自愈水凝胶
疏水效应
韧性
氢键
化学
化学工程
极限抗拉强度
纤维
材料科学
应力松弛
高分子化学
复合材料
分子
有机化学
蠕动
工程类
生物化学
作者
Koki Nishida,Ryohei Ikura,Kenji Yamaoka,Osamu Urakawa,Takashi Konishi,Tadashi Inoue,Go Matsuba,Masaru Tanaka,Yoshinori Takashima
标识
DOI:10.1021/acs.macromol.4c00732
摘要
To reveal the synergic effects of movable and reversible cross-links, we fabricated movable cross-linked hydrogels with hydrophobic acetylated cyclodextrins (CDs). The obtained hydrogels showed high toughness based on the broad range of relaxation times achieved by the high mobility of movable cross-links and reversible hydrophobic interaction. The high mobility of movable cross-links resulted from the lack of hydrogen bonds between the triacetylated γCD (TAcγCD) units and main chains. High mobility also occurred because TAcγCD units were not hydrated. The localization of hydration forms hydrophobic domains with the distribution of TAcγCD units. The hydrophobic domains also disperse the stress upon tensile deformation. The low water content (Wc = 15 wt %) achieved further high toughness (36.8 MJ·m–3) by the triple-synergic effects of movable cross-links, reversible hydrophobic interaction, and craze/fibril-like structures upon deformation. The mobility of movable cross-links and the reformation of reversible hydrophobic interaction achieved high self-restoring properties.
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