自愈水凝胶
胶粘剂
材料科学
水下
粘附
单宁酸
共聚物
纳米技术
化学工程
复合材料
高分子化学
聚合物
化学
有机化学
图层(电子)
工程类
地质学
海洋学
作者
Baotong Ye,Yongxin Ma,Difei Zhang,Jieyu Gu,Ziyan Wang,Yan Zhang,Jinghua Chen
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2023-11-28
卷期号:9 (12): 6891-6901
被引量:2
标识
DOI:10.1021/acsbiomaterials.3c01539
摘要
With the fast development of soft electronics, underwater adhesion has become a highly desired feature for various sensing uses. Currently, most adhesive hydrogels are based on catechol-based structures, such as polydopamine, pyrogallol, and tannic acid, with very limited structural variety. Herein, a new type of glycopolymer-based underwater adhesive hydrogel has been prepared straightforwardly by random copolymerization of acrylic acid, acetyl-protected/unprotected glucose, and methacrylic anhydride in dimethyl sulfoxide (DMSO). By employing a DMSO–water solvent exchange strategy, the underwater adhesion was skillfully induced by the synergetic effects of hydrophobic aggregation and hydrogen bonding, leading to excellent adhesion behaviors on various surfaces, including pig skins, glasses, plastics, and metals, even after 5 days of storage in water. In addition, the underwater adhesive hydrogels with simple and low-cost protected/unprotected carbohydrate compositions showed good mechanical and rheological properties, together with cytocompatibility and antiswelling behavior in water, all of which are beneficial for underwater adhesions. In application as a flexible strain sensor, the adhesive hydrogel exhibited stable and reliable sensing ability for monitoring human motion in real time, suggesting great potential for intelligent equipment design.
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