材料科学
天然橡胶
三元乙丙橡胶
韧性
共价键
复合材料
氢键
弹性体
分子
有机化学
化学
作者
Chengjie Li,Yujie Wang,Zun Yuan,Lin Ye
标识
DOI:10.1016/j.apsusc.2019.04.064
摘要
Through a facile method in the process of milling/hot pressing of ethylene-propylene-diene monomer (EPDM) rubber in solid state, the hybrid networks formed by covalent crosslinks, hydrogen bonds and Zn2+-carboxyl units were successfully designed and constructed in EPDM rubber system (EPDM-g-ZnGlu) by incorporation of carboxyl groups onto EPDM backbone and coordination with ZnCl2. The dynamic features capable of reversibly breaking and reforming for the sacrificial hydrogen bonds and Zn2+-carboxyl units endowed EPDM-g-ZnGlu with remarkable hysteresis loss, evident residual strain and rapid stress relaxation, which can be preferentially ruptured before breaking of covalent bonds upon deformation, thus resulting in high energy dissipation and significantly enhanced mechanical strength and toughness of EPDM rubber. Compared with EPDM, the mechanical strength and toughness of EPDM-g-ZnGlu-1/1 increased by 288% and 156%, respectively. Meanwhile, the reprocessing ability was imparted to EPDM-g-ZnGlu samples cured by the sacrificial bonds, further confirming the dynamic characteristics of the sacrificial bonds. Such efficient strategy shows a promising perspective in rational design of EPDM rubbers for practical applications in diverse fields.
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