Highly stretchable and tough alginate-based cyclodextrin/Azo-polyacrylamide interpenetrating network hydrogel with self-healing properties

被引:38
|
作者
He, Furui [1 ]
Wang, Longzheng [1 ]
Yang, Shujuan [1 ]
Qin, Wenqi [1 ]
Feng, Yuhong [1 ]
Liu, Yuanyuan [1 ]
Zhou, Yang [1 ]
Yu, Gaobo [1 ]
Li, Jiacheng [1 ]
机构
[1] Hainan Univ, Key Lab Adv Mat Trop Isl Resources, Minist Educ, Sch Chem Engn & Technol, 58 Renmin Rd, Haikou 570228, Hainan, Peoples R China
基金
中国国家自然科学基金;
关键词
Highly stretchable and tough gel; Self-healing; Sodium alginate; Beta-cyclodextrin; Interpenetrating network polymer gels; SUPRAMOLECULAR HYDROGELS; MECHANICAL-PROPERTIES; CONTROLLED-RELEASE; BEADS; CHITOSAN; TEMPERATURE; ADSORPTION; DELIVERY; WATER; ACID;
D O I
10.1016/j.carbpol.2020.117595
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Most structural self-healing materials were developed based on either reversible supramolecular interaction or dynamic covalent bonding. It seems a good idea to incorporate self-healing properties into high-performance materials. In this study, we fabricated the alginate-based cyclodextrin and polyacrylamide azobenzene highly stretchable and tough interpenetrating composite hydrogel with self-repairing behavior under light irradiation. Initially, the alginate-based cyclodextrin and polyacrylamide azobenzene were designed and synthesized. The corresponding structural, thermal, and morphological properties of hydrogels were characterized. The reversible transformation of the sol-gel can be achieved by the irradiation upon ultraviolet light and visible light. The self healing behavior of this composited gel is based on the host-guest interaction between cyclodextrin and azobenzene. The recovery gel elongation at 48 h healing in the dark condition was is 0.04 MPa, with an elongation of 1140 %. Therefore, this gel can achieve self-healing ability while maintaining highly stretchable and tough performance.
引用
收藏
页数:9
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