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1 Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, U.K.
2 Institute for Mineralogy and Petrography, ETH Zurich, Sonneggstrasse 5, 8092 Zurich, Switzerland
Correspondence: * E-mail: george{at}geology.bristol.ac.uk
Simple polythermal extensions to two widely used isothermal equations of state, the Murnaghan and the Birch-Murnaghan, can lead to non-physical material behavior without proper parameterization: the thermal expansivity at high pressure can become negative. We show how this arises and propose a remedy using an approximation to the thermal relaxation of the bulk modulus. Using the revised equation of state for thermodynamic equilibrium calculations leads to low-pressure and -temperature behavior indistinguishable from the unmodified equation of state, yet extrapolates to high pressure and temperature without non-physical behavior.
Key Words: Thermodynamics equation of state properties phase equilibria calculation high-pressure studies expansivity measurements negative expansivity
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