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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 836-839 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 7 (1986), S. 911-922 
    ISSN: 1572-9567
    Keywords: carbon dioxide ; critical region ; equation of state ; hydrocarbons ; scaling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A critical scaling method for equations of state developed by Fox at the National Bureau of Standards has been extended to predict thermodynamic properties and all of the first and second derivatives of the chemical potential and density. This is done by using a new damping function and developing expressions which avoid all numerical evaluations of the derivatives needed in calculating thermodynamic properties. Using this procedure, an analytical 32-constant equation of state was scaled in the critical region for pure light hydrocarbons and for carbon dioxide. The BWRS equation was scaled for heavier hydrocarbons. Calculations of the saturated vapor and liquid densities of methane in the region from 175 K to the critical temperature of 190.5 K were improved, and the mean absolute error decreased from 0.153 without scaling to 0.031 with scaling. Other derivative properties were also improved in the critical region for several of the lighter pure hydrocarbons.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 7 (1986), S. 331-341 
    ISSN: 1572-9567
    Keywords: Activity coefficients ; corresponding states ; group contributions ; hard-sphere theory ; polar contributions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A new method has been developed for predicting liquid activity coefficients in ternary mixtures from group contributions. In this method, activity coefficients are obtained from the excess Gibbs free energy of mixing at constant temperature and pressure. In calculating this excess function, the constituent and mixture Gibbs free energies are each represented by an expansion about a pure reference fluid in powers of ratios of hard-sphere diameters and molecular attraction parameters. When the pure component differs from the reference by a single structural group, these ratios represent, respectively, the size contribution and the attraction contribution of this group to the thermodynamic property of the pure fluid. Contributions of intermolecular repulsion to the excess Gibbs free energy are calculated directly from hard-sphere equations of state for the mixture and pure components. The effect of polar contributions calculated by a Padé approximant is also examined. Results indicate that the method developed from the hard-sphere expansion corresponding-states theory is useful for predicting activity coefficients in ternary mixtures when unlike-pair interaction parameters are fitted to binary activity coefficient data. Furthermore, the method shows promise in providing a theoretical basis for applying group contributions to activity coefficients.
    Type of Medium: Electronic Resource
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