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by Vladimir Evgenievich
The equation of state relates the pressure p, volume V and temperature T of a physically
homogeneous system in the state of thermodynamic equilibrium f(p, V, T) = 0. The equation called
the thermic equation of state allows the expression of pressure in terms of volume and temperature
p = p(V, T) and the definition of an elementary work δA = pδV at an infinitesimal change of system
volume δV. As distinguished from thermic equations, the caloric equation of state specifies the
dependence of the internal energy of the system E on volume V and temperature T (either p and V
or p and T).
The equation of state is a fundamental characteristic of a substance which makes possible the
application of the general principles of thermodynamics and hydrodynamics to particular physical
objects.
Equations of state cannot be derived from thermodynamic relations alone but rely also on either
experimental measurements or on theoretical calculations by the methods of statistical physics,
using various models of interparticle interactions in a system. The First Law of Thermodynamics
suggests that there exists a caloric equation of state while the Second, a relation between the
thermodynamic and the caloric equations of state in the form ∂E/∂V T = T(∂p/∂T)V − p. The
thermodynamic relationship allows the determination of the thermic and caloric equations of state,
if the thermodynamic potential, specified in the form of a function of appropriate variables, is
known. Thus, for instance, for Helmholtz free energy F as a function of volume V and temperature
T, we have:
A simple example of the equation of state for gases is the Clapeyron-Mendeleev equation pν = RT,
where R is the gas constant and v is the volume of one mole. For real gases, and considering the
interaction between particles, virial equations of state pν = RT(1 + B(T)/ν + C(T)/ν 2 + ... ) are
widely used, where B(T), C(T), ... , are the second, third, etc. virial coefficients. These coefficients
are the functions of temperature alone and, depend on the forces of two, three or more particles
interacting in the system. This equation of state for real gases is the most theoretically-substantiated
one, but the calculation of higher order virial coefficients is limited by the difficulties presented by
multiple integrals. With a rise in density, the character of the convergence of the virial expansion
also deteriorates drastically. In dense systems, nonadditivity of interparticle interaction becomes
significant which, when considered, changes drastically the values of the higher order virial
coefficients.
A qualitatively accurate picture of a phase diagram of real gases yields the van der Waals equation
of state (p + a/ν2)(ν − b) = RT, in which a and b are constants whose values are determined from the
adequate description of experimental data. This equation considers both the existence of attractive
forces between the gas molecules, which brings about a decrease in pressure, and the presence of
repulsive forces, which appears when the distances between molecules are small, preventing an
infinite compression of the gas. The van der Waals equation of state has made it possible for the
first time to obtain a thermodynamically-consistent description of a phase gas-liquid transition,
which terminates at the critical point with parameters p c, νc, and Tc —where the difference between
the liquid and gaseous states disappears. If the equation of state is represented in a reduced form,
i.e., in dimensionless parameters p/pc, ν/νc, T/Tc, then the equations of state of various substances
differ only slightly (the so-called law of corresponding states) within the limits of a definite group
(simple liquids, alkali metals) over a reasonably large near-the-critical area.
The weak dependence of liquid structure on temperature at constant density is the decisive factor in
creating models of equations of state for a liquid.
Molten metals, ionic systems and dielectrics, having substantially different attractive forces, and
this testifies to the small role these forces play in forming the equilibrium properties of a liquid.
These facts reveal the leading contribution of repulsive potential, while attractive forces and
accounting for the temperature effects in a liquid bring about only minor corrections. A simple
potential of interaction of solid spheres with radius a is widely used as a model for the description
of repulsive forces in the system:
which characterizes the limit state of a highly-compressed and hot liquid. The model for hard
spheres, being the simplest nontrivial model of the equation of state of a liquid, is widely used in
Integral Equations, numerical Monte-Carlo methods and in molecular dynamics. Using different
methods, the calculation of a system of particles with the potential of solid spheres is made over the
entire range of a liquid state. This can be represented with high accuracy by the Pade analytic
Carnahon-Starling approximation
which has a free parameter ν = 4πa 3n/3 (n is the number density of the particles) that characterizes
the degree of solid sphere packing. It must be noted that numerical calculations of the potential of
solid spheres, with density approximating the dense packing of spheres ν ≤ 1, have shown a
tendency towards the appearance of a long-range order in the system which is associated with
crystallization.
Considerable progress in describing the thermodynamic properties of a liquid phase have been
attained with the help of a soft sphere model. This model uses a power potential of repulsion
which is also the basis for carrying out numerical calculations by the Monte-Carlo method and by
the molecular dynamics method. The resulting calculations of the equation of state of soft spheres is
described for any 4 ≤ n ≤ 12 by the approximating formula
where η = a3n/√2 and ε and n are the additional free parameters of the model. The power potential
of repulsion, like the potential of hard spheres, brings about crystallization—whose characteristics
depend strongly on the value of n.
A modified van der Waals’ model based on the combination of an approximate formula for the
potential of soft spheres and an approximated average field considerably improves the description
of the thermodynamic properties of a dense gaseous phase and a liquid. Greater accuracy in
describing experimental data is achieved by using the results of calculations for the
thermodynamics of a system of soft spheres and introducing adjusting parameters into the average
field model. The modified van der Waals’ equations of state can be equally useful for calculating the
thermodynamic properties of liquids and dense gaseous phase. They have asymptotics of an ideal
gas, which makes it possible to use them successfully for expressing a wide-range of semiempirical
equations of state. These models can also define the equilibrium liquid-vapor line and the critical
point. But as a whole, they are quantitative and do not give a detailed description of the fine
characteristics of a liquid; in particular, the dual correlation function g(r) which defines all
equilibrium properties of a liquid phase for a given potential of interparticle interaction φ(r).
The density of a liquid near the melting point curve differs slightly (by 10–20%) from that of a
crystal, which explains the success of equations of state for describing solid-state models. The
notion of liquid molecules localizing in a small area in space under the action of an average field of
neighbors forms the basis for the lattice model, or for the unconfined space theory. Such an
approach, however, is applied only for a strongly-compressed liquid at low temperatures when
kinetic energy forms a small fraction of total energy, a condition which, in general, does not
correspond to a liquid state. A combination of solid-state and gaseous notions brings about a
multistructural model, according to which an actual liquid is an equilibrium mixture of gaseous and
solid bodies, whose properties can be described by a dual distribution function. Similar notions are
used in a cell model where the liquid is divided into molecular cells, which are filled depending on
thermodynamic conditions. Such models describe only schematically the thermodynamic properties
of a real liquid.
Models of hard and soft spheres properly take into account the basic qualitative characteristics of
multiparticle interactions in a dense liquid. This makes it possible to use them as a zero
approximation model in calculating equations of state. The details of real potential of interparticle
interaction are carried out within the framework of the thermodynamic perturbation theory, the
chaotic phase approximation or on the basis of the variational method of perturbation theory. The
variational method is most convenient for calculating the thermodynamics of particular liquids over
a wide range of parameters and is especially effective in describing the properties of a dense liquid
phase. Gibb’s-Bogolyubov’s inequality is used in finding the free energy F(V, T) of a system of
particles with an arbitrary potential of interaction φ(r)
where F0 and g0 are the free energy and a dual correlation function of the original system with
interparticle interaction potential φ0(k), respectively. The equation of state of an arbitrary system is
defined by averaging the perturbation over the structural characteristics of an initial approximation
and further minimizing a free parameter of this approximation λ according to (∂F/∂λ) V,T = 0. It is
good practice to take a system of solid spheres as the zero approximation, for there are analytical
expressions defining the free energy and dual correlation functions. This allows the explicit
calculation of the thermodynamic characteristics of an arbitrary potential of the interparticle
interaction. The radius of solid spheres is, in this case, the minimizing parameter λ. But at large
densities, use of the solid spheres system as the initial one brings about essential errors, caused by
the strong repulsion of particles at small distances. The choice, as the zero approximation model, of
“soft” power potential φ(r) = C/r12 is usually favored here. Use of the soft and solid spheres model
for the original approximation results in equations of state of inert liquids or molecular gases and
simple metals that are of high accuracy.
The development of the variational method of perturbation theory for calculating the equation of
state of liquid metals has led to the use of the results obtained from the Monte-Carlo method for a
single-component plasma as the zero approximation. The model of a single-component plasma is
based on numerical simulation of a simple system of point-like particles with Coulomb interaction,
located, for its stability, on a homogeneous background of a balance charge with an opposite sign.
In this case, there exists an analytical expression for F 0, with the Coulomb nonideality parameter Γ
= e/kTrws as the minimizing quantity, and the average interparticle distance rws = (3/4πn)1/3. Results
of calculating the equations of state have shown that for liquids with slight repulsion (alkali metals,
solt melts, alloys), a single-component plasma model is best suited. It should be noted that the final
expression for the equation of state of liquid metals—in addition to the configurational term
determined by the variational method, the expression for energy—must include terms according to
the Coulomb interaction energy and the kinetic energy of particles of the system, whose total value
at high temperatures becomes significant. In simple liquids, the same holds true when accounting
for electron excitation at high temperatures.
Additional information on equations of state are given in the article PVT Relationships.
To form equations of state for a solid body, phonon and electron components are distinguished and
are considered separately to a large degree. A distinguishing feature of solid bodies is their atoms
which oscillate about the nodes of a crystal lattice. A quasi-harmonic model of a solid body is based
on the representation of a crystal lattice in the form of 3N oscillators. The most widespread
interpolation of the Debye equation for a solid body has been obtained in the approximation of a
sound spectrum of heat variations, which yields the following expression for heat components of
energy and pressure:
where is the Debye function, θD is the Debye temperature dependent on
volume and γ = − d lnθD/d lnV is the Grüneisen coefficient. The Debye function D(θ D/T) ensures in