自愈水凝胶
粘附
共价键
材料科学
胶粘剂
拓扑(电路)
非共价相互作用
高分子科学
分子
化学
聚合物
纳米技术
高分子化学
复合材料
有机化学
图层(电子)
氢键
数学
组合数学
作者
Jason Steck,Jiawei Yang,Zhigang Suo
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2019-06-07
卷期号:8 (6): 754-758
被引量:76
标识
DOI:10.1021/acsmacrolett.9b00325
摘要
Tough adhesion between wet materials (i.e., synthetic hydrogels and biological tissues) is undergoing intense development, but methods reported so far either require functional groups from the wet materials, involve toxic chemicals, or result in unstable adhesion. Here, we present a method to achieve biocompatible, covalent adhesion, without requiring any functional groups from the wet materials. We use two hydrogels as model adherends that have covalent polymer networks, but have no functional groups for adhesion. We use an aqueous solution of biopolymers and bioconjugate agents as a model adhesive. When the solution is spread at the interface of the hydrogels, the biopolymers diffuse into both hydrogels and cross-link into a covalent network in situ, in topological entanglement with the two polymer networks of the hydrogels. We characterize the chemistry and mechanics of the covalent topological adhesion. In a physiological fluid, the covalent topological adhesion is stable, but a noncovalent topological adhesion separates. Covalent topological adhesion presents immediate opportunities to advance the art of adhesion in diverse and complex environments.
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