自愈水凝胶
互穿聚合物网络
材料科学
肿胀 的
共价键
极限抗拉强度
聚丙烯酰胺
离子键合
聚合物
离子强度
聚电解质
化学工程
复合材料
预聚物
高分子化学
水溶液
化学
聚氨酯
有机化学
离子
工程类
作者
Yali Li,Chaoxia Wang,Wan Zhang,Yunjie Yin,Qingqing Rao
摘要
ABSTRACT In order to fabricate tough hydrogels with superior formability, polyacrylamide/sodium alginate (PAM/SA) interpenetrating polymer network (IPN) hydrogels were produced with ionically crosslinked SA interpenetrated in covalently crosslinked PAM. TGA results show that the heat resistance of PAM/SA IPN hydrogel is improved as compared to that of the individual component. Swelling studies indicate that increasing either chemical crosslinker content or ionic crosslinking via adding more N , N ′‐methylenebisacrylamide (MBA) or SA results in lower ESR. It is concluded by tensile test that loosely crosslinked PAM coupled with tightly crosslinked SA improve mechanical strength for hydrogels based on covalent/ionic crosslinking. PAM/SA hydrogels via “one‐pot” method can form different complex shapes with mechanical properties comparable to conventional double network (DN) gels. The fracture strength of PAM 0.05 /SA 20 reaches level of MPa, approaching 2.0 MPa. The work strives to provide method to tune mechanical and physical properties for hydrogels, which is hopefully to guide the design of hydrogel material with desirable properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41342.
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