The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Reprocessable Acid-Degradable Polycarbonate Vitrimers
Open accessAbstract
Abstract Vitrimers are cross-linked polymer networks containing linkages that undergo thermally activated, associative exchange reactions, such that the cross-link density and overall network connectivity are preserved. Polycarbonates are industrially relevant polymers that, to our knowledge, have not yet been explored as vitrimers. We developed hydroxyl-functionalized polycarbonate networks that undergo transcarbonation exchange reactions at elevated temperatures in the presence of catalytic Ti(IV) alkoxides. The rate of transcarbonation within the networks, estimated through stress relaxation experiments, was tuned by adjusting the catalyst loading or hydroxyl group concentration in the networks. The polymer networks exhibit recovery of their tensile strength and plateau storage modulus (71–133%) after reprocessing. In addition to being reprocessable, the networks were hydrolyzed and decarboxylated in aqueous acid to recover 80 wt % of the precursor to the bifunctional cyclic carbonate monomer. These observations demonstrate that PC vitrimers are a novel class of strong, repairable polymers with more facile end-of-life degradation compared to other vitrimers and conventional thermosets. These characteristics, along with the high likelihood of deriving their monomers from bio-based sources, make PC vitrimers outstanding candidates for sustainable manufacture and use.
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Cites
Silica-Like Malleable Materials from Permanent Organic Networks
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High-performance vitrimers from commodity thermoplastics through dioxaborolane metathesis
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Mechanically Activated, Catalyst-Free Polyhydroxyurethane Vitrimers
Fortman, D. J., Brutman, J. P., Cramer, C. J., Hillmyer, M. A., & Dichtel, W. R. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b08084 · Cited by 811
Self-citationAlternating Copolymerization of Limonene Oxide and Carbon Dioxide
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Renewable, Degradable, and Chemically Recyclable Cross-Linked Elastomers
Brutman, J. P., De Hoe, G. X., Schneiderman, D. K., Le, T. N., & Hillmyer, M. A. (2016) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.6b02931 · Cited by 92
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Wang, S., & Urban, M. W. (2020) · Nature Reviews Materials · doi:10.1038/s41578-020-0202-4 · Cited by 1,374
Scheutz, G. M., Lessard, J. J., Sims, M. B., & Sumerlin, B. S. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b07922 · Cited by 934
Dynamic covalent chemistry in polymer networks: a mechanistic perspective
Winne, J. M., Leibler, L., & Du Prez, F. E. (2019) · Polymer Chemistry · doi:10.1039/c9py01260e · Cited by 736
Vitrimers: Permanently crosslinked polymers with dynamic network topology
Van Zee, N. J., & Nicolaÿ, R. (2020) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2020.101233 · Cited by 734
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
Metadata
- Authors
- Snyder, R. L., Fortman, D. J., De Hoe, G. X., Hillmyer, M. A., & Dichtel, W. R.
- Venue
- Macromolecules
- Publisher
- American Chemical Society (ACS)
- Published
- 2018-01-04
- Volume
- 51
- Issue
- 2
- Pages
- 389-397
- ISSN
- 0024-9297 (ISSN-L)
- 1520-5835
- OpenAlex
- W2781765098
- Cited by
- 390
- References
- 7
- FWCI
- 19.58
- Type
- journal article
- Language
- en
- Open access
- hybrid
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