首页> 外文期刊>The Journal of Chemical Physics >Response to 'Comment on 'Direct determination of the fragility indices of glassforming liquids by differential scanning calorimetry: Kinetic versus thermodynamic fragilities'' [J. Chem, Phys. 118, 10351 (2003)]
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Response to 'Comment on 'Direct determination of the fragility indices of glassforming liquids by differential scanning calorimetry: Kinetic versus thermodynamic fragilities'' [J. Chem, Phys. 118, 10351 (2003)]

机译:回应“关于“通过差示扫描量热法直接确定玻璃成型液的脆性指数:动力学与热力学脆性”的评论” [J.化学,物理学。 118,10351(2003)]

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摘要

We give a brief review of how activation energies from scan-rate-dependent T_g studies have been correlated with those for viscosity and other relaxation processes, in order to place the present study in context with previous work, including that referred to in the comment. Then we examine the ensuing question of the extent to which kinetic fragility can be predicted from thermodynamic data. We present a new correlation involving only the entropy of fusion and the jump in heat capacity at T_g, that is followed by most nonchain liquids. Polymer liquids, as the comment authors have shown, have different behavior, consistent with earlier failures to identify Kauzmann and Vogel temperatures in these materials.
机译:我们简要回顾一下依赖于扫描速率的T_g研究的活化能如何与粘度和其他松弛过程的活化能相关联,以使本研究与以前的工作相结合,包括评论中提到的那些。然后,我们研究了随后的问题,即可以从热力学数据预测动力学脆性的程度。我们提出了一种新的相关性,仅涉及聚变熵和T_g处的热容量跳跃,大多数非链状液体都紧随其后。正如评论作者所显示的,聚合物液体具有不同的行为,这与早期未能确定这些材料中的考兹曼和沃格尔温度有关。

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