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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 11 (1990), S. 503-513 
    ISSN: 1572-9567
    Keywords: equation of state ; molecular gases ; nonspherical interactions ; second virial coefficients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A self-consistent scheme is given for the calculation of the contributions of nonspherical molecular interactions to second virial coefficients. The usual longrange nonspherical interactions, which are asymptotically valid only at large separations, are modified by damping functions that render them valid at small separations as well. Numerical tables of new auxiliary functions J n D (T*) are given for 6⩽n⩽30 and 0.5⩽T *⩽10. These are designed to be used in the identical statistical-mechanical formalism for the second virial coefficient that had been developed for the undamped long-range nonspherical interactions.
    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. 1115-1133 
    ISSN: 1572-9567
    Keywords: equation of state ; molecular gases ; nonspherical interactions ; second virial coefficients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A set of improved numerical tables is given for use in calculating the effects of nonspherical molecular interactions on the second virial coefficients of simple molecular gases. The second virial coefficients are given as a spherical-core contribution (not discussed in this paper) plus a series of nonspherical perturbation terms. The tables give easy-to-interpolate auxiliary functions that occur in the perturbation terms. These functions depend on the form assumed for the spherical-core part of the interaction potential, but only in a relatively insensitive way, so that the tables should be adequate for almost all calculations that are likely to occur in this connection. The auxiliary functions J nT are tabulated for n from 6 to 30 and T from 0.5 to 10, where T* = kT/ɛe 0 and ɛe 0 is the well depth of the spherical-core potential. Explicit formulas are given for the simple cases of axially symmetric molecules, but the tabulated functions can also be used for more complex cases.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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