Recyclable Polymethacrylate Networks Containing Dynamic Dialkylamino Disulfide Linkages and Exhibiting Full Property Recovery
Reprocessable polymer networks with dynamic covalent bonds exhibit thermoplastic-like properties at elevated processing temperatures while maintaining thermoset responses under service conditions, offering a sustainable solution to the recycling of conventional, permanently cross-linked polymers. Mo...
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Published in | Macromolecules Vol. 53; no. 19; pp. 8367 - 8373 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
13.10.2020
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Online Access | Get full text |
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Summary: | Reprocessable polymer networks with dynamic covalent bonds exhibit thermoplastic-like properties at elevated processing temperatures while maintaining thermoset responses under service conditions, offering a sustainable solution to the recycling of conventional, permanently cross-linked polymers. Most studies on reprocessable networks that report full cross-link density recovery after recycling have focused on step-growth polymer networks; no study has previously reported full cross-link density recovery of reprocessable networks prepared directly from only monomers via addition polymerization. Here, we report the utilization of dialkylamino disulfide chemistry as a fast, robust dynamic chemistry in the synthesis of reprocessable networks from monomers and/or polymers with carbon–carbon double bonds that are amenable to free-radical polymerization. In particular, we have employed a simple one-step method to design a bifunctional bis(dialkylamino) disulfide cross-linker. With this dynamic cross-linker, we synthesized a catalyst-free, reprocessable polymethacrylate network that exhibits full property recovery (within error) associated with cross-link density after multiple reprocessing steps. This achievement could allow for the facile development of chemically recyclable versions of common, commercially important addition-type polymer networks. |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/acs.macromol.0c01539 |