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Cure Kinetics and Activation Energy Studies of Modified Bismaleimide Resins

机译:改性双马来酰亚胺树脂的固化动力学和活化能研究

摘要

The cure kinetics and activation energy (Ea) of bismaleimide homopolymer and modified bismaleimide resin systems with different chain extenders were investigated. The bismaleimide resin under investigation was bismaleimidodiphenyl methane (BMPM) and the chain extenders were (i) O-O� diallyl bisphenol A (DABA) and (ii) methylenedianiline (MDA). Dynamic multiheating DSC method was used to study the kinetics of the curing process. Activation energies were determined for bothudunmodified and modified resins from nonisothermalmultiheating rate DSC tests by using Ozawa and Kissinger models. Activation energy for BMPM homopolymer increased from 95 kJ/mol to 125 kJ/mol as a function of conversion. For the MDA-modified system the activation energy was independent of percentage conversion, at 108 kJ/mol. In the case of DABA-modified bismaleimideudthe activation energy increased steadily at 6 kJ/mol from 10 to 100% conversion.
机译:研究了具有不同扩链剂的双马来酰亚胺均聚物和改性双马来酰亚胺树脂体系的固化动力学和活化能(Ea)。被研究的双马来酰亚胺树脂为双马来酰亚胺二苯甲烷(BMPM),扩链剂为(i)O-O-二烯丙基双酚A(DABA)和(ii)亚甲基二苯胺(MDA)。动态多重加热DSC方法用于研究固化过程的动力学。通过使用Ozawa和Kissinger模型通过非等温多升温速率DSC测试确定了 udun改性和改性树脂的活化能。 BMPM均聚物的活化能从95 kJ / mol增加到125 kJ / mol,这是转化率的函数。对于MDA修饰的系统,活化能与转化百分数无关,为108 kJ / mol。在DABA修饰的双马来酰亚胺中,活化能以6 kJ / mol的速率稳定地从10%转换为100%。

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