A General Model for Thermodynamic Properties of Fluid Mixtures Based on Helmholtz Energy Formulations for the Components. Virial Expansion and Reduction to van der Waals \nMixing Rules

0577496 - ÚT 2024 RIV US eng J - Článek v odborném periodiku
Hrubý, Jan
A General Model for Thermodynamic Properties of Fluid Mixtures Based on Helmholtz Energy Formulations for the Components. Virial Expansion and Reduction to van der Waals
Mixing Rules.
International Journal of Thermophysics. Roč. 44, č. 8 (2023), č. článku 130. ISSN 0195-928X. E-ISSN 1572-9567
Grant CEP: GA ČR(CZ) GA22-03380S
Institucionální podpora: RVO:61388998
Klíčová slova: fluid mixtures * multiparameter equation of state * thermodynamic properties * virial coefficient
Obor OECD: Fluids and plasma physics (including surface physics)
Impakt faktor: 2.2, rok: 2022
Způsob publikování: Open access
https://link.springer.com/article/10.1007/s10765-023-03237-8

Over the recent decades, Helmholtz energy formulations became available for a broad range of fluids. These multiparameter equations of state (R. Span, Springer 2000) allow computation of thermodynamic properties essentially within the experimental errorbars. Corresponding states-based model by Lemmon and Tillner-Roth (Fluid Phase Equilib 165:1, 1999) enabled construction of Helmholtz energy formulations for mixtures. However, we show that this model generates a non-physical dependence of virial coefficients on composition, which can be strong when the components are dissimilar. We propose a new mixture model that overcomes this deficiency. It has two main ingredients: (i) Quadratic mixing of 'Helmholtz volumities'. This quantity with units of molar volume is introduced as a ratio of the molar residual Helmholtz energy to a product of gas constant, thermodynamic temperature, and molar density. It reduces to the second virial coefficient in the zero-density limit. Helmholtz volumities are considered for components and 'cross-components', hypothetical fluids representing the binary interactions. (ii) Replacing the variables-reduced reciprocal temperatures and reduced densities-with temperature and density scaling functions. Different scaling functions can be used for different components and cross-components, thus providing a highly flexible framework for representing the properties of mixtures. The scaling functions must be expandable into Taylor series in terms of molar concentrations in the zero-density limit. For the proposed mixture model, we develop formulas for computing virial coefficients up to the fourth order. Furthermore, we show that when the proposed mixture model is applied to a cubic equation of state, the conventional van der Waals mixing rules can be retrieved. These findings allow to consider the new model as a viable alternative to the corresponding states method of modeling thermodynamic properties of fluid mixtures.
Trvalý link: https://hdl.handle.net/11104/0349223