材料科学
氢键
海水
聚合物
儿茶酚
自愈
化学工程
有机化学
分子
复合材料
化学
海洋学
医学
病理
替代医学
地质学
工程类
作者
Jincai Li,Hirotaka Ejima,Naoko Yoshie
标识
DOI:10.1021/acsami.6b04075
摘要
It is highly desirable to prevent crack formation in polymeric materials at an early stage and to extend their lifespan, particularly when repairs to these materials would be difficult for humans. Here, we designed and synthesized catechol-functionalized polymers that can self-heal in seawater through hydrogen bonding and coordination. These bioinspired acrylate polymers are originally viscous materials, but after coordination with environmentally safe, common metal cations in seawater, namely, Ca(2+) and Mg(2+), the mechanical properties of the polymers were greatly enhanced from viscous to tough, hard materials. Reduced swelling in seawater compared with deionized water owing to the higher osmotic pressure resulted in greater toughness (∼5 MPa) and self-healing efficiencies (∼80%).
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