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Highly stretchable and tough alginate-based cyclodextrin/Azo-polyacrylamide interpenetrating network hydrogel with self-healing properties
被引:43
|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.
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页数:9
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