极限抗拉强度
自愈水凝胶
琼脂糖
聚丙烯酰胺
材料科学
复合材料
延伸率
缩颈
压缩(物理)
化学
高分子化学
色谱法
作者
Tingrui Lin,Qingwen Bai,Jing Peng,Ling Xu,Jiuqiang Li,Maolin Zhai
标识
DOI:10.1016/j.carbpol.2018.07.070
摘要
A facile one-step radiation method is first developed to synthesize agarose/polyacrylamide (AG/PAM) double-network (DN) hydrogel. Compared to other synthetic methods of DN hydrogels, our synthesis method endows the resultant AG/PAM DN hydrogel with not only top-level tensile properties with a tensile strength of 1263 ± 59 kPa and an elongation at break of 3406 ± 143%, but also highest compression properties with a compression strength of 140 ± 3 MPa and a fracture compression strain of above 99.9%. An expanding-necking phenomenon during compression process of AG/PAM DN hydrogel were observed. We propose a chain pushing-in model to interpret the energy dissipation mechanism accounting for the super-compressibility of AG/PAM DN hydrogel. This novel radiation synthesis strategy provides an insight into the development of DN hydrogels with extremely excellent mechanical properties.
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