论文标题
玻璃的结构放松是否由平衡剪切粘度控制?
Is the Structural Relaxation of Glasses Controlled by Equilibrium Shear Viscosity?
论文作者
论文摘要
放松过程的知识在玻璃科学技术中至关重要,因为放松本质上与玻璃的玻璃化以及退火和SEV积有关。但是,有相互矛盾的报告 - 在此处汇总了不同眼镜 - 关于是否可以使用Maxwell方程来计算玻璃的结构放松时间,这将放松时间与剪切粘度和剪切模量有关。因此,这项研究旨在验证这两个放松时间是否可比。通过测量在虚拟温度以下5到25 K之间的温度下,在温度下的温度下,研究了铅氧化液的结构弛豫动力学,最初将其设置在玻璃过渡温度低于5 K的温度下。平衡剪切粘度在玻璃过渡范围的上方和下方测量,从一个数量级扩展了当前知识。 Kohlrausch方程很好地描述了整个调查的温度范围内实验性结构弛豫动力学,而Kohlrausch指数随温度升高,与对其他眼镜的研究一致。如预期的那样,实验平均结构放松时间比从同生粘度计算出的值要长得多。尽管如此,它们还是比通过Maxwell方程计算的平均松弛时间高的数量级,该平均松弛时间依赖于平衡剪切粘度。因此,这些结果是,结构弛豫过程不受同源粘度的控制,而平衡剪切粘度仅为结构弛豫动力学提供了下边界。
Knowledge of relaxation processes is fundamental in glass science and technology because relaxation is intrinsically related to vitrification, tempering as well as to annealing and sev-eral applications of glasses. However, there are conflicting reports -- summarized here for different glasses -- on whether the structural relaxation time of glass can be calculated using the Maxwell equation, which relates relaxation time with shear viscosity and shear modulus. Hence, this study aimed to verify whether these two relaxation times are comparable. The structural relaxation kinetics of a lead metasilicate glass were studied by measuring the re-fractive index variation over time at temperatures between 5 and 25 K below the fictive temperature, which was initially set 5 K below the glass transition temperature. Equilibrium shear viscosity was measured above and below the glass transition range, expanding the current knowledge by one order of magnitude. The Kohlrausch equation described very well the experimental structural relaxation kinetics throughout the investigated temperature range and the Kohlrausch exponent increased with temperature, in agreement with studies on other glasses. The experimental average structural relaxation times were much longer than the values computed from isostructural viscosity, as expected. Still, they were less than one order of magnitude higher than the average relaxation time computed through the Maxwell equation, which relies on equilibrium shear viscosity. Thus, these results demon-strate that the structural relaxation process is not controlled by isostructural viscosity, and that equilibrium shear viscosity only provides a lower boundary for structural relaxation kinetics.