Calculation of the second virial coefficient and molecular radius of polar and non-polar substances using a new potential function

2019 ◽  
Vol 492 ◽  
pp. 88-100 ◽  
Author(s):  
Hamed Peyrovedin ◽  
Feridun Esmaeilzadeh ◽  
Mojtaba Binazadeh
1954 ◽  
Vol 32 (12) ◽  
pp. 759-763 ◽  
Author(s):  
C. F. A. Beaumont

A new potential function for liquid helium is obtained by modifying the Margenau potential function and summing over a suggested structure for the liquid. The new potential function leads to fair agreement with the first peak of the radial distribution curve for liquid helium, with the isothermal compressibility, and with second virial coefficient data at high temperatures.


1971 ◽  
Vol 24 (8) ◽  
pp. 1567 ◽  
Author(s):  
CHJ Johnson ◽  
TH Spurling

Pairwise additive third virial coefficients for axially symmetric multipolar molecules have been calculated using a non-product multidimensional integration formula. Results for the Stockmayer potential agree with the corrected results of Rowlinson. It is found that the inclusion of the dipole-quadrupole and quadrupole-quadrupole terms in the potential function has a marked qualitative effect on the shape of the C-T curve. Values of the third virial coefficient for water vapour calculated using a potential function derived from gaseous viscosity and second virial coefficient data are in good agreement with the experimental values.


2013 ◽  
Vol 2013 ◽  
pp. 1-29 ◽  
Author(s):  
Seung-Kyo Oh

The three-parameter Lennard-Jones (12-6) potential function is proposed to calculate thermodynamic property (second virial coefficient) and transport properties (viscosity, thermal conductivity, and diffusion coefficient) of noble gases (He, Ne, Ar, Kr, and Xe) and their mixtures at low density. Empirical modification is made by introducing a reduced temperature-correction parameter τ to the Lennard-Jones potential function for this purpose. Potential parameters (σ, ε, and τ) are determined individually for each species when the second virial coefficient and viscosity data are fitted together within the experimental uncertainties. Calculated thermodynamic and transport properties are compared with experimental data by using a single set of parameters. The present study yields parameter sets that have more physical significance than those of second virial coefficient methods and is more discriminative than the existing transport property methods in most cases of pure gases and of gas mixtures. In particular, the proposed model is proved with better results than those of the two-parameter Lennard-Jones (12-6) potential, Kihara Potential with group contribution concepts, and other existing methods.


2020 ◽  
Vol 49 (3) ◽  
pp. 261-278
Author(s):  
MASOUMEH KIANI

In this study, the density of nanoparticles, nanofluids containing a base fluid and nanofluids containing a mixture of two base fluids in the compressive range of 0.1-45 MPa and a temperature range of 273-363 K were calculated and predicted. The equation of state used in this work is the Ihm-Sang-Mason equation of state. According to the quantum properties of nanoparticles, a part of quantum correction was used to calculate the second virial coefficient. The potential function of Morse three-parameters was used which is more flexible than the usual potential functions of two-parameters such as Lenard Jones 12-6.


1995 ◽  
Vol 60 (10) ◽  
pp. 1641-1652 ◽  
Author(s):  
Henri C. Benoît ◽  
Claude Strazielle

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.


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