壳聚糖
丙烯酰胺
自愈水凝胶
丙烯酸
聚电解质
极限抗拉强度
高分子化学
材料科学
化学工程
复合材料
聚合物
共聚物
工程类
作者
Aihua Shi,Xiangyi Dai,Zhanxin Jing
出处
期刊:Polymer Science Series A
[Springer Nature]
日期:2020-05-01
卷期号:62 (3): 228-239
被引量:22
标识
DOI:10.1134/s0965545x20030128
摘要
Chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels based on non-covalent bond and winding between molecular chains were synthesized by copolymerization reaction in the presence of Fe3+. The formation mechanism of chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels was analyzed using UV–Vis spectra and FTIR, revealing that Fe3+ could form the electrostatic interaction with –COO– group in poly(acrylamide-co-acrylic acid) chains, and the –COOH form also the hydrogen bond also with –CONH2 in poly(acrylamide-co-acrylic acid) chains or –NH2 in chitosan chains. Mechanical properties of the prepared double network hydrogels were investigated by rheological and mechanical measurements. These results indicated that the chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels present good recovery ability. The tensile strength and elongation at break of the synthesized hydrogel could reach 141.9 kPa and 18.2 mm/mm, respectively, their compressive strength could reach 1.76 MPa at strain of 85%. In addition, the synthesized hydrogels can maintain good self-healing capacity owing to the dynamically reversible bonds (ionic bond and hydrogel bonding). This work provides a facile method for the synthesis of hydrogels with toughness and self-healing capacity. The synthesized chitosan/poly(acrylamide-co-acrylic acid) double network hydrogels would have a great potential applications in a diverse range.
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