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Using mechanical spectroscopies to study the glass transition dynamics in unsaturated polyester resins cured with different styrene contents

机译:使用机械光谱学研究不同苯乙烯含量的不饱和聚酯树脂的玻璃化转变动力学

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摘要

The control of chemical architecture has been one relevant parameter in the study of glass transition dynamics in macromolec-ular systems.In this study,two polyester resins differing in the styrene content that was added in the curing process were studied using two complementary mechanical spectroscopy techniques:dynamic mechanical analysis (DMA) and thermally stimulated recovery (TSR).Both techniques showed that the alpha-relaxation is shifted to higher temperatures (longer times) with increasing styrene content.Master curves were obtained from the DMA data.The shift factors were used to obtain the temperature dependence of the apparent activation energy,E_a(T).The TSR results also permitted to obtain E_a(T) that also exhibited a maximum around T_g.This behaviour,apparently universally observed in thermally stimulated techniques,was explained by the shift from a Vogel-Fulcher-Tam-man-Hesse to an Arrhenius regime.The data also allowed to calculate the fragility index of the two materials,which was found to be higher for the one with higher styrene content.Remarks are made on the dependency of the values of this parameter obtained from different techniques.
机译:化学结构的控制已成为研究大分子体系玻璃化转变动力学的一个相关参数。在这项研究中,使用两种互补的机械光谱技术研究了固化过程中添加的两种苯乙烯含量不同的聚酯树脂动态力学分析(DMA)和热激发采收率(TSR)两种技术均表明,随着苯乙烯含量的增加,α-松弛转变到更高的温度(更长的时间),从DMA数据获得了主曲线。用于获得表观活化能E_a(T)的温度依赖性。TSR结果还允许获得在T_g附近也表现出最大值的E_a(T)。这种行为在热刺激技术中普遍观察到,解释为从Vogel-Fulcher-Tam-Man-Hesse到Arrhenius政权的转变。该数据还允许计算两个材料的脆性指数ls,对于苯乙烯含量较高的那些被发现更高。注释是依赖于从不同技术获得的该参数的值。

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