材料科学
聚乙烯醇
自愈水凝胶
极限抗拉强度
韧性
复合材料
乙烯醇
微观结构
琼脂
化学工程
聚合物
高分子化学
遗传学
生物
工程类
细菌
作者
Xinxin Sun,Chunhui Luo,Faliang Luo
标识
DOI:10.1016/j.eurpolymj.2019.109465
摘要
Developing hydrogels with excellent mechanical properties and functions is important and challenging. Herein, commercial available materials, polyvinyl alcohol (PVA) and agar, are used to synthesize ultra-strong, self-healable and conductive hydrogels by freezing-thawing cycles and soaking in the ammonium sulfate (AS) solution. The relationship between microstructures and mechanical properties of the obtained PVA-Agar hydrogel is analyzed. The results show that the tensile stress and toughness of PVA-Agar precursor hydrogel are only 0.2 MPa and 0.3 MJ/m3, respectively, due to the uneven network with a pore size between 1 and 8 μm and the lower crosslink density of network. After soaking in AS solution, the network becomes dense and uniform with a pore size of 1–3 μm, accompanied by the formation of stronger hydrogen bonds between PVA and agar. As a result, the tensile stress and toughness increase to 18.0 MPa and 42.3 MJ/m3, respectively. Due to the efficient energy dissipation mechanism endowed by dynamic junctions, the hydrogel also has good anti-fatigue property and high self-healing efficiencies (>80%), and the dissipative energy can reach 18.5 MJ/m3, which accounts for 94.9% of the total energy. Furthermore, the hydrogel exhibits electrical conductivity. The full-fledged starting materials, PVA and agar, and easy-operated process, freeze/thaw cycle, provide our method great potentials to scale up and promising applications as a biocompatible and bioactive material.
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