scholarly journals Re-evaluation of experimental data on the second virial coefficient for steam and development of its analytical representation as a function of the internal energy

2013 ◽  
Vol 45 ◽  
pp. 01024 ◽  
Author(s):  
M. Duška ◽  
J. Hrubý
2001 ◽  
Vol 66 (6) ◽  
pp. 833-854 ◽  
Author(s):  
Ivan Cibulka ◽  
Lubomír Hnědkovský ◽  
Květoslav Růžička

Values of adjustable parameters of the Bender equation of state evaluated for chloromethane, dichloromethane, trichloromethane, tetrachloromethane, and chlorobenzene from published experimental data are presented. Experimental data employed in the evaluation included the data on state behaviour (p-ρ-T) of fluid phases, vapour-liquid equilibrium data (saturated vapour pressures and orthobaric densities), second virial coefficients, and the coordinates of the gas-liquid critical point. The description of second virial coefficient by the equation of state is examined.


Author(s):  
E. Somuncu ◽  
B.A. Mamedov

An analytical expression for the second virial coefficient based on an exponent-spline-Morse-spline-van der Waals (ESMSV) potential is presented here for use in defining the thermodynamic properties of rare gases. Our method is established based on a series expansion of the exponential function, Meijer function, gamma function, binomial function, and hypergeometric function. Numerical approaches have commonly been used for the evaluation of the second virial coefficient with the ESMSV potential in the literature. The general formula obtained here can be applied to estimate the thermal properties of rare gases. Our results for the second virial coefficient based on the ESMSV potential of He-He, He-Ne, He-Ar, and He-Xe rare gases are compared with numerical calculations and experimental data, and it is shown that our analytical expression can be successfully used for other gases.


1980 ◽  
Vol 45 (9) ◽  
pp. 2375-2383 ◽  
Author(s):  
Miloš Ševčík ◽  
Tomáš Boublík

The second virial coefficient in systems with permanent and induced multipole interactions was studied by using a statistical-thermodynamics correlation based on the perturbation theory of fluids. Several pair potential combinations of the Lennard-Jones function with different, subsequently more complex anisotropic contributions, were considered; the improvement in the description of intermolecular interactions due to these non-central contributions brought about an improvement in the interpretation of experimental data. The characteristic dependence of the parameters ε/k on σ at different temperatures was obtained for all of the three systems studied (Ar, CH4 and CH3F). It was found that if experimental values of the second virial coefficient of methyl fluoride are correlated by a relation derived from the Stockmayer potential, two sets of the ε/k and σ can be employed.


1967 ◽  
Vol 45 (4) ◽  
pp. 409-412 ◽  
Author(s):  
Jacques Léonard ◽  
Hubert Daoust

Osmotic pressures of polymethylmethacrylate in solution in ethylene dichloride and in dioxane have been measured at 25 °C for concentrations up to 24%. In both cases, the apparent second virial coefficient, S, increases rapidly with concentration to reach a plateau at approximately 8% in polymer, and then increases monotonically as predicted by the well-known Flory–Huggins theory. The theoretical treatments of Fixman and Yamakawa on moderately concentrated polymer solutions give very good correlations with the experimental data up to the plateau region.However, both theories cannot use the same set of molecular dimension parameters in order to obtain the best fit.


PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0258429
Author(s):  
Fan Yin ◽  
Domarin Khago ◽  
Rachel W. Martin ◽  
Carter T. Butts

Static light scattering is a popular physical chemistry technique that enables calculation of physical attributes such as the radius of gyration and the second virial coefficient for a macromolecule (e.g., a polymer or a protein) in solution. The second virial coefficient is a physical quantity that characterizes the magnitude and sign of pairwise interactions between particles, and hence is related to aggregation propensity, a property of considerable scientific and practical interest. Estimating the second virial coefficient from experimental data is challenging due both to the degree of precision required and the complexity of the error structure involved. In contrast to conventional approaches based on heuristic ordinary least squares estimates, Bayesian inference for the second virial coefficient allows explicit modeling of error processes, incorporation of prior information, and the ability to directly test competing physical models. Here, we introduce a fully Bayesian model for static light scattering experiments on small-particle systems, with joint inference for concentration, index of refraction, oligomer size, and the second virial coefficient. We apply our proposed model to study the aggregation behavior of hen egg-white lysozyme and human γS-crystallin using in-house experimental data. Based on these observations, we also perform a simulation study on the primary drivers of uncertainty in this family of experiments, showing in particular the potential for improved monitoring and control of concentration to aid inference.


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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