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Investigation on Self-healing Property of Epoxy Resins Based on Disulfide Dynamic Links

环氧树脂 缩水甘油醚 材料科学 自愈 极限抗拉强度 复合材料 粘结强度 聚合物 乙二醇 胶粘剂 高分子化学 双酚A 有机化学 化学 医学 病理 图层(电子) 替代医学
作者
Zijian Li,Jiang Zhong,Mao-Chen Liu,Jinchuang Rong,Kun Yang,Jiyong Zhou,Liang Shen,Fei Gao,Haifeng He
出处
期刊:Chinese Journal of Polymer Science [Springer Nature]
卷期号:38 (9): 932-940 被引量:81
标识
DOI:10.1007/s10118-020-2406-x
摘要

Self-healing polymers based on dynamic crosslinkers have drawn rapidly increasing interest over the last decade. Here, a self-healable epoxy network with exchangeable disulfide bonds was synthesized by polymerizing two epoxies with an aromatic amine containing a disulfide bond. The bisphenol A diglycidyl ether (DGEBA) and poly(ethylene glycol) diglycidyl ether (DER736) were used as rigid and soft components, respectively. The crosslinking densities of studied polymers decreased with the increasing amount of DER736, resulting in the lower glassy temperature and weaker mechanical strength. The dynamic covalent network character of disulfide bond and its low active energy were also investigated through stress relaxation experiments at various temperatures. The self-healing performance of healable epoxy resins with varied flexibility was measured by tensile tests. The tensile strength of a full-cut sample was restored to 84% (13 MPa) of the initial values (16 MPa) at moderate temperature. Its healed fracture strain was up to 505%. Moreover, the effect of healing time and temperature on the self-healing properties was also studied. A model was proposed to investigate the self-repairing efficiency evolution with healing time, suggesting that hydrogen bonds mainly contributed to the initial sticking or interfacial adhesion while disulfide links and chain interdiffusion assisted time dependent reformation of networks to restore the original mechanical strength.
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