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The Adam-Gibbs equation and the out-of-equilibrium alpha relaxation of glass forming systems

机译:Adam-Gibbs方程和玻璃成型系统的非平衡α弛豫

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The temperature dependence of the alpha-relaxation time out of equilibrium has been investigated by means of dielectric relaxation in a series of fragile glass formers including several polymers.The influence of physical aging on this behavior has also been studied.The experimental results have been quantitatively compared with the predictions of the Adam-Gibbs equation.It has been found that,whereas for small molecule glass formers the experimental values of the apparent activation energy agree quite well with the prediction of the Adam-Gibbs equation,for polymers the experimental activation energy values are systematically higher.Moreover,whereas for small molecule glass formers the experimental values of the apparent activation energy remains essentially unaffected by physical aging,for polymers a pronounced reduction of the experimental apparent activation energy is observed.These results are found to be consistent with the Adam-Gibbs equation if a significant temperature variation of the configurational entropy in the investigated temperature range would occur for nonannealed polymers,being the possible variation hardly noticeable for the small molecules.With this assumption,all the obtained results would support the validity of the Adam-Gibbs equation for describing the temperature dependence of the time scale of the a-relaxation also out of equilibrium,at least for fragile glass formers.
机译:通过介电弛豫的方法研究了一系列包含几种聚合物的易碎玻璃成型机中α-松弛时间不平衡的温度依赖性,还研究了物理老化对其行为的影响,并定量地对实验结果进行了定量分析与Adam-Gibbs方程的预测值相比,已经发现,对于小分子玻璃成型体,表观活化能的实验值与Adam-Gibbs方程的预测值非常吻合,而聚合物的实验活化能与此外,虽然对于小分子玻璃成型体,表观活化能的实验值基本上不受物理老化的影响,但对于聚合物,观察到的表观活化能明显降低。这些结果与如果温度变化很大,则使用Adam-Gibbs方程对于非退火聚合物来说,在研究的温度范围内会发生构型熵的变化,因为对于小分子来说,这种变化可能很难察觉。在此假设下,所有获得的结果都将支持描述亚当-吉布斯方程对温度的依赖性的有效性。至少对于易碎玻璃制造商而言,α松弛的时间尺度也不平衡。

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