EXPERIMENTAL STUDY OF THE DEPENDENCE OF THERMODYNAMIC PROPERTIES OF THE (PROPANOL-1 + N-OCTANE) SYSTEM IN LIQUID, GASEOUS, AND SUPERCRITICAL STATES
Bazaev E.A., Bazaev A.R., Osmanova B.K., Dzhapparov T.A.-G.
Institute for Geothermal Research and Renewable Energy
of the Joint Institute for High Temperatures RAS
367030, Makhachkala, Imama Shamilya st., 39a
Experimental data on the p, ,T,x - dependences of 1-propanol + n-octane mixtures at various compositions (0.2, 0.5, and 0.8 mole fractions of n-octane) in the temperature range of 373.15–623.15 K, density range of 1–680 kg/m³, and pressures up to 56 MPa, obtained using a constant-volume piezometer [1], are described by a virial-type thermal equation of state by expanding the compressibility factor Z = p/RT into series in terms of reduced density and temperature:
Here, is the molar density (mol/m³); ω = ρ/ρк, τ = T/Tк are the reduced density and reduced temperature, respectively; ρc, Tc are the critical density and critical temperature; R = 8.314 J/(mol⋅K) is the universal (molar) gas constant. The mean relative deviation of the pressure values calculated using the equation from the experimental data is 0.8%.
Furthermore, based on this equation and thermodynamic relations [2], the principal thermodynamic properties of the investigated mixtures were calculated in the liquid, gaseous, and supercritical states. The figure illustrates the dependence of the Helmholtz energy F on density and temperature T for the composition x = 0.5.
1. E. A. Bazaev, A. R. Bazaev, T. A.-G. Dzhapparov, and B. K. Osmanova, "Phase Transformations and Critical Properties of the C₃H₇OH–C₈H₁₈ System," High Temperature, 2025, Vol. 63, No. 3, pp. 368–374.
2. E. E. Shpilrain and P. M. Kesselman, Fundamentals of the Theory of Thermophysical Properties of Substances, Moscow: Energiya, 1977, 248 p.