Derivation of Interatomic Potentials for Inert‐Gas Atoms from the Second Virial Coefficient

1965 ◽  
Vol 42 (2) ◽  
pp. 719-722 ◽  
Author(s):  
A. E. Kingston
Keyword(s):  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Inert Gas ◽  
Interatomic Potentials

Predicting the borderline between the classical and quantum regimes in 4He gas from the second virial coefficient

2014 ◽  
Vol 92 (9) ◽  
pp. 997-1001 ◽  
Author(s):  
H.B. Ghassib ◽  
A.S. Sandouqa ◽  
B.R. Joudeh ◽  
S.M. Mosameh
Keyword(s):  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Quantum Mechanical ◽  
Interatomic Potentials ◽  
Number Density ◽  
Temperature Range ◽  
Interparticle Potential ◽  
Main Input ◽  
Effective Phase ◽  
Full Quantum

The second Virial coefficient in both classical and quantum regimes of 4He gas is investigated in the temperature range 4.2–10 K. Full quantum mechanical and classical treatments are undertaken to calculate this coefficient. The main input in computing the quantum coefficient is the “effective” phase shifts. These are determined within the framework of the Galitskii–Migdal–Feynman formalism, using two interatomic potentials. The borderline between the classical and quantum regimes is found to depend on the temperature, the number density, and the interparticle potential.

Interpretation of Preferential Adsorption Using Random Phase Approximation Theory

1995 ◽  
Vol 60 (10) ◽  
pp. 1641-1652 ◽  
Author(s):  
Henri C. Benoît ◽  
Claude Strazielle
Keyword(s):  
Approximation Theory ◽  
Random Phase Approximation ◽  
Virial Coefficient ◽  
Random Phase ◽  
Second Virial Coefficient ◽  
Solvent Mixture ◽  
Gyration Radius ◽  
Thermodynamic Quantities ◽  
Phase Approximation ◽  
Preferential Adsorption

It has been shown that in light scattering experiments with polymers replacement of a solvent by a solvent mixture causes problems due to preferential adsorption of one of the solvents. The present paper extends this theory to be applicable to any angle of observation and any concentration by using the random phase approximation theory proposed by de Gennes. The corresponding formulas provide expressions for molecular weight, gyration radius, and the second virial coefficient, which enables measurements of these quantities provided enough information on molecular and thermodynamic quantities is available.

Scattering of anyons with hard-disk repulsion and the second virial coefficient

1991 ◽  
Vol 44 (19) ◽  
pp. 10731-10735 ◽  
Author(s):  
Akira Suzuki ◽  
M. K. Srivastava ◽  
R. K. Bhaduri ◽  
J. Law
Keyword(s):  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Hard Disk

GENERAL FORMULA FOR THE SECOND VIRIAL COEFFICIENT

1961 ◽  
Vol 39 (11) ◽  
pp. 1563-1572 ◽  
Author(s):  
J. Van Kranendonk
Keyword(s):  
Phase Shift ◽  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Resolvent Operators ◽  
Simple Derivation ◽  
Scattering Phase ◽  
Scattering Phase Shifts ◽  
Quantization Volume ◽  
Mechanical Expression ◽  
The Waves

A simple derivation is given of the quantum mechanical expression for the second virial coefficient in terms of the scattering phase shifts. The derivation does not require the introduction of a quantization volume and is based on the identity R(z)−R0(z) = R0(z)H1R(z), where R0(z) and R(z) are the resolvent operators corresponding to the unperturbed and total Hamiltonians H0 and H0 + H1 respectively. The derivation is valid in particular for a gas of excitons in a crystal for which the shape of the waves describing the relative motion of two excitons is not spherical, and, in general, varies with varying energy. The validity of the phase shift formula is demonstrated explicitly for this case by considering a quantization volume with a boundary the shape of which varies with the energy in such a way that for each energy the boundary is a surface of constant phase. The density of states prescribed by the phase shift formula is shown to result if the enclosed volume is required to be the same for all energies.

Theoretical Assessment of Compressibility Factor of Gases by Using Second Virial Coefficient

2018 ◽  
Vol 73 (2) ◽  
pp. 121-125
Author(s):  
Bahtiyar A. Mamedov ◽  
Elif Somuncu ◽  
Iskender M. Askerov
Keyword(s):  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Compressibility Factor ◽  
Analytical Approximation ◽  
Accurate Evaluation ◽  
Numerical Examples ◽  
Lennard Jones ◽  
Theoretical Assessment ◽  
Good Agreement

AbstractWe present a new analytical approximation for determining the compressibility factor of real gases at various temperature values. This algorithm is suitable for the accurate evaluation of the compressibility factor using the second virial coefficient with a Lennard–Jones (12-6) potential. Numerical examples are presented for the gases H2, N2, He, CO2, CH4 and air, and the results are compared with other studies in the literature. Our results showed good agreement with the data in the literature. The consistency of the results demonstrates the effectiveness of our analytical approximation for real gases.

Quantum Mechanical Second Virial Coefficient of a Lennard‐Jones Gas. Helium

1969 ◽  
Vol 50 (9) ◽  
pp. 4034-4055 ◽  
Author(s):  
M. E. Boyd ◽  
S. Y. Larsen ◽  
J. E. Kilpatrick
Keyword(s):  
Virial Coefficient ◽  
Second Virial Coefficient ◽  
Quantum Mechanical ◽  
Lennard Jones
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