Thermodynamical scaling of the glass transition dynamics

R. Casalini and C. M. Roland
Phys. Rev. E 69, 062501 – Published 28 June 2004

Abstract

Classification of glass-forming liquids based on the dramatic change in their properties upon approach to the glassy state is appealing, since this is the most conspicuous and often-studied aspect of the glass transition. Herein, we show that a generalized scaling, log(τ)T1Vγ, where γ is a material constant, yields superpositioning for ten glass formers, encompassing van der Waals molecules, associated liquids, and polymers. The exponent γ reflects the degree to which volume governs the temperature and pressure dependence of the relaxation times.

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  • Received 9 December 2003

DOI:https://doi.org/10.1103/PhysRevE.69.062501

©2004 American Physical Society

Authors & Affiliations

R. Casalini1,2,* and C. M. Roland1,†

  • 1Naval Research Laboratory, Code 6120, Washington, DC 20375-5342, USA
  • 2George Mason University, Fairfax, Virginia 22030, USA

  • *Electronic address: casalini@ccs.nrl.navy.mil
  • Electronic address: roland@nrl.navy.mil

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Issue

Vol. 69, Iss. 6 — June 2004

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