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Polyester-Based (Bio)degradable Polymers as Environmentally Friendly Materials for Sustainable Development
Open accessAbstract
This review focuses on the polyesters such as polylactide and polyhydroxyalkonoates, as well as polyamides produced from renewable resources, which are currently among the most promising (bio)degradable polymers. Synthetic pathways, favourable properties and utilisation (most important applications) of these attractive polymer families are outlined. Environmental impact and in particular (bio)degradation of aliphatic polyesters, polyamides and related copolymer structures are described in view of the potential applications in various fields.
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![Figure 1 Alkaline-catalysed hydrolysis of polyesters, originally published in [9].](/paper-figures/b1a75b7e6009469487639b619326a402/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-1.jpg)
![Figure 2 Acid-catalysed hydrolysis of polyesters, originally published in [9].](/paper-figures/f3575083005644c5874dcf89c9bcfd0f/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-2.jpg)
![Figure 3 Scheme of general mechanism of enzymatic catalysed hydrolytic polymer degradation, originally published in [14].](/paper-figures/c9d3ab3e323e45119da5897a120a9b79/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-3.jpg)
![Figure 4 Strategies used to enhance the sustainability of polyhydroxyalkanoates (PHA) production processes, originally published in [21] under CC BY 3.0 license.](/paper-figures/7b3b1c4f373848e6bb2194df5fc9102a/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-4.jpg)
![Figure 5 Preparation of block copolymers PHA-block-aPHB from low-molar mass macroinitiators, originally published in [61].](/paper-figures/dec8249be5574af795b682d171e45df0/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-5.jpg)
![Figure 6 Zoe B Beach Toys, Compostable Shopping Bag, based on Metabolix, Inc. [67].](/paper-figures/bbb2f755f61f47978559fb54163259fc/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-6.jpg)
![Figure 7 Polylactide market size in 2013 by application [154].](/paper-figures/fc2164b8cbd74988b9c0c86e63caf443/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-7.jpg)
![Figure 8 Establishment of hydrogen bonds between Nylon-56 molecular chains, (a) scheme of the unfavourable hydrogen-bond geometry between odd diamide units of Nylon-56 molecular chains with an all trans conformation and (b) scheme of the establishment of hydrogen bonds along two directions when consecutive amide planes of a molecular chain slightly rotate in opposite directions from the plane defined by the methylene carbon atoms (nitrogen, blue; oxygen, red; carbon, gray; hydrogen, brown), originally published in [180].](/paper-figures/126393a1787b4dd788ae1dcab9bcfdaf/polyester-based-bio-degradable-polymers-as-environmentally-friendly-materials-figure-8.jpg)
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“Additionally, PLLA and its enantiomer PDLA can form a stereocomplex (sc-PLA).”
From Correlative characterization of stereocomplex formation in blends of aliphatic polyester P(PCL m - b -PLLA n ) multiblock-copolymers and PDLA (2026) · cites this paper as [8]
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“sc-PLA formation is driven by nucleation through CH 3 •••O=C hydrogen bonding and/or van der Waals forces between L-lactide and D-lactide unit sequences.8”
From Correlative characterization of stereocomplex formation in blends of aliphatic polyester P(PCL m - b -PLLA n ) multiblock-copolymers and PDLA (2026) · cites this paper as [8]
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In the citing paper
“The structure-phase and structure-property relations in multiblock copolymers (MBCs) of PLA are not fully understood, compared to homopolymers, copolymers and DCs, though studies on other MBCs suggest similarities as well as peculiarities of MBCs compared to diblock copolymers.8,17,21”
From Correlative characterization of stereocomplex formation in blends of aliphatic polyester P(PCL m - b -PLLA n ) multiblock-copolymers and PDLA (2026) · cites this paper as [8]
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Metadata
- Authors
- Rydz, J., Sikorska, W., Kyulavska, M., & Christova, D.
- Affiliations
- Bulgarian Academy of Sciences (BG)
- Centre of Polymer and Carbon Materials (PL)
- Corresponding author
- Rydz, Joanna
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2014-12-29
- Volume
- 16
- Issue
- 1
- Pages
- 564-596
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC4307263
- OpenAlex
- W2055520654
- Cited by
- 303
- References
- 185
- Citations by year
- 2026: 17 · 2025: 31 · 2024: 23 · 2023: 35 · 2022: 36 · 2021: 28 · 2020: 23 · 2019: 39 · 2018: 32 · 2017: 28 · 2016: 4 · 2015: 7
- FWCI
- 0.89
- Type
- journal article
- Language
- en
- Open access
- gold
- dx.doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- European Commission (316086)
- European Regional Development Fund (POIG.01.03.01-00-018/08)
- Topics
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer crystallization and properties
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer composites and self-healing
- Keywords
- polylactic acid, polyhydroxyalkanoates, polyamide, aliphatic polyesters, polymer synthesis, biodegradation, environmental impact of polymers, sustainable materials, polymer applications
- MeSH terms
- Bacteria, Biodegradation, Environmental, Environmental Pollutants, Fungi, Hydrolysis, Models, Molecular, Nylons, Polyesters
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