A Rational Equation of State for Water and Water Vapor in the Critical Region

1964 ◽  
Vol 86 (3) ◽  
pp. 320-326 ◽  
Author(s):  
E. S. Nowak

A parametric equation of state was derived for water and water vapor in the critical region from experimental P-V-T data. It is valid in that part of the critical region encompassed by pressures from 3000 to 4000 psia, specific volumes from 0.0400 to 0.1100 ft3/lb, and temperatures from 698 to 752 deg F. The equation of state satisfies all of the known conditions at the critical point. It also satisfies the conditions along certain of the boundaries which probably separate “supercritical liquid” from “supercritical vapor.” The equation of state, though quite simple in form, is probably superior to any equation heretofore derived for water and water vapor in the critical region. Specifically, the deviations between the measured and computed values of pressure in the large majority of the cases were within three parts in one thousand. This coincides approximately with the overall uncertainty in P-V-T measurements. In view of these factors, the author recommends that the equation be used to derive values for such thermodynamic properties as specific heat at constant pressure, enthalpy, and entropy in the critical region.

1995 ◽  
pp. 358-364
Author(s):  
J. M. H. Levelt Sengers ◽  
W. L. Greer ◽  
J. V. Sengers

1973 ◽  
Vol 15 (2) ◽  
pp. 132-143 ◽  
Author(s):  
B. M. Burnside

Thermodynamic properties of five halogenated hydrocarbons, of importance as working fluids for small vapour power units, have been studied. The compounds are monochlorobenzene, hexafluorobenzene, o-dichlorobenzene, perfluoro-2-butyltetrahydrofuran and perfluorodecalin. With the aid of the Martin-Hou equation of state the properties of each compound, including sonic velocities and specific heat ratios, have been correlated. By comparison with the well established data for steam the accuracy of the sonic velocity and specific heat ratio values has been indicated. The information is presented in a manner which facilitates either the production of saturation and superheat tables or diagrams, or direct inclusion of the data in computer design and simulation studies of Rankine plant.


1967 ◽  
Vol 34 (2) ◽  
pp. 478-483 ◽  
Author(s):  
R. J. Zaworski ◽  
J. H. Keenan

An equation of state and expressions for enthalpy and entropy are presented for water in the region of maximum density (from freezing to about 30 deg C for pressures up to about 2500 bars). A table of thermodynamic properties computed from these expressions (Table 1) is included, and comparisons of calculated values with the data from which the equation of state was derived, and other formulations, are presented.


2005 ◽  
Vol 127 (1) ◽  
pp. 83-87 ◽  
Author(s):  
George A. Adebiyi

This article presents a procedure for formulation for the thermodynamic properties of pure substances using two primary sets of data, namely, the pvT data and the specific heat data, such as the constant-pressure specific heat cp as a function of pressure and temperature. The method makes use of a linkage, on the basis of the laws of thermodynamics, between the virial coefficients for the pvT data correlation and those for the corresponding specific heat data correlation for the substance. The resulting equations of state take on remarkably simple analytic forms that give accurate predictions over the range of input data employed.


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