نتایج جستجو برای: virial coefficient

تعداد نتایج: 171755  

Journal: :Journal of Research of the National Bureau of Standards Section A: Physics and Chemistry 1967

Journal: :physical chemistry and electrochemistry 0

in this work an analytical equation of state has been employed to calculate the pvt properties ofternary refrigerant mixtures. the theoretical eos is that of ihm, song and mason, which is based onstatistical-mechanical perturbation theory, and the two constants are enthalpy of vaporization δhvapand molar density ρnb, both at the normal boiling temperature. the following three temperaturedepende...

Journal: :The Journal of chemical physics 2015
Mariano López de Haro Carlos F Tejero Andrés Santos Santos B Yuste Giacomo Fiumara Franz Saija

The problem of demixing in the Asakura-Oosawa colloid-polymer model is considered. The critical constants are computed using truncated virial expansions up to fifth order. While the exact analytical results for the second and third virial coefficients are known for any size ratio, analytical results for the fourth virial coefficient are provided here, and fifth virial coefficients are obtained ...

Journal: :Physical review letters 1994
Murthy Shankar

We show that the particles in the Calogero-Sutherland Model obey fractional exclusion statistics as defined by Haldane. We construct anyon number densities and derive the energy distribution function. We show that the partition function factorizes in the form characteristic of an ideal gas. The virial expansion is exactly computable and interestingly it is only the second virial coefficient tha...

Journal: :journal of physical & theoretical chemistry 2013
m. aghaie f. naderi a. menatian

an interaction potential at different orientation for the ch4 and co2 complex was derived at theb3lyp level of theory and 6-31+g* basis sets. the potential energy surface was computed on somemolecular geometries. the complete basis set limit of the interaction energies were fitted to wellknownanalytical functions. to determine the second virial coefficients b, u(r) is used to obtain themodel’s ...

A revised analysis of the effect of long-range nonspherical terms in the intermolecular potential on the second virial coefficient is presented with a preferred Hartree-Fock-Dispersion functional (HFD-C) spherical core treatment of the integrations for small intermolecular distances. A set of modified numerical tables for the accurate calculation of the nonspherical contribution to the sec...

1998
B. L. Neal D. Asthagiri E. W. Kaler

A molecular basis is presented for characterizing the osmotic second virial coefficient, B 22 , of dilute protein solutions, which provides a measure of the nature of protein—protein interactions and has been shown to be correlated with crystallization behavior. Experimental measurements of the second virial coefficient of lysozyme and bovine a-chymotrypsinogen A were performed by static light ...

2001

The recently discovered attractive force between hydrophobic surfaces is incorporated in a theory of polyelectrolyte solutions. Ita influence on the second and third virial coefficients is estimated. Binary collisions between two polyions are virtually unaffected by attractive forces of long range whereas the impact on the third virial coefficient is enormous. The theoretical coefficients are c...

Journal: :Physical review. E, Statistical, nonlinear, and soft matter physics 2009
Eelco Eggen Marjolein Dijkstra René van Roij

We explicitly calculate the orientation-dependent second virial coefficient of short charged rods in an electrolytic solvent, assuming the rod-rod interactions to be a pairwise sum of hard-core and segmental screened-Coulomb repulsions. From the parallel and isotropically averaged second virial coefficient, we calculate the effective length and diameter of the rods, for charges and screening le...

2004
H. Grajek J. Choma M. Jaroniec E. Michalski

Adsorption isotherms and specific retention volumes of benzene on MCM41C16 mesoporous silica and F4O porous carbon were determined at different temperatures by employing inverse gas chromatography. The differential isosteric enthalpies, -∆Hads , and entropies, -∆Sads , of adsorption were calculated from the retention time data and compared with the results obtained from the adsorption second vi...

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