2 to synthesize a variety of block copolymers with great sequence control and predictable compositions in the polymer chains.
“Recently, this approach was extended to a monomer mixture of epoxide, lactone, anhydride, and CO2 to synthesize a variety of block copolymers with great sequence control and predictable compositions in the polymer chains.323”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [323] source
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- Premisecitation
Coulembier developed a zwitterionic ammonium betaine catalyst that exhibited high selectivity for the ROP of lactide.
“Coulembier developed a zwitterionic ammonium betaine catalyst that exhibited high selectivity for the ROP of lactide.333”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [333] source
Not checked in the free run.
- Premisenone given
The synthesis of well-defined linear polyesters or polycarbonates with molecular weights over 100 kDa has been difficult using organocatalysts due to the competitive catalyst-initiated process at low alcohol initiator concentrations.
“The synthesis of well-defined linear polyesters or polycarbonates with molecular weights over 100 kDa has been difficult using organocatalysts due to the competitive catalyst-initiated process at low alcohol initiator concentrations.”
Quote in the paperNot a substantial claim - Premisecitation
PLA of Mn = 97 kDa (DP = 750) with molecular weight conformed to the monomer-to-alcohol ratios and Mw/Mn = 1.18 can be synthesized by this catalyst.
“PLA of Mn = 97 kDa (DP = 750) with molecular weight conformed to the monomer-to-alcohol ratios and Mw/Mn = 1.18 can be synthesized by this catalyst.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [333] source
Not checked in the free run.
- Premisecitation
Alternatively, organic bases can activate the monomer through nucleophilic addition.
“Alternatively, they can activate the monomer through nucleophilic addition.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [326] source
Not checked in the free run.
- Premisecitation
Repetitive introduction and removal of CO2 resulted in the formation of multiblock poly(carbonate-block-ester).
“Thus, repetitive introduction and removal of CO2 resulted in the formation of multiblock poly(carbonateblock-ester).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [322] source
Not checked in the free run.
- Premisereasoning
Despite the weak basicity of aryloxide, these catalysts showed good reactivity toward L-LA owing to the supplementary ionic activation.
“Despite the weak basicity of aryloxide, these catalysts showed good reactivity toward L-LA owing to the supplementary ionic activation.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [333] source
Not checked in the free run.
- Premisecitation
Williams developed a strategy using CO2 as a chemical switch as well as a co-monomer for the one-pot chemoselective polymerization of epoxide and CL.
“Williams developed a strategy using CO2 as a chemical switch as well as a co-monomer for the one-pot chemoselective polymerization of epoxide and CL (Scheme 8C).322”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [322] source
Not checked in the free run.
- Premisenone given
Catalytic systems combining both H-bond donor and H-bond acceptor moieties, such as thiourea/amine, can simultaneously activate the monomer and alcohol initiator/chain end.
“Catalytic systems combining both H-bond donor and H-bond acceptor moieties, such as thiourea/amine, can simultaneously activate the monomer and alcohol initiator/chain end.”
Quote in the paperNot a substantial claim - Premisecitation
The living polymerizations of VL and CL mediated by NHO-1/Al(C6F5)3 generated linear polyesters with high molecular weights up to 855 kDa (DP = 3200) and narrow molecular weight distributions (Ð = 1.03-1.63).
“The living polymerizations of VL and CL mediated by NHO-1/Al(C6F5)3 generated linear polyesters with high molecular weights up to 855 kDa (DP = 3200) and narrow molecular weight distributions (Ð = 1.03 -1.63).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [335] source
Not checked in the free run.
- Premisecitation
They proposed a charged-assisted hydrogen-bonding mechanism for this catalyst where it activates the alcohol initiator/chain-end through a combination of hydrogen bonding between the aryloxide group and the H(d+) of ROH and the Coulomb attraction between the ammonium group and the O(d-) of ROH.
“They proposed a charged-assisted hydrogen-bonding mechanism for this catalyst where it activates the alcohol initiator/chain-end through a combination of hydrogen bonding between the aryloxide group and the H(d+) of ROH and the Coulomb attraction between the ammonium group and the O(d-) of ROH (Scheme 10).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [333] source
Not checked in the free run.
- Premisecitation
Organic bases such as N-heterocyclic carbenes and amidines can activate the alcohol initiator/chain ends through hydrogen bonding interactions.
“Organic bases such as N-heterocyclic carbenes (NHCs) and amidines can activate the alcohol initiator/chain ends through hydrogen bonding interactions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [326] source
Not checked in the free run.
- Premisenone given
The replacement of metal catalysts with organic catalysts has emerged for the synthesis of plastics, especially for those used in biomedical and microelectronic applications.
“The replacement of metal catalysts with organic catalysts has emerged for the synthesis of plastics, especially for those used in biomedical and microelectronic applications.”
Quote in the paperNot a substantial claim - Premisecitation
A class of (thio)urea anions catalysts were disclosed that exhibit both high activity and selectivity for the ROP of a variety of cyclic esters and carbonates.
“Recently a class of (thio)urea anions catalysts were disclosed that exhibit both high activity and selectivity for the ROP of a variety of cyclic esters and carbonates (Scheme 12).321,336”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
As soon as CO2 was removed, the catalyst turned on the ROP of CL with no incorporation of epoxide.
“But as soon as CO2 was removed, the catalyst turned on the ROP of CL with no incorporation of epoxide.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [322] source
Not checked in the free run.
- Interpretationreasoning
Several attributes of organic catalysts, including their low cost and wide availability, easy removal from polymers, low toxicity, and versatile catalytic mechanisms, make possible a greener and more versatile synthesis of polyesters and polycarbonates.
“Several attributes of organic catalysts, including their low cost and wide availability, easy removal from polymers, low toxicity, and versatile catalytic mechanisms, make possible a greener and more versatile synthesis of polyesters and polycarbonates.”
Quote in the paperSubstantial claim - Premisereasoning
This has led to the development of zwitterionic ring-opening polymerization for the synthesis of high molecular weight polyesters and polycarbonates with cyclic topology.
“This has led to the development of zwitterionic ring-opening polymerization for the synthesis of high molecular weight polyesters 327 and polycarbonates 284 with cyclic topology.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Depending on the nature of the catalyst, organocatalysts can operate through a variety of mechanisms.
“Depending on the nature of the catalyst, organocatalysts can operate through a variety of mechanisms (Scheme 9).326”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [326] source
Not checked in the free run.
- Premisenone given
Their catalytic behavior largely depends on the ring size, (un)saturation of the backbone, and sterics on the exocyclic carbon.
“Their catalytic behavior largely depends on the ring size, (un)saturation of the backbone, and sterics on the exocyclic carbon.”
Quote in the paperNot a substantial claim - Premisecitation
N-heterocyclic olefins have emerged as a class of active and versatile catalysts for the ROP of cyclic esters and carbonates.
“Recently, N-heterocyclic olefins (NHOs) have emerged as a class of active and versatile catalysts for the ROP of cyclic esters and carbonates.334,335”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Chen recently combined NHOs with a Lewis acid Al(C6F5)3 to develop a highly efficient catalytic system.
“Chen recently combined NHOs with a Lewis acid Al(C6F5)3 to develop a highly efficient catalytic system.335”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [335] source
Not checked in the free run.
- Premisecitation
This catalyst exerts double stereo-differentiation for the ROP of rac-LA with kL/kD up to 53 (for TU-ICD).
“This catalyst exerts double stereo-differentiation for the ROP of rac-LA with kL/kD up to 53 (for TU-ICD, Figure 9).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [341] source
Not checked in the free run.
- Premisecitation
The rate of the polymerization can be tuned over several orders of magnitude by modifying the urea or thiourea substituents.
“The rate of the polymerization can be tuned over several orders of magnitude by modifying the urea or thiourea substituents.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [336] source
Not checked in the free run.
- Premisecitation
DFT calculations suggested a bifunctional mechanism analogous to that of TBD, where the (thio)imidiates behave as a proton shuttle to pick up the proton from the initiator/chain end, to stabilize the tetrahedral intermediate via double H-bonds, and to deliver the proton back to the chain end after ring-opening.
“DFT calculations suggested a bifunctional mechanism analogous to that of TBD, 321 where the (thio)imidiates behave as a proton shuttle to pick up the proton from the initiator/chain end, to stabilize the tetrahedral intermediate via double H-bonds, and to deliver the proton back to the chain end after ring-opening.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [321] source
Not checked in the free run.
- Interpretationreasoning
The operational simplicity of these urea or thiourea anions coupled with their high activity, selectivity, and versatility illustrate the potential of these catalysts for the sustainable synthesis of polyesters and polycarbonates.
“The operational simplicity of these urea or thiourea anions coupled with their high activity, selectivity, and versatility illustrate the potential of these catalysts for the sustainable synthesis of polyesters and polycarbonates.”
Quote in the paperSubstantial claim - Premisecitation
The ROP of rac-LA mediated by TU-ICD generated isotactic PLAs (Pm = 0.88) at 25 °C and 50% conversion.
“The ROP of rac-LA mediated by TU-ICD generated isotactic PLAs (Pm = 0.88) at 25 °C and 50% conversion.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [341] source
Not checked in the free run.
- Premisecitation
Mecerreyes and Cossío found that a cocatalytic system consisting of a densely substituted proline and DBU was able to kinetically resolve racemic lactide.
“Mecerreyes and Cossío found that a cocatalytic system consisted of a densely substituted proline (PRO, Figure 9) and DBU was able to kinetically resolve racemic lactide.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [342] source
Not checked in the free run.
- Interpretationnone given
The success of ROCP is largely driven by the development of efficient and selective catalysts.
“The success of ROCP is largely driven by the development of efficient and selective catalysts.”
Quote in the paperSubstantial claim - Premisecitation
Early studies focused on heterogeneous catalysts such as zinc glutarate and double metal cyanides.
“Early studies focused on heterogeneous catalysts such as zinc glutarate 353,354 and double metal cyanides 355,356 .”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisereasoning
ROCP is often the only route to polycarbonates whose carbonates are 2 carbons apart since these polymers are otherwise difficult to obtain from the ROP or step-growth method.
“On the other hand, it is often the only route to polycarbonates whose carbonates are 2 carbons apart since these polymers are otherwise difficult to obtain from the ROP or stepgrowth method for the reasons mentioned above.”
Quote in the paperNot a substantial claim - Premisenone given
An alternative chain-growth route to aliphatic polyesters and polycarbonates is the alternating copolymerization of epoxides and cyclic anhydrides (for polyesters) or epoxides and CO2 (for polycarbonates).
“An alternative chain-growth route to aliphatic polyesters and polycarbonates is the alternating copolymerization of epoxides and cyclic anhydrides (for polyesters) or epoxides and CO2 (for polycarbonates).”
Quote in the paperNot a substantial claim - Premisereasoning
Because of the large economic and environmental benefits of this process, it has stimulated a number of commercialization efforts, such as QPAC by Empower Materials and Converge by Saudi Aramco.
“Because of the large economic and environmental benefits of this process, it has stimulated a number of commercialization, such as QPAC® by Empower Materials 70 and Converge® by Saudi Aramco.71”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [70] Coca-Cola.http://www.coca-colacompany.com/plantbottle-technology(accessed February 10, 2017).
Not checked in the free run.
- cites [71] Empower Materials.http://www.empowermaterials.com/(accessed February 10, 2017).
Not checked in the free run.
- Premisereasoning
Because of the limitation on the ring size of epoxides (3,4-membered) and cyclic anhydrides (mainly 5,6-membered) that can be incorporated, ROCP is restricted to the synthesis of polyesters and polycarbonates whose ester/carbonate moieties are 2 or 3 carbons apart.
“Because of the limitation on the ring size of epoxides (3,4membered) and cyclic anhydrides (mainly 5,6-membered) that can be incorporated, ROCP is restricted to the synthesis of polyesters and polycarbonates whose ester/carbonate moieties are 2 or 3 carbons apart.”
Quote in the paperNot a substantial claim - Premisecitation
Because of the mechanistic similarities between epoxide/CO2 copolymerization and epoxide/cyclic anhydride copolymerization, the two can be mediated by a similar array of catalysts.
“Because of the mechanistic similarities between epoxide/CO2 copolymerization and epoxide/cyclic anhydride copolymerization, the two can be mediated by a similar array of catalysts.343”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [343] source
Not checked in the free run.
- Premisecitation
The development of single-site metal complexes with ancillary ligands has largely boosted the understanding and the scope of ROCP.
“The development of single-site metal complexes with ancillary ligands has largely boosted the understanding and the scope of ROCP.343”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [343] source
Not checked in the free run.
- Premisecitation
This leads to a metal bound alkoxide to which CO2 (or cyclic anhydride) readily inserts to form a metal carbonate (or carboxylate) species.
“This leads to a metal bound alkoxide to which CO2 (or cyclic anhydride) readily inserts to form a metal carbonate (or carboxylate) species.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [344] source
Not checked in the free run.
- Premisecitation
Protic impurities such as water and alcohol can cause the molecular weight of resulting polymers to be lower than expected.
“This can cause the molecular weight of the resulting polymers to be lower than that expected.[357][358][359]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [357][358][359]
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- Premisecitation
Although the exact mechanism for each catalytic system may vary, ROCP of epoxide with CO2 or cyclic anhydride generally follows the coordination-insertion mechanism.
“Although the exact mechanism for each catalytic system may vary, ROCP of epoxide with CO2 or cyclic anhydride generally follows the coordination-insertion mechanism shown in Scheme 14. 344”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [344] source
Not checked in the free run.
- Interpretationreasoning
ROCP of cyclohexene oxide/CO2 is less susceptible to backbiting than that of propylene oxide/CO2 due to the unfavorable ring strain of cyclohexene carbonate.
“ROCP of cyclohexene oxide/CO2 is less susceptible to backbiting than that of propylene oxide/CO2 due to the unfavorable ring strain of cyclohexene carbonate.”
Quote in the paperNot a substantial claim - Premisecitation
One detrimental side reaction for the ROCP of epoxide/CO2 is the formation of five-membered cyclic carbonates (5CCs) as a result of intramolecular cyclization.
“One detrimental side reaction for the ROCP of epoxide/CO2 is the formation of fivemembered cyclic carbonates (5CCs) as a result of intramolecular cyclization (Scheme 14, yellow box).352”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [352] source
Not checked in the free run.
- Premisecitation
The extent of 5CC formation depends on the nature of the epoxide, the catalyst, and the reaction conditions.
“The extent of this reaction depends on the nature of the epoxide, the catalyst, and the reaction conditions.83,361”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisenone given
Recently, a series of multi-nuclear catalysts have been shown to display superior performance than their mono-nuclear analogues.
“Recently, a series of multi-nuclear catalysts have been shown to display superior performance than their mono-nuclear analogues.”
Quote in the paperNot a substantial claim - Premisecitation
Introduction of positively charged moieties (e.g. ammonium) to the ligand can suppress 5CC formation.
“For example, the introduction of positively charged moieties (e.g.ammonium) to the ligand can suppress the 5CC formation.[362][363][364]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [362][363][364]
Not checked in the free run.
- Premisecitation
The polymerization is initiated by the nucleophilic attack of a ligand (X) or an exogenous nucleophile onto a coordinated epoxide.
“The polymerization is initiated by the nucleophilic attack of a ligand (X) or an exogenous nucleophile onto a coordinated epoxide.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [344] source
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- Premisenone given
Among the different metal catalysts, β-diiminate zinc complexes and metal complexes (Al, Cr, Co) with Schiff-base ligands are the most successful ones.
“Among the different metal catalysts, b-diiminate (BDI) zinc complexes and metal complexes (Al, Cr, Co) with Schiff-base ligands (salen and their derivatives) are the most successful ones (Figure 10).”
Quote in the paperNot a substantial claim - Premisecitation
This selectivity is attributed to the faster rate of anhydride insertion than CO2 insertion into the metal-alkoxide intermediate.
“This selectivity is attributed to the faster rate of anhydride insertion than CO2 insertion into the metal-alkoxide intermediate.367”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [367] source
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- Premisecitation
Incineration is the most suitable way for dealing with highly mixed plastics.
“Nevertheless, it is the most suitable way for dealing with highly mixed plastics.388”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [388] source
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- Premisecitation
Copolymerization of different epoxides or anhydrides provides even more possibilities of structures and properties that can be tuned by the ratios of different monomers.
“Copolymerization of different epoxides or anhydrides provides even more possibilities of structures and properties that can be tuned by the ratios of different monomers.83”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [83] source
Not checked in the free run.
- Interpretationreasoning
For polymers derived from less exergonic polymerization reactions, chemical recycling can provide an attractive option to recover value, provided that efficient processes can be developed and implemented.
“However, for polymers derived from less exergonic polymerization reactions, chemical recycling can provide an attractive option to recover value, provided that efficient processes can be developed and implemented.”
Quote in the paperSubstantial claim - Interpretationreasoning
The large variety of structures yields a diverse set of polymer properties that can be easily controlled by the choice of monomer.
“The large variety of structures yields a diverse set of polymer properties that can be easily controlled by the choice of monomer.”
Quote in the paperNot a substantial claim - Premisecitation
When the two blocks are miscible, only one intermediate Tg higher than that of the pure polyester and lower than the polycarbonate is obtained.
“When the two blocks are miscible, only one intermediate Tg higher than that of the pure polyester and lower than the polycarbonate is obtained.368”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [368] source
Not checked in the free run.
- Premisecitation
For certain bacteria under optimized growth conditions, the yield of PHA obtained from the intracellular inclusions can be as high as 89% of the organism's dry weight.
“For certain bacteria under optimized growth condition, the yield of PHA obtained from the intracellular inclusions can be as high as 89% of the organism's dry weight.380”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [380] source
Not checked in the free run.
- Interpretationnone given
One important advantage of this biosynthetic route is that the feedstock can be completely sourced from biomass (sugars, oils) or methane waste.
“One important advantage of this biosynthetic route is that the feedstock can be completely sourced from biomass (sugars, oils) or methane waste.”
Quote in the paperNot a substantial claim - Premisecitation
By using a different combination of epoxide and cyclic anhydride, Tg of polyesters can be tuned to almost any value from -44 to 184 °C.
“By using a different combination of epoxide and cyclic anhydride, Tg of polyesters can be tuned to almost any value from -44 to 184 °C.211”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [211] source
Not checked in the free run.
- Premisecitation
Only PET and HDPE in the form of relatively pure packaging materials are currently recycled routinely.
“only PET and HDPE in the form of relatively pure packaging materials are currently recycled routinely, 388”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [388] source
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- Premisecitation
The majority of the recyclates is repurposed for lower grade materials.
“and the majority of the recyclates is repurposed for lower grade materials.389”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [389] source
Not checked in the free run.
- Interpretationreasoning
This provides an opportunity for transforming waste gas to valuable plastic materials.
“This provides an opportunity for transforming waste gas to valuable plastic materials.383”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [383] The use of methane waste as a feedstock for PHAs has been tested by Mango Materials.https://www.biobasedworldnews.com/ask-the-industry-dr.molly-morse-ceo-and-co-founder-mango-materials(accessed May 8, 2017).
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- Premisecitation
Chemical recycling is considered uneconomical for petroleum plastics due to the low price of petrochemical feedstock compared with the process costs incurred to depolymerize and recover the monomer.
“This approach is considered uneconomical for petroleum plastics due to the low price of petrochemical feedstock compared with the process costs incurred to depolymerize and recover the monomer.388”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [388] source
Not checked in the free run.
- Premisecitation
High level of recycling can potentially allow for lower energy and material inputs for a given level of products and thus improve eco-efficiency.
“High level of recycling can potentially allow for lower energy and material inputs for a given level of products and thus improve eco-efficiency.387”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [387] The term “Eco-efficiency” was coined by the World Business Council for Sustainable Development (WBCSD) in its 1992, publication “Changing Course”.
Not checked in the free run.
- Interpretationreasoning
Addition of CO2 to an epoxide/cyclic anhydride copolymerization is a simple way to improve the thermal properties of polyesters for many applications that do not require pure polyesters.
“Therefore, the addition of CO2 to an epoxide/cyclic anhydride copolymerization is a simple way to improve the thermal properties of polyesters for many applications that do not require pure polyesters.”
Quote in the paperSubstantial claim - Premisecitation
Switching the epoxide from PO to CHO significantly increases the Tg of polycarbonates from 30-40 °C to 80-120 °C.
“For example, switching the epoxide from PO to CHO significantly increases the Tg of polycarbonates from 30-40 °C to 80-120 °C.351”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [351] source
Not checked in the free run.
- Premisecitation
Microbial synthesis by naturally occurring or genetically modified microorganisms has been practiced industrially for the production of bioplastics.
“The microbial synthesis by naturally occurring or genetically modified microorganisms has been practiced industrially for the production of bioplastics.369,370”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
A number of companies have implemented PET depolymerization at pilot or commercial level, including Loop Industries, Carbios, Ioniqa, and Gr3n Project.
“A number of companies have implemented PET depolymerization at pilot or commercial level, including Loop Industries, 398 Carbios, 399 Ioniqa, 400 and Gr3n Project.401”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [398] loop Industries: Leading the sustainable plastic revolution. http://www.loopindustries.com/en/(accessed August 5, 2017).
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- cites [399] CARBIOS: Reinvent Polymers Lifecycle. https://carbios.fr/en/(accessed August 5, 2017).
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- cites [400] Ioniqa Technologies. http://www.ioniqa.com/(accessed August 5, 2017).
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- Premisecitation
This is due to a common downgrading problem of mechanical recycling, that is, the recovered plastics tend to lose some quality attributes of the virgin plastics, such as color, clarity, or mechanical properties.
“This is due to a common downgrading problem of mechanical recycling, that is, the recovered plastics tend to lose some quality attributes of the virgin plastics, such as color, clarity, or mechanical properties.395”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [395] source
Not checked in the free run.
- Premisecitation
In one example of glycolytic depolymerization of PET by TBD or DBU, Horn et al showed that the rate-determining step for the depolymerization is the ethylene glycol involved nucleophilic attack.
“In one example of glycolytic depolymerization of PET by TBD or DBU, Horn et al 408 showed that the rate-determining step for the depolymerization is the ethylene glycol involved nucleophilic attack.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [408] source
Not checked in the free run.
- Premisecitation
Glycolysis of PET by a variety of metal or organic catalysts yields bis(2-hydroxyethyl)terephthalester (BHET) as the major product.
“Glycolysis of PET by a variety of metal or organic catalysts yields bis(2-hydroxyethyl)terephthalester (BHET) as the major product.403,407”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Calculations suggest that these reactions likely involve a bifunctional mechanism in which the alcohol reactant activates the carbonyl group of these polyesters while the organocatalyst activates the reacting alcohol.
“The calculations suggest that these reactions likely involve a bifunctional mechanism in which the alcohol reactant activates the carbonyl group of these polyesters while the organocatalyst activates the reacting alcohol.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [408] source
Not checked in the free run.
- Premisecitation
Catalyst-free depolymerization of PET and PC in supercritical alcohol or high-pressure steam has also proven efficient for recovering high-quality monomers equivalent to the virgin monomers produced from petroleum.
“The catalyst-free depolymerization of PET and PC in supercritical alcohol 410,411 or high-pressure steam 412,413 has also proven efficient for recovering high-quality monomers equivalent to the virgin monomers produced from petroleum.”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [410] Genta, M.; Yano, F.; Kondo, Y.; Matsubara, W.; Oomoto, S.Technical Review;Mitsubishi Heavy Industries, Ltd., 2003, Vol.40, pp1–4.
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- cites [411] source
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- cites [412] source
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- cites [413] source
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- Premisecitation
Alkali-catalyzed methanolysis of PC in THF at 40 °C provides BPA and dimethyl carbonate in over 95% yield within 35 min.
“For example, the alkali-catalyzed methanolysis of PC in THF at 40 °C provides BPA and dimethyl carbonate in over 95% yield within 35 min.404”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [404] source
Not checked in the free run.
- Premisecitation
A small amount of PVC contaminant present in a PET recycle stream will degrade the recycled PET resin owing to evolution of hydrochloric acid gas from the PVC at a higher temperature required to melt and reprocess PET.
“For example, a small amount of PVC contaminant present in a PET recycle stream will degrade the recycled PET resin owing to evolution of hydrochloric acid gas from the PVC at a higher temperature required to melt and reprocess PET.388”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [388] source
Not checked in the free run.
- Premisecitation
Solvolysis using water, methanol and glycol has been the most common chemical recycling strategy for step-growth polyesters and polycarbonates.
“Solvolysis using water, methanol and glycol has been the most common chemical recycling strategy for step-growth polyesters and polycarbonates.41,397”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [41] Francis R., 2017
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- cites [397] source
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- Premisecitation
The presence of water could result in chain scission and decrease in molecular weight during the melting reprocessing of PET.
“The presence of water could result in chain scission and decrease in molecular weight during the melting reprocessing.395”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [395] source
Not checked in the free run.
- Premisecitation
Different solvolysis processes of PETs and bisphenol A (BPA)-type PCs have been developed to recover suitable monomers for the production of new PETs and PCs.
“Different solvolysis processes of PETs and bisphenol A (BPA)-type PCs have been developed to recover suitable monomers for the production of new PETs and PCs.402,403”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
The obtained copolyesters demonstrate properties suitable for powder coating applications.
“The obtained copolyesters demonstrate properties suitable for powder coating applications.415”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [415] source
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- Premisecitation
Alkyl lactates, the alcoholysis products of PLAs, are green substitutes for petroleum-derived esters in applications such as solvents or diluents for polymeric resins, low-temperature lubricants, and emulsifiers or dispersants in pharmaceutical compositions.
“For example, alkyl lactates, the alcoholysis products of PLAs, are green substitutes for petroleumderived esters in applications such as solvents 429 or diluents for polymeric resins, 430 lowtemperature lubricants, 431 and emulsifiers or dispersants in pharmaceutical compositions.432”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [429] source
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- cites [430] Bakker, H. R.; Kranz, M. T. C.Paint Composition Based on a Chemical Cross Linking System and/or Oxidative Drying, With Lactates As Solvent and Thinner. E.P. Patent 1023405 A1, 1999.
Not checked in the free run.
- cites [431] Morgan, J. D.Low-Temperature Lubricants. U.S. Patent 2389924 A, 1945.
Not checked in the free run.
- Premisecitation
The degradation of polyesters and polycarbonates is in general much faster under basic conditions than acidic than neutral conditions.
“The degradation of polyesters and polycarbonates is in general much faster under basic conditions than acidic than neutral conditions.421”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [421] source
Not checked in the free run.
- Interpretationreasoning
This is attributed to the hydrophilic nature of the COOH and OH chain ends compared to the hydrophobic backbone.
“This is attributed to the hydrophilic nature of the COOH and OH chain ends compared to the hydrophobic backbone.”
Quote in the paperSubstantial claim - Premisecitation
Recently, a quantitative one-step transformation of PC into high-value poly(aryl ether sulfone)s in the presence of a carbonate salt was developed as another strategy for repurposing these plastic wastes.
“Recently, a quantitative one-step transformation of PC into high-value poly(aryl ether sulfone)s in the presence of a carbonate salt was developed as another strategy for repurposing these plastic wastes.417”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [417] source
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- Premisecitation
Colonna reported a two-step one-pot strategy for converting PET to new polyesters using monomers available from renewable sources.
“Colonna reported a two-step one-pot strategy for converting PET to new polyesters using monomers available from renewable sources.414”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [414] source
Not checked in the free run.
- Premisecitation
The overall degradation process is a complicated interplay between the intrinsic degradation kinetics and the diffusive rate of water to the polymer.
“The overall degradation process is a complicated interplay between the intrinsic degradation kinetics and the diffusive rate of water to the polymer.419,420”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Hodge showed that the depolymerization of polyundecanoate in 2% w/v chlorobenzene in the presence of a tin catalyst produced 90% yield of cyclic oligomers with cyclic dimer being the major product (56%).
“Hodge showed that the depolymerization of polyundecanoate in 2% w/v chlorobenzene in the presence of a tin catalyst produced 90% yield of cyclic oligomers with cyclic dimer being the major product (56%).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [459] source
Not checked in the free run.
- Premisecitation
The diols or diamines were quantitatively incorporated into the degradation products.
“The diols or diamines were quantitatively incorporated into the degradation products.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
- Premisecitation
In all cases, the products obtained are not pure triblock structures but contain some molar fraction of homopolymers of PLA.
“In all cases, the products obtained are not pure triblock structures but contain some molar fraction of homopolymers of PLA.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
- Premisecitation
Plichta showed that the degradation of PLA with less than 10 wt% diols or diamines occurred readily in xylene at reflux or in bulk at 180-200 °C in the presence of Sn(Oct)2, affording hydroxyl-terminated PLAs with molecular weights significantly lower than the pristine samples.
“Plichta showed that the degradation of PLA with less than 10 wt% diols or diamines occurred readily in xylene at reflux or in bulk at 180-200 °C in the presence of Sn(Oct)2, affording hydroxylterminated PLAs with molecular weights significantly lower than the pristine samples.443”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
- Premisecitation
The isolated cyclic dimer can undergo ROP in neat with a tin catalyst to regenerate polyundecanoates.
“The isolated cyclic dimer can undergo ROP in neat with a tin catalyst to regenerate polyundecanoates.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [459] source
Not checked in the free run.
- Premisecitation
When macrodiols such as PEG are used, a variety of triblock copolymers can be synthesized.
“When macrodiols such as PEG are used, a variety of triblock copolymers can be synthesized.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
- Premisecitation
When the depolymerization of PCL was performed in toluene with Bu2Sn(OMe)2 at 110 °C, the products were a mixture of cyclic oligomers with little formation of CL.
“When the depolymerization of PCL was performed in toluene with Bu2Sn(OMe)2 at 110 °C, the products were, however, a mixture of cyclic oligomers with little formation of CL. 455”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [455] source
Not checked in the free run.
- Premisecitation
Noda found that the yield and selectivity for L-LA were dependent on the nature of the metal and increased in an order of Al < Ti < Zr < Zn < Sn.
“They found that the yield and selectivity for L-LA were dependent on the nature of the metal and increased in an order of Al < Ti < Zr < Zn < Sn.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [450] source
Not checked in the free run.
- Premisecitation
Thermal depolymerization of PCL and poly(2,2-dimethyl trimethylene carbonate) can be achieved in bulk at temperature around 250 °C in the presence of a transesterification catalyst.
“For example, the thermal depolymerization of PCL and poly(2,2-dimethyl trimethylene carbonate) can be achieved in bulk at temperature around 250 °C in the presence of a transesterification catalyst.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [454] source
Not checked in the free run.
- Premisecitation
Back in 1939, Carothers described the selective depolymerization of polydecanoate, polytridecanoate and polytetradecanoate at 270 °C and 1 mm Hg pressure using MgCl2 or SnCl2 as the catalyst.
“Back in 1939, Carothers has described the selective depolymerization of polydecanoate, polytridecanoate and polytetradecanoate at 270 °C and 1 mm Hg pressure using MgCl2 or SnCl2 as the catalyst.456,457”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Depending on the starting polyesters, either cyclic monomer or dimer were obtained in moderate yield (50-70%) and selectivity (50~90%).
“Depending on the starting polyesters, either cyclic monomer or dimer were obtained in moderate yield (50-70%) and selectivity (50 ~ 90%).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
The use of multihydroxyl compounds such as dipentaerythritol results in star polymers with six short arms of PLA.
“For example, the use of multihydroxyl compounds such as dipentaerythritol results in star polymers with six short arms of PLA.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
- Premisecitation
In the presence of 1 wt% Sn(Oct)2 or zinc naphthenate, L-LA was recovered within 2 h in ~90% yield and over 95% selectivity.
“In the presence of 1 wt% Sn(Oct)2 or zinc naphthenate, L-LA was recovered within 2 h in ~ 90% yield and over 95% selectivity.450”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [450] source
Not checked in the free run.
- Premisecitation
The molecular weights of these polymers can be significantly higher than the original step-growth polymers.
“The molecular weights of these polymers can be significantly higher than the original step-growth polymers.459”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [459] source
Not checked in the free run.
- Interpretationreasoning
Using monomers with low polymerization enthalpies has an advantage for the feedstock-recycling process.
“These examples clearly demonstrate the advantage of using monomers with low polymerization enthalpies for the feedstock-recycling process.”
Quote in the paperSubstantial claim - Interpretationcitation
Chemical recycling of PHAs to the constituent monomers can provide a time-efficient option.
“While the closed-loop recycling of PHA can be realized by several biotic pathways 463,464 , the chemical recycling of PHAs to the constituent monomers can provide a time-efficient option.375”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [375] source
Not checked in the free run.
- Premisereasoning
Because of the low polymerization enthalpy of the monomer, polymerization reactions and formulation/processing must be performed at low temperature, often below room temperature, to achieve decent yields.
“First, because of the low polymerization enthalpy of the monomer, the polymerization reactions and formulation/processing have to be performed at low temperature (often below room temperature) in order to achieve decent yields.”
Quote in the paperNot a substantial claim - Interpretationcitation
Polyesters with integrated aromatic groups are potential recyclable alternatives for commodity polyesters like PET.
“The resulting polyesters with integrated aromatic groups are potential recyclable alternatives for commodity polyesters like PET.”
Quote in the paperSubstantial claim - Premisecitation
A clean and quantitative thermal recycling of these polymers was achieved by simply heating the bulk material at 220 °C (for the linear polymer) or 300 °C (for the cyclic polymer).
“A clean and quantitative thermal recycling of these polymers was achieved by simply heating the bulk material at 220 °C (for the linear polymer) or 300 °C (for the cyclic polymer).”
Quote in the paperSubstantial claim0 of 2 sources checked - Interpretationreasoning
The low thermal stability of these materials could limit their practical use and shelf life.
“The low thermal stability of these materials could limit their practical use and shelf live.”
Quote in the paperNot a substantial claim - Premisecitation
Shaver established a clean and selective polymerization and recycling process for benzodioxipinone using an aluminum-salen catalyst.
“Another monomer-benzodioxipinone -was utilized by Shaver to establish a clean and selective polymerization and recycling process using an aluminum-salen catalyst.462”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [462] source
Not checked in the free run.
- Premisecitation
Closed-loop recycling of PHA can be realized by several biotic pathways.
“While the closed-loop recycling of PHA can be realized by several biotic pathways 463,464 , the chemical recycling of PHAs to the constituent monomers can provide a time-efficient option.375”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Bacteria are responsible for degradation of plastics that end up in the environment and in industrial composting settings.
“Microbial degradation has attracted considerable interest, as bacteria are responsible for any degradation occurring to plastics that end up in the environment, 75,76 as well as in industrial composting settings.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Uncatalytic pyrolysis performed by heating the polymer to 500 °C under vacuum or N2 leads to the formation of PHA oligomers, crotonic acid, and several volatile side products.
“While uncatalytic pyrolysis performed by heating the polymer to 500 °C under vacuum or N2 leads to the formation of PHA oligomers, crotonic acid, and several volatile side products (Scheme 22A), 465”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [465] source
Not checked in the free run.
- Premisecitation
The use of MgO or Mg(OH)2 as the catalyst enables selective thermal degradation of PHB to trans-crotonic acids.
“For example, the use of MgO or Mg(OH)2 as the catalyst enables a selective thermal degradation of PHB to trans-crotonic acids (Scheme 22B).466”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [466] source
Not checked in the free run.
- Interpretationcitation
A time- and energy-efficient recycling between monomers (hydroxyalkanoate or alkenoic acids) and PHAs is established.
“In this way, a time-and energy-efficient recycling between monomers (hydroxyalkanoate or alkenoic acids) and PHAs is established.”
Quote in the paperSubstantial claim - Premisecitation
A similar trend was observed for Ca2+ containing PHB.
“Similar trend was observed for Ca 2+ containing PHB. 467”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [467] source
Not checked in the free run.
- Interpretationreasoning
Catalytic pyrolysis provides a more efficient and selective degradation behavior than uncatalytic pyrolysis.
“catalytic pyrolysis provides a more efficient and selective degradation behavior.”
Quote in the paperSubstantial claim - Premisecitation
Enoki et al. isolated Pseudomonas, Alcanivorax, and Tenacibaculum which were able to partially degrade PCL and PHB fibers in deep sea water.
“Enoki et al. isolated Pseudomonas, Alcanivorax, and Tenacibaculum which were able to partially degrade PCL and PHB fibers in deep sea water.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [485] source
Not checked in the free run.
- Premisenone given
Microorganisms degrade polymers to use the degradation products as carbon and/or energy sources.
“Microorganisms degrade polymers to use the degradation products as carbon and/or energy source(s).”
Quote in the paperNot a substantial claim - Premisecitation
Numerous studies have focused on degradation of aliphatic polyesters and polycarbonates by microbes or cell extracts in laboratory settings or in the environment.
“Since then, numerous studies have focused on the degradation of aliphatic polyesters and polycarbonates by microbes (mainly bacteria, yeast and fungi) or cell extracts from these organisms, in laboratory settings or in the environment (e.g.marine 470 or soil degradation 471 ).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
The occurrence of polyesters-degrading microorganisms in the environment has been classified as PCL = PHB > PES > PBS > PLA.
“The occurrence of polyesters-degrading microorganisms in the environment has been classified as follows: PCL = PHB > PES (polyethylene succinate) > PBS (polybutylene succinate) > PLA.472”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [472] source
Not checked in the free run.
- Interpretationreasoning
Depending on experimental conditions, isolation of the microorganisms/enzymes responsible for polyester degradation can be beneficial or detrimental.
“Depending on the experimental conditions, the isolation of the microorganisms/enzymes that are thought to be responsible for the polyesters degradation can be beneficial or detrimental.”
Quote in the paperNot a substantial claim - Premisecitation
Faster mineralization of PLLA was demonstrated in thermophilic conditions because of the close proximity of experimental temperatures to the Tg of PLLA.
“Moreover, faster mineralization of PLLA was demonstrated in thermophilic conditions because of the close proximity of experimental temperatures to the Tg of PLLA.479”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [479] source
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- Premisecitation
Mineralization rates of polyesters in aerobic tests decreased as PHAs > PCL > PLA.
“The mineralization of polyesters has been evaluated using soil (i.e.compost) or diluting the inoculum in growing medium enriched with minerals and the rates decreased as follows: PHAs > PCL > PLA.[481][482][483][484]”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
PHB granules isolated from microbial cell extracts could be hydrolyzed to β-hydroxybutyric acid while the polymer was incubated with part of the cell extracts it had been purified from.
“Merrick, Doudoroff et al. noticed that polyhydroxybutyrate (PHB)”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisereasoning
Degradation of polyesters and polycarbonates by enzymes generally proceeds through surface erosion: the bulk of the material is not affected and properties are maintained, while lower molar mass fragments are released from the surface.
“For the same reason, the degradation of polyesters and polycarbonates by enzymes generally proceeds through surface erosion: the bulk of the material is not affected and the properties (e.g.molar mass, crystallinity, etc.) are maintained, while lower molar mass fragments are released from the surface.”
Quote in the paperNot a substantial claim - Premisecitation
Fukushima et al. found that isolation of microorganisms was advantageous to the mineralization of PLA and PLA nanocomposites.
“In contrast, Fukushima et al. found that the isolation of microorganisms was advantageous to the mineralization of PLA and PLA nanocomposites.488”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [488] source
Not checked in the free run.
- Interpretationnone given
The nature and provenance of the inoculum, as well as the experimental setup, considerably influence the biodegradation's efficiency.
“Similarly to anaerobic conditions, the nature and provenance of the inoculum, as well as the experimental setup, considerably influence the biodegradation's efficiency.”
Quote in the paperNot a substantial claim - Interpretationcitation
Experimental settings and the origin of the inoculum have a tremendous impact on the rate of degradation.
“In contrast, Massardier-Nageotte et al. reported that their inoculum was inefficient to biodegrade both PLA and PCL in anaerobic conditions, evidencing that the experimental settings, as well as the origin of the inoculum have a tremendous impact on the rate of degradation.480”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [480] source
Not checked in the free run.
- Premisecitation
Massardier-Nageotte et al. reported that their inoculum was inefficient to biodegrade both PLA and PCL in anaerobic conditions.
“In contrast, Massardier-Nageotte et al. reported that their inoculum was inefficient to biodegrade both PLA and PCL in anaerobic conditions, evidencing that the experimental settings, as well as the origin of the inoculum have a tremendous impact on the rate of degradation.480”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [480] source
Not checked in the free run.
- Premisecitation
Bacteria after isolation were more efficient in experimental conditions close to their natural occurrence, low temperature (4-10 oC) and high pressure (30 MPa).
“They found that the bacteria, after isolation, were more efficient in experimental conditions close to their natural occurrence -i.e.low temperature (4 -10 ºC) and high pressure (30 MPa).485”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [485] source
Not checked in the free run.
- Premisecitation
Lee et al. showed that enantiomerically pure (R)-(-)-3-hydroxycarboxylic acids could be produced by in vivo depolymerization of P3HB, both in anaerobic and aerobic conditions, in Alcaligenes latus.
“Lee et al. showed that enantiomerically pure (R)-(-)-3-hydroxycarboxylic acids could be produced by in vivo depolymerization of P3HB, both in anaerobic and aerobic conditions, in Alcaligenes latus.489”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [489] source
Not checked in the free run.
- Premisecitation
Lipases were shown to degrade PCL, PLLA, poly(g-butyrolactone), PHB, poly(butylene succinate adipate), PCL/PBS blend and poly(propylene carbonate) in PBS at 37 °C, producing mainly short oligomers.
“Lipases were shown to degrade PCL, [504][505][506][507][508]504,505 PLLA,509 poly(g-butyrolactone), 507 PHB, 508,510 poly(butylene succinate adipate), 511 PCL/PBS blend 511 and poly(propylene carbonate) 508 in PBS at 37 °C, producing mainly short oligomers.”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationcitation
Useful chemicals that could be re-used as monomers or in other chemical industries could be the end-products of microbial degradation.
“This contribution elegantly showed that useful chemicals that could be re-used as monomers or in other chemical industries could be the end-products of microbial degradation.”
Quote in the paperSubstantial claim - Premisecitation
Ren et al. extended the concept to a broader range of PHAs, allowing synthesis of a variety of R-hydroxyalkanoic acids whose structures depend on the parent PHA.
“Ren et al. later extended this concept to a broader range of PHAs, allowing for the synthesis of a variety of R-hydroxyalkanoic acids, the structures of which depend on the parent PHA.490”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [490] source
Not checked in the free run.
- Interpretationreasoning
Microbes first express extracellular enzymes to decrease the polymer's molar mass and allow solubilization and assimilation of oligomers through their cellular membrane.
“Therefore, microbes first express extracellular enzymes, in order to decrease the polymer's molar mass and allow for solubilization and assimilation of the oligomers through their cellular membrane.”
Quote in the paperNot a substantial claim - Premisecitation
A variety of soil microorganisms have been isolated and proved efficient for mineralization of PLLA on agar plates or in growing medium.
“A variety of soil microorganisms have also been isolated and proved efficient for the mineralization of PLLA on agar plates or in growing medium.486,487”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisenone given
In all cases, enzymes naturally occurring in microbes (hydrolases) catalyze the material's hydrolysis.
“In all cases, enzymes, which are naturally occurring in microbes (i.e.hydrolases), catalyze the material's hydrolysis.”
Quote in the paperNot a substantial claim - Premisecitation
Enzymes exhibit different efficacies depending on the nature of the ester/carbonate bonds.
“These enzymes were shown to exhibit different efficacies depending on the nature of the ester/carbonate bonds and are summarized in Figure 13.471,473”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisenone given
Depolymerization of poly(glycolic acid), PCL, PHB or poly(trimethylene carbonate) with proteinase K is slower than with the aforementioned enzymes.
“In contrast, the depolymerization of poly(glycolic acid), 525 PCL, 523,524 PHB 523 or poly(trimethylene carbonate) 525 with proteinase K is slower than with the aforementioned enzymes.”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationnone given
Organocatalysts have emerged as an efficient alternative to metal-based catalysts.
“While metal-based catalysts are in general more competent in tackling the aforementioned challenges, organocatalysts have emerged as an efficient alternative.”
Quote in the paperSubstantial claim - Interpretationnone given
Many catalytic approaches have been developed to transform renewable raw materials to versatile monomers and to further convert these monomers to existing or new polymer materials.
“Many catalytic approaches have been developed to transform renewable raw materials to versatile monomers and to further convert these monomers to existing or new polymer materials.”
Quote in the paperSubstantial claim - Interpretationnone given
Aliphatic polyesters and aliphatic polycarbonates can be derived from renewable resources.
“Among the potentially sustainable alternatives to current commodity plastics, aliphatic polyesters and aliphatic polycarbonates are highlighted as they can be derived from renewable resources, they can be produced by a variety of versatile synthetic methods, they exhibit a wide range of useful properties and can be repurposed to versatile synthetic intermediates or environmentally degraded if they”
Quote in the paperSubstantial claim - Premisecitation
Using the same lipase, Joly et al. demonstrated that PBS could be transformed to succinic acid (44% yield) by reactive extrusion at 120 oC (30 min, 10 wt% lipase).
“Using the same lipase, Joly et al. demonstrated that PBS could be transformed to succinic acid (44% yield) by reactive extrusion at 120 ºC (30 min, 10 wt% lipase).521”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [521] source
Not checked in the free run.
- Premisecitation
Crystalline PLA could not be degraded by proteinase K.
“For instance, crystalline PLA could not be degraded by proteinase K. 525,526”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisereasoning
In many cases, depolymerization may be kinetically slow or unselective, requiring the use of a catalyst.
“Even so, in many cases the depolymerization may be kinetically slow or unselective, requiring the use of a catalyst.”
Quote in the paperSubstantial claim - Premisenone given
The efficiency of proteinase K at degrading semi-crystalline polymers increases with decreasing crystallinity contents.
“As for most enzymes, the efficiency of proteinase K at degrading semi-crystalline polymers increases with decreasing crystallinity contents.”
Quote in the paperNot a substantial claim - Premisecitation
PTMC could be depolymerized to TMC in acetonitrile at 70 °C with recovery yields up to 80%.
“PTMC could be depolymerized to TMC in acetonitrile at 70 °C with recovery yields up to 80%.518”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [518] source
Not checked in the free run.
- Premisecitation
After solvent evaporation, the oligomers could be repolymerized in bulk using the same lipase catalyst.
“After solvent evaporation, these oligomers could be repolymerized in bulk using the same lipase catalyst.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [515] source
Not checked in the free run.
- Premisereasoning
For polymerization reactions that are highly exergonic at normal operating temperatures, the reverse processes are energy intensive under similar conditions.
“However, controlled depolymerization through chain-end unzipping (the exact reverse process of chain-growth) depends on the thermodynamics of the polymerization: for polymerization reactions that are highly exergonic (∆G°p << 0) at normal operating temperatures, the reverse processes are energy intensive under similar conditions.”
Quote in the paperSubstantial claim - Interpretationnone given
A variety of active and selective catalysts are available for converting renewable monomers into well-defined polymers.
“While a variety of active and selective catalysts are available for converting renewable monomers into well-defined polymers, data to assess their environmental impacts or sustainability are incomplete.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Catalysts developed for polymerization can also be used for depolymerization because they reduce the kinetic barrier of both polymerization and depolymerization to the same extent.
“Catalysts developed for polymerization can also be used for depolymerization as they reduce the kinetic barrier of both polymerization and depolymerization to the same extent.”
Quote in the paperNot a substantial claim - Premisereasoning
Controlled depolymerization through chain-end unzipping depends on the thermodynamics of the polymerization.
“However, controlled depolymerization through chain-end unzipping (the exact reverse process of chain-growth) depends on the thermodynamics of the polymerization: for polymerization reactions that are highly exergonic (∆G°p << 0) at normal operating temperatures, the reverse processes are energy intensive under similar conditions.”
Quote in the paperSubstantial claim - Premisecitation
In flow conditions (15 MPa) with 80% sCO2 and 20% toluene at 40 °C, more than 99% of the products were cyclic oligomers (210 < Mn < 1010 g/mol).
“In flow conditions (15 MPa) with 80% sCO2 and 20% toluene at 40 °C, more than 99% of the products were cyclic oligomers (210 < Mn < 1010 g/mol).519”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [519] source
Not checked in the free run.
- Premisecitation
In a study on the influence of PLA chirality on proteinase K degradation activity, LL, DL, and LD diads could be cleaved, but not DD diads.
“In a thorough study on the influence of the chirality of PLA on the degradation activity of proteinase K, they also evidenced that LL, DL, and LD diads could be cleaved, but not DD diads.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [527] source
Not checked in the free run.
- Premisecitation
The ability of lipases to degrade polycarbonates in buffer has been linked to the glass transition temperature of the polymer.
“Finally, the ability of lipases to degrade polycarbonates in buffer has been linked to the glass transition temperature of the polymer.513”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [513] source
Not checked in the free run.
- Premisenone given
The specific chain cleavage of lipases, as compared to random scission for uncatalyzed hydrolysis, was demonstrated.
“The specific chain cleavage of lipases, as compared to random scission for uncatalyzed hydrolysis, was demonstrated.”
Quote in the paperNot a substantial claim - Interpretationnone given
End-of-life options of plastics are critical for the development of circular plastics economies.
“The end-of-life options of plastics are critical for the development of circular plastics economies, but economic disincentives have contributed to the modest rates of recycling and material recovery.”
Quote in the paperSubstantial claim - Premisecitation
For polyesters and polycarbonates with large polymerization enthalpies, a simple pyrolysis process leads to undesired products.
“For polyesters and polycarbonates with large polymerization enthalpies, a simple pyrolysis process leads to undesired products.”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
In Kopinke et al.'s comparison, thermal degradation of PLAs without catalyst was slow and uncontrolled.
“Kopinke et al. compared the thermal degradation of PLAs in the absence and presence of Sn(Oct)2.446 While the degradation without the assistance of catalyst was slow and uncontrolled, the presence of residual Sn (from the polymerization process) reduced the depolymerization”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [446] source
Not checked in the free run.
- Premisecitation
Pyrolysis of PLLA at ambient pressure leads to uncontrolled degradation through various non-radical and radical pathways that yield a mixture of L-LA, meso-LA, cyclic oligomers, acetaldehyde, acrylic acid, CO, CO2.
“For example, pyrolysis of PLLA at ambient pressure leads to uncontrolled degradation through various non-radical and radical pathways that yield a mixture of products consisted of L-LA, meso-LA, cyclic oligomers, acetaldehyde, acrylic acid, CO, CO2.444- 446”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
Use of a transesterification catalyst is a key factor in promoting selective depolymerization under milder conditions.
“The use of a transesterification catalyst is a key factor in promoting the selective depolymerization under milder conditions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [446] source
Not checked in the free run.
- Premisereasoning
Thermal recycling is often performed at lower temperature and reduced pressure to distill volatile monomer from the polymer melt and suppress unwanted degradation reactions.
“To drive the equilibrium toward the formation of monomer and suppress other unwanted degradation reactions, the thermal recycling is often performed at lower temperature and reduced pressure to distill the volatile monomer from the polymer melt.”
Quote in the paperNot a substantial claim - Premisecitation
Adding a higher amount of enzyme increases the efficiency of degradation up to an inhibitory concentration that is detrimental to degradation rates, owing to saturation of the substrate that prevents the catalytic site from interacting with the polymer.
“Because of this mechanism of action, adding a higher amount of enzyme increases the efficiency of the degradation up to an inhibitory concentration that is detrimental to the degradation rates, owing to saturation of the substrate that prevents the catalytic site from interacting with the polymer.497”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [497] source
Not checked in the free run.
- Premisecitation
Depending on the provenance of the PHB depolymerase, either monomer and dimer of 3-hydroxybutyric acid or oligomers can be obtained.
“Depending on the provenance of the PHB depolymerase, either monomer and dimer of 3-hydroxybutyric acid 497 or oligomers can be obtained.[498][499][500]”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
The rates for the best depolymerase/polyester pairs were up to 0.28 g/h/cm2.
“The rates for the best depolymerase/polyester pairs were up to 0.28 g/h/cm 2 .”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [493] source
Not checked in the free run.
- Classified as probably not a substantial claim. 76
- May combine two claims. 158
- The quote only partly states this claim. 2
Probably not a substantial claim: may not pass S4 (based).
Premisenone givenAliphatic polyesters and polycarbonates are promising materials due to their renewable resources and excellent biodegradability.
“Among potential candidates, aliphatic polyesters and polycarbonates are promising materials due to their renewable resources and excellent biodegradability.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenThe amount of landfill space available for discarded plastic wastes is finite.
“However, the amount of landfill space available for discarded plastic wastes is finite.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenEven under optimized circular economies, some fraction of products will end up in the environment.
“Even under the most highly optimized circular materials economies, some fraction of the products will eventually end up in the environment.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationcitationThe point of maximum leverage is the socioeconomic system that has led to our current model of resource utilization.
“While considerable research has focused on replacing petroleum raw materials with renewable sources and developing biodegradable or recyclable polymers that minimize waste disposal, 16 ultimately the point of maximum leverage 44 is the socioeconomic system that has led to our current model of resource utilization.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationLife-cycle assessment results are variable across studies with quantification strongly tied to modeling assumptions and feedstock choice.
“Life-cycle assessment has been used to assess the environmental impacts resulting from the production, use, and disposal of a polymer product (see section 1.5.2) but the results are variable across studies with quantification being strongly tied to modeling assumptions and feedstock choice.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningBiodegradable plastics can mitigate some environmental consequences but are only one of several end-of-life strategies.
“However, while biodegradable plastics can mitigate some of the environmental consequences of plastics that find their way into the environment, it is only one of the several end-of-life strategies to minimize the environmental impact of plastics.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationCurrent rates of plastics recycling are exceedingly low (<10%) and are not keeping pace with increased production volumes.
“Thus, while many petrochemically-based polymers are recyclable, the current rates of plastics recycling are exceedingly low (<10%) and, on a volume basis, are not keeping pace with the increased volumes of production.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningPlastics that end up in the environment should be biodegradable.
“To mitigate the environmental impact of plastics that end up in the environment, these plastics should be biodegradable.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningNew scientific and technological innovations are needed for efficient catalytic strategies to convert renewable resources into platform chemicals, monomers, polymers, and products economically.
“As the chemical composition of renewable resources are quite different from those derived from petroleum-based resources, new scientific and technological innovations are needed for the development of efficient catalytic strategies for converting these resources into platform chemicals, monomers, polymers, and products that can be produced economically on a scale sufficient for commodity materials”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationIncineration of recovered plastic provides a potential source of energy but generates CO2 and requires purification to avoid hazardous releases.
“Incineration of recovered plastic provides a potential source of energy, 39 but generates CO2; moreover, rigorous purification and process controls are needed to insure that the hazardous substances are not released into the atmosphere.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationLCA provides a standardized methodology to compare different product choices and identifies unintended environmental trade-offs.
“LCA provides a standardized methodology to compare different product choices, and identifies unintended environmental trade-offs between impact categories.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenSupport from public and government including favorable policy and legislation is the key stimulator for technological innovations on sustainable polymers.
“Support from public and government including favorable policy and legislation is the key stimulator for technological innovations on sustainable polymers and for businesses and customers to transition towards more sustainable products.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSeveral other reviews discuss sustainable polymers from the end-of-use perspective.
“Several other reviews discuss the topic from the end-of-use perspective, covering different families of recyclable and biodegradable polymers.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Interpretationnone givenCatalysis presents an enabling tool to facilitate the development of sustainable polymers.
“Catalysis presents an enabling tool to facilitate the development of sustainable polymers.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningBiodegradation is arguably not the optimal end-of-life option because energy invested is wasted.
“It is arguably not the optimal end-of-life option in that the energy invested to create these materials is wasted and provides benefit only to the microbes.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisereasoningMany biomass-derived polymers have oxygen-rich backbones and are more readily degraded than all-carbon backbones of most petroleum-based polymers.
“Although there is no direct correlation between a plastic's ability to biodegrade and the resource from which is derived, many biomass-derived polymers have oxygen-rich backbones and are thus more readily degraded than the all-carbon backbones of most petroleum-based polymers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningNew strategies are needed for selective depolymerization of plastics to monomers or useful intermediates.
“New strategies are needed for the selective depolymerization of plastics either to their constituent monomers or other useful intermediates that could be used as resources for other chemical processes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenMore sustainable alternatives must meet a high bar in cost and performance to be economically competitive.
“One of the most significant challenges is that the plastics of modern society are quite remarkable materials; more sustainable alternatives will have to meet a high bar in terms of the cost and performance in order to be economically competitive.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationOilseed crops such as soybean, rapeseed, and oil palm are the major supply of oils at present.
“Oilseed crops such as soybean, rapeseed, and oil palm are the major supply of oils at present, but algae has turned up as a cheaper alternative due to its non-food nature, fast production and recycle rate, and low use of production inputs.82”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [82] source
Not checked in the free run.
May combine two claims.
PremisecitationTransition to non-food sources such as lignocellulosic biomass is an important direction to lower production costs and avoid resource competition with the food supply.
“Transition to non-food sources such as lignocellulosic biomass is an important direction to lower the production costs [78][79][80] and to avoid resource competition with the food supply.”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationSuccinic acid is used in the production of bio-based PBS and is a versatile precursor for monomers such as 1,4-butanediol (BDO), g-butyrolactone (g-BL), maleic anhydride, and maleic acid.
“Succinic acid is used in the production of bio-based PBS; it is also a versatile precursor for monomers such as 1,4-butanediol (BDO), g-butyrolactone (g-BL), maleic anhydride, and maleic acid.91”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [91] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationFatty acids obtained from transesterification of plant oils have been a long-standing biofeedstock for polymer production.
“Fatty acids obtained from transesterification of plant oils have been a long-standing biofeedstock for polymer production.25,98”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Premisenone givenThe conversion of renewable monomers to polyesters and polycarbonates can be achieved via a variety of polymerization methods, enabling diverse backbone structures and side-chain functionalities that give rise to versatile physical properties.
“Second, the conversion of these renewable monomers to polyesters and polycarbonates can be achieved via a variety of polymerization methods, which enables diverse backbone structures and side-chain functionalities that in turn give rise to versatile physical properties of these polymers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenIn the last decade, a number of synthetic bio-derived plastics have been commercialized.
“In the last decade, a number of synthetic bio-derived plastics have been commercialized.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
InterpretationreasoningTwo important criteria for sustainable polymers are the use of renewable feedstock and the degradability or recyclability of the polymer.
“While the sustainability of a polymer should be considered on a systems level that encapsulate a variety of factors in its feedstock, synthesis, and end-of-use options, two important criteria are the use of renewable feedstock and the degradability or recyclability of the polymer.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenConversion of renewable feedstocks to monomers focuses on replacing existing petroleum-derived monomers with renewable counterparts and developing new bio-derived monomers and polymers with unique structures and properties.
“The conversion of renewable feedstocks to monomers focuses on two directions: to replace the existing petroleum-derived monomers with their renewable counterparts, and to develop new bio-derived monomers and polymers with unique structures and properties that current commodity plastics do not have.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationAlthough bio-based polymers save non-renewable resources and generally emit less greenhouse gases, studies have shown they may exert higher environmental impacts in eutrophication and stratospheric ozone depletion.
“Although bio-based polymers save non-renewable resources and generally emit less greenhouse gases for their production, studies have shown that they may exert higher environmental impacts in the categories of eutrophication and stratospheric ozone depletion.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationIn 2014, only 1.7 megatons of more than 300 megatons of polymers produced globally were bio-derived, with the three main products being PLA, biopolyethylene, and bioPET.
“For example, in 2014 only 1.7 megatons of more than 300 megatons of polymers produced globally were bio-derived, of which the three main products were PLA, biopolyethylene, and bioPET.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThese are attractive candidates for feedstock recycling as polymerization thermodynamics are not as exergonic as those of conventional commodity plastics.
“Alternatively, these are attractive candidates for feedstock recycling as the polymerization thermodynamics are not as exergonic as those of conventional commodity plastics (PE, PS, PVC).”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationDiacids and hydroxyl acids are key monomers for various commodity polyesters and polycarbonates, and serve as a platform for high-value added products by chemical and biological transformations.
“They are not only key monomers for various commodity polyesters and polycarbonates, but also serve as a platform for a multitude of highvalue added products by means of chemical and biological transformations.77”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [77] source
Not checked in the free run.
May combine two claims.
Premisenone givenAmong polymers that can be both renewable and degradable, polyesters and polycarbonates have attracted the most attention and many have been used as substitutes for petroleum-based plastics.
“Among the families of polymers that can be both renewable and degradable (upper right quadrant), polyesters and polycarbonates have attracted the most attention, with a great many of them been successfully used as substitutes for plastics of petroleum origin.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPoly(ethylene furandicarboxylate) (PEF) produced from FDCA is regarded as a renewable substitute for PET.
“Poly(ethylene furandicarboxylate) (PEF) produced from FDCA is regarded as a renewable substitute for PET.104”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [104] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone givenPLA produced from starch-rich crops is an important example, developed by Natureworks LLC under the brand name Ingeo.
“One important example is PLA produced from starch-rich crops such as corn; for example, that developed by Natureworks LLC under the brand name Ingeo TM .60”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationAdipic acid is one of the most important diacids in industry and about 2.5 million tons are produced annually from petrochemicals.
“Adipic acid, a monomer used for the production of nylon, polyurethane, and polyesters, is one of the most important diacids in industry and ~2.5 million tons are produced annually from petrochemicals.96”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [96] Bohnet M., 2003
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe role of catalysis in these conversions is critical and many research efforts are focusing on developing green catalytic processes with high efficiency and low cost.
“The role of catalysis in these conversions is critical and many research efforts are focusing on developing green catalytic processes with high efficiency and low cost.[84][85][86]”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
InterpretationreasoningPolyesters and polycarbonates have met several key principles for a sustainable polymer, enabling a potentially cyclic model of resource utilization.
“They have met several key principles outlined for a sustainable polymer (section 1.3), which enables a potentially cyclic model of resource utilization.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone givenTraditional polymers are derived from fossil fuels and are non-degradable, whereas sustainable polymers are sourced from renewables and can readily degrade.
“Traditional polymers are derived from fossil fuels and are non-degradable in nature (lower left quadrant), whereas sustainable polymers are sourced from renewables and can readily degrade in the environment.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationIn Landis's analysis, biopolymers such as PLA and PHA were ranked highest based on green design metrics but in the middle of LCA rankings, whereas petroleum polymers such as PE and PP were ranked highest in LCA but in the middle of green design rankings.
“In this analysis, biopolymers such as polylactide (PLA) and polyhydroxyalkanoate (PHA) were ranked the highest based on green design metrics but in the middle of the LCA rankings whereas petroleum polymers such as PE and PP were ranked the highest in the LCA rankings but in the middle of green design rankings.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPlant oil is converted to fatty acids and glycerol for biodiesel and oleochemical production.
“Another common renewable resource is plant oil, which is converted to fatty acids and glycerol for biodiesel and oleochemical production.16,25,81”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
InterpretationreasoningThis allows a faster rate of resource regeneration than resource consumption.
“This allows a faster rate of resource regeneration than resource consumption.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThe two metrics focus on different aspects of sustainability, so evaluations can give different results.
“Since the two metrics focus on different aspects of sustainability, the evaluation based on these metrics can give different results.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSynthetic plastics on the market can be classified into four categories according to feedstock renewability and polymer degradability.
“As summarized in Figure 2, synthetic plastics on the market can be classified into four categories according to their feedstock renewability and polymer degradability.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationSugar fermentations to produce polyols such as sorbitol, mannitol, xylitol are feasible although they cannot yet compete with chemical reduction economically.
“Sugar fermentations to produce these polyols are also feasible although it cannot yet compete with the chemical reduction economically.[149][150][151]”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationThe coupling of diols with CO2 occurred at 25 °C and ambient pressure, affording cyclic carbonates in 40-70% yields.
“The coupling of diols with CO2 occurred at 25 °C and ambient pressure, affording cyclic carbonates in 40-70% yields.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [202] source
Not checked in the free run.
May combine two claims.
InterpretationcitationThe use of halide is crucial for the conversion, highlighting the importance of the leaving group.
“The use of halide is crucial for the conversion, highlighting the importance of the leaving group.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationLactic acid is a well-recognized bio-based chemical, currently produced from starch crops via bacteria fermentation.
“Lactic acid is a well-recognized bio-based chemical, currently produced from starch crops via bacteria fermentation.91”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [91] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBuchard reported an efficient two-step procedure using DBU as the base in the first step to activate the hydroxyl group toward carbonylation and NH3/TsCl in the second step to facilitate the cyclization.
“Recently, Buchard reported an efficient two-step procedure using DBU as the base in the first step to activate the hydroxyl group toward carbonylation and NH3/TsCl in the second step to facilitate the cyclization.202”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [202] source
Not checked in the free run.
May combine two claims.
InterpretationcitationThe yields of biological or chemical production of glycolic acid are typically low, which makes them hard to compete with the current petroleum-based synthesis.
“However, the yields of these processes are typically low, which makes them hard to compete with the current petroleum-based synthesis.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [158] Dischert, W.; Colomb, C.; Soucaille, P.Fermentation Process for Producing Glycolic Acid. U.S. 20120178136A1, 2012.
Not checked in the free run.
- cites [159] source
Not checked in the free run.
May combine two claims.
PremisecitationThe second step of lactide production requires the use of a selective catalyst, typically tin octoate, and continuous removal of lactide to achieve good yield.
“This second step requires the use of a selective catalyst, typically tin octoate, 156 and continuous removal of lactide (e.g. by distillation) to achieve good yield.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [156] source
Not checked in the free run.
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Premisenone givenDehydrative condensation of CO2 and alcohols is the most straightforward and green route to dialkyl carbonates but the reaction is severely limited by the unfavorable equilibrium.
“Dehydrative condensation of CO2 and alcohols is the most straightforward and green route to dialkyl carbonates but the reaction is severely limited by the unfavorable equilibrium.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenThe most successful cyclic ester derived from biomass is lactide (LA), the monomer for commodity polylactides (PLAs).
“The most successful cyclic ester derived from biomass is lactide (LA), the monomer for commodity polylactides (PLAs).”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationThese monomers can undergo polymerizations at both the alkene and ester site, making them potential substitutes for petroleum-based polyacrylates and polyesters.
“These monomers can undergo polymerizations at both the alkene and ester site, making them potential substitutes for petroleum-based polyacrylates and polyesters.176,177”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenEthylene glycol (EG), a component for PET, is traditionally produced from petroleum-based ethylene, via the intermediate ethylene oxide.
“Ethylene glycol (EG), a component for PET, is traditionally produced from petroleum-based ethylene, via the intermediate ethylene oxide.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationHydrogenolysis of sugar-derived polyols (glycerol, xylitol, sorbitol) catalyzed by supported transition-metal catalysts, mostly Ru, Cu, Ni, under basic conditions, provides a direct and potentially cheaper route to EG but is complicated by concurrent generation of other polyols like propylene glycol.
“Another promising route is the hydrogenolysis of sugarderived polyols (glycerol, xylitol, sorbitol) catalyzed by supported transition-metal catalysts, mostly Ru, Cu, Ni, under basic conditions.126,127 This process provides a direct and potentially cheaper route to EG but is complicated by the concurrent generation of other polyols, like propylene glycol (PG).”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThe shape-selective property of zeolites enables high selectivity for LA (~79% at full conversion), devoid of racemization and side-product formation.
“The shape-selective property of zeolites enables high selectivity for LA (~79% at full conversion), devoid of racemization and side-product formation.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [157] source
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InterpretationreasoningBoth steps of lactide production are time- and energy-intensive owing to their reliance on high temperatures and vacuum.
“Both steps are time-and energy-intensive owing to their reliance on high temperatures and vacuum.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenThe syntheses of cyclic esters directly from sugar precursors typically involve elaborate protecting group chemistry, which compromises the atom economy and production cost of these monomers.
“Their syntheses typically involve elaborate protecting group chemistry, which compromises the atom economy and production cost of these monomers.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationSince furfural is industrially produced from lignocellulose on a scale of 400 kilotons a year, producing FDCA from furfural provides a potentially cheaper route to FDCA.
“Since furfural is industrially produced from lignocellulose on a scale of 400 kilotons a year, this provides a potentially cheaper route to FDCA.115”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [115] source
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PremisecitationThe thermodynamics of the dehydrative cyclization reaction to cyclic carbonates from CO2 is unfavorable, similar to the synthesis of dialkyl carbonate from CO2.
“The thermodynamics of this dehydrative cyclization reaction is unfavorable, similar to the synthesis of dialkyl carbonate from CO2. 184”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [184] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenThe development of petroleum-based plastics has been driven by the innovations in catalytic petrochemistry and polymerization methods.
“The development of petroleum-based plastics has been driven by the innovations in catalytic petrochemistry and polymerization methods.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningDue to the wide availability of diols, diacids or hydroxy acids, SGP provides easy access to polyesters and polycarbonates with diverse backbone structures and side-chain functionalities.
“Due to the wide availability of diols, diacids or hydroxy acids, SGP provides easy access to polyesters and polycarbonates with diverse backbone structures and side-chain functionalities.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenMost bio-derived epoxides are prepared by catalytic epoxidation of alkene group present in a renewable substrate.
“Most bio-derived epoxides are prepared by catalytic epoxidation of alkene group present in a renewable substrate.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationEpichlorohydrin (ECH), an important industrial chemical produced on a 1.8 million tons scale annually, can be derived from glycerin through a two-step reaction.
“Epichlorohydrin (ECH), an important industrial chemical produced on a 1.8 million tons scale annually, can be derived from glycerin through a two-step reaction.208,209”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
InterpretationcitationThe removal of by-products, water or alcohol, from polycondensation reactions necessitates the use of high temperatures and often vacuum conditions, which makes this approach very energy-intensive.
“In addition, the removal of by-products, water or alcohol, from the polycondensation reactions necessitates the use of high temperatures and often times vacuum conditions, which makes this approach very energy-intensive.218”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [218] Odian G., 2004 source
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Premisenone givenThe traditional way of synthesizing polyesters and polycarbonates is by step-growth polymerization.
“The traditional way of synthesizing polyesters and polycarbonates is by step-growth polymerization.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningAlthough these approaches use cheap, safe, and renewable feedstocks and operate under relatively mild conditions, the generation of stoichiometric wastes and the moderate yields of these reactions limit their atomic efficiencies.
“Although these approaches use cheap, safe, and renewable feedstocks and operate under relatively mild conditions, the generation of stoichiometric wastes and the moderate yields of these reactions limit their atomic efficiencies.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based).
Premisenone givenThe effective uses and transformations of renewable feedstocks to sustainable polymers rely on the development of innovative and green catalytic chemistries.
“Similarly, the effective uses and transformations of renewable feedstocks to sustainable polymers rely on the development of innovative and green catalytic chemistries.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisereasoningBecause the water by-product is expelled out of the hydrophobic interior of micelles, the DBSA-mediated emulsion polycondensation can proceed effectively at low temperature (40-80 °C) and 1 atm.
“Since the water by-product is expelled out of the hydrophobic interior of micelles, this reaction can proceed effectively at low temperature (40-80 °C) and 1 atm.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationThe use of a chemoselective catalyst is critical to eliminate the need for tedious and uneconomical protection chemistry and to enhance product specificity.
“The use of a chemoselective catalyst is critical to eliminate the need for tedious and uneconomical protection chemistry 239,240 and to enhance the product specificity.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationBismuth triflate has received particular attention due to its low toxicity, low cost, and stability.
“Among different metals, bismuth triflate (Bi(OTf)3) has received particular attention due to its low toxicity (Bi 3+ is among the least toxic heavy metal ions), low cost, and stability.234”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [234] source
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May combine two claims.
PremisecitationOrganic carbonates can be produced on a large scale from CO, or potentially from CO2.
“They can be produced on a large scale from CO, or potentially from CO2. 183,184”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
InterpretationreasoningThe development of catalytic processes that can operate at lower temperatures will reduce the energy input and thus increase the sustainability of step-growth synthesis.
“The development of catalytic processes that can operate at lower temperatures will reduce the energy input, and thus increase the sustainability of the step-growth synthesis.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationPendant hydroxyl groups not only enable post-polymerization functionalization but also provide a handle to tailor the crystallinity of these aliphatic polyesters.
“The pendant hydroxyl groups not only enable post-polymerization functionalization but also provide a handle to tailor the crystallinity of these aliphatic polyesters.242”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [242] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenTo date, the activity of organocatalysts for step-growth polymerization and the molecular weights of the resulting polyesters and polycarbonates are not yet comparable to the most efficient metal catalysts.
“To date, the activity of organocatalysts for SGP and the molecular weights of the resulting polyesters and polycarbonates are not yet comparable to the most efficient metal catalysts.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone givenThe direct coupling of CO2 and diols is severely limited by the reaction equilibrium and requires an effective dehydration system.
“The direct coupling of CO2 and diols is severely limited by the reaction equilibrium and requires an effective dehydration system.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationFurther modification of the resulting unsaturated polyesters by Michael addition yielded polyesters with different substituents dangling off the backbone, which provided a means to tune the thermal property of the materials.
“Further modification of the resulting unsaturated polyesters by Michael addition yielded polyesters with different substituents dangling of the backbone, which provided a means to tune the thermal property of the materials.233”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [233] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenFor the step-growth synthesis of polycarbonates, the replacement of hazardous phosgene with more renewable and eco-friendly carbonyl reagents is a subject of intensive research.
“For the step-growth synthesis of polycarbonates, the replacement of hazardous phosgene with more renewable and eco-friendly carbonyl reagents is a subject of intensive research.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationHigh yields (>90%) and high molecular weights (Mn in the range of 10-40 kDa) were achieved for a variety of diols and dihalides substrates with Feng and Gnanou's system.
“High yields (> 90%) and high molecular weights (Mn in the range of 10-40 kDa) were achieved for a variety of diols and dihalides substrates.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [265] source
Not checked in the free run.
May combine two claims.
Premisenone givenWhile the ROP of five-membered cyclic carbonates is enthalpically disfavored, six- and seven-membered cyclic carbonates can undergo facile and controlled ROP under mild conditions.
“While the ROP of fivemembered cyclic carbonates is enthalpically disfavored, six-and seven-membered cyclic carbonates (6CCs, 7CCs) can undergo facile and controlled ROP under mild conditions.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationFour-, six-, and seven-membered rings are favorable for ROP due to their large ring strains, while five-membered lactones such as γ-butyrolactone exhibit a less favorable enthalpy of polymerization and are usually considered nonpolymerizable.
“Four-, six-, and seven-membered rings are favorable for ROP due to their large ring strains while five-membered lactones such as γ-butyrolactone (γ-BL) exhibits a less favorable enthalpy of polymerization and is usually considered as nonpolymerizable.277”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [277] source
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May combine two claims.
PremisecitationThe synthetic versatility of six-membered cyclic carbonates allows the incorporation of a wide range of functional groups to the resulting polycarbonates, which has led to a versatile material platform for biomedical applications.
“The synthetic versatility of 6CCs allows the incorporation of a wide range of functional groups to the resulting polycarbonates, which has led to a versatile material platform for biomedical applications.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [282] source
Not checked in the free run.
May combine two claims.
Premisenone givenWith the proper choice of an initiating/catalytic system, ROP of cyclic esters and carbonates can be performed under mild conditions (room temperature, ambient pressure) to give high yield and 100% atom economy, making ROP a highly efficient and green route for the synthesis of polyesters and polycarbonates.
“With the proper choice of an initiating/catalytic system, ROP of cyclic esters and carbonates can be performed under mild conditions (room temperature, ambient pressure) to give high yield and 100% atom economy, which makes ROP a highly efficient and green route for the synthesis of polyesters and polycarbonates.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationQuantitative conversions of diols were achieved under 5 MPa CO2 with Tomishige's system, but the molecular weights of the obtained polycarbonates were extremely low (Mn < 1700 Da).
“Quantitative conversions of diols were achieved under 5 MPa CO2 but the molecular weights of the obtained polycarbonates were extremely low (Mn < 1700 Da).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [263] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenSimilar limitations on ring size exist for cyclic carbonates.
“Similar limitations on ring size exist for cyclic carbonates.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationDu employed CH2Cl2 as the dihalide and condensed it with various diols and 1 atm of CO2 to give polymers with Mn up to 11 kDa.
“In another study, Du employed CH2Cl2 as the dihalide and condensed it with various diols and 1 atm of CO2 to give polymers with Mn up to 11 kDa (Scheme 5e).266”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [266] source
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May combine two claims.
PremisecitationN-substitution not only enhances the ring strain but also provides a synthetic handle to introduce functionality to these polycarbonates.
“The N-substitution not only enhances the ring strain but also provides a synthetic handle to introduce functionality to these polycarbonates.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationOnly moderate yields (<60%) and low molecular weights (Mn up to 6 kDa) were achieved with Kadokawa's PR3/CBr4/base system.
“Only moderate yields (< 60%) and low molecular weights (Mn up to 6 kDa) were achieved.”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing), S4 (based).
Interpretationnone givenCatalytic processes performed at mild temperature, low catalyst loading, and solvent-free conditions are particularly attractive from a sustainability standpoint.
“In addition, catalytic processes performed at mild temperature, low catalyst loading, and solvent-free conditions are particularly attractive from a sustainability standpoint.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationIntramolecular chain transfer such as cyclization and backbiting of chain end onto an internal ester group leads to the formation of cyclic polyesters; intermolecular chain transfer (transesterification) results in chain scrambling and broadens the molecular weight distribution.
“As depicted in Scheme 6, intramolecular chain transfer such as cyclization (kcy) and backbiting (kbb) of chain end onto an internal ester group leads to the formation of cyclic polyesters; intermolecular chain transfer (transesterification) results in chain scrambling (ksc) and broadens the molecular weight distribution.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [273] Duda A., 2009
Not checked in the free run.
May combine two claims.
PremisecitationSome metal catalysts show extremely high reactivity (TOF > 1000 h-1) and high regio-/stereoselectivity for the ROP of asymmetric monomers.
“Some of these catalysts show not only extremely high reactivity (TOF > 1000 h -1 ) but also high regio-/stereoselectivity for the ROP of asymmetric monomers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe aggregation of alkali metal salts, lithium in particular, often complicates the polymerization kinetics.
“The aggregation of alkali metal salts, lithium in particular, often complicates the polymerization kinetics.287”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [287] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone givenSimple metal alkoxides and carboxylates such as tin octoate are cheap and convenient catalysts for ROPs and are used industrially to produce PLA.
“Simple metal alkoxides and carboxylates such as tin octoate are cheap and convenient catalysts for ROPs and are used industrially to produce PLA.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe most commonly used catalysts for ROP are transition and posttransition metal complexes, which mediate ROP through a coordination-insertion type mechanism.
“The most commonly used catalysts for ROP are transition and posttransition metal complexes, which mediate the ROP through a “coordination-insertion” type mechanism (Scheme 7).289”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [289] source
Not checked in the free run.
The quote only partly states this claim.
PremisereasoningWhen it comes to selectivity, especially stereoselectivity, well-defined single-site metal catalysts with ancillary ligands are more competent than simple metal alkoxides and carboxylates.
“However, when it comes to selectivity, especially stereoselectivity, those well-defined single-site metal catalysts with ancillary ligands are more competent.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisereasoningThe ancillary ligand has proven to be an important element in ROP catalysis to fine tune the electronic and steric properties of the metal center and to control the selectivity of polymerization.
“The ancillary ligand has proven to be an important element in ROP catalysis to fine tune the electronic and steric properties of the metal center and to control the selectivity of polymerization.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationAluminum complexes supported by SALEN-type ligands are some of the most stereoselective catalysts for the ROP of racemic LA, but their low reactivities limit their applicability.
“Aluminum complexes supported by SALEN-type ligands [301][302][303][304][305][306][307][308][309] are some of the most stereoselective catalysts for the ROP of racemic LA but their low reactivities (typical reaction conditions: Al loading >1 mol%, 70-130 °C, and long reaction time) limit their applicability.”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationUnlike the previous case, the two monomers exhibited orthogonal reactivity with one being completely inactive during the polymerization of the other.
“Unlike the previous case, the two monomers exhibited orthogonal reactivity with one being completely inactive during the polymerization of the other.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [320] source
Not checked in the free run.
May combine two claims.
PremisecitationPHAs are naturally produced by various bacteria but only isotactic microstructures are made biologically.
“PHAs are naturally produced by various bacteria (section 3.3) but only isotactic microstructures are made biologically.317”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [317] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
PremisereasoningAmong all chiral monomers, the stereoselective ROP of lactide has been most extensively studied because of the important application of PLAs.
“Among all chiral monomers, the stereoselective ROP of lactide has been most extensively studied because of the important application of PLAs.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningThis provides new possibilities for engineering the properties and applications for these plastics.
“This provides new possibilities for engineering the properties and applications for these plastics.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationRare-earth metal catalysts supported by phosphasalen ligands displayed both high reactivity and stereoselectivity (Pi up to 0.84 at 25 °C) with the ability to produce high molecular weight isotactic PLAs (Mn > 100 kDa) with extremely narrow polydispersities (Ð < 1.1).
“Rare-earth metal catalysts supported by phosphasalen ligands (such as Ln-phosSALEN in Figure 8) displayed both high reactivity and stereoselectivity (Pi up to 0.84 at 25°C) with the ability to produce high molecular weight isotactic PLAs (Mn > 100 kDa) with extremely narrow polydispersities (Ð <1.1).310,311”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThey found that the reduced form was much more active towards LA than CL while the oxidized form had the opposite selectivity.
“They found that the reduced form was much more active towards LA than CL while the oxidized form had the opposite selectivity.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [319] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationreasoningGiven that many cyclic esters and carbonates monomers derived from plants contain stereocenters, stereoselective ROP is an important aspect for the controlled synthesis of sustainable polymers.
“Given that many cyclic esters and carbonates monomers derived from plants contain stereocenters, the stereoselective ROP is an important aspect for the controlled synthesis of sustainable polymers.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationNo appreciable amount of ether linkage was detected in the resulting polymers, indicating the absence of decarboxylation reaction.
“No appreciable amount of ether linkage was detected in the resulting polymers, indicating the absence of decarboxylation reaction.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [297] source
Not checked in the free run.
May combine two claims.
PremisecitationEnd-group analysis revealed an imidazolium enol-like chain end of the final polymers, indicative of an intramolecular proton transfer within the zwitterionic intermediates generated from the nucleophilic addition of NHOs to the monomer.
“End-group analysis revealed an imidazolium enol-like chain end of the final polymers, indicative of an intramolecular proton transfer within the zwitterionic intermediates generated from the nucleophilic addition of NHOs to the monomer (Scheme 11D).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [335] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenOrganic acids such as sulfonic or phosphoric acid can catalyze the polymerization through electrophilic activation of monomers.
“Organic acids such as sulfonic or phosphoric acid can catalyze the polymerization through electrophilic activation of monomers.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone givenTypical nucleophilic organocatalytic ROP is subject to a trade-off between rate and selectivity: the most active catalysts, i.e. NHCs and TBD, tend to promote side reactions such as chain transfer and epimerization especially at high conversions while the most selective systems, such as TU/amines, suffer from slow kinetics.
“Typical nucleophilic organocatalytic ROP is subject to a trade-off between rate and selectivity: the most active catalysts, i.e.NHCs, TBD, tend to promote side reactions such as chain transfer and epimerization especially at high conversions while the most selective systems, such as TU/amines, suffer from slow kinetics.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationWhile non-substituted NHOs were ineffective for ROP due to catalyst deactivation, NHO bearing dimethyl substituents proved highly active for the ROP of LA and VL.
“While non-substituted NHOs (at the exocyclic carbon, NHO-1,3) were ineffective for ROP due to catalyst deactivation (Scheme 11C), NHO bearing dimethyl substituents (NHO-2) proved highly active for the ROP of LA and VL.334”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [334] source
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May combine two claims.
PremisecitationUnder the same conditions, the ROP of VL is fast but poorly controlled due to the more significant enolate-based initiation.
“Under the same conditions, the ROP of VL is fast but poorly controlled due to the more significant enolate-based initiation.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [334] source
Not checked in the free run.
May combine two claims.
InterpretationreasoningThe high activity and the ability to operate through different polymerization mechanisms make NHO an attractive motif for future catalyst design and optimization.
“The high activity and the ability to operate through different polymerization mechanisms make NHO an attractive motif for future catalyst design and optimization.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationThey found that the dizinc acetate catalyst was an excellent catalyst for the ring-opening copolymerization of epoxide and CO2 but not for the ROP of CL.
“They found that the dizinc acetate catalyst (Zn-OAc) was an excellent catalyst for the ring-opening copolymerization of epoxide and CO2 but not for the ROP of CL.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [322] source
Not checked in the free run.
May combine two claims.
PremisecitationIn the presence of an alcohol initiator, the ROP of 50 equiv L-LA by as low as 0.2 mol% NHO-2 reached quantitative conversion in less than a minute, resulting in PLAs with low molecular weight distributions (Ð < 1.2).
“In the presence of an alcohol initiator, the ROP of 50 equiv.L-LA by as low as 0.2 mol% NHO-2 reached quantitative conversion in less than a minute, resulting in PLAs with low molecular weight distributions (Ð <1.2).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [334] source
Not checked in the free run.
May combine two claims.
PremisecitationSince the pioneering work of Hedrick in 2001, the application of organic catalysts to ROP has witnessed significant progress in the last 15 years and this field has grown to the point that it now provides a powerful and, in some cases, better alternative to the use of traditional metal-based catalysts.
“Since the pioneering work of Hedrick in 2001, 324 the application of organic catalysts to ROP has witnessed significant progress in the last 15 years and this field has grown to the point that it now provides a powerful and, in some cases, better alternative to the use of traditional metal-based catalysts.325,326”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThese ionic catalysts are prepared by simple deprotonation of the neutral ureas or thioureas.
“These ionic catalysts are prepared by simple deprotonation of the neutral ureas or thioureas.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Interpretationnone givenThe diversity in mechanistic pathways not only provides new opportunities for enhancing the rate and selectivity of polymerization but also enables the synthesis of polymer architectures that are difficult to access by metal-mediated processes.
“The diversity in mechanistic pathways not only provides new opportunities for enhancing the rate and selectivity of polymerization but also enable the synthesis of polymer architectures that are difficult to access by metal-mediated processes.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone givenThese systems have proven especially selective for chain propagation over transesterification, affording narrowly dispersed polyesters and polycarbonates.
“These systems have proven especially selective for chain propagation over transesterification, affording narrowly dispersed polyesters and polycarbonates.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone givenWhile low stereo-control at ambient temperature has been a long-standing problem for organocatalytic ROP, recent advances in catalyst design have demonstrated the potential of organocatalysts to rival the state-of-the-art metal catalysts.
“While low stereo-control at ambient temperature has been a long-standing problem for organocatalytic ROP, recent advances in catalyst design have demonstrated the potential of organocatalysts to rival the state-of-the-art metal catalysts.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationChen developed a bifunctional catalyst that combines β-isocupreidine, a previously reported chiral ROP catalyst with low enantioselectivity (kL/kD = 4.4), and a chiral thiourea based on the binaphthyl scaffold.
“Chen developed a bifunctional catalyst that combines b-isocupreidine, a previously reported chiral ROP catalyst with low enantioselectivity (kL/kD = 4.4), 340 and a chiral thiourea based on the binaphthyl scaffold.341”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationUrea anions are more active than the corresponding thiourea anions, with the ability to polymerize all tested monomers in just seconds (<12 s) with excellent control on molecular weight distributions (Ð = 1.06-1.14).
“The urea anions are more active than the corresponding thiourea anions, with the ability to polymerize all tested monomers in just seconds (<12s) with excellent control on molecular weight distributions (Ð =1.06 ~ 1.14).336”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [336] source
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PremisecitationThe most active one, a trisurea/MTBD, is approximately 100 times faster than mono-TU/MTBD for the ROP of CL, with equally good control on molecular weights and molecular weight distributions (Ð < 1.05).
“The most active one, a trisurea/MTBD, is approximately 100 times faster than mono-TU/MTBD for the ROP of CL, with equally good control on molecular weights and molecular weight distributions (Ð < 1.05).”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Premisecitationexo-PRO exhibited a strong preference for L-LA and the ROP of rac-LA by this catalyst at 50% conversion generates highly isotactic PLAs with Pm up to 0.96 at 25 °C.
“exo-PRO exhibited a strong preference for L-LA and the ROP of rac-LA by this catalyst at 50% conversion generates a highly isotactic PLAs with Pm up to 0.96 at 25 °C.342”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [342] source
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PremisecitationKiesewetter reported a series of bis- and tris-(thio)urea based H-bond donors, which exhibited dramatic rate acceleration compared to the mono-TU/amine systems, yet retaining the high selectivity for propagation over transesterification.
“Kiesewetter reported a series of bis-and tris-(thio)urea based H-bond donors (Scheme 13), which exhibited dramatic rate acceleration compared to the mono-TU/amine systems, yet retaining the high selectivity for propagation over transesterification. 337,338”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThe rate acceleration is proposed to arise from an "activated (thio)urea" mechanism in which each additional (thio)urea moiety enhances the acidity via intramolecular H-bond activation, supported by DFT calculations.
“The rate acceleration is proposed to arise from an “activated (thio)urea” mechanism in which each additional (thio)urea moiety enhances the acidity via intramolecular H-bond activation (Scheme 13), supported by DFT calculations.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationWhile these heterogeneous catalysts can show good reactivities, they lack sufficient control on the polymerizations and the structures of the active species are ill-defined.
“While these catalysts can show good reactivities, they lack sufficient control on the polymerizations and the structures of the active species are ill-defined.”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenOne obvious advantage of epoxide/CO2 copolymerization is the utilization of CO2 as a monomer.
“One obvious advantage of epoxide/CO2 copolymerization is the utilization of CO2 as a monomer.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationWhile the field of epoxide/CO2 copolymerization is quite mature, with several technologies commercialized, the progress in epoxide/cyclic anhydride copolymerization is more recent.
“While the field of epoxide/CO2 copolymerization is quite mature, with several technologies been commercialized, the progress in epoxide/cyclic anhydride copolymerization is more recent.211,343”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Premisenone givenDepending on the epoxide, epoxide/CO2 copolymerization enables 30-50% of a polymer's mass to be derived from CO2, with the rest derived from cheap platform petrochemicals, or potentially from renewable biomass.
“Depending on the epoxide, this method enables 30-50% of a polymer's mass to be derived from CO2, with the rest derived from cheap platform petrochemicals, or potentially from renewable biomass.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationUpcycling of waste gases such as CO2 to useful and valuable plastics has long been of interest, and the ROCP of epoxides and CO2 represents one of the most successful examples of CO2 utilization in polymer synthesis.
“Upcycling of waste gases such as CO2 to useful and valuable plastics has long been of interest to researchers, and the ROCP of epoxides and CO2 represents one of the most successful examples of CO2 utilization in polymer synthesis.83,[344][345][346][347][348][349][350][351][352]”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
InterpretationreasoningBecause 5CCs are thermodynamically stable and cannot be re-incorporated into the chains, this elimination causes irreversible loss of yield.
“Because 5CCs are thermodynamically stable and cannot be re-incorporated into the chains, this elimination causes irreversible loss of yield.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenOne appealing aspect of the ROCP approach is the common availability and structural diversity of epoxide and cyclic anhydride monomers, which can be easily prepared from olefins and dicarboxylic acids, respectively.
“One appealing aspect of the ROCP approach is the common availability and structural diversity of epoxide and cyclic anhydride monomers, which can be easily prepared from olefins and dicarboxylic acids, respectively.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationChain propagation proceeds by the alternative insertion of epoxide and CO2 (or cyclic anhydride) to the metal-oxygen chain end, which leads to the desired formation of polycarbonate (or polyesters) backbones.
“Chain propagation proceeds by the alternative insertion of epoxide and CO2 (or cyclic anhydride) to the metal-oxygen chain end, which leads to the desired formation of polycarbonate (or polyesters) backbones.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [344] source
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PremisecitationIn most cases, a nucleophilic cocatalyst is used to increase the activity of the metal complexes, the most common ones being bis(triphenylphosphine) iminium salts and 4-dimethylaminopyridine.
“In most cases, a nucleophilic cocatalyst is used to increase the activity of the metal complexes, the most common ones being bis(triphenylphosphine) iminium salts ([PPN]X) and 4-dimethylaminopyridine (DMAP).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [343] source
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PremisecitationThe exploitation of chain transfer phenomenon enables immortal polymerization conditions, where chain transfer agents are added in large excess compared to the catalyst to increase the polymerization rate and control the molecular weight of products.
“On the other hand, the exploitation of chain transfer phenomenon enables immortal polymerization conditions, where the chain transfer agents are added in large excess compared to the catalyst to increase the polymerization rate and control the molecular weight of products.360”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [360] source
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PremisecitationSome epoxides and anhydrides can be prepared from biomass such as limonene oxide (from terpene) and maleic anhydride (from furfuraldehyde), which are attractive monomers for fully renewable aliphatic polyesters and polycarbonates.
“Some epoxides and anhydrides can be prepared from biomass (Figure 7) such as limonene oxide (from terpene) 365,366 and maleic anhydride (from furfuraldehyde) 138 , which are attractive monomers for fully renewable aliphatic polyesters and polycarbonates.”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPHAs are produced by a variety of microorganisms as a carbon and energy storage material in times of unbalanced nutrient availability.
“PHAs are produced by a variety of microorganisms as a carbon and energy storage material in times of unbalanced nutrient availability.376”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [376] source
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationCollectively, heterotrophic bacteria have led to the biosynthesis of over 150 different types of PHA copolymers.
“Collectively, these bacteria have led to the biosynthesis of over 150 different types of PHA copolymers.385”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [385] source
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InterpretationreasoningBiological recycling is the longest path for building a circular flow of plastics, and the energy and environmental prices paid to build the chemical complexity of monomers are completely lost during the degradation processes.
“However, this is the longest path for building a circular flow of the plastics (Scheme 17), and the energy and environmental prices paid to build the chemical complexity of monomers are completely lost during the degradation processes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenRecycling is one of the most important end-of-use options to reduce the environmental impacts and resources depletion of plastics.
“Recycling is one of the most important end-of-use options to reduce the environmental impacts and resources depletion of plastics.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationWhile efficient processes have been developed, sophisticated purification and process controls are needed to insure that hazardous substances are not released into the atmosphere during incineration.
“In addition, while efficient processes have been developed, sophisticated purification and process controls are needed to insure that the hazardous substances are not released into the atmosphere.41”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [41] Francis R., 2017
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationDepending on the organism and the conditions of growth, the molecular weight of PHBs can vary from 50,000 Da to over a million Da.
“Depending on the organism and the conditions of growth, the molecular weight of PHBs can vary from 50,000 Da to over a million Da. 384”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [384] Bugnicourt E., 2015
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PremisecitationMethanotrophic bacteria that produce PHAs can be found at wastewater treatment plants, which are often geographically close to sources of waste methane.
“The methanotrophic bacteria that produce PHAs can be found at wastewater treatment plants, which are often geographically close to sources of waste methane.375,381,382”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationMany epoxides and cyclic anhydrides contain unsaturated moieties that can be utilized for post-polymerization modifications and crosslinking, which increases the range of architectures and functionalities achievable through the ROCP method.
“Additionally, many epoxides and cyclic anhydrides contain unsaturated moieties that can be utilized for post-polymerization modifications and crosslinking, 211 which increases the range of architectures and functionalities that can be achieved through the ROCP method.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [211] source
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPHAs are an important class of biodegradable plastics commonly used for packaging, bottles, cutlery, furniture, biomedical implants, drug delivery vehicles, and animal food supplements.
“PHAs are an important class of biodegradable plastics commonly used for packaging, bottles, cutlery, furniture, biomedical implants, drug delivery vehicles, and animal food supplements.[371][372][373][374]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [371][372][373][374]
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PremisecitationTerpolymerization of epoxide, cyclic anhydride, and CO2 is a facile strategy for the one-pot synthesis of poly(ester-carbonate), a class of biodegradable polymers that have garnered considerable interest due to their possible superior properties than pure polyesters and polycarbonates.
“Terpolymerization of epoxide, cyclic anhydride, and CO2 is a facile strategy for the onepot synthesis of poly(ester-carbonate), 211,343 a class of biodegradable polymers that have garnered considerable interest due to their possible superior properties than pure polyesters and polycarbonates.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThe majority (>70%) of recycled PET (rPET) is used for production of lower-grade products, mainly polyester fibers, and only a small fraction (~10%) is used for closed-loop bottle-to-bottle recycling.
“The majority (> 70%) of recycled PET (rPET) is used for production of lower-grade products, mainly polyester fibers, and only a small fraction (~10%) is used for closed-loop bottle-to-bottle recycling.394”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [394] Data from Noone A., Collected PET bottles, Proceedings of 13th International Polyester Recycling Forum, 2008.
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAccording to the National Association for PET Container Resources (NAPCOR), ~30.1% PET plastic bottles were mechanically recycled in 2015 in the United States.
“According to the National Association for PET Container Resources (NAPCOR), ~30.1% PET plastic bottles were mechanically recycled in 2015 in the United States.393”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [393] NAPCOR Recycling Rate Reports. http://www.napcor.com/PET/pet_reports.html(accessed May 8, 2017).
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May combine two claims.
InterpretationreasoningSince the ability to substitute recycled plastic for virgin polymer depends on the purity of the recovered plastic feed, mechanical recycling of rigid plastic bottles consisting of a single polymer is much simpler and more economical than multi-layer and multi-component packages.
“Since the ability to substitute recycled plastic for virgin polymer depends on the purity of the recovered plastic feed, mechanical recycling of rigid plastic bottles consisting of a single polymer are much simpler and more economical than those multi-layer and multi-component packages.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationSince closed-loop mechanical recycling requires the polymers to be effectively separated from sources of contaminations and stable during reprocessing, the only postconsumer plastic wastes that have routinely been recycled in a closed-loop fashion are clear PET bottles and more recently HDPE bottles.
“Since closed-loop mechanical recycling requires the polymers to be effectively separated from sources of contaminations (other plastics, metals, pigments, adhesives, etc.) and stable during reprocessing (grinding, melting), the only postconsumer plastic wastes that have routinely been recycled in a closed-loop fashion are clear PET bottles and more recently HDPE bottles.388”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [388] source
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Interpretationnone givenThe most challenging step in mechanical recycling of PET is sorting/separation, which limits the type of polymers that can be recycled and also determines the quality of recyclates.
“The most challenging step is sorting/ separation, which limits the type of polymers that can be recycled and also determines the quality of recyclates.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationIn the first step, PET was depolymerized using isosorbide to oligomers, which were chain extended by succinic acid in the second step to form a novel copolyester.
“In the first step, PET was depolymerized using isosorbide to oligomers, which were chain extended by succinic acid in the second step to form a novel copolyester (Scheme 18).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [414] source
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May combine two claims.
PremisecitationComputational studies revealed that this reaction proceeds by the nucleophilic attack of the metal carbonate on the PC and the evolution of CO2 gas as the by-product.
“Computational studies revealed that this reaction proceeds by the nucleophilic attack of the metal carbonate on the PC and the evolution of CO2 gas as the by-product.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [417] source
Not checked in the free run.
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PremisecitationThe alcoholysis of PLAs have been achieved under different conditions and the efficiency of these processes is highly condition-dependent.
“The alcoholysis of PLAs have been achieved under different conditions [433][434][435][436] and the efficiency of these processes is highly condition-dependent.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [433][434][435][436]
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PremisecitationMonobutyltin oxide was identified as the most active catalyst for both steps and resulted in minimal discoloration.
“Monobutyltin oxide was identified as the most active catalyst for both steps and resulted in minimal discoloration.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [415] source
Not checked in the free run.
May combine two claims.
PremisecitationThese mechanisms are supported by the fact that when the OH chain end is capped via acetylation, the degradation rate significantly decreases and the relatively slow random chain scission become dominant.
“These mechanisms are supported by the fact that when the OH chain end is capped via acetylation, the degradation rate significantly decreases and the relatively slow random chain scission become dominant.428”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [428] source
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PremisecitationJung found that PPC was less susceptible to degradation in acidic medium than PCL and PLA, with increased degradation rate as PPC << PLA < PCL.
“They found that PPC was less susceptible to degradation in acidic medium than PCL and PLA, with increased degradation rate as PPC << PLA < PCL.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [425] source
Not checked in the free run.
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PremisereasoningAlthough the two mechanisms operate simultaneously during hydrolysis, several studies have found that the chain-end scission is significantly faster than the random backbone cleavage.
“Although the two mechanisms operate simultaneously during hydrolysis, several studies have found that the chainend scission is significantly faster than the random backbone cleavage.424,426,427”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationIn contrast, PPC was more readily hydrolyzed in basic conditions, with increased degradation rate being PCL << PLA < PPC.
“In contrast, PPC was more readily hydrolyzed in basic conditions, with increased degradation rate being PCL << PLA < PPC.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [425] source
Not checked in the free run.
May combine two claims.
PremisecitationThe rate of water diffusion depends on the hydrophobicity of the polymer and its shape or surface area while the intrinsic degradation kinetics is affected by the pH and temperature of the medium as well as the molecular weight and microstructures of the polymer.
“The rate of water diffusion depends on the hydrophobicity of the polymer and its shape or surface area while the intrinsic degradation kinetics is affected by the pH 421 and temperature of the medium 422 as well as the molecular weight 423 and microstructures of the polymer.424”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationAt acidic pH the hydrolysis proceeds through a preferential scission of the end groups and spits out one lactic acid unit at a time, while the base catalyzed hydrolysis proceeds preferentially via a backbiting process from the OH chain end leading to the formation of lactide, which is eventually hydrolyzed to lactate.
“While at acidic pH the hydrolysis proceeds through a preferential scission of the end groups and spits out one lactic acid unit at a time, the base catalyzed hydrolysis proceeds preferentially via a backbiting process from the OH chain end leading to the formation of lactide, which is eventually hydrolyzed to lactate.”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationComputational investigation showed that stoichiometric amounts of metal carbonate is needed for the reaction to proceed to completion, but insights provided by investigating the mechanism also led them to develop a catalytic process using 12 mol% K2CO3 with lower reaction efficiency.
“The computational investigation showed that stoichiometric amounts of metal carbonate is needed for the reaction to proceed to completion, but insights provided by investigating the mechanism also led them to develop a catalytic process using 12 mol% K2CO3 with lower reaction efficiency.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [417] source
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAcid- or base-catalyzed hydrolysis of aliphatic polyester and polycarbonates has also been widely explored, the results of which have been used to guide the design and application of these polymers for therapeutic delivery and medical implants.
“The acid-or base-catalyzed hydrolysis of aliphatic polyester and polycarbonates has also been widely explored, the results of which have been used to guide the design and application of these polymers for therapeutic delivery and medical implants.418”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [418] Kumar M. N. V. R., 2016
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May combine two claims.
PremisecitationThe use of Bu2Sn(OMe)2 or NaOH facilitated a nearly quantitative depolymerization to CL, while Ti(OiPr)4 gave almost equal amounts of CL and its cyclic dimer.
“The use of Bu2Sn(OMe)2 or NaOH facilitated a nearly quantitative depolymerization to CL, while Ti(O i Pr)4 gave almost equal amounts of CL and its cyclic dimer.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [454] source
Not checked in the free run.
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PremisecitationIt was shown that both the depolymerization rate and selectivity increased with Sn concentration.
“It was shown that both the depolymerization rate and selectivity increased with Sn concentration.[447][448][449]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [447][448][449]
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PremisecitationAcetylation of the OH chain end significantly increased the polymer stability and impeded the thermal recycling, consistent with an unzipping mechanism initiated from the OH chain end.
“Acetylation of the OH chain end significantly increased the polymer stability and impeded the thermal recycling, consistent with an unzipping mechanism initiated from the OH chain end.444”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [444] source
Not checked in the free run.
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PremisecitationFor Sn < 20 ppm, the degradation proceeded mainly via random intra- and intermolecular ester exchange, generating a significant amount of diastereomers and cyclic oligomers.
“For Sn < 20 ppm, the degradation proceeded mainly via random intra-and intermolecular ester exchange, generating a significant amount of diastereomers and cyclic oligomers.448”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [448] source
Not checked in the free run.
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InterpretationcitationCompared to the traditional bulk production of lactate esters based on the esterification of lactic acid, these catalytic alcoholyses of PLAs provide a number of advantages, including starting materials derived from PLA wastes, reduced reaction time and high yield, simple purification, and retention of stereochemistry.
“Compared to the traditional bulk production of lactate esters based on the esterification of lactic acid 441,442 , these catalytic alcoholyses of PLAs provide a number of advantages, including starting materials derived from PLA wastes, reduced reaction time and high yield, simple purification, and retention of stereochemistry.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [441] source
Not checked in the free run.
- cites [442] Martino-Gauchi, G.; Teissier, R.Continuous Esterification Process for the Preparation of Ethyl Lactate from Lactic Acid and Ethanol. U.S. Patent 20060041165 A1, 2004.
Not checked in the free run.
May combine two claims.
PremisecitationHowever, this method exerts little control over the chain length of each block as the insertion of the diols to the PLA is random.
“However, this method exerts little control over the chain length of each block as the insertion of the diols to the PLA is random.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [443] source
Not checked in the free run.
May combine two claims.
PremisecitationLeibfarth reported a very efficient way to recycle PLAs and PGA to small esters using TBD as the catalyst; with only 1.5 equivalents of alcohol per ester bond, quantitative alcoholysis to small esters was observed in only 2 min at room temperature with nearly complete retention of stereochemistry.
“Leibfarth reported a very efficient way to recycle PLAs and PGA to small esters using TBD as the catalyst.439 With only 1.5 equivalents of alcohol per ester bond, quantitative alcoholysis to small esters was observed in only 2 min at room temperature with nearly complete retention of stereochemistry.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [439] source
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PremisecitationThe functional group tolerance of TBD allows the introduction of different polymerizable groups (e.g. olefin) to the ester products, which provides a number of opportunities in the production of new polymer materials.
“The functional group tolerance of TBD allows the introduction of different polymerizable groups (e.g.olefin) to the ester products (Scheme 21), which provides a number of opportunities in the production of new polymer materials.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [439] source
Not checked in the free run.
May combine two claims.
PremisecitationThe presence of catalyst enables milder reaction conditions and among the screened metal catalysts, magnesium and calcium alkoxides generated in situ from the metallic precursors and alcohols gave the best yields (>90%) and negligible epimerization.
“The presence of catalyst enables milder reaction conditions and among the screened metal catalysts, magnesium and calcium alkoxides generated in situ from the metallic precursors and alcohols gave the best yields (>90%) and negligible epimerization.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [440] source
Not checked in the free run.
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PremisecitationIn the early 1990s, Du Pont developed a method using 2-3 equiv. of alcohol per polymer unit at 150-190 °C with H2SO4 as the catalyst, achieving 69-87% conversion of high-molecular-weight PLA to lactates within 2 h.
“In the early 1990s, Du Pont developed a method using 2-3 equiv. of alcohol (ROH for R = Me, Et, Bu) per polymer unit at 150-190 °C with H2SO4 as the catalyst.69-87% conversion of high-molecular-weight PLA to lactates is achieved within 2 h.437,438”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [437] Brake, L. D.Recovery of polyhydroxy acids. U.S. Patent 5264614 A, 1993.
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- cites [438] Brake, L. D.Preparation of alkyl esters by depolymerization of poly(hydroxy acids). U.S. Patent 5264617 A, 1993.
Not checked in the free run.
May combine two claims.
PremisecitationIn contrast, for samples with Sn > 480 ppm, the degradation kinetics indicated an unzipping depolymerization mechanism along with minor bimolecular transesterification reactions, leading to the predominant production of L-LA.
“In contrast, for samples with Sn > 480 ppm, the degradation kinetics indicated an unzipping depolymerization mechanism along with minor bimolecular transesterification reactions, leading to the predominant production of L-LA.448,449”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationIn general, substituted lactones have relatively low polymerizability compared to the unsubstituted ones and are thus potential candidates for thermal recycling.
“In general, substituted lactones have relatively low polymerizability compared to the unsubstituted ones and are thus potential candidates for thermal recycling.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationThe topologies of the products can be controlled by the La[N(SiMe3)2]3/ROH ratios, with excess ROH favoring the formation of linear chains.
“The topologies of the products can be controlled by the La[N(SiMe3)2]3/ROH ratios, with excess ROH favoring the formation of linear chains.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationUsing similar conditions (-60 °C, Ln/ROH = 1/3) to that of γ-BL, they were able to achieve the selective ROP of MBL to produce poly(MBL) with Mn up to 21 kDa, which can be facilely recycled back to the monomer MBL by heating the polymer ≥ 100 °C for 1 h in the presence of catalysts.
“Using similar conditions (-60 °C, Ln/ROH = 1/3) to that of γ-BL, they were able to achieve the selective ROP of MBL to produce poly(MBL) with Mn up to 21 kDa, which can be facilely recycled back to the monomer MBL by heating the polymer ≥ 100 °C for 1 h in the presence of catalysts.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [177] source
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Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Premisenone givenPolymers made from monomers with low polymerization enthalpy are intrinsically unstable and tend to degrade under environmental stresses such as heat or moisture.
“Second, the polymers are intrinsically unstable and tend to degrade in the environmental stresses such as heat or moisture.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationAt -40 °C and ambient pressure, the ROP of γ-BL proceeded smoothly in the presence of a catalyst (La[N(SiMe3)2]3 or tert-Bu-P4) to high conversions within 24 h, generating poly(γ-BL) with Mn up to 30 kDa and Ð ~ 2.0.
“At -40 °C and ambient pressure, the ROP of γ-BL proceeded smoothly in the presence of a catalyst (La[N(SiMe3)2]3 or tert-Bu-P4) to high conversions within 24 h, generating poly(γ-BL) with Mn up to 30 kDa and Ð ~ 2.0.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationBased on this chemistry, they developed chemically recyclable thermoplastic polyurethanes and novel polyester elastomers.
“Based on this chemistry, they developed chemically recyclable thermoplastic polyurethanes 161 and novel polyester elastomers 162 .”
Quote in the paperSubstantial claim0 of 2 sources checkedThe quote only partly states this claim.
InterpretationreasoningPerforming polymerization and processing at low temperature increases the energy cost of the products.
“This increases the energy cost of the products.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe presence of catalyst allowed pyrolysis to be conducted at lower temperature than without a catalyst and suppressed the formation of oligomeric species.
“The presence of catalyst not only allowed the pyrolysis to be conducted at lower temperature than without a catalyst, but also suppressed the formation of oligomeric species.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [466] source
Not checked in the free run.
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InterpretationreasoningThe Lewis acidic nature of Ca2+ and Mg2+ facilitates activation of the six-membered transition state in the unzipping depolymerization of PHA, leading to more selective degradation than in the absence of catalysts.
“It is proposed that the Lewis acidic nature of Ca 2+ and Mg 2+ facilitates the activation of the six-membered transition state in the unzipping depolymerization of PHA (Scheme 23), and thus leads to a more selective degradation process than in the absence of catalysts.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationCatalytic pyrolysis using Mg(OH)2 as the catalyst was used to recycle a variety of short- and medium-chain length PHAs and proved the utility of the recovered monomers as feedstocks for microbial synthesis of PHAs.
“This catalytic pyrolysis strategy (using Mg(OH)2 as the catalyst) was used to recycle a variety of short-and medium-chain length PHAs and further proved the utility of the recovered monomers as feedstocks for the microbial synthesis of PHAs.375,381”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisereasoningBecause most aliphatic polyesters and polycarbonates are hydrophobic, enzymes exhibit a substrate binding domain (SBD) in addition to their catalytic domain, which facilitates adsorption of the enzyme on water-insoluble polymers.
“Since most aliphatic polyesters and polycarbonates are hydrophobic, enzymes exhibit a substrate binding domain (SBD) in addition to their catalytic domain, which facilitates the adsorption of the enzyme on the water-insoluble polymers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenWhen cell extracts are used to depolymerize water-insoluble polymers, only steps 2 and 3 are observed.
“Noteworthy, when cell extracts are used to depolymerize water-insoluble polymers, only steps 2 and 3 are observed (see Figure 14).”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationMineralization of PHVB was faster in fertile soil than with isolated enzymes, owing to a more diverse population of degrading enzymes in the soil.
“For instance, the mineralization of PHVB was shown to be faster in fertile soil vs. isolated enzymes, owing to a more diverse population of degrading enzymes in the soil.484”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [484] source
Not checked in the free run.
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Interpretationnone givenOverall, anaerobic microbial degradation of aliphatic polyesters and polycarbonates remains poorly studied, despite advantages such as high efficiency, especially for PLA and PHAs, and fast rates.
“Overall, anaerobic microbial degradation of aliphatic polyesters and polycarbonates remains poorly studied, despite several advantages such as high efficiency, especially for PLA and PHAs, and fast rates.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenWhen chains are short enough to be soluble in the media and cross the membrane, further degradation/digestion might take place with the help of intracellular enzymes.
“When the chains are short enough to be soluble in the media and cross the membrane, further degradation/digestion might take place with the help of intracellular enzymes.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe rate of degradation was faster for PLA nanocomposites than for pure PLA, owing to the presence of hydroxyl moieties at the surface of nanoclay that can act as nucleophiles.
“Moreover, the rate of degradation was found to be faster for PLA nanocomposites than for pure PLA, owing to the presence of hydroxyl moieties at the surface of nanoclay that can act as nucleophiles.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [488] source
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May combine two claims.
Premisenone givenHigh molar mass polymers are unable to penetrate the membrane of microbial organisms and so are not susceptible to microbial attack by intracellular enzymes as such.
“High molar masses polymers are unable to penetrate the membrane of microbial organisms, and so are not susceptible to microbial attack by intracellular enzymes as such.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
PremisereasoningBecause the microorganism has access to O2 in aerobic conditions, the end products of mineralization are CO2 and H2O, instead of CO2 and CH4 in anaerobic conditions.
“Because the microorganism has access to O2 in aerobic conditions, the endproducts of mineralization are CO2 and H2O, instead of CO2 and CH4 in anaerobic conditions.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPCL and PHB could also be biodegraded in similar settings, up to 90% degradation after 14 days for PHB, while PBS remained mostly intact, 3% degradation after 96 days.
“PCL and PHB could also be biodegraded in similar settings (up to 90% degradation after 14 days for PHB), while PBS remained mostly intact (3% degradation after 96 days).478”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [478] source
Not checked in the free run.
May combine two claims.
PremisecitationPLA and PLLA could be degraded by soil bacteria in aquatic conditions, up to 90% after 60 days for PLA and 50% after 40 days for PLLA.
“showed that PLA and PLLA, respectively, could be degraded by soil bacteria in aquatic conditions (up to 90% after 60 days for PLA and 50% after 40 days for PLLA).[477][478][479]”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenConsiderable efforts have been focused on biodegradable polymers that can be decomposed naturally or in composting sites by microorganisms.
“Considerable efforts have been focused on biodegradable polymers that can be decomposed naturally or in composting sites by microorganisms.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenRecently, catalytic systems that enable control of polymerization on a more sophisticated level such as architectures and monomer sequences are emerging.
“Recently, catalytic systems that enable the control of polymerization on a more sophisticated level such as architectures and monomer sequences are emerging.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThe end products of biodegradable polymers are primarily CO2, H2O, and other metabolites that can re-enter the life cycle.
“The end products are primarily CO2, H2O, and other metabolites that can re-enter the life cycle.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenMetal-based catalysts are in general more competent in tackling the aforementioned challenges.
“While metal-based catalysts are in general more competent in tackling the aforementioned challenges, organocatalysts have emerged as an efficient alternative.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThermally recyclable polymers can be depolymerized to their monomers in high yields and reused to produce virgin quality polymers.
“An emerging frontier in sustainable polymers is the design and synthesis of thermally recyclable polymers that can be depolymerized to their monomers in high yields, which can then be reused to produce virgin quality polymers.23”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [23] source
Not checked in the free run.
Classified as probably not a substantial claim.
Interpretationnone givenData to assess the environmental impacts or sustainability of catalysts are incomplete.
“While a variety of active and selective catalysts are available for converting renewable monomers into well-defined polymers, data to assess their environmental impacts or sustainability are incomplete.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Interpretationnone givenAliphatic polyesters and aliphatic polycarbonates can be repurposed to versatile synthetic intermediates or environmentally degraded if they end up in the environment.
“Among the potentially sustainable alternatives to current commodity plastics, aliphatic polyesters and aliphatic polycarbonates are highlighted as they can be derived from renewable resources, they can be produced by a variety of versatile synthetic methods, they exhibit a wide range of useful properties and can be repurposed to versatile synthetic intermediates or environmentally degraded if they”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenAliphatic polyesters and aliphatic polycarbonates exhibit a wide range of useful properties.
“Among the potentially sustainable alternatives to current commodity plastics, aliphatic polyesters and aliphatic polycarbonates are highlighted as they can be derived from renewable resources, they can be produced by a variety of versatile synthetic methods, they exhibit a wide range of useful properties and can be repurposed to versatile synthetic intermediates or environmentally degraded if they”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Interpretationnone givenCatalysis is an enabling science that impacts every step of the plastics life cycle.
“Catalysis is an enabling science that impacts every step of the plastics life cycle.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenAddition of organic solvents is advantageous to solubilization of polymers but can have a detrimental effect on the stability of the enzyme.
“The addition of organic solvents is advantageous to the solubilization of the polymers but can have a detrimental effect on the stability of the enzyme.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenAliphatic polyesters and aliphatic polycarbonates can be produced by a variety of versatile synthetic methods.
“Among the potentially sustainable alternatives to current commodity plastics, aliphatic polyesters and aliphatic polycarbonates are highlighted as they can be derived from renewable resources, they can be produced by a variety of versatile synthetic methods, they exhibit a wide range of useful properties and can be repurposed to versatile synthetic intermediates or environmentally degraded if they”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone givenSignificant progress has been made in increasing catalytic activity (turnover frequency), productivity (turnover number), selectivity toward desired product formation over side reactions, and regio- or stereoselectivity.
“Significant progress has been made in increasing the catalytic activity (turnover frequency), productivity (turnover number), selectivity toward desired product formation over side reactions, regio-or stereoselectivity.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningUse of a proper catalyst allows milder depolymerization conditions and can improve the selectivity of depolymerization reactions.
“It will be seen from the examples below that the use of a proper catalyst not only allows milder depolymerization conditions but can also improve the selectivity of depolymerization reactions.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationLipases are thought to only trigger esterification and transesterification reactions in dry organic solvents, while the presence of water allows hydrolysis.
“Lipases are thought to only trigger esterification and transesterification reactions in dry organic solvents, while the presence of water allows for hydrolysis.514”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [514] source
Not checked in the free run.
Classified as probably not a substantial claim. May combine two claims.
InterpretationreasoningAlthough the biodegradable end-of-life option mitigates some issues associated with indiscriminate disposal of plastics in the environment, it is not the only or even best option for capturing value.
“Although this end-of-life option mitigates some of the issues associated with indiscriminate disposal of plastics in the environment, it is not the only or even best option for capturing value.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenOverall PCL degrades fastest with quantitative depolymerization obtained with Pseudomonas lipase after 4 days in aqueous media, and addition of PLA or PPC to PCL greatly decreases this rate.
“Overall PCL degrades the fastest with quantitative depolymerization obtained with Pseudomonas lipase after 4 days in aqueous media and, the addition of PLA or PPC to PCL greatly decreases this rate.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationTraces of H2O in sCO2 (18 MPa) triggered formation of dicaprolactone from PCL in yields higher than 90%, allowing a full recycling cycle.
“In contrast, traces of H2O in sCO2 (18 MPa), triggered the formation of dicaprolactone (i.e.1,8dioxacyclotetradecane-2,9-dione) from PCL in yields higher than 90%, therefore allowing for a full recycling cycle.520”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [520] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenSome sustainability metrics and indicators such as green design principles can be used to assess different catalytic methods based on their adherence to green design principles.
“Nevertheless, some sustainability metrics and indicators such as green design principles can be used to assess different catalytic methods based on their adherence to green design principles.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenEconomic disincentives have contributed to the modest rates of recycling and material recovery.
“The end-of-life options of plastics are critical for the development of circular plastics economies, but economic disincentives have contributed to the modest rates of recycling and material recovery.”
Quote in the paperNot a substantial claim- Rests on an assumption: Economic disincentives have contributed to the modest rates of recycling and material recovery.
May combine two claims.
PremisecitationWei, Li et al. showed that proteinase K degraded PLLA faster than PDLA, mostly owing to higher adsorption of the enzyme at the surface of PLLA as compared to PDLA.
“However, Wei, Li et al. showed that proteinase K degraded PLLA faster than PDLA, mostly owing to higher adsorption of the enzyme at the surface of PLLA as compared to PDLA.527”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [527] source
Not checked in the free run.
May combine two claims.
PremisecitationVert et al. showed that Pseudomonas lipase could break down the crystalline domains of PCL within days, in contrast to hydrolytic degradation that would take several years.
“Noteworthy, Vert et al. showed that Pseudomonas lipase could break down the crystalline domains of PCL within days in contrast to hydrolytic degradation that would take several years to do the same.504”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [504] source
Not checked in the free run.
May combine two claims.
PremisecitationAcetone allowed faster degradation and DMSO was the less efficient solvent, evidencing that overall the depolymerization rate increased with higher solvent polarity and lower solvent viscosity.
“Acetone allowed for the faster degradation and DMSO was the less efficient solvent, evidencing that overall, the depolymerization rate increased with higher solvent polarity and lower solvent viscosity.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationProteinase K is stable in the 8-8.6 pH range and is particularly efficient to degrade PLA.
“Proteinase K is stable in the 8-8.6 pH range and is particularly efficient to degrade PLA.523,524”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationDepolymerase and esterase could digest inclusion bodies of Bacillus megaterium containing PHB to produce D(-)-β-hydroxybutyric ester, with up to 90% hydrolysis after 100 min.
“depolymerase”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [469] Merrick J. M., 1964, J. Bacteriol. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPHA depolymerases usually exhibit a catalytic domain containing an esterase sequence (often similar to lipase) and a substrate-binding domain (SBD) to enable adsorption of the enzyme at the surface of hydrophobic PHAs.
“PHA depolymerases usually exhibit a catalytic domain containing an esterase sequence -often similar to lipase -and a substrate-binding domain (SBD) to enable adsorption of the enzyme at the surface of hydrophobic PHAs.493”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [493] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationSeveral PHA depolymerases have been isolated mainly from Alcaligenes, Pseudomonas, and Comamonas, and their structures and properties have been extensively reviewed.
“Since this first report, several PHA depolymerases have been isolated on agar plates, mainly from Alcaligenes, Pseudomonas and Comamonas and their structures and properties have been extensively reviewed.491,492”
Quote in the paperNot a substantial claim0 of 2 sources checked
The authors state this as an assumption.
The definition of sustainable polymers as materials with closed-loop life cycles is adopted as an aspirational goal.
“We have adopted this definition as an aspirational goal in the spirit of sustainable development.”
The paper relies on this without support.
Cellulose and hemicellulose can provide an almost unlimited source of C5 and C6 sugars if efficient strategies are devised to recover and purify these feedstocks effectively.
“The two major components of lignocellulose, cellulose and hemicellulose, provide an almost unlimited source of C5 and C6 sugars, provided efficient strategies can be devised to recover and purify these feedstocks effectively.”
The paper relies on this without support.
Identifying the best pathway to convert a given feedstock to a given monomer is one of the first challenges for the development of sustainable polymers.
“Identifying the best pathway to convert the aforementioned feedstock to a given monomer is one of the first challenges for the development of sustainable polymers.”
The paper relies on this without support.
Economic disincentives have contributed to the modest rates of recycling and material recovery.
“economic disincentives have contributed to the modest rates of recycling and material recovery.”
The paper relies on this without support.
Direct pyrolysis cannot achieve monomer recovery for step-growth polyesters and polycarbonates.
“While monomer recovery cannot be achieved through direct pyrolysis for step-growth polyesters and polycarbonates, this is an attractive recycling option for chain-growth polymers.”
The paper relies on this without support.
Direct pyrolysis is an attractive recycling option for chain-growth polymers.
“While monomer recovery cannot be achieved through direct pyrolysis for step-growth polyesters and polycarbonates, this is an attractive recycling option for chain-growth polymers.”
The paper relies on this without support.
Plastic sorting and tolerance to contaminants in plastics feeds presents a significant challenge for chemical recycling.
“Similar to mechanical recycling, plastic sorting and tolerance to contaminants in the plastics feeds presents a significant challenge for chemical recycling.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Glycolide forms the hydrophilic polymer polyglycolide (PGA), leading to faster degradation.
“The set of comonomers is completed by glycolide (GG), which forms the hydrophilic polymer polyglycolide (PGA) leading e.g., to a faster degradation. [13]”
From Master of Chaos and Order: Opposite Microstructures of PCL‐<i>co</i>‐PGA‐<i>co</i>‐PLA Accessible by a Single Catalyst** (2022) · cites this paper as [13]
Cites
Plastic waste inputs from land into the ocean
Jambeck, J. R., Geyer, R., Wilcox, C., Siegler, T. R., Perryman, M., Andrady, A., Narayan, R., & Law, K. L. (2015) · Science · doi:10.1126/science.1260352 · Cited by 13,163 · see citing works
Chitin and chitosan: Properties and applications
Rinaudo, M. (2006) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2006.06.001 · Cited by 8,378 · see citing works
Odian, G. (2004) · doi:10.1002/047147875x · Cited by 7,158 · see citing works
Chemical Routes for the Transformation of Biomass into Chemicals
Corma, A., Iborra, S., & Velty, A. (2007) · Chemical Reviews · doi:10.1021/cr050989d · Cited by 5,970 · see citing works
The Path Forward for Biofuels and Biomaterials
Ragauskas, A. J., Williams, C. K., Davison, B. H., Britovsek, G., Cairney, J., Eckert, C. A., Frederick, W. J., Hallett, J. P., Leak, D. J., Liotta, C. L., et al. (2006) · Science · doi:10.1126/science.1114736 · Cited by 5,741 · see citing works
Bozell, J. J., & Petersen, G. R. (2010) · Green Chemistry · doi:10.1039/b922014c · Cited by 4,566 · see citing works
An Overview of Polylactides as Packaging Materials
Auras, R., Harte, B., & Selke, S. (2004) · Macromolecular Bioscience · doi:10.1002/mabi.200400043 · Cited by 3,454 · see citing works
Plastics Recycling: Challenges and Opportunities
Hopewell, J., Dvorak, R., & Kosior, E. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0311 · Cited by 3,201 · see citing works
Ullmann's Encyclopedia of Industrial Chemistry
(2012) · Choice Reviews Online · doi:10.5860/choice.50-1224 · Cited by 3,067 · see citing works
Chitosan Chemistry and Pharmaceutical Perspectives
Kumar, M. N. V. R., Müzzarelli, R. A. A., Muzzarelli, C., Sashiwa, H., & Domb, A. J. (2004) · Chemical Reviews · doi:10.1021/cr030441b · Cited by 2,945 · see citing works
Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources
van Putten, R.-J., van der Waal, J. C., de Jong, E., Rasrendra, C. B., Heeres, H. J., & de Vries, J. G. (2013) · Chemical Reviews · doi:10.1021/cr300182k · Cited by 2,886 · see citing works
Biological degradation of plastics: A comprehensive review
Shah, A. A., Hasan, F., Hameed, A., & Ahmed, S. (2008) · Biotechnology Advances · doi:10.1016/j.biotechadv.2007.12.005 · Cited by 2,765 · see citing works
Sustainable polymers from renewable resources
Zhu, Y., Romain, C., & Williams, C. K. (2016) · Nature · doi:10.1038/nature21001 · Cited by 2,762 · see citing works
Azizi Samir, M. A. S., Alloin, F., & Dufresne, A. (2005) · Biomacromolecules · doi:10.1021/bm0493685 · Cited by 2,311 · see citing works
Controlled Ring-Opening Polymerization of Lactide and Glycolide
Dechy-Cabaret, O., Martin-Vaca, B., & Bourissou, D. (2004) · Chemical Reviews · doi:10.1021/cr040002s · Cited by 2,257 · see citing works
Biodegradable Polymers for the Environment
Gross, R. A., & Kalra, B. (2002) · Science · doi:10.1126/science.297.5582.803 · Cited by 1,983 · see citing works
Tokiwa, Y., Calabia, B. P., Ugwu, C. U., & Aiba, S. (2009) · International Journal of Molecular Sciences · doi:10.3390/ijms10093722 · Cited by 1,782 · see citing works
Conversion of Biomass into Chemicals over Metal Catalysts
Besson, M., Gallezot, P., & Pinel, C. (2014) · Chemical Reviews · doi:10.1021/cr4002269 · Cited by 1,780 · see citing works
Green and sustainable manufacture of chemicals from biomass: state of the art
Sheldon, R. A. (2013) · Green Chemistry · doi:10.1039/c3gc41935e · Cited by 1,685 · see citing works
Synthesis of polycaprolactone: A review
Labet, M., & Thielemans, W. (2009) · Chemical Society Reviews · doi:10.1039/b820162p · Cited by 1,673 · see citing works
From Glycerol to Value‐Added Products
Pagliaro, M., Ciriminna, R., Kimura, H., Rossi, M., & Pina, C. D. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200604694 · Cited by 1,653 · see citing works
Darensbourg, D. J. (2007) · Chemical Reviews · doi:10.1021/cr068363q · Cited by 1,593 · see citing works
Recent Developments in Ring Opening Polymerization of Lactones for Biomedical Applications
Albertsson, A.-C., & Varma, I. K. (2003) · Biomacromolecules · doi:10.1021/bm034247a · Cited by 1,582 · see citing works
Trends in bioconversion of lignocellulose: Biofuels, platform chemicals & biorefinery concept
Menon, V., & Rao, M. (2012) · Progress in Energy and Combustion Science · doi:10.1016/j.pecs.2012.02.002 · Cited by 1,562 · see citing works
Simple Chemical Transformation of Lignocellulosic Biomass into Furans for Fuels and Chemicals
Binder, J. B., & Raines, R. T. (2009) · Journal of the American Chemical Society · doi:10.1021/ja808537j · Cited by 1,491 · see citing works
Organocatalytic Ring-Opening Polymerization
Kamber, N. E., Jeong, W., Waymouth, R. M., Pratt, R. C., Lohmeijer, B. G. G., & Hedrick, J. L. (2007) · Chemical Reviews · doi:10.1021/cr068415b · Cited by 1,489 · see citing works
Self-citationPlant oil renewable resources as green alternatives in polymer science
Meier, M. A. R., Metzger, J. O., & Schubert, U. S. (2007) · Chemical Society Reviews · doi:10.1039/b703294c · Cited by 1,487 · see citing works
Polymer biodegradation: Mechanisms and estimation techniques – A review
Lucas, N., Bienaime, C., Belloy, C., Queneudec, M., Silvestre, F., & Nava-Saucedo, J.-E. (2008) · Chemosphere · doi:10.1016/j.chemosphere.2008.06.064 · Cited by 1,384 · see citing works
Shaikh, A.-A. G., & Sivaram, S. (1996) · Chemical Reviews · doi:10.1021/cr950067i · Cited by 1,381 · see citing works
Anastas, P. T., & Warner, J. C. (2000) · doi:10.1093/oso/9780198506980.001.0001 · Cited by 1,356 · see citing works
Transesterification of vegetable oils: a review
Schuchardt, U. F., Sercheli, R., & Vargas, R. M. (1998) · Journal of the Brazilian Chemical Society · doi:10.1590/s0103-50531998000300002 · Cited by 1,346 · see citing works
Furfural—A Promising Platform for Lignocellulosic Biofuels
Lange, J., van der Heide, E., van Buijtenen, J., & Price, R. (2012) · ChemSusChem · doi:10.1002/cssc.201100648 · Cited by 1,323 · see citing works
A microbial polyhydroxyalkanoates (PHA) based bio- and materials industry
Chen, G. (2009) · Chemical Society Reviews · doi:10.1039/b812677c · Cited by 1,302 · see citing works
Peer Reviewed: Design Through the 12 Principles of Green Engineering
Anastas, P. T., & Zimmerman, J. B. (2003) · Environmental Science & Technology · doi:10.1021/es032373g · Cited by 1,273 · see citing works
Ethylene glycol: properties, synthesis, and applications
Yue, H., Zhao, Y., Ma, X., & Gong, J. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15359a · Cited by 1,180 · see citing works
Coates, G. W., & Moore, D. R. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200460442 · Cited by 1,154 · see citing works
Metabolic engineering of Escherichia coli for direct production of 1,4-butanediol
Yim, H. H., Haselbeck, R. J., Niu, W., Pujol-Baxley, C., Burgard, A. P., Boldt, J., Khandurina, J., Trawick, J. D., Osterhout, R. E., Stephen, R., et al. (2011) · Nature Chemical Biology · doi:10.1038/nchembio.580 · Cited by 1,119 · see citing works
The synthesis of organic carbonates from carbon dioxide
Sakakura, T., & Kohno, K. (2009) · Chemical Communications · doi:10.1039/b819997c · Cited by 1,067 · see citing works
Low-pressure hydrogenolysis of glycerol to propylene glycol
Dasari, M. A., Kiatsimkul, P.-P., Sutterlin, W. R., & Suppes, G. J. (2005) · Applied Catalysis A General · doi:10.1016/j.apcata.2004.11.033 · Cited by 1,014 · see citing works
50th Anniversary Perspective : There Is a Great Future in Sustainable Polymers
Schneiderman, D. K., & Hillmyer, M. A. (2017) · Macromolecules · doi:10.1021/acs.macromol.7b00293 · Cited by 1,005 · see citing works
Plastics derived from biological sources: present and future: a technical and environmental review
Chen, G.-Q., & Patel, M. K. (2012) · Chemical Reviews · doi:10.1021/cr200162d · Cited by 997 · see citing works
TRACI 2.0: the tool for the reduction and assessment of chemical and other environmental impacts 2.0
Bare, J. (2011) · Clean Technologies and Environmental Policy · doi:10.1007/s10098-010-0338-9 · Cited by 988 · see citing works
Diversity of bacterial polyhydroxyalkanoic acids
Steinbüchel, A., & Valentin, H. E. (1995) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1995.tb07528.x · Cited by 981 · see citing works
Polymers from Renewable Resources: A Perspective for a Special Issue of Polymer Reviews
Williams, C. K., & Hillmyer, M. A. (2008) · Journal of macromolecular science. Part C, Reviews in macromolecular chemistry and physics/Journal of macromolecular science. Reviews in macromolecular chemistry and physics · doi:10.1080/15583720701834133 · Cited by 979 · see citing works
Biodegradable and compostable alternatives to conventional plastics
Song, J. H., Murphy, R. J., Narayan, R., & Davies, G. B. H. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0289 · Cited by 971 · see citing works
Organocatalysis: Opportunities and Challenges for Polymer Synthesis
Kiesewetter, M. K., Shin, E. J., Hedrick, J. L., & Waymouth, R. M. (2010) · Macromolecules · doi:10.1021/ma9025948 · Cited by 907 · see citing works
Self-citationBacterial polymers: biosynthesis, modifications and applications
Rehm, B. H. A. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2354 · Cited by 899 · see citing works
Stereocontrolled ring-opening polymerisation of lactide
Stanford, M. J., & Dove, A. P. (2009) · Chemical Society Reviews · doi:10.1039/b815104k · Cited by 878 · see citing works
Chemically recyclable polymers: a circular economy approach to sustainability
Hong, M., & Chen, E. Y.-X. (2017) · Green Chemistry · doi:10.1039/c7gc01496a · Cited by 876 · see citing works
Vegetable oil-based polymeric materials: synthesis, properties, and applications
Xia, Y., & Larock, R. C. (2010) · Green Chemistry · doi:10.1039/c0gc00264j · Cited by 864 · see citing works
Lactic acid as a platform chemical in the biobased economy: the role of chemocatalysis
Dusselier, M., Wouwe, P. V., Dewaele, A., Makshina, E. V., & Sels, B. F. (2013) · Energy & Environmental Science · doi:10.1039/c3ee00069a · Cited by 827 · see citing works
From Multisite Polymerization Catalysis to Sustainable Materials and All-Polyolefin Composites
Stürzel, M., Mihan, S., & Mülhaupt, R. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00310 · Cited by 822 · see citing works
Catalysts for CO <sub>2</sub> /epoxide copolymerisation
Kember, M. R., Buchard, A., & Williams, C. K. (2011) · Chem. Commun. · doi:10.1039/c0cc02207a · Cited by 797 · see citing works
Bacterial Polyesters: Biosynthesis, Biodegradable Plastics and Biotechnology
Lenz, R. W., & Marchessault, R. H. (2005) · Biomacromolecules · doi:10.1021/bm049700c · Cited by 780 · see citing works
Bacterial synthesis of biodegradable polyhydroxyalkanoates
Verlinden, R. A. J., Hill, D. J., Kenward, M. A., Williams, C. D., & Radecka, I. (2007) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03335.x · Cited by 775 · see citing works
Alternative Monomers Based on Lignocellulose and Their Use for Polymer Production
Delidovich, I., Hausoul, P. J. C., Deng, L., Pfützenreuter, R., Rose, M., & Palkovits, R. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00354 · Cited by 773 · see citing works
Progress of Polymers from Renewable Resources: Furans, Vegetable Oils, and Polysaccharides
Gandini, A., Lacerda, T. M., Carvalho, A. J. F., & Trovatti, E. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00264 · Cited by 755 · see citing works
Recycling of Polymers: A Review
Ignatyev, I. A., Thielemans, W., & Vander Beke, B. (2014) · ChemSusChem · doi:10.1002/cssc.201300898 · Cited by 753 · see citing works
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review
Fenouillot, F., Rousseau, A., Colomines, G., Saint-Loup, R., & Pascault, J.-P. (2010) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2009.10.001 · Cited by 752 · see citing works
Li, S. M., Garreau, H., & Vert, M. (1990) · Journal of Materials Science: Materials in Medicine · doi:10.1007/bf00700871 · Cited by 733 · see citing works
Handbook on life cycle assessment — operational guide to the ISO standards
Guinée, J. B. (2001) · The International Journal of Life Cycle Assessment · doi:10.1007/bf02978784 · Cited by 715 · see citing works
Ovitt, T. M., & Coates, G. W. (2002) · Journal of the American Chemical Society · doi:10.1021/ja012052+ · Cited by 713 · see citing works
Recent advances in CO2/epoxide copolymerization—New strategies and cooperative mechanisms
Klaus, S., Lehenmeier, M. W., Anderson, C. E., & Rieger, B. (2010) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2010.12.002 · Cited by 709 · see citing works
Hong, M., & Chen, E. Y.-X. (2016) · Nature Chemistry · doi:10.1038/nchem.2391 · Cited by 677 · see citing works
Replacing fossil based PET with biobased PEF; process analysis, energy and GHG balance
Eerhart, A. J. J. E., Faaij, A. P. C., & Patel, M. K. (2012) · Energy & Environmental Science · doi:10.1039/c2ee02480b · Cited by 666 · see citing works
Chemical Recycling of Poly(ethylene terephthalate)
Paszun, D., & Spychaj, T. (1997) · Industrial & Engineering Chemistry Research · doi:10.1021/ie960563c · Cited by 661 · see citing works
CO2 Copolymers from Epoxides: Catalyst Activity, Product Selectivity, and Stereochemistry Control
Lu, X., Ren, W., & Wu, G. (2012) · Accounts of Chemical Research · doi:10.1021/ar300035z · Cited by 654 · see citing works
Spassky, N., Wisniewski, M., Pluta, C., & Le Borgne, A. (1996) · Macromolecular Chemistry and Physics · doi:10.1002/macp.1996.021970902 · Cited by 627 · see citing works
From monomers to polymers from renewable resources: Recent advances
Gandini, A., & Lacerda, T. M. (2015) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2014.11.002 · Cited by 621 · see citing works
Thermal decomposition of biodegradable polyesters—II. Poly(lactic acid)
Kopinke, F.-D., Remmler, M., Mackenzie, K., Möder, M., & Wachsen, O. (1996) · Polymer Degradation and Stability · doi:10.1016/0141-3910(96)00102-4 · Cited by 614 · see citing works
Longo, J. M., Sanford, M. J., & Coates, G. W. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00553 · Cited by 596 · see citing works
Ring-opening copolymerization (ROCOP): synthesis and properties of polyesters and polycarbonates
Paul, S., Zhu, Y., Romain, C., Brooks, R., Saini, P. K., & Williams, C. K. (2015) · Chemical Communications · doi:10.1039/c4cc10113h · Cited by 593 · see citing works
Recent advances in the synthesis of aliphatic polyesters by ring-opening polymerization☆
JEROME, C., & LECOMTE, P. (2008) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2008.02.008 · Cited by 590 · see citing works
Organic Catalysis for Ring-Opening Polymerization
Dove, A. P. (2012) · ACS Macro Letters · doi:10.1021/mz3005956 · Cited by 545 · see citing works
Handbook of Ring‐Opening Polymerization
(2009) · doi:10.1002/9783527628407 · Cited by 544 · see citing works
Ethyl lactate as a solvent: Properties, applications and production processes – a review
Pereira, C. S. M., Silva, V. M. T. M., & Rodrigues, A. E. (2011) · Green Chemistry · doi:10.1039/c1gc15523g · Cited by 544 · see citing works
Sustainability assessments of bio-based polymers
Hottle, T. A., Bilec, M. M., & Landis, A. E. (2013) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2013.06.016 · Cited by 537 · see citing works
Marine microplastics spell big problems for future generations
Galloway, T. S., & Lewis, C. N. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1600715113 · Cited by 534 · see citing works
The quest for sustainable polyesters – insights into the future
Vilela, C., Sousa, A. F., Fonseca, A. C., Serra, A. C., Coelho, J. F. J., Freire, C. S. R., & Silvestre, A. J. D. (2014) · Polym. Chem. · doi:10.1039/c3py01213a · Cited by 527 · see citing works
Cohen, C. T., Chu, T., & Coates, G. W. (2005) · Journal of the American Chemical Society · doi:10.1021/ja051744l · Cited by 524 · see citing works
Doi, Y., Kanesawa, Y., Kunioka, M., & Saito, T. (1990) · Macromolecules · doi:10.1021/ma00203a006 · Cited by 515 · see citing works
Open-loop recycling: A LCA case study of PET bottle-to-fibre recycling
Shen, L., Worrell, E., & Patel, M. K. (2010) · Resources, Conservation and Recycling · doi:10.1016/j.resconrec.2010.06.014 · Cited by 514 · see citing works
Controlled and Stereoselective Polymerization of Lactide: Kinetics, Selectivity, and Microstructures
Zhong, Z., Dijkstra, P. J., & Feijén, J. (2003) · Journal of the American Chemical Society · doi:10.1021/ja0347585 · Cited by 503 · see citing works
Aliphatic cyclic carbonates and spiroorthocarbonates as monomers
Rokicki, G. (2000) · Progress in Polymer Science · doi:10.1016/s0079-6700(00)00006-x · Cited by 499 · see citing works
Metal-catalyzed immortal ring-opening polymerization of lactones, lactides and cyclic carbonates
Ajellal, N., Carpentier, J.-F., Guillaume, C., Guillaume, S. M., Helou, M., Poirier, V., Sarazin, Y., & Trifonov, A. (2010) · Dalton Transactions · doi:10.1039/c001226b · Cited by 494 · see citing works
Biotechnological production of itaconic acid and its biosynthesis in Aspergillus terreus
Okabe, M., Lies, D., Kanamasa, S., & Park, E. Y. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2132-3 · Cited by 488 · see citing works
Microbial production of 1,3-propanediol: Recent developments and emerging opportunities
Saxena, R. K., Anand, P., Saran, S., & Isar, J. (2009) · Biotechnology Advances · doi:10.1016/j.biotechadv.2009.07.003 · Cited by 486 · see citing works
Controlled Polymerization of Next-Generation Renewable Monomers and Beyond
Yao, K., & Tang, C. (2013) · Macromolecules · doi:10.1021/ma3019574 · Cited by 485 · see citing works
Poirier, Y., Nawrath, C., & Somerville, C. (1995) · Nature Biotechnology · doi:10.1038/nbt0295-142 · Cited by 480 · see citing works
Nomura, N., Ishii, R., Akakura, M., & Aoi, K. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0175789 · Cited by 478 · see citing works
Buntara, T., Noel, S., Phua, P. H., Melián‐Cabrera, I., de Vries, J. G., & Heeres, H. J. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201102156 · Cited by 477 · see citing works
Stereoselective Epoxide Polymerization and Copolymerization
Childers, M. I., Longo, J. M., Van Zee, N. J., LaPointe, A. M., & Coates, G. W. (2014) · Chemical Reviews · doi:10.1021/cr400725x · Cited by 471 · see citing works
Papageorgiou, G. Z., Papageorgiou, D. G., Terzopoulou, Z. N., & Bikiaris, D. Ν. (2016) · European Polymer Journal · doi:10.1016/j.eurpolymj.2016.08.004 · Cited by 459 · see citing works
Strengths and weaknesses of common sustainability indices for multidimensional systems
Mayer, A. L. (2008) · Environment International · doi:10.1016/j.envint.2007.09.004 · Cited by 456 · see citing works
Life cycle assessments of biodegradable, commercial biopolymers—A critical review
Yates, M. R., & Barlow, C. Y. (2013) · Resources Conservation and Recycling · doi:10.1016/j.resconrec.2013.06.010 · Cited by 444 · see citing works
Catalytic synthesis of α-methylene-γ-valerolactone: a biomass-derived acrylic monomer
Manzer, L. E. (2004) · Applied Catalysis A General · doi:10.1016/j.apcata.2004.05.048 · Cited by 441 · see citing works
Oxidation of 5-hydroxymethylfurfural over supported Pt, Pd and Au catalysts
Davis, S. E., Houk, L. R., Tamargo, E., Datye, A. K., & Davis, R. J. (2010) · Catalysis Today · doi:10.1016/j.cattod.2010.06.004 · Cited by 434 · see citing works
Carbon dioxide utilization via carbonate-promoted C–H carboxylation
Banerjee, A., Dick, G. R., Yoshino, T., & Kanan, M. W. (2016) · Nature · doi:10.1038/nature17185 · Cited by 431 · see citing works
Alternating Copolymerization of Limonene Oxide and Carbon Dioxide
Byrne, C. M., Allen, S. D., Lobkovsky, E. B., & Coates, G. W. (2004) · Journal of the American Chemical Society · doi:10.1021/ja0472580 · Cited by 428 · see citing works
Synthesis of biodegradable polymers from renewable resources
Tschan, M. J. ‐., Brûlé, E., Haquette, P., & Thomas, C. M. (2011) · Polymer Chemistry · doi:10.1039/c2py00452f · Cited by 426 · see citing works
Biodegradability of polylactide bottles in real and simulated composting conditions
Kale, G., Auras, R., Singh, S. P., & Narayan, R. (2007) · Polymer Testing · doi:10.1016/j.polymertesting.2007.07.006 · Cited by 421 · see citing works
Present and future development in plastics from biomass
Shen, L., Worrell, E., & Patel, M. K. (2009) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.189 · Cited by 418 · see citing works
Sustainability Metrics: Life Cycle Assessment and Green Design in Polymers
Tabone, M. D., Cregg, J., Beckman, E. J., & Landis, A. E. (2010) · Environmental Science & Technology · doi:10.1021/es101640n · Cited by 416 · see citing works
Nomura, N., Ishii, R., Yamamoto, Y., & Kondo, T. (2007) · Chemistry - A European Journal · doi:10.1002/chem.200601308 · Cited by 410 · see citing works
McNeill, I. C., & Leiper, H. A. (1985) · Polymer Degradation and Stability · doi:10.1016/0141-3910(85)90035-7 · Cited by 404 · see citing works
Manabe, K., Iimura, S., Sun, X.-M., & Kobayashi, S. (2002) · Journal of the American Chemical Society · doi:10.1021/ja026241j · Cited by 401 · see citing works
Single site catalysts for stereoselective ring-opening polymerization of lactides
Dijkstra, P. J., Du, H., & Feijén, J. (2010) · Polymer Chemistry · doi:10.1039/c0py00204f · Cited by 401 · see citing works
Stempfle, F., Ortmann, P., & Mecking, S. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00705 · Cited by 397 · see citing works
A Review of the Environmental Impacts of Biobased Materials
Weiss, M., Haufe, J., Carus, M., Brandão, M., Bringezu, S., Hermann, B. G., & Patel, M. K. (2012) · Journal of Industrial Ecology · doi:10.1111/j.1530-9290.2012.00468.x · Cited by 396 · see citing works
Challenges in the catalytic synthesis of cyclic and polymeric carbonates from epoxides and CO2
Pescarmona, P. P., & Taherimehr, M. (2012) · Catalysis Science & Technology · doi:10.1039/c2cy20365k · Cited by 392 · see citing works
Industrial ecology: concepts and approaches.
Jelinski, L. W., Graedel, T. E., Laudise, R. A., McCall, D. W., & Patel, C. K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.3.793 · Cited by 389 · see citing works
Nakano, K., Kamada, T., & Nozaki, K. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200603132 · Cited by 389 · see citing works
Sustainable Polymers: Opportunities for the Next Decade
Miller, S. A. (2013) · ACS Macro Letters · doi:10.1021/mz400207g · Cited by 385 · see citing works
Research core and framework of sustainability science
Kajikawa, Y. (2008) · Sustainability Science · doi:10.1007/s11625-008-0053-1 · Cited by 384 · see citing works
Shape-selective zeolite catalysis for bioplastics production
Dusselier, M., Van Wouwe, P., Dewaele, A., Jacobs, P. A., & Sels, B. F. (2015) · Science · doi:10.1126/science.aaa7169 · Cited by 376 · see citing works
A Theoretical Model of Erosion and Macromolecular Drug Release from Biodegrading Microspheres
Batycky, R. P., Hanes, J., Langer, R., & Edwards, D. A. (1997) · Journal of Pharmaceutical Sciences · doi:10.1021/js9604117 · Cited by 374 · see citing works
Update and challenges in organo-mediated polymerization reactions
Ottou, W. N., Sardón, H., Mecerreyes, D., Vignolle, J., & Taton, D. (2015) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2015.12.001 · Cited by 370 · see citing works
Biodegradation of poly(lactic acid) and its nanocomposites
Fukushima, K., Abbate, C., Tabuani, D., Gennari, M., & Camino, G. (2009) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2009.07.001 · Cited by 368 · see citing works
Erosion kinetics of hydrolytically degradable polymers.
Tamada, J. A., & Langer, R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.2.552 · Cited by 356 · see citing works
Tempelaar, S., Mespouille, L., Coulembier, O., Dubois, P., & Dove, A. P. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35268k · Cited by 345 · see citing works
Circular economy design considerations for research and process development in the chemical sciences
Clark, J. H., Farmer, T. J., Herrero‐Davila, L., & Sherwood, J. R. (2016) · Green Chemistry · doi:10.1039/c6gc00501b · Cited by 345 · see citing works
Carothers, W. H. (1929) · Journal of the American Chemical Society · doi:10.1021/ja01383a041 · Cited by 344 · see citing works
Furandicarboxylic Acid (FDCA), A Versatile Building Block for a Very Interesting Class of Polyesters
de Jong, E., Dam, M. A., Sipos, L., & Gruter, G.-J. M. (2012) · ACS Symposium Series · doi:10.1021/bk-2012-1105.ch001 · Cited by 344 · see citing works
Chemistry and Technology of Biodegradable Polymers
(1994) · Springer eBooks · doi:10.1007/978-94-011-1330-4 · Cited by 343 · see citing works
Brannigan, R. P., & Dove, A. P. (2016) · Biomaterials Science · doi:10.1039/c6bm00584e · Cited by 340 · see citing works
Zhu, J., Cai, J., Xie, W., Chen, P.-H., Gazzano, M., Scandola, M., & Gross, R. A. (2013) · Macromolecules · doi:10.1021/ma3023298 · Cited by 333 · see citing works
A Highly Active and Recyclable Catalytic System for CO2/Propylene Oxide Copolymerization
Sujith, S., Min, J. K., Seong, J. E., Na, S. J., & Lee, B. Y. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200801852 · Cited by 330 · see citing works
What's new with CO2? Recent advances in its copolymerization with oxiranes
Darensbourg, D. J., & Poland, S. J. (2012) · Green Chemistry · doi:10.1039/c2gc35928f · Cited by 318 · see citing works
Noh, E. K., Na, S. J., Sujith, S., Kim, S., & Lee, B. Y. (2007) · Journal of the American Chemical Society · doi:10.1021/ja071290n · Cited by 315 · see citing works
Plastics recycling and waste management in the US
Subramanian, P. M. (2000) · Resources Conservation and Recycling · doi:10.1016/s0921-3449(99)00049-x · Cited by 313 · see citing works
Science and Technology for Sustainable Well-Being
Holdren, J. P. (2008) · Science · doi:10.1126/science.1153386 · Cited by 303 · see citing works
Discrete Cationic Complexes for Ring-Opening Polymerization Catalysis of Cyclic Esters and Epoxides
Sarazin, Y., & Carpentier, J. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00033 · Cited by 301 · see citing works
Development of a commercial scale process for production of 1,4-butanediol from sugar
Burgard, A. P., Burk, M. J., Osterhout, R. E., Dien, S. V., & Yim, H. H. (2016) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2016.04.016 · Cited by 297 · see citing works
Sauer, A., Kapelski, A., Fliedel, C., Dagorne, S., Kol, M., & Okuda, J. (2013) · Dalton Transactions · doi:10.1039/c3dt00010a · Cited by 294 · see citing works
Water soluble polyhydroxyalkanoates: future materials for therapeutic applications
Li, Z., & Loh, X. J. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00089k · Cited by 291 · see citing works
Aliphatic Polyester Block Polymer Design
Schneiderman, D. K., & Hillmyer, M. A. (2016) · Macromolecules · doi:10.1021/acs.macromol.6b00211 · Cited by 290 · see citing works
Hydrogen-bonding organocatalysts for ring-opening polymerization
Thomas, C., & Bibal, B. (2013) · Green Chemistry · doi:10.1039/c3gc41806e · Cited by 278 · see citing works
Urea Anions: Simple, Fast, and Selective Catalysts for Ring-Opening Polymerizations
Lin, B., & Waymouth, R. M. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.6b11864 · Cited by 278 · see citing works
Self-citationMicrobial succinic acid production: Natural versus metabolic engineered producers
Beauprez, J. J., Mey, M. D., & Soetaert, W. (2010) · Process Biochemistry · doi:10.1016/j.procbio.2010.03.035 · Cited by 277 · see citing works
Biodegradation of polylactide in aerobic and anaerobic thermophilic conditions
Itävaara, M., Karjomaa, S., & Selin, J.-F. (2002) · Chemosphere · doi:10.1016/s0045-6535(01)00163-1 · Cited by 269 · see citing works
Llevot, A., Dannecker, P., von Czapiewski, M., Over, L. C., Söyler, Z., & Meier, M. A. R. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201602068 · Cited by 266 · see citing works
Metabolic Engineering of Candida Tropicalis for the Production of Long–Chain Dicarboxylic Acids
Picataggio, S. K., Rohrer, T., Deanda, K., Lanning, D., Reynolds, R., Mielenz, J. R., & Eirich, L. D. (1992) · Nature Biotechnology · doi:10.1038/nbt0892-894 · Cited by 265 · see citing works
Wang, X., Thevenon, A., Brosmer, J. L., Yu, I., Khan, S. I., Mehrkhodavandi, P., & Diaconescu, P. L. (2014) · Journal of the American Chemical Society · doi:10.1021/ja505883u · Cited by 263 · see citing works
Aerobic and anaerobic biodegradability of polymer films and physico-chemical characterization
Massardier-Nageotte, V., Pestre, C., Cruard-Pradet, T., & Bayard, R. (2006) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2005.02.029 · Cited by 263 · see citing works
Tsuji, H., & Suzuyoshi, K. (2002) · Polymer Degradation and Stability · doi:10.1016/s0141-3910(01)00240-3 · Cited by 260 · see citing works
Environmental biodegradation of synthetic polymers II. Biodegradation of different polymer groups
Eubeler, J. P., Bernhard, M., & Knepper, T. P. (2010) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2009.09.005 · Cited by 259 · see citing works
Hong, M., & Chen, E. Y. ‐. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201601092 · Cited by 259 · see citing works
Jeske, R. C., Rowley, J. M., & Coates, G. W. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200801415 · Cited by 258 · see citing works
Chemoselective Polymerizations from Mixtures of Epoxide, Lactone, Anhydride, and Carbon Dioxide
Romain, C., Zhu, Y., Dingwall, P., Paul, S., Rzepa, H. S., Buchard, A., & Williams, C. K. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b13070 · Cited by 258 · see citing works
Zwitterionic Ring-Opening Polymerization for the Synthesis of High Molecular Weight Cyclic Polymers
Brown, H. A., & Waymouth, R. M. (2013) · Accounts of Chemical Research · doi:10.1021/ar400072z · Cited by 255 · see citing works
Self-citationGuillaume, S. M., Kirillov, E., Sarazin, Y., & Carpentier, J. (2015) · Chemistry – A European Journal · doi:10.1002/chem.201500613 · Cited by 251 · see citing works
Thermodynamic Presynthetic Considerations for Ring-Opening Polymerization
Olsén, P., Odelius, K., & Albertsson, A.-C. (2016) · Biomacromolecules · doi:10.1021/acs.biomac.5b01698 · Cited by 244 · see citing works
Poly(3-hydroxyalkanoate)s: Diversification and biomedical applications
Hazer, D. B., Kılıçay, E., & Hazer, B. (2012) · Materials Science and Engineering C · doi:10.1016/j.msec.2012.01.021 · Cited by 242 · see citing works
Haywood, G. W., Anderson, A. J., & DAWES, E. A. (1989) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1989.tb03210.x · Cited by 242 · see citing works
Life cycle assessment and green chemistry: the yin and yang of industrial ecology
Anastas, P. T., & Lankey, R. L. (2000) · Green Chemistry · doi:10.1039/b005650m · Cited by 242 · see citing works
Potential Synergies and Challenges in Refining Cellulosic Biomass to Fuels, Chemicals, and Power
Wyman, C. E. (2003) · Biotechnology Progress · doi:10.1021/bp025654l · Cited by 239 · see citing works
Chemoselective Polymerization Control: From Mixed‐Monomer Feedstock to Copolymers
Romain, C., & Williams, C. K. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201309575 · Cited by 238 · see citing works
How well can renewable resources mimic commodity monomers and polymers?
Mathers, R. T. (2011) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.24939 · Cited by 238 · see citing works
Kinetics and Time−Temperature Equivalence of Polymer Degradation
Lyu, Schley, J., Loy, B., Lind, D., Hobot, C., Sparer, R., & Untereker, D. (2007) · Biomacromolecules · doi:10.1021/bm070313n · Cited by 237 · see citing works
Grassie, N., Murray, E. J., & Holmes, P. A. (1984) · Polymer Degradation and Stability · doi:10.1016/0141-3910(84)90016-8 · Cited by 235 · see citing works
Material Recycling - Trends and Perspectives
(2012) · doi:10.5772/2003 · Cited by 235 · see citing works
Enzyme-catalysis breathes new life into polyester condensation polymerizations
Gross, R. A., Ganesh, M., & Lu, W. (2010) · Trends in Biotechnology · doi:10.1016/j.tibtech.2010.05.004 · Cited by 233 · see citing works
Tsuji, H., & Suzuyoshi, K. (2002) · Polymer Degradation and Stability · doi:10.1016/s0141-3910(01)00239-7 · Cited by 232 · see citing works
Biotechnological production of succinic acid: current state and perspectives
Cheng, K., Zhao, X., Zeng, J. H., & Zhang, J. (2012) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.1327 · Cited by 229 · see citing works
Bakewell, C., Cao, T.-P.-A., Long, N., Le Goff, X. F., Auffrant, A., & Williams, C. K. (2012) · Journal of the American Chemical Society · doi:10.1021/ja310003v · Cited by 226 · see citing works
Controlled Cationic Polymerization of Lactide
Bourissou, D., Martin-Vaca, B., Dumitrescu, A., Graullier, M., & Lacombe, F. (2005) · Macromolecules · doi:10.1021/ma051646k · Cited by 226 · see citing works
Structure–properties relationship of fatty acid-based thermoplastics as synthetic polymer mimics
Maisonneuve, L., Lebarbé, T., Grau, E., & Cramail, H. (2013) · Polymer Chemistry · doi:10.1039/c3py00791j · Cited by 220 · see citing works
Noordover, B. A. J., van Staalduinen, V. G., Duchateau, R., Koning, C. E., van Benthem, Mak, M., Heise, A., Frissen, A. E., & van Haveren, J. (2006) · Biomacromolecules · doi:10.1021/bm060713v · Cited by 219 · see citing works
Algae as a source of renewable chemicals: opportunities and challenges
Foley, P. M., Beach, E. S., & Zimmerman, J. B. (2011) · Green Chemistry · doi:10.1039/c1gc00015b · Cited by 219 · see citing works
Stereoselective Polymerization of rac-Lactide Using a Monoethylaluminum Schiff Base Complex
Tang, Z., Chen, X., Pang, X., Yang, Y., Zhang, X., & Jing, X. (2004) · Biomacromolecules · doi:10.1021/bm034467o · Cited by 215 · see citing works
Self-citationMcNeill, I. C., & Leiper, H. A. (1985) · Polymer Degradation and Stability · doi:10.1016/0141-3910(85)90050-3 · Cited by 215 · see citing works
Manabe, K., Sun, X.-M., & Kobayashi, S. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016338q · Cited by 215 · see citing works
Environmental biodegradation of synthetic polymers I. Test methodologies and procedures
Eubeler, J. P., Zok, S., Bernhard, M., & Knepper, T. P. (2009) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2009.06.007 · Cited by 214 · see citing works
Ree, M., Bae, J. Y., Jung, J. H., & Shin, T. J. (1999) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/(sici)1099-0518(19990615)37:12 · Cited by 213 · see citing works
Sanders, D. P., Fukushima, K., Coady, D. J., Nelson, A., Fujiwara, M., Yasumoto, M., & Hedrick, J. L. (2010) · Journal of the American Chemical Society · doi:10.1021/ja105332k · Cited by 213 · see citing works
Chemically Recyclable Biobased Polyurethanes
Schneiderman, D. K., Vanderlaan, M. E., Mannion, A. M., Panthani, T. R., Batiste, D. C., Wang, J. Z., Bates, F. S., Macosko, C. W., & Hillmyer, M. A. (2016) · ACS Macro Letters · doi:10.1021/acsmacrolett.6b00193 · Cited by 213 · see citing works
Lopes, A. M. D. C., & Bogel‐Łukasik, R. (2015) · ChemSusChem · doi:10.1002/cssc.201402950 · Cited by 208 · see citing works
Basel, Y., & Häßner, A. (2000) · The Journal of Organic Chemistry · doi:10.1021/jo000257f · Cited by 205 · see citing works
A review: Conversion of bioglycerol into 1,3-propanediol via biological and chemical method
Lee, C. S., Aroua, M. K., Daud, W. M. A. W., Cognet, P., Pérès, Y., Fabre, P., Reynes, O., & Latapie, L. (2014) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2014.10.033 · Cited by 204 · see citing works
Renewable polycarbonates and polyesters from 1,4-cyclohexadiene
Winkler, M., Romain, C., Meier, M. A. R., & Williams, C. K. (2014) · Green Chemistry · doi:10.1039/c4gc01353k · Cited by 204 · see citing works
Stempfle, F., Quinzler, D., Heckler, I., & Mecking, S. (2011) · Macromolecules · doi:10.1021/ma200627e · Cited by 203 · see citing works
Scalable production of mechanically tunable block polymers from sugar
Xiong, M., Schneiderman, D. K., Bates, F. S., Hillmyer, M. A., & Zhang, K. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404596111 · Cited by 203 · see citing works
Catalysts for CO <sub>2</sub> /epoxide ring-opening copolymerization
Trott, G., Saini, P. K., & Williams, C. K. (2016) · Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences · doi:10.1098/rsta.2015.0085 · Cited by 201 · see citing works
Recent Advances in Catalytic Conversion of Glycerol
Zhou, C. H., Zhao, H., Tong, D. S., Wu, L. M., & Yu, W. H. (2013) · Catalysis Reviews · doi:10.1080/01614940.2013.816610 · Cited by 200 · see citing works
Cellulose‐Based Sustainable Polymers: State of the Art and Future Trends
Rose, M., & Palkovits, R. (2011) · Macromolecular Rapid Communications · doi:10.1002/marc.201100230 · Cited by 198 · see citing works
Mishra, D. K., Lee, H. J., Kim, J., Lee, H.-S., Cho, J. K., Suh, Y.-W., Yi, Y., & Kim, Y. J. (2017) · Green Chemistry · doi:10.1039/c7gc00027h · Cited by 198 · see citing works
Green polycarbonates prepared by the copolymerization of CO<sub>2</sub> with epoxides
Taherimehr, M., & Pescarmona, P. P. (2014) · Journal of Applied Polymer Science · doi:10.1002/app.41141 · Cited by 194 · see citing works
Acid- and base-catalyzed hydrolyses of aliphatic polycarbonates and polyesters
Jung, J. H., Ree, M., & Kim, H. (2006) · Catalysis Today · doi:10.1016/j.cattod.2006.02.060 · Cited by 194 · see citing works
Standardization and certification in the area of environmentally degradable plastics
Kržan, A., Hemjinda, S., Miertuš, S., Corti, A., & Chiellini, E. (2006) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2006.04.034 · Cited by 194 · see citing works
Carpentier, J. (2010) · Macromolecular Rapid Communications · doi:10.1002/marc.201000114 · Cited by 192 · see citing works
Nakano, K., Nakamura, M. J., & Nozaki, K. (2009) · Macromolecules · doi:10.1021/ma9012626 · Cited by 190 · see citing works
Cherubini, F., & Strømman, A. H. (2011) · Biofuels, Bioproducts and Biorefining · doi:10.1002/bbb.297 · Cited by 186 · see citing works
Directions for environmentally biodegradable polymer research
Swift, G. (1993) · Accounts of Chemical Research · doi:10.1021/ar00027a005 · Cited by 185 · see citing works
DEPOLYMERIZATION OF POLY-β-HYDROXYBUTYRATE BY AN INTRACELLULAR ENZYME SYSTEM
Merrick, J. M., & Doudoroff, M. (1964) · Journal of Bacteriology · doi:10.1128/jb.88.1.60-71.1964 · Cited by 185 · see citing works
Kinetics of the hydrolytic degradation of poly(lactic acid)
Codari, F., Lazzari, S., Soos, M., Storti, G., Morbidelli, M., & Moscatelli, D. (2012) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2012.06.026 · Cited by 184 · see citing works
Zinc-Catalyzed Highly Isoselective Ring Opening Polymerization of rac -Lactide
Abbina, S., & Du, G. (2014) · ACS Macro Letters · doi:10.1021/mz5002959 · Cited by 184 · see citing works
Chemicals from biomass: technological <i>versus</i> environmental feasibility. A review
Fiorentino, G., Ripa, M., & Ulgiati, S. (2017) · Biofuels, Bioproducts and Biorefining · doi:10.1002/bbb.1729 · Cited by 184 · see citing works
Carpentier, J. (2015) · Organometallics · doi:10.1021/acs.organomet.5b00540 · Cited by 183 · see citing works
Fatty Acid Derived Monomers and Related Polymers Via Thiol‐ene (Click) Additions
Türünç, O., & Meier, M. A. R. (2010) · Macromolecular Rapid Communications · doi:10.1002/marc.201000291 · Cited by 182 · see citing works
Solvothermal Alcoholysis Routes for Recycling Polylactide Waste as Lactic Acid Esters
Petrus, R., Bykowski, D., & Sobota, P. (2016) · ACS Catalysis · doi:10.1021/acscatal.6b01009 · Cited by 181 · see citing works
Flagged first, then by citations
5 of the 475 references couldn’t be matched to a known paper.
Research works printed but not linked: 17
- Francis R., 2017, Recycling of Polymers: Methods, Characterization and Applications
- Valuing Plastic: The Business Case for Measuring, Managing and Disclosing Plastic Use in the Consumer Goods Industry, 2014, United Nations Environment Programme (UNEP).http://hdl.handle.net/20.500.11822/9238(accessed August 5, 2017).
- Kaenzig, J.; H, G.; Rocher, M.Proceedings of the 2nd World Conference and Technology Exhibition on Biomass For Energy, Industry and Climate Change, Rome, Italy, 2004.
- 10.1039/c3py01213a · DOI · Paper page
- Werpy T., 2004, Top Value Added Chemicals from Biomass. Vol. I - Results of Screening for Potential Candidates from Sugars and Synthesis Gas
- Kassaian J.-M., 2002, Ullmann’s Encyclopedia of Industrial Chemistry
- Sivasankaran C., 2016, J. Env. Biol., 37, 1539
- 2008, Biodiesel from Triglycerides via Transesterification
- 10.1039/b922014c · DOI · Paper page
- Wang L. S., 2005, Chin. Chem. Lett., 16, 572
- 10.1002/macp.201200332 · DOI · Paper page
- 10.1039/c5py01843a · DOI
- 10.1021/ma200685u · DOI · Paper page
- Dove A. P., 2009, Handbook of Ring-Opening Polymerization
- Data from Noone A., Collected PET bottles, Proceedings of 13th International Polyester Recycling Forum, 2008.
- Genta, M.; Yano, F.; Kondo, Y.; Matsubara, W.; Oomoto, S.Technical Review;Mitsubishi Heavy Industries, Ltd., 2003, Vol.40, pp1–4.
- 10.1073/pnas.1404596111 · DOI · Paper page
Cited by
Sorted by citations
Bright Side of Lignin Depolymerization: Toward New Platform Chemicals
Sun, Z., Fridrich, B., Santi, A. D., Elangovan, S., & Barta, K. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00588 · Cited by 2,200 · see citing works
Chemical recycling to monomer for an ideal, circular polymer economy
Coates, G. W., & Getzler, Y. D. Y. L. (2020) · Nature Reviews Materials · doi:10.1038/s41578-020-0190-4 · Cited by 1,644 · see citing works
Chemical and biological catalysis for plastics recycling and upcycling
Ellis, L. D., Rorrer, N. A., Sullivan, K. P., Otto, M., McGeehan, J. E., Román‐Leshkov, Y., Wierckx, N. J. P., & Beckham, G. T. (2021) · Nature Catalysis · doi:10.1038/s41929-021-00648-4 · Cited by 1,228 · see citing works
Bio-based polymers with performance-advantaged properties
Cywar, R. M., Rorrer, N. A., Hoyt, C. B., Beckham, G. T., & Chen, E. Y.-X. (2021) · Nature Reviews Materials · doi:10.1038/s41578-021-00363-3 · Cited by 811 · see citing works
Closed-loop recycling of polyethylene-like materials
Häußler, M., Eck, M., Rothauer, D., & Mecking, S. (2021) · Nature · doi:10.1038/s41586-020-03149-9 · Cited by 753 · see citing works
Advances in the use of CO 2 as a renewable feedstock for the synthesis of polymers
Grignard, B., Gennen, S., Jérôme, C., Kleij, A. W., & Detrembleur, C. (2019) · Chemical Society Reviews · doi:10.1039/c9cs00047j · Cited by 727 · see citing works
A synthetic polymer system with repeatable chemical recyclability
Zhu, J.-B., Watson, E. M., Tang, J., & Chen, E. Y.-X. (2018) · Science · doi:10.1126/science.aar5498 · Cited by 709 · see citing works
Dogu, O., Pelucchi, M., de Vijver, R. V., Steenberge, P. H. M. V., D’hooge, D., Cuoci, A., Mehl, M., Frassoldati, A., Faravelli, T., & Geem, K. M. V. (2021) · Progress in Energy and Combustion Science · doi:10.1016/j.pecs.2020.100901 · Cited by 708 · see citing works
Closed-loop recycling of plastics enabled by dynamic covalent diketoenamine bonds
Christensen, P. R., Scheuermann, A. M., Loeffler, K. E., & Helms, B. A. (2019) · Nature Chemistry · doi:10.1038/s41557-019-0249-2 · Cited by 676 · see citing works
A unified view on catalytic conversion of biomass and waste plastics
Lee, K., Jing, Y., Wang, Y., & Yan, N. (2022) · Nature Reviews Chemistry · doi:10.1038/s41570-022-00411-8 · Cited by 602 · see citing works
Approaches to Sustainable and Continually Recyclable Cross-Linked Polymers
Fortman, D. J., Brutman, J. P., De Hoe, G. X., Snyder, R. L., Dichtel, W. R., & Hillmyer, M. A. (2018) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.8b02355 · Cited by 559 · see citing works
Sustainable Fiber‐Reinforced Composites: A Review
Maiti, S., Islam, M. R., Uddin, M. A., Afroj, S., Eichhorn, S. J., & Karim, N. (2022) · Advanced Sustainable Systems · doi:10.1002/adsu.202200258 · Cited by 525 · see citing works
Plastics recycling with a difference
Sardón, H., & Dove, A. P. (2018) · Science · doi:10.1126/science.aat4997 · Cited by 516 · see citing works
Designing a circular carbon and plastics economy for a sustainable future
Vidal, F., van der Marel, E. R., Kerr, R. W. F., McElroy, C. A., Schroeder, N., Mitchell, C., Rosetto, G., Chen, T. T. D., Bailey, R. M., Hepburn, C. J., et al. (2024) · Nature · doi:10.1038/s41586-023-06939-z · Cited by 509 · see citing works
Bio-based and biodegradable polymers - State-of-the-art, challenges and emerging trends
Saranya, R., Shaiju, P., O’Connor, K. E., & Babu, R. P. (2019) · Current Opinion in Green and Sustainable Chemistry · doi:10.1016/j.cogsc.2019.12.005 · Cited by 489 · see citing works
Reducing environmental plastic pollution by designing polymer materials for managed end-of-life
Law, K. L., & Narayan, R. (2021) · Nature Reviews Materials · doi:10.1038/s41578-021-00382-0 · Cited by 488 · see citing works
Seawater‐Degradable Polymers—Fighting the Marine Plastic Pollution
Wang, G., Huang, D., Ji, J., Völker, C., & Wurm, F. R. (2020) · Advanced Science · doi:10.1002/advs.202001121 · Cited by 444 · see citing works
Payne, J., & Jones, M. D. (2021) · ChemSusChem · doi:10.1002/cssc.202100400 · Cited by 428 · see citing works
Recyclable and (Bio)degradable Polyesters in a Circular Plastics Economy
Shi, C., Quinn, E. C., Diment, W. T., & Chen, E. Y. ‐. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00848 · Cited by 418 · see citing works
Jing, Y., Wang, Y., Furukawa, S., Xia, J., Sun, C., Hülsey, M. J., Wang, H., Guo, Y. Q., Liu, X., & Yan, N. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202011063 · Cited by 402 · see citing works
Continuous Flow Upgrading of Selected C2–C6 Platform Chemicals Derived from Biomass
Gérardy, R., Debecker, D. P., Estager, J., Luis, P., & Monbaliu, J. M. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.9b00846 · Cited by 397 · see citing works
Toward Infinitely Recyclable Plastics Derived from Renewable Cyclic Esters
Tang, X., & Chen, E. Y. ‐. (2018) · Chem · doi:10.1016/j.chempr.2018.10.011 · Cited by 389 · see citing works
A circular economy approach to plastic waste
Payne, J., McKeown, P., & Jones, M. D. (2019) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2019.05.014 · Cited by 385 · see citing works
Mohanty, A. K., Wu, F., Mincheva, R., Hakkarainen, M., Raquez, J., Mielewski, D. F., Narayan, R., Netravali, A. N., & Misra, M. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00124-8 · Cited by 383 · see citing works
Catalytic methods for chemical recycling or upcycling of commercial polymers
Kosloski-Oh, S. C., Wood, Z. A., Manjarrez, Y., Rios, J. P. D. L., & Fieser, M. E. (2020) · Materials Horizons · doi:10.1039/d0mh01286f · Cited by 377 · see citing works
Westhues, S., Idel, J., & Klankermayer, J. (2018) · Science Advances · doi:10.1126/sciadv.aat9669 · Cited by 348 · see citing works
Sustainability of bioplastics: Opportunities and challenges
Thakur, S., Chaudhary, J., Sharma, B., Verma, A., Tamulevicius, S., & Thakur, V. K. (2018) · Current Opinion in Green and Sustainable Chemistry · doi:10.1016/j.cogsc.2018.04.013 · Cited by 345 · see citing works
Zhang, Q., Deng, Y., Shi, C., Feringa, B. L., Tian, H., & Qu, D. (2021) · Matter · doi:10.1016/j.matt.2021.01.014 · Cited by 327 · see citing works
Organocatalysis for depolymerisation
Jehanno, C., Pérez‐Madrigal, M. M., Demarteau, J., Sardón, H., & Dove, A. P. (2018) · Polymer Chemistry · doi:10.1039/c8py01284a · Cited by 325 · see citing works
Deacy, A. C., Kilpatrick, A. F. R., Regoutz, A., & Williams, C. K. (2020) · Nature Chemistry · doi:10.1038/s41557-020-0450-3 · Cited by 325 · see citing works
Polymerization of Polar Monomers Mediated by Main-Group Lewis Acid–Base Pairs
Hong, M., Chen, J., & Chen, E. Y. ‐. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00352 · Cited by 322 · see citing works
Zhi, M., Yang, X., Fan, R., Yue, S., Zheng, L., Liu, Q., & He, Y. (2022) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2022.109976 · Cited by 317 · see citing works
Yuan, J., Xiong, W. H., Zhou, X., Zhang, Y., Shi, D., Li, Z., & Lu, H. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b00031 · Cited by 316 · see citing works
Tripathi, N., Misra, M., & Mohanty, A. K. (2021) · ACS Engineering Au · doi:10.1021/acsengineeringau.1c00011 · Cited by 314 · see citing works
Upcycling to Sustainably Reuse Plastics
Zhao, X. Y., Boruah, B., Chin, K. F., Đokić, M., Modak, J. M., & Soo, H. S. (2021) · Advanced Materials · doi:10.1002/adma.202100843 · Cited by 309 · see citing works
Designing Biobased Recyclable Polymers for Plastics
Hatti‐Kaul, R., Nilsson, L. J., Zhang, B., Rehnberg, N., & Lundmark, S. (2019) · Trends in biotechnology · doi:10.1016/j.tibtech.2019.04.011 · Cited by 298 · see citing works
Iglesias, J., Martínez-Salazar, I., Maireles-Torres, P., Martin Alonso, D., Mariscal, R., & López Granados, M. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00177e · Cited by 292 · see citing works
100th Anniversary of Macromolecular Science Viewpoint: Redefining Sustainable Polymers
Fagnani, D. E., Tami, J. L., Copley, G., Clemons, M. N., Getzler, Y. D. Y. L., & McNeil, A. J. (2020) · ACS Macro Letters · doi:10.1021/acsmacrolett.0c00789 · Cited by 279 · see citing works
Jehanno, C., Flores, I., Dove, A. P., Müller, A. J., Ruipérez, F., & Sardón, H. (2018) · Green Chemistry · doi:10.1039/c7gc03396f · Cited by 276 · see citing works
Roadmap to Biodegradable Plastics—Current State and Research Needs
Ghosh, K., & Jones, B. H. (2021) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.1c00801 · Cited by 264 · see citing works
Recent Trends in Catalytic Polymerizations
Walsh, D. J., Hyatt, M. G., Miller, S. A., & Guironnet, D. (2019) · ACS Catalysis · doi:10.1021/acscatal.9b03226 · Cited by 258 · see citing works
Future Directions for Sustainable Polymers
Hong, M., & Chen, E. Y. ‐. (2019) · Trends in Chemistry · doi:10.1016/j.trechm.2019.03.004 · Cited by 250 · see citing works
Bioadhesive Technology Platforms
Wu, S. J., & Zhao, X. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00380 · Cited by 228 · see citing works
Krystosik, A., Njoroge, G., Odhiambo, L. A., Forsyth, J. E., Mutuku, F. M., & LaBeaud, A. D. (2020) · Frontiers in Public Health · doi:10.3389/fpubh.2019.00405 · Cited by 226 · see citing works
Bulk network polymers with dynamic B–O bonds: healable and reprocessable materials
Bapat, A. P., Sumerlin, B. S., & Sutti, A. (2019) · Materials Horizons · doi:10.1039/c9mh01223k · Cited by 225 · see citing works
Design principles for intrinsically circular polymers with tunable properties
Shi, C., Reilly, L. T., Phani Kumar, V. S., Coile, M. W., Nicholson, S. R., Broadbelt, L. J., Beckham, G. T., & Chen, E. Y.-X. (2021) · Chem · doi:10.1016/j.chempr.2021.10.004 · Cited by 219 · see citing works
Afewerki, S., Wang, X., Ruiz‐Esparza, G. U., Tai, C., Kong, X., Zhou, S., Welch, K., Huang, P. J., Bengtsson, R., Xu, C., et al. (2020) · ACS Nano · doi:10.1021/acsnano.0c06346 · Cited by 216 · see citing works
Yadav, N., Seidi, F., Crespy, D., & D’Elia, V. (2018) · ChemSusChem · doi:10.1002/cssc.201802770 · Cited by 215 · see citing works
Yu, Q., Weng, Z., Kou, Y., Song, L., Li, J., Wang, J., Zhang, S., Liu, C., & Jian, X. (2020) · Chemical Engineering Journal · doi:10.1016/j.cej.2020.126881 · Cited by 215 · see citing works
Chemically recyclable polymer materials: polymerization and depolymerization cycles
Xu, G., & Wang, Q. (2022) · Green Chemistry · doi:10.1039/d1gc03901f · Cited by 214 · see citing works
Xiong, W. H., Chang, W.-Y., Shi, D., Yang, L., Tian, Z., Wang, H., Zhang, Z., Zhou, X., Chen, E., & Lu, H. (2020) · Chem · doi:10.1016/j.chempr.2020.06.003 · Cited by 213 · see citing works
From terpenes to sustainable and functional polymers
Monica, F. D., & Kleij, A. W. (2020) · Polymer Chemistry · doi:10.1039/d0py00817f · Cited by 212 · see citing works
Wan, J., Zhao, J., Zhang, X., Fan, H., Zhang, J., Hu, D., Jin, P., & Wang, D. (2020) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2020.101287 · Cited by 210 · see citing works
Self-citationToward Green Atom Transfer Radical Polymerization: Current Status and Future Challenges
Dworakowska, S., Lorandi, F., Gorczyński, A., & Matyjaszewski, K. A. (2022) · Advanced Science · doi:10.1002/advs.202106076 · Cited by 210 · see citing works
High-performance pan-tactic polythioesters with intrinsic crystallinity and chemical recyclability
Shi, C., McGraw, M. L., Li, Z., Cavallo, L., Falivene, L., & Chen, E. Y. ‐. (2020) · Science Advances · doi:10.1126/sciadv.abc0495 · Cited by 208 · see citing works
Sustainable developments in polyolefin chemistry: Progress, challenges, and outlook
Wang, X., Gao, Y., & Tang, Y. J. (2023) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2023.101713 · Cited by 207 · see citing works
Catalytic Approaches to Monomers for Polymers Based on Renewables
Stadler, B. M., Wulf, C., Werner, T., Tin, S., & de Vries, J. G. (2019) · ACS Catalysis · doi:10.1021/acscatal.9b01665 · Cited by 205 · see citing works
Recent developments in recycling of polystyrene based plastics
Thakur, S., Verma, A., Sharma, B., Chaudhary, J., Tamulevičius, S., & Thakur, V. K. (2018) · Current Opinion in Green and Sustainable Chemistry · doi:10.1016/j.cogsc.2018.03.011 · Cited by 203 · see citing works
Synthesis and Deconstruction of Polyethylene-type Materials
Schwab, S. T., Baur, M., Nelson, T. F., & Mecking, S. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00587 · Cited by 203 · see citing works
Innovations to decarbonize materials industries
Daehn, K., Basuhi, R., Gregory, J. R., Berlinger, M., Somjit, V., & Olivetti, E. (2021) · Nature Reviews Materials · doi:10.1038/s41578-021-00376-y · Cited by 197 · see citing works
Chen, Z., Wang, Y., Cheng, Y., Wang, X., Tong, S., Yang, H., & Wang, Z. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.136138 · Cited by 194 · see citing works
Multifunctional Catalysts for Ring-Opening Copolymerizations
Lidston, C. A. L., Severson, S. M., Abel, B. A., & Coates, G. W. (2022) · ACS Catalysis · doi:10.1021/acscatal.2c02524 · Cited by 193 · see citing works
Nasrollahzadeh, M., Shafiei, N., Nezafat, Z., Bidgoli, N. S. S., & Soleimani, F. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.116353 · Cited by 190 · see citing works
Biobased High-Performance Aromatic–Aliphatic Polyesters with Complete Recyclability
Tu, Y., Wang, X., Yang, X., Fan, H., Gong, F.-L., Cai, Z., & Zhu, J. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c10162 · Cited by 187 · see citing works
Yuan, P., Sun, Y., Xu, X., Luo, Y., & Hong, M. (2021) · Nature Chemistry · doi:10.1038/s41557-021-00817-9 · Cited by 183 · see citing works
Zhou, Y., Li, J., Wang, T., Wu, Y., & Luo, Z. (2022) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2022.101555 · Cited by 172 · see citing works
A circular polyester platform based on simple gem-disubstituted valerolactones
Li, X., Clarke, R. W., Jiang, J., Xu, T., & Chen, E. Y. ‐. (2022) · Nature Chemistry · doi:10.1038/s41557-022-01077-x · Cited by 172 · see citing works
Biomass-derived chemical substitutes for bisphenol A: recent advancements in catalytic synthesis
Liguori, F., Moreno‐Marrodán, C., & Barbaro, P. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00179a · Cited by 171 · see citing works
ZnO nanodispersion as pseudohomogeneous catalyst for alcoholysis of polyethylene terephthalate
Du, J.-T., Sun, Q., Zeng, X., Wang, D., Wang, J., & Chen, J. (2020) · Chemical Engineering Science · doi:10.1016/j.ces.2020.115642 · Cited by 169 · see citing works
Li, M., Tao, Y., Tang, J., Wang, Y., Zhang, X., Tao, Y., & Wang, X. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b09739 · Cited by 167 · see citing works
Self-citationPoly(lactic acid) Degradation into Methyl Lactate Catalyzed by a Well-Defined Zn(II) Complex
Román‐Ramírez, L. A., McKeown, P., Jones, M. D., & Wood, J. (2018) · ACS Catalysis · doi:10.1021/acscatal.8b04863 · Cited by 164 · see citing works
Yang, G., Xu, C., Xie, R. J., Zhang, Y., Zhu, X.-F., & Wu, G. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.0c12425 · Cited by 163 · see citing works
Sajwan, D., Sharma, A., Sharma, M., & Krishnan, V. (2024) · ACS Catalysis · doi:10.1021/acscatal.4c00290 · Cited by 162 · see citing works
Shi, C., Li, Z.-C., Caporaso, L., Cavallo, L., Falivene, L., & Chen, E. Y. ‐. (2021) · Chem · doi:10.1016/j.chempr.2021.02.003 · Cited by 160 · see citing works
Tschan, M. J. ‐., Gauvin, R. M., & Thomas, C. M. (2021) · Chemical Society Reviews · doi:10.1039/d1cs00356a · Cited by 157 · see citing works
Cui, W. Q., Li, J., Sun, Y., Wang, H., Jiang, G., Lee, S., & Dong, F. (2018) · Applied Catalysis B: Environmental · doi:10.1016/j.apcatb.2018.06.071 · Cited by 154 · see citing works
O’Dea, R. M., Willie, J. A., & Epps, T. H. I. (2020) · ACS Macro Letters · doi:10.1021/acsmacrolett.0c00024 · Cited by 153 · see citing works
Zhu, J., & Chen, E. Y. ‐. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201808003 · Cited by 151 · see citing works
Chen, Z., Duan, R., Xiao, Y., Wei, Y., Zhang, H., Sun, X., Wang, S., Cheng, Y., Wang, X., Tong, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34908-z · Cited by 148 · see citing works
Shi, C., Clarke, R. W., McGraw, M. L., & Chen, E. Y. ‐. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.1c12278 · Cited by 147 · see citing works
Sustaining the Transition from a Petrobased to a Biobased Chemical Industry with Flow Chemistry
Gérardy, R., Morodo, R., Estager, J., Luis, P., Debecker, D. P., & Monbaliu, J. M. (2018) · Topics in Current Chemistry · doi:10.1007/s41061-018-0222-3 · Cited by 146 · see citing works
Li, C., Wang, L., Qin, Y. F., Liu, F., Shen, Y., & Li, Z. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202201407 · Cited by 143 · see citing works
Yang, R., Xu, G., Dong, B., Guo, X., & Wang, Q. (2022) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.2c01708 · Cited by 136 · see citing works
Zhang, C., Wu, H., Li, Y., Yang, J., & Zhang, X. (2018) · Nature Communications · doi:10.1038/s41467-018-04554-5 · Cited by 135 · see citing works
Self-citationOpportunities for organocatalysis in polymer synthesis via step-growth methods
Bossion, A., Heifferon, K. V., Meabe, L., Zivic, N., Taton, D., Hedrick, J. L., Long, T. E., & Sardón, H. (2018) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2018.11.003 · Cited by 134 · see citing works
Catalytic depolymerization of polyester plastics toward closed-loop recycling and upcycling
Weng, Y., Hong, C., Zhang, Y., & Liu, H. (2023) · Green Chemistry · doi:10.1039/d3gc04174c · Cited by 133 · see citing works
Degradation of plastic wastes to commercial chemicals and monomers under visible light
Meng, J., Zhou, Y., Li, D., & Jiang, X. (2023) · 中国科学通报:英文版 · doi:10.1016/j.scib.2023.06.024 · Cited by 132 · see citing works
Bobbink, F. D., van Muyden, A. P., & Dyson, P. J. (2018) · Chemical Communications · doi:10.1039/c8cc07907b · Cited by 131 · see citing works
Chemical aspects of polymer recycling
Chanda, M. (2021) · Advanced Industrial and Engineering Polymer Research · doi:10.1016/j.aiepr.2021.06.002 · Cited by 131 · see citing works
Phosphazene Bases as Organocatalysts for Ring‐Opening Polymerization of Cyclic Esters
Liu, S., Ren, C., Zhao, N., Shen, Y., & Li, Z. (2018) · Macromolecular Rapid Communications · doi:10.1002/marc.201800485 · Cited by 128 · see citing works
A brief overview of renewable plastics
Chen, X., & Yan, N. (2019) · Materials Today Sustainability · doi:10.1016/j.mtsust.2019.100031 · Cited by 128 · see citing works
Bio‐based and Degradable Block Polyester Pressure‐Sensitive Adhesives
Chen, T. T. D., Carrodeguas, L. P., Sulley, G. S., Gregory, G. L., & Williams, C. K. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202006807 · Cited by 127 · see citing works
H 2 ‐free Plastic Conversion: Converting PET back to BTX by Unlocking Hidden Hydrogen
Lu, S., Jing, Y., Feng, B., Guo, Y. Q., Liu, X., & Wang, Y. (2021) · ChemSusChem · doi:10.1002/cssc.202100196 · Cited by 127 · see citing works
Zhang, Y., Liu, Z., Xu, Y., Li, J., Shi, S. Q., Li, J., & Gao, Q. (2021) · Chemical Engineering Journal · doi:10.1016/j.cej.2021.130852 · Cited by 126 · see citing works
Liu, S., Bai, T., Ni, K., Chen, Y., Zhao, J., Ling, J., Ye, X., & Zhang, G. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201908904 · Cited by 125 · see citing works
Ring-Opening Polymerization of Lactones to Prepare Closed-Loop Recyclable Polyesters
Li, Z., Shen, Y., & Li, Z. (2024) · Macromolecules · doi:10.1021/acs.macromol.3c01912 · Cited by 123 · see citing works
Easy access to oxygenated block polymers via switchable catalysis
Stößer, T., Sulley, G. S., Gregory, G. L., & Williams, C. K. (2019) · Nature Communications · doi:10.1038/s41467-019-10481-w · Cited by 118 · see citing works
Gregory, G. L., Sulley, G. S., Carrodeguas, L. P., Chen, T. T. D., Santmartí, A., Terrill, N. J., Lee, K., & Williams, C. K. (2020) · Chemical Science · doi:10.1039/d0sc00463d · Cited by 118 · see citing works
Alkyl borane-mediated metal-free ring-opening (co)polymerizations of oxygenated monomers
Zhang, C., Geng, X., Zhang, X., Gnanou, Y., & Feng, X. (2022) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2022.101644 · Cited by 117 · see citing works
Self-citationGao, J., Zhu, D., Zhang, W., Solan, G. A., Ma, Y., & Sun, W. (2019) · Inorganic Chemistry Frontiers · doi:10.1039/c9qi00855a · Cited by 116 · see citing works
- Authors
- Zhang, X., Fevre, M., Jones, G. O., & Waymouth, R. M.
- Affiliations
- Stanford University (US)
- IBM Research−Almaden, 650 Harry Road, San Jose, California 95120, United States
- IBM Research - Almaden (US)
- Corresponding author
- Waymouth, Robert M.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2017-10-19
- Volume
- 118
- Issue
- 2
- Pages
- 839-885
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2765471533
- Semantic Scholar
- cee5814ab26e29aa779b2c3b6eaac0d596cea68a
- Cited by
- 936
- References
- 475
- Citations by year
- 2026: 63 · 2025: 106 · 2024: 116 · 2023: 131 · 2022: 141 · 2021: 127 · 2020: 118 · 2019: 77 · 2018: 55 · 2017: 1
- FWCI
- 4.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.osti.gov
- Locations
- Chemical Reviews (publishedVersion)
- PubMed (publishedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- Division of Chemistry (CHE-1607092)
- LAM Foundation
- Stanford University
- U.S. Department of Energy (DE-SC0005430)
- Topics
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Chemical Engineering › Process Chemistry and Technology › Carbon dioxide utilization in catalysis
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer crystallization and properties
- Keywords
- sustainable polymers, catalysis, renewable raw materials, aliphatic polyesters, polycarbonate, renewable monomers, biodegradable polymers, polymer synthesis, biocatalysis
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