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Cure reaction for modified diallylbisphenol A/diaminodiphenylsulfone/bismaleimide

机译:改性二烯丙基双酚A /二氨基二苯砜/双马来酰亚胺的固化反应

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摘要

The glass-transition temperature as a function of curing conversion for a modified diallylbisphenol A/diaminodiphenylsulfone/bismaleimide (BMI) resin was investigated at different temperature regimes and modeled using a modified Di Benedetto equation. Although the relationship between the glass-transition temperature and conversion of the BMI system conforms to the Di Benedetto equation for alpha < 0.6 and at lower cure temperatures, at higher cure temperatures the results deviated significantly from the equation; thus, it was an inadequate model for the system. Fourier transform IR analysis showed that the major crosslinking reactions did not occur during cure for the modified BMI at and below 150degreesC. However, as the cure temperature was increased, the crosslinking reactions responsible for 3-dimensional network structures became more dominant. At 190degreesC the C-N-C-stretch vibration of the uncured maleimide ring converted into succinimide rings in the curing process. Simultaneously, a decrease was observed for the absorbance bands of ==C-H-bending (maleimide). The higher cure temperatures induced a significantly faster initial crosslinking rate and also resulted in a shorter period of time after which further crosslinking was retarded, because the increase in the crosslinks also physically slowed further crosslinking activity. (C) 2002 Wiley Periodicals, Inc. [References: 34]
机译:在不同温度下研究了改性二烯丙基双酚A /二氨基二苯砜/双马来酰亚胺(BMI)树脂的玻璃化转变温度与固化转化率的关系,并使用改进的Di Benedetto方程进行了建模。尽管玻璃化转变温度与BMI系统转化率之间的关系符合α<0.6且在较低固化温度下的Di Benedetto方程,但在较高固化温度下,结果与方程明显不同。因此,这是该系统的不足模型。傅里叶变换红外光谱分析表明,在改性的BMI于150℃或低于150℃固化期间,没有发生主要的交联反应。但是,随着固化温度的升高,负责3维网络结构的交联反应变得更加重要。在固化过程中,未固化的马来酰亚胺环在190℃的C-N-C拉伸振动转化为琥珀酰亚胺环。同时,观察到== C-H-弯曲(马来酰亚胺)的吸收带下降。较高的固化温度引起明显更快的初始交联速率,并且还导致更短的时间,在此之后进一步的交联受到阻碍,因为交联的增加还物理上减慢了进一步的交联活性。 (C)2002 Wiley Periodicals,Inc. [参考:34]

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