Seawater-Assisted Self-Healing of Catechol Polymers via Hydrogen Bonding and Coordination Interactions

被引:148
作者
Li, Jincai [1 ]
Ejima, Hirotaka [1 ]
Yoshie, Naoko [1 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
关键词
bioinspired polymers; seawater; catechol; self-healing metallopolymers; CROSS-LINKING; ADHESIVE; STATE;
D O I
10.1021/acsami.6b04075
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
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, Ca2+ and Mg2+, 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 (similar to 5 MPa) and self-healing efficiencies (similar to 80%).
引用
收藏
页码:19047 / 19053
页数:7
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