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Cited by 390

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 access
Snyder, Rachel L., Fortman, David J., De Hoe, Guilhem X., Hillmyer, Marc A., Dichtel, William R.·2018·Macromolecules

Abstract

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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Crossref · 10.1021/acs.macromol.7b02299

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Metadata

Authors
Snyder, R. L., Fortman, D. J., De Hoe, G. X., Hillmyer, M. A., & Dichtel, W. R.
Venue
Macromolecules
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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