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Repulsive segregation of fluoroalkyl side chains turns a cohesive polymer into a mechanically tough, ultrafast self-healable, nonsticky elastomer

Dynamic crosslinking of flexible polymer chains via attractive and reversible interactions is widely employed to obtain autonomously self-healable elastomers. However, this design leads to a trade-off relationship between the strength and self-healing speed of the material, i.e., strong crosslinks p...

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Detalles Bibliográficos
Autores principales: Miwa, Yohei, Udagawa, Taro, Kutsumizu, Shoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314360/
https://www.ncbi.nlm.nih.gov/pubmed/35879386
http://dx.doi.org/10.1038/s41598-022-16156-9
Descripción
Sumario:Dynamic crosslinking of flexible polymer chains via attractive and reversible interactions is widely employed to obtain autonomously self-healable elastomers. However, this design leads to a trade-off relationship between the strength and self-healing speed of the material, i.e., strong crosslinks provide a mechanically strong elastomer with slow self-healing property. To address this issue, we report an “inversion” concept, in which attractive poly(ethyl acrylate-random-methyl acrylate) chains are dynamically crosslinked via repulsively segregated fluoroalkyl side chains attached along the main chain. The resulting elastomer self-heals rapidly (> 90% within 15 min) via weak but abundant van der Waals interactions among matrix polymers, while the dynamic crosslinking provides high fracture stress (≈2 MPa) and good toughness (≈17 MJ m(−3)). The elastomer has a nonsticky surface and selectively self-heals only at the damaged faces due to the surface segregation of the fluoroalkyl chains. Moreover, our elastomer strongly adheres to polytetrafluoroethylene plates (≈60 N cm(−2)) via hot pressing.