环氧树脂
热固性聚合物
缩水甘油醚
材料科学
动态力学分析
胶粘剂
玻璃化转变
降级(电信)
双酚A
复合材料
共价键
极限抗拉强度
聚合物
交叉连接
化学工程
高分子化学
化学
有机化学
计算机科学
电信
图层(电子)
工程类
作者
Lin Zhou,Lin Zhou,Linfang Zhou,Linfang Zhou,Shipeng Xiang,Kuibao Zhang,Mao Chen
出处
期刊:Polymer
[Elsevier BV]
日期:2023-08-06
卷期号:283: 126234-126234
被引量:4
标识
DOI:10.1016/j.polymer.2023.126234
摘要
Covalent adaptable networks relying on dynamic cross-links have been developed to make the conventional thermosets degradable and reprocessable, but the greater challenge lies in how to overcome the trade-off between excellent degradability and mechanical properties. It remains a formidable challenge to achieve complete degradation of high mechanical materials (such as epoxy) especially at more moderate conditions. Herein, dual-responsive epoxy thermosets that were serially cross-linked by double dynamic bonds of disulfide bonds and cation-π interactions were prepared from diglycidyl ether of bisphenol A (DGEBA), dithiodianiline (DTDA), N-expoxypropane-indole (EIN) and MgCl2. The dual-responsive epoxy exhibited moderate mechanical properties with the tensile strength of 55 MPa, while the glass transition temperature (Tg) was 85 °C. In addition, the dual-responsive epoxy could be degraded by either DTT or PPi, due to the thiol-disulfide oxidation/reduction reaction and the complexation reaction of PPi and Mg2+. Furthermore, the degradation times could be controlled from <100 to 2700 min with optimal conditions by varying the concentration of reactive molecules and temperature. Meanwhile, the dual-responsive epoxy also exhibited excellent reprocessing properties. The dual-responsive dynamic epoxy thermoset is expected to be useful for coatings, adhesives, and matrix polymers of composites that require controlled degradation and recyclability.
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