scholarly journals Critical phenomena in gases - I

The exact measurements of the isotherms of gases have proved extremely valuable in the determination of interatomic forces. For this purpose it has been found necessary to express the pv values of a gas as a finite power series in the density or in the pressure, and the coefficients so obtained have been compared with theoretical expressions in terms of interatomic fields. Many accounts of the method have been given and it is not necessary to give further details here (cf. Lennard-Jones 1931). While these methods are valid for gases at low densities where binary encounters are predominant, they fail for gases at high densities such as obtain in the neighbourhood of the critical point. Michels and his collaborators (Michels and others 1937) have recently studied the isotherms of gases at pressures as high as 3000 atm., and they find that the usual method of representing isotherms as simple functions of density or pressure ceases to be useful. The equation of state of van der Waals was astonishingly successful in accounting for the critical phenomena of gases and the form of the isotherms for temperatures below the critical temperature. Other empirical equations of state, for example that of Dieterici, were even more successful in reproducing the observed relations between the critical pressure, volume and temperature, and their very success has often obscured the fact that they were not logical theories of critical phenomena in gases, based as they were on arguments which were valid only for gases of low concentration. Thus the van der Waals equation, valuable as it has been and useful as it still is, implies that the internal energy of a vapour and its liquid phase is proportional only to the first power of the density, and this cannot be true for gases or vapours at densities comparable with those of liquids. The problem still remains of explaining why gases exhibit critical properties and of correlating the observed values of the critical temperature with the forces which atoms or molecules exert on each other.

In a paper recently published by Professor Lennard-Jones and the author (Lennard-Jones and Devonshire 1937) the equation of state of a gas at high concentrations has been calculated in terms of the interatomic fields. The equation found had the right kind of properties and, in particular, using the interatomic fields previously determined from the observed equation of state at low concentrations (Lennard-Jones 1931), the critical temperature was given correctly to within a few degrees for the inert gases. In this paper we shall apply the same method to determine the equation of state of a two-dimensional gas. Although such a gas cannot strictly be obtained in practice, an inert gas adsorbed on a surface (or in fact any gas held by van der Waals’ forces only) would probably behave very much like one, the fluctuations of the potential field over the surface not being of much importance. In confirmation of this it may be noted that the specific heat of argon adsorbed on charcoal was found by Simon (Simon 1935) to be equal to that of a perfect two-dimensional gas down to 60° K. A gas adsorbed on a liquid would be an even better representation of a two-dimensional one. Some measurements on the adsorption of krypton and xenon on liquid mercury have been made by Cassel and Neugebauer (Cassel and Neugebauer 1936), and they found no trace of any critical phenomena though they worked at temperatures considerably below the critical temperature of xenon. Our results are in agreement with this, for they show that the critical temperature of a two-dimensional gas should be about half that of the corresponding three-dimensional one.


2021 ◽  
Author(s):  
Simon Stephan ◽  
Jens Staubach ◽  
Hans Hasse

The Lennard-Jones (LJ) potential is widely used for describing simple fluids; it is also a point of departure for developing models of complex fluids. Thermodynamic properties of the LJ fluid have been studied by molecular simulations by many authors and a critical review of the available data, which comprises about 35,000 data points, has been published recently [J. Chem. Inf. Mod. 59 (2019) 4248–4265]. The importance of the LJ fluid has also triggered the development of a large number of equations of state (EOS). In the present work, 20 LJ EOS were critically assessed by comparing their results with consolidated data from computer experiments. A large variety of thermophysical properties was considered: vapor pressure; saturated densities; enthalpy of vaporization; critical properties; thermal, caloric, and entropic properties at homogeneous state points; and second and third virial coefficients. It was found that none of the available LJ EOS meets the following two criteria: (1) it does not yield unphysical artifacts when used for extrapolations, and (2) it describes data from computer experiments within their statistical uncertainty in most fluid regions. Furthermore, a re-parameterization of the monomer term of the PC-SAFT EOS was carried out by fitting it to data of the LJ fluid. The new LJ EOS yields good results for the LJ fluid, but does not outperform the best existing LJ EOS.


1980 ◽  
Vol 45 (4) ◽  
pp. 977-983 ◽  
Author(s):  
Jan Sýs ◽  
Anatol Malijevský

An empirical equation of state was proposed, which is based on pseudoexperimental data on the state behaviour. The equation can be used at reduced temperatures from the range 0.7-100.0 and reduced densities up to 2. Calculated compressibility factors and critical properties agree well with available literature data.


2021 ◽  
Vol 154 (19) ◽  
pp. 194302
Author(s):  
Jean Demaison ◽  
Natalja Vogt ◽  
Yan Jin ◽  
Rizalina Tama Saragi ◽  
Marcos Juanes ◽  
...  

1981 ◽  
Vol 13 (11) ◽  
pp. 993-1002 ◽  
Author(s):  
Koichi Fujisawa ◽  
Tomoo Shiomi ◽  
Fumiyuki Hamada ◽  
Akio Nakajima

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