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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

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An Errata to this article was published on 01 October 2010

Abstract

A brief review is presented of the concepts regarding the nature of α and β 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.

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Original Russian Text © S.V. Nemilov, 2010, published in Fizika i Khimiya Stekla.

An erratum to this article can be found at http://dx.doi.org/10.1134/S1087659610050147

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Nemilov, S.V. Relaxation processes in inorganic melts and glasses: An elastic continuum model as a promising basis for the description of the viscosity and electrical conductivity. Glass Phys Chem 36, 253–285 (2010). https://doi.org/10.1134/S1087659610030028

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