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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 17 (1996), S. 391-404 
    ISSN: 1572-9567
    Keywords: coexistence curve ; equation of state ; Lennard Jones fluid ; thermodynamic properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A new equation of state (EOS) is proposed for the Helmholtz energyF of the Lennard Jones fluid which represents the thermodynamic properties over a wide range of temperatures and densities. The EOS is written in the form of a generalized van der Waals equation.F =F u +F v. WhereF u is a hard body contribution andF A an anttractive dispersion force contribution. The expression forF H is closely related to the hybrid Barker Henderson pertubation theory. The construction ofF A is accomplished with the Setzmann Wagner optimization procedure on the basis of virial coefficients and critically assessed computer simulation data. A comparison with the EOS of Johnson et al. shows improvement in the description of the vapor liquid coexistence properties, thepvT data. and in peculiar, of the calorie properties. A comparison with the EOS of Kolafa and Nezbeda which appeared after the bulk of this work was finished shows still by about 30%.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 19 (1998), S. 1121-1132 
    ISSN: 1572-9567
    Keywords: caloric properties ; density ; equation of state ; nitrogen ; thermodynamic properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A new formulation describing the thermodynamic properties of nitrogen has been developed. New data sets which have been used to improve the representation of the p–ρ–T surface of gaseous, liquid and supercritical nitrogen, including the saturated states are now available. New measurements on the speed of sound from spherical resonators have been used to improve the accuracy of caloric properties in gaseous and supercritical nitrogen. State-of-the-art algorithms for the optimization of the mathematical structure of the equation and special functional forms for an improved description of the critical region were used to represent even the most accurate data within their experimental uncertainty. The uncertainty in density of the new reference equation of state ranges from ±0.01% between 270 and 350 K at pressures less than 12MPa, within ±0.02% over all other temperatures less than 550 K and pressures less than 12 MPa, and up to a maximum of ±0.6% at the highest pressures. The equation is valid from the triple point to temperatures of 1000 K and pressures up to 2200 MPa. The new formulation yields a reasonable extrapolation up to the limits of chemical stability of nitrogen as indicated by comparison to experimental shock tube data. Constraints regarding the structure of the equation ensure reasonable extrapolated properties up to temperatures and pressures of 5000 K and 25 GPa. For typical calibration applications, the new reference equation is supplemented by a simple but also highly accurate formulation, valid only for supercritical nitrogen between 270 and 350 K at pressures up to 30 MPa.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 14 (1993), S. 699-725 
    ISSN: 1572-9567
    Keywords: argon ; caloric properties ; density ; equation of state ; Helmholtz function ; methane ; nitrogen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract In order to describe the thermodynamic behavior of methane, argon, and nitrogen in the so-called “natural-gas region,” namely, from 270 to 350 K at pressures up to 30 MPa as accurate as possible with equations of a very simple form, new equations of state for these three substances have been developed. These equations are in the form of a fundamental equation in the dimensionless Helmholtz energy; for calculating the pressure or the density, the corresponding equations explicit in pressure are also given. The residual parts of the Helmholtz function representing the behavior of the real gas contain 12 fitted coefficients for methane, 8 for argon, and 7 for nitrogen. The thermodynamic relations between the Helmholtz energy and the most important thermodynamic properties and the needed derivatives of the equations are explicitly given; to assist the user there is also a table with values for computer-program verification. The uncertainties when calculating the density ρ, the speed of sound w, the isobaric specific heat capacity c p, and the isochoric specific heat capacity c v are estimated as follows. For all three substances it is Δρ/ρ≤±0.02 % for p≤ 12 MPa and Δρ/ρ ≤ ±0.05% for higher pressures. For methane it is Δw/w≤±0.02% for p≤10 MPa and Δw/w≤+-0.1% for higher pressures; for argon it is Δw/w≲-0.1 % for p≤ 7 MPa, Δw/w≤±0.3 % for 7 〈p≤30 MPa; and for nitrogen it is Δw/w≤±0.1% for p≤1.5 MPa and Δw/w±0.5% for higher pressures. For all three substances it is Δc p/c p≤±1 % and ΔC v/C v≤±1 % in the entire range.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 10 (1989), S. 1103-1126 
    ISSN: 1572-9567
    Keywords: correlation equation ; equation of state ; least-squares principle ; optimization method ; search method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract An optimization strategy is presented for optimizing the structure of empirical thermodynamic correlation equations. Based on a comprehensive functional expression for the physical dependence considered, which is called a “bank of terms,” the new procedure optimizes the structure and the length of the equation as well. The application of this method results in an equation which meets the quality wanted for representing the experimental data with the lowest number of fitted coefficients. The procedure can be used for the determination of the structure of any equation where the method of the linear least squares is applicable. A detailed description of the algorithm is given which includes values for the control parameters for different applications in the field of thermodynamics (vapor pressure equations, equations of state, etc.) and also for applications in other fields. The optimization steps are described using an equation which represents a relationship between variables in a general form. It is demonstrated how even the complex problem of the optimization of a fundamental equation for the Heimholtz energy can be written in terms of this general equation.
    Type of Medium: Electronic Resource
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