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首页> 外文期刊>Journal of Applied Polymer Science >Blends of Bisphenol A-Based Cyanate Ester and Bismaleimide:Cure and Thermal Characteristics
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Blends of Bisphenol A-Based Cyanate Ester and Bismaleimide:Cure and Thermal Characteristics

机译:双酚A基氰酸酯和双马来酰亚胺的共混物:固化和热学特性

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摘要

A dicyanate ester,namely,2,2-bis-(4-cyanatophenyl)propane,and a bismaleimide,namely,2,2-bis[4-(4-maleimido phenoxy) phenyl] propane,possessing closely resembling backbone structures,were cured together to derive bismaleimide-triazine network polymers of varying compositions.The blend manifested a eutectic melting behavior at a 1 : 1 composition with a eutectic melting point of 15 deg C.The cure characterization of the blends was done by DS and dynamic mechanical analyses (DMA).The near simultaneous cure of the blend could be transformed to a clear sequential one by catalyzing the dicyanate cure to lower temperature using dibutyl tin dilaurate.The two-stage,independent cure of the components of the blend evidenced in DSC was confirmed by DMA.The cure profile of the bismaleimide component predicted from the kinetic data derived from nonisothermal DSC was found to be in league with the isothermal DMA behavior.Both techniques led to optimization of the cure schedule of the blends.The cured polymers were characterized by FTIR and TGA.The cured blends underwent decomposition in two stages,each corresponding to the polycyanu-rate and poluybismaleimide.Enhancing the bismaleimide component did not alter the initial decomposition temperature,but led to reduced rate of thermal degradation at higher temperature.Interlinking of the two networks and enhancing crosslink density through coreaction of the blend with 4-cyantophenylmaleimide unaffected the initial decomposition properties but was conducive for increasing the char residue signifi-cantly.Computation of activation parameters for the thermal decomposition of the polymers confirmed that the first step in the degradation of the blends is caused by the polycyanurate compnent.
机译:具有与骨架结构非常相似的二氰酸酯,即2,2-双-(4-氰基苯基)丙烷和双马来酰亚胺,即2,2-双[4-(4-马来酰亚胺基苯氧基)苯基]丙烷固化后可得到组成不同的双马来酰亚胺-三嗪网络聚合物。共混物在1:1组成下的共熔熔点为15摄氏度,共晶熔融行为。通过DS和动态力学分析对共混物进行了固化表征(DMA)。通过使用二月桂酸二丁锡催化双氰酸酯固化至更低的温度,可以将共混物的近乎同时固化转变为清晰的顺序固化。证实了DSC中证明的共混物组分的两阶段独立固化根据非等温DSC的动力学数据预测的双马来酰亚胺组分的固化曲线与等温DMA行为相吻合,这两种技术均优化了共混物的固化时间表。 FTIR和TGA对聚合物进行了表征。固化后的共混物经历了两个阶段的分解,每个阶段分别对应于聚氰尿酸酯和多双马来酰亚胺。提高双马来酰亚胺组分不会改变初始分解温度,但导致高温下的热降解速率降低。通过共混物与4-氰基苯基马来酰亚胺的共聚作用,这两个网络相互连接并提高了交联密度,但未影响其初始分解性能,但有利于显着增加炭残基。共混物降解的第一步是由聚氰尿酸酯成分引起的。

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