详细信息

Super tough, ultra-stretchable, and fast recoverable double network hydrogels physically crosslinked by triple non-covalent interactions  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Super tough, ultra-stretchable, and fast recoverable double network hydrogels physically crosslinked by triple non-covalent interactions

作者:Zhou, Linjie[1,2,3];Pei, Xinjie[3];Fang, Kun[3];Zhang, Rui[1];Fu, Jun[2,3]

机构:[1]East China Univ Sci & Technol, State Key Lab Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China;[2]Sun Yat Sen Univ, Sch Mat Sci & Engn, Guangzhou 510275, Peoples R China;[3]Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, 1219 Zhongguan West Rd, Ningbo 315201, Peoples R China

年份:2020

卷号:192

外文期刊名:POLYMER

收录:;EI(收录号:20200908243015);WOS:【SCI-EXPANDED(收录号:WOS:000519993100023)】;

基金:This study was supported by National Natural Science Foundation of China (51873224, 21574145), and National Key Research and Development Program of China (2016YFC1101902).

语种:英文

外文关键词:Tough hydrogels; Non-covalent crosslinking; Self-recovery; Metal coordination; Double network hydrogels

摘要:Incorporating sacrificial bonds into hydrogels networks has been demonstrated an efficient way to obtain ultrahigh strength, but is usually at the expense of flexibility and recoverability. This study demonstrates novel triple physically crosslinked hydrogels with very high stretchability, toughness and rapid self-recovery at ambient conditions. Physically crosslinked kappa-carrageenan acts as the first network to host free radical copolymerization of polymers with Pluronic F127 diacrylate micelles. Hydrophobic association of micelles in the second network contributes to outstanding stretchability (over 1100%) and toughness (10.83 MJ/m(3)). Further crosslinking of the second network through tridentate Fe3+-COO- coordination significantly enhances the fracture strength up to 2.7 MPa, and elastic modulus 1171 kPa. Systematic investigations demonstrate the key roles played by non-covalent crosslinking on energy dissipation during loadings and the damaged non-covalent networks could recover 40% toughness in 1 min at ambient conditions. These hydrogels are promising for applications as biocompatible load-bearing materials.

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