A new non-extensive equation of state for the fluid phases of argon including the metastable states, from the melting line to 2300 K and 50 GPa
arXiv:1504.00633 · doi:10.3390/fluids9050102
Abstract
A new equation of state for argon has been developed in view to extend the range of validity of the equation of state previously proposed by Tegeler et al. (Ref. 4) and to obtain a better physical description of the experimental thermodynamic data for the whole fluid region (single-phase, metastable and saturation states). As proposed by Tegeler et al., this equation is also based on a functional form of the residual part of the reduced Helmholtz free energy. However in this work, the fundamental equation for the Helmholtz free energy has been derived from the measured quantities CV(rho,T) and P(rho,T). The empirical description of the isochoric heat capacity CV(rho,T) is based on an original empirical description containing explicitly the metastable states. The thermodynamic properties (internal energy, entropy, free energy) are then obtained by combining integration of CV(rho,T). The arbitrary functions introduced by the integration process have been deduced from a comparison between calculated and experimental pressure P(rho,T) data. The new formulation is valid for the whole fluid region from the melting line to 2300 K and for pressures up to 50 GPa. It also predicts existence of a maximum of the isochoric heat capacity CV along isochors as experimentally observed in several other fluids. For many applications, an approximate form of the equation of state for the liquid phase may be sufficient. A Tait-Tammann equation is therefore proposed between the triple point temperature and 148 K.
arXiv comment93 pages, 53 figures, 12 tables, 3 appendix
References in corpus (4)
- A New Single Equation of State to describe the Dynamic Viscosity and Self-Diffusion Coefficient for all Fluid Phases of Water from 200 K to 1800 K based on a New Original Microscopic Model
- A novel general modeling of the viscoelastic properties of fluids: application to mechanical relaxation and low frequency oscillation measurements of liquid water
- New Equations of State describing both the Dynamic Viscosity and Self-Diffusion Coefficient for Potassium and Thallium in their fluid phases
- A novel approach for modeling the non-Newtonian behavior of simple liquids: application to liquid water viscosity from low to high shear rates