环氧树脂
共价键
缩水甘油醚
材料科学
亚胺
双酚A
热固性聚合物
香兰素
极限抗拉强度
有机化学
双酚
高分子化学
化学工程
乙醚
环氧化物
复合材料
胺气处理
粘结强度
化学
动态共价化学
动态力学分析
胶粘剂
交叉连接
合成树脂
聚合物
二胺
作者
Shichang Wang,Zhengzhuo Li,Yuan Ji,Hong Wu,Shishang Guo
标识
DOI:10.1021/acs.iecr.5c04625
摘要
The incorporation of dynamic covalent networks into epoxy resins is an effective strategy to overcome their inherent limitations of nonreprocessability and nondegradability, leading to a class of materials known as epoxy vitrimers. Despite recent progress in achieving rapid reprocessability and degradability, epoxy vitrimers still face challenges, including inadequate mechanical properties and the prevalent use of the toxic precursor bisphenol A diglycidyl ether (BADGE). Herein, we report a one-pot synthesis of a biobased epoxy vitrimer using vanillin, diamino-functionalized phenylenediboronic ester (DPDBE), and polyether amine (PEA), which incorporates dual dynamic covalent bonds of the imine and boronic ester. The resulting vitrimer exhibits a remarkable combination of high mechanical strength and good toughness, achieving a tensile strength of 73 MPa with an elongation at break of 23%. This excellent mechanical performance is attributed to the molecular design: the conjugation between the imine bonds and benzene rings, the rigidity of the boronic ester five-membered rings, and the flexible ether bonds and long methylene chains from PEA. Furthermore, the synergistic effect between the imine and boronate ester bonds enables an exceptionally low activation energy (Ea) of 58.1 kJ/mol for the bond exchange reactions, resulting in rapid reprocessability within 5 min and complete degradation within 30 min. This work presents a promising strategy for developing high-performance, environmentally friendly epoxy vitrimers from sustainable resources.
科研通智能强力驱动
Strongly Powered by AbleSci AI