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Contributions of Dipolar Relaxation Processes and Ionic Transport to the Response of Liquids to Electrical Perturbation Fields

机译:偶极弛豫过程和离子输运对液体对电微扰场响应的贡献

摘要

The objective of this work was to study the influence of small variations in theudchemical structure on the molecular dynamics of liquids using as models bis(cyclohexylmethyl)ud2-methyl- and dicyclohexyl 2-methylsuccinate. The dielectric behavior of the low molecularudweight liquids was studied over a wide range of frequencies and temperatures. The results showudthat the temperature dependence of the dielectric strengths, relaxation times, and shapeudparameters of the secondary and glass liquid relaxations are very sensitive to the slightuddifferences in the structures of the liquids. Significant changes take place in the dielectricudstrength of the β relaxation in the glass liquid transition. Moreover, the temperature dependenceudof the β relaxation exhibits Arrhenius behavior in the glassy state and departs from this behaviorudin the liquid state. Special attention is paid to the temperature dependence of low-frequencyudrelaxations produced by the motion of a macrodipole arising from charges located near the liquid electrode boundaries.
机译:这项工作的目的是使用2-甲基琥珀酸双(环己基甲基) ud2-甲基和二环己基酯作为模型研究 udchemical结构中的小变化对液体分子动力学的影响。在很宽的频率和温度范围内研究了低分子量/超重液体的介电性能。结果表明, u200b u200b介电强度,弛豫时间以及次级和玻璃液体弛豫的形状参数的温度依赖性对液体结构中的轻微 u差异非常敏感。在玻璃液体转变过程中,β弛豫的介电强度/强度发生了重大变化。而且,β弛豫的温度依赖性 ud表现出在玻璃态下的阿累尼乌斯行为,而在液态下则偏离该行为。要特别注意由偶极子的运动引起的低频松弛的温度依赖性,该偶极子运动是由位于液体电极边界附近的电荷引起的。

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