环氧树脂
材料科学
缩水甘油醚
固化(化学)
异氰酸酯
动态力学分析
复合材料
乙二醇
双酚A
三甘醇
聚丙烯乙二醇
高分子化学
聚氨酯
聚合物
化学
有机化学
聚乙二醇
作者
Bluma G. Soares,Viviane Gonçalez,Rurik Galimberti,Alex da Silva Sirqueira,Fábio L. Barcia,Renata Antoun Simão
摘要
Abstract A low‐molar‐mass, hydroxyl‐terminated polyether [polypropylene glycol/poly(ethylene glycol) copolymer (POPE)] was functionalized with isocyanate groups and used to improve the impact resistance of a diglycidyl ether of bisphenol A based epoxy resin cured with triethylene tetramine (TETA). The effect of polyether‐based modifiers (with and without NCO groups) on the curing rate of the epoxy/TETA system was investigated with rheological techniques. The NCO‐functionalized polyether reduced the gel time, and this indicated an accelerating effect of the curing process. In addition, a significant improvement in the impact resistance was observed with only a slightly detrimental effect on the stiffness and mechanical strength. Scanning electron microscopy of the corresponding epoxy network revealed a homogeneous morphology with no phase separation. The miscibility of NCO‐modified POPE and the epoxy resin was also confirmed with atomic force microscopy. The glass‐transition temperature of the epoxy networks was also investigated with dynamic mechanical techniques. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
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