A general equation of state for dense fluids

Abstract

A general equation of state, originally proposed for compressed solids by Parsafar and Mason, has been successfully applied to dense fluids. The equation was tested with experimental data for 13 fluids, including polar, nonpolar, saturated and unsaturated hydrocarbons, strongly hydrogen bonded, and quantum fluids. This equation works well for densities larger than the Boyle density ρB [1/ρB=T B d B 2(T B)/T], where B2(TB) is the second virial coefficient at the Boyle temperature, at whichB 2=0 and for a wide temperature range, specifically from the triple point to the highest temperature for which the experimental measurements have been reported. The equation is used to predict some important known regularities for dense fluids, like the common bulk modulus and the common compression points, and the Tait-Murnaghan equation. Regarding the common points, the equation of state predicts that such common points are only a low-temperature characteristic of dense fluids as verifed experimentally. It is also found that the temperature dependence of the parameters of the equation of state differs from those given for the compressed solids. Specifically they are given byA 1 (T)=a 1+b1T+c1T2-d1 T ln (T).