自愈水凝胶
乙烯醇
材料科学
极限抗拉强度
离子电导率
羟丙基纤维素
化学工程
纤维素
复合数
复合材料
生物高聚物
聚电解质
羧甲基纤维素
化学
电导率
高分子化学
电解质
聚合物
钠
电极
物理化学
工程类
冶金
作者
Shuchun Gan,Shihang Bai,Cheng Chen,Yongliang Zou,Yingjuan Sun,Jianhao Zhao,Jianhua Rong
标识
DOI:10.1016/j.ijbiomac.2021.03.068
摘要
Ionic conductive hydrogels with both high-performance in conductivity and mechanical properties have received increasing attention due to their unique potential in artificial soft electronics. Here, a dual physically cross-linked double network (DN) hydrogel with high ionic conductivity and tensile strength was fabricated by a facile approach. Hydroxypropyl cellulose (HPC) biopolymer fibers were embedded in a poly (vinyl alcohol)‑sodium alginate (PVA/SA) hydrogel, and then the prestretched PVA-HPC/SA composite hydrogel was immersed in a CaCl2 solution to prepare PVA-HPCT/SA-Ca DN hydrogels. The obtained composite hydrogel has an excellent tensile strength up to 1.4 MPa. Importantly, the synergistic effect of hydroxypropyl cellulose (HPC) and prestretching reduces the migration resistance of ions in the hydrogel, and the conductivity reaches 3.49 S/ m. In addition, these composite hydrogels are noncytotoxic, and they have a low friction coefficient and an excellent wear resistance. Therefore, PVA-HPCT/SA-Ca DN hydrogels have potential applications in nerve replacement materials and biosensors.
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