材料科学
环氧树脂
复合材料
热塑性塑料
抗弯强度
聚合物
聚合
玻璃化转变
苯胺
原位聚合
催化作用
高分子化学
有机化学
化学
作者
Chong Cheng,Jun Wang,Shuang Yang,Jingsheng Wang,Xi Chen,Yue Jia,Qiufei Chen,Pengzong Guo,Wang Xiao,Fu Liu
摘要
Thermoplastic resins have been widely used in fiber reinforced polymer composites because of its recyclability and short cycle times. However, the high viscosity after heating and melting restricts its infiltration on the surface of fiber. In this study, a series of thermoplastic epoxy resins were prepared via the chain extension reaction of epoxy groups with liquid aniline using triphenylphosphine (TPP) as catalyst. The relationship between polymer network structure and performance was comprehensively investigated. The solubility tests indicated that excessive aniline or TPP facilitated the crosslinking of resins. Besides, on the premise of thermoplasticity, appropriate TPP could increase the degree of chain extension, molecular weight, and glass transition temperature of resins. Furthermore, the in‐situ polymerization process facilitated infiltration between epoxy resin and the fibers before chain extension reaction. The bending test showed that the flexural performance of the sample with 2 phr of TPP was improved by 38.8%. Therefore, this work provides a feasible method to prepare the thermoplastic epoxy resins and its fiber‐reinforced composites with good mechanical properties.
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