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首页> 外文期刊>International Journal of Polymeric Materials >Curing Kinetics of Liquid Crystalline Epoxy Resins Based on Bisphenol-S Mesogen with DDE by Nonisothermal DSC Data
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Curing Kinetics of Liquid Crystalline Epoxy Resins Based on Bisphenol-S Mesogen with DDE by Nonisothermal DSC Data

机译:非等温DSC法研究双酚S介晶和DDE对液晶环氧树脂的固化动力学

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摘要

The curing kinetics for a system of Sulfonyl bis(4,1-phenylene)bis[4-(2,3-epoxypro pyloxy)benzoate] (p-SBPEPB) with 4,4'-diaminodiphenyl ether (DDE) were investigated by nonisothermal differential scanning calorimetry (DSC). The dependencies of the apparent activation energy Ea and the conversion a during overall curing reaction were revealed by Ozawa's method. The results shown the Ea decreased drastially from 107 to 75KJ/mol with α in the initial stages (α = 0-20%), the average apparent activation energy Ea of p-SBPEPB/DDE is 82.81KJ/mol and was relatively constant in the 0.5 to 0.9 conversion interval. Some parameters were evaluated using the two kinetic models of Sestdk-Berggren (S-B) equation and JMA model. The liquid crystalline (LC) phase had formed and was fixed in the system during the curing process.
机译:通过非等温研究了磺酰基双(4,1-亚苯基)双[4-(2,3-环氧丙氧基苯甲酸)苯甲酸酯](p-SBPEPB)与4,4'-二氨基二苯醚(DDE)的固化动力学。差示扫描量热法(DSC)。 Ozawa方法揭示了在整个固化反应过程中表观活化能Ea和转化率a的依赖性。结果表明,在初始阶段(α= 0-20%),Ea从107急剧降低至75KJ / mol,p-SBPEPB / DDE的平均表观活化能Ea为82.81KJ / mol,并且相对稳定。 0.5至0.9的转换间隔。使用Sestdk-Berggren(S-B)方程和JMA模型这两个动力学模型评估了一些参数。液晶(LC)相已形成并在固化过程中固定在系统中。

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