极限抗拉强度
自愈水凝胶
壳聚糖
离子强度
聚合
聚合物
单体
材料科学
化学工程
离子键合
韧性
水溶液
离子电导率
聚电解质
丙烯酸
高分子化学
化学
复合材料
离子
有机化学
物理化学
电解质
工程类
电极
作者
Jinfeng Cao,Yang Wang,Chen He,Yun Jin Kang,Jinping Zhou
标识
DOI:10.1016/j.carbpol.2020.116420
摘要
A dual physically crosslinking (DPC) strategy is used to construct hydrogels with ultrahigh strength. First, polyelectrolyte complex (PEC) hydrogels were prepared through in situ polymerization of acrylic acid monomers in chitosan solutions. Subsequently, cations and anions were introduced into the PEC hydrogels to form strong electrostatic interactions with the polymer chains. The mechanical properties of the DPC hydrogels strongly depended on the ionic concentration and the valence state of the loading ions. The tensile strength of DPC-Na 8-20-2.0, DPC-Mg 8-20-2.0, DPCAl 8-20-2.0 and DPC-Sul 8-20-0.8 reached to 2.36, 12.59, 65.1 and 2.80 MPa, respectively, which were significantly higher than that of PEC 8-20 (0.29 MPa). Moreover, DPC-Na, DPC-Mg and DPC-Sul still maintained a good flexibility. Specifically, hydrogels of DPC-Ca exhibited ionic conductivity and freeze tolerance, which could be cooled to −20 °C without freezing. The DPC strategy opens an avenue to fabricate hydrogels with outstanding mechanical properties.
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