Thermodynamic properties derived from the free volume model of liquids

An equation of state and expressions for the isothermal compressibility, thermal expansion coefficient, heat capacity and entropy of liquids have been derived from the Free Volume Model partition function suggested by Turnbull. The simple definition of the free volume is used and it is assumed that the specific volume is directly related to the cube of the inter-molecular separation by a proportionality factor which is found to be a function of temperature and pressure as well as specific volume. When values of the proportionality factor are calculated from experimental data for real liquids, it is found to be approximately constant over ranges of temperature and pressure which correspond to the dense liquid phase. This result provides a single-parameter method for calculating dense liquid thermodynamic properties and is consistent with the fact that the Free Volume Model is designed to describe liquids near the solidification point. Calculated values ofβ, α, C _p andS for nine liquids are compared to experimental data when possible, and agree with these data within an order of magnitude.