Ultrastrong and High‐Tough Thermoset Epoxy Resins from Hyperbranched Topological Structure and Subnanoscaled Free Volume

环氧树脂 热固性聚合物 材料科学 韧性 复合材料 缩水甘油醚 聚合物 双酚A 酰亚胺 高分子化学
作者
Xin Liu,Huanghu Wu,Wei Xu,Yu Jiang,Junheng Zhang,Bangjiao Ye,Hongjun Zhang,Sufang Chen,Menghe Miao,Daohong Zhang
出处
期刊:Advanced Materials [Wiley]
卷期号:36 (9): e2308434-e2308434 被引量:86
标识
DOI:10.1002/adma.202308434
摘要

The strength and toughness of thermoset epoxy resins are generally mutually exclusive, as are the high performance and rapid recyclability. Experimentally determined mechanical strength values are usually much lower than their theoretical values. The preparation of thermoset epoxy resins with high modulus, high toughness, ultrastrong strength, and highly efficient recyclability is still a challenge. Here, novel hyperbranched epoxy resins (Bn, n = 6, 12, 24) with imide structures by a thiol-ene click reaction. Bn shows an excellent comprehensive function in simultaneously improving the strength, modulus, toughness, low-temperature resistance, and degradability of diglycidyl ether of bisphenol-A (DGEBA). All the mechanical properties first increase and then decrease with minimization of the free volume properties. The improvement is attributable to uniform molecular holes or free volume by a molecular mixture of linear and hyperbranched topological structures. The precise measurement and controllability of the molecular free volume properties of epoxy resins is first discovered, as well as the imide structure degradation of crosslinked epoxy resins. The two conflicts are successfully resolved between strength and toughness and between high performance during service and high efficiency during degradation. These findings provide a route for designing ultrastrong, tough, and recyclable thermoset epoxy resins.
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