Covalent Adaptable Networks: Reprocessable Cross-Linked PolymersClick to copy article linkArticle link copied!
- Molly SunMolly SunDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by Molly Sun
- Lillian M. FelsenthalLillian M. FelsenthalDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by Lillian M. Felsenthal
- Subeen KimSubeen KimDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by Subeen Kim
- Elizabeth Y. ChoiElizabeth Y. ChoiDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by Elizabeth Y. Choi
- Laura J. ReedLaura J. ReedDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by Laura J. Reed
- Benjamin R. EllingBenjamin R. EllingDepartment of Chemistry, Wesleyan University, 52 Lawn Avenue, Middletown, Connecticut 06459, United StatesMore by Benjamin R. Elling
- William R. Dichtel*William R. Dichtel*William R. Dichtel. Email: wdichtel@northwestern.eduDepartment of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United StatesMore by William R. Dichtel
Abstract
Thermoset polymers have desirable properties, such as excellent thermal and mechanical stability, but their covalent cross-links typically prevent repair or recycling. By enabling and controlling dynamic exchange reactions within polymer networks, their covalent bonds rearrange and allow the polymer to be reshaped. These viscoelastic polymer networks, now known as covalent adaptable networks (CANs), are an important frontier for improving plastic circularity, as well as for designing valuable stimuli-responsive materials. This Review describes the history of CANs, dating back to the early days of polymer science, and the evolution of their classification and nomenclature. A comprehensive survey of dynamic reactions and linkage chemistries is provided, as well as methods to characterize and reprocess CANs. Beyond straightforward reprocessing, many advanced applications of CANs and their composites are now emerging. Finally, we provide perspective on how the development of new chemistries, strategies to control stimuli-responsive bond exchange and mechanical properties, and a deep understanding of exchange reactions will advance this field toward scalable, sustainable, and high-value materials.
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