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首页> 外文期刊>Glass Physics and Chemistry: A Journal on the Structural, Physical, and Chemical Properties and Nature of Inorganic Glasses and Glass-Forming Melts >Relaxation Processes in Inorganic Melts and Glasses: An Elastic Continuum Model as a Promising Basis for the Description of the Viscosity and Electrical Conductivity
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Relaxation Processes in Inorganic Melts and Glasses: An Elastic Continuum Model as a Promising Basis for the Description of the Viscosity and Electrical Conductivity

机译:无机熔体和玻璃中的弛豫过程:弹性连续体模型作为描述粘度和电导率的有前途的基础

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摘要

A brief review is presented of the concepts regarding the nature of a and P relaxation processes in melts and glasses. Experimental data have been used to show that different types of relaxation in oxide systems can be interrelated to each other. The molecular mechanism of viscous flow in inorganic systems has been discussed in detail with the use of continuum theories (elasticity and hydrodynamics) developed in the works by the author in 1967-2007. A rigorous relationship between the volumes of atoms overcoming the activation barrier, the instantaneous shear modulus, and the barrier itself (free activation energy) has been derived. This relationship allows one to calculate the sizes of atoms involved in the viscous flow with a deviation that does not exceed 10% of the values determined by direct structural methods. In this case, empirically chosen constants are absent. Based on the results obtained by Anderson and Stewart (1954) and the author (1974), it has been established that the activation energy for ionic conduction can be calculated using similar notions. It has been demonstrated for the first time that the universal relation between the viscosity and conductivity over a wide range of temperatures (for alkali-containing oxide melts) i.e., the Littleton equation, finds a simple quantitative explanation in the framework of the same models, even though the mechanisms of both processes do not depend on each other.
机译:简要回顾了有关熔体和玻璃中a和P弛豫过程的性质的概念。实验数据已被用来表明氧化物体系中不同类型的弛豫可以相互关联。作者利用1967-2007年在工作中开发的连续论(弹性和流体动力学),详细讨论了无机系统中粘性流动的分子机理。已经得出了克服活化势垒的原子体积,瞬时剪切模量和势垒本身(自由活化能)之间的严格关系。这种关系使得计算粘性流中原子的大小的偏差不超过直接结构方法确定的值的10%。在这种情况下,没有经验选择的常数。基于Anderson和Stewart(1954)和作者(1974)的结果,可以确定可以使用类似的概念来计算离子传导的活化能。首次证明,在很宽的温度范围内(对于含碱氧化物熔体)粘度和电导率之间的通用关系,即利特尔顿方程,在相同模型的框架内找到了简单的定量解释,即使两个过程的机制都不相互依赖。

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