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

Author:

Miwa Yohei,Udagawa Taro,Kutsumizu Shoichi

Abstract

AbstractDynamic 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.

Funder

Precursory Research for Embryonic Science and Technology

The Eno Science Foundation

The Tatematsu Foundation

Japan Society for the Promotion of Science

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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