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Correlation function, inhomogeneous

The equilibrium theory of homogeneous fluids may be constructed by using the hierarchy of the direct correlation functions [48]. This approach has been of much utility for the development of the theory of inhomogeneous simple fluids. The hierarchy of the direct correlation functions is defined by the following relation... [Pg.171]

A set of equations (15)-(17) represents the background of the so-called second-order or pair theory. If these equations are supplemented by an approximate relation between direct and pair correlation functions the problem becomes complete. Its numerical solution provides not only the density profile but also the pair correlation functions for a nonuniform fluid [55-58]. In the majority of previous studies of inhomogeneous simple fluids, the inhomogeneous Percus-Yevick approximation (PY2) has been used. It reads... [Pg.175]

The multidensity Ornstein-Zernike equation (70) and the self-consistency relation (71) actually describe a nonuniform system. To solve these equations numerically for inhomogeneous fluids one needs only an appropriate generalization of the Lowett-Mou-Buff-Wertheim equation (14). Such a generalization, employing the concept of the partial correlation function has been considered in Refs. 34,35. [Pg.200]

First we are looking for the adsorption of a fluid consisting of particles of species m, in a slit-like pore of width H. The pore walls are chosen normal to the z axis and the pore is centered at z = 0. Adsorption of the fluid m, i.e., the matrix, occurs at equihbrium with its bulk counterpart at the chemical potential The matrix fluid is then characterized by the density profile, p (z) and by the inhomogeneous pair correlation function A (l,2). The structure of that fluid is considered... [Pg.330]

Now, we would like to investigate adsorption of another fluid of species / in the pore filled by the matrix. The fluid/ outside the pore has the chemical potential at equilibrium the adsorbed fluid / reaches the density distribution pf z). The pair distribution of / particles is characterized by the inhomogeneous correlation function /z (l,2). The matrix and fluid species are denoted by 0 and 1. We assume the simplest form of the interactions between particles and between particles and pore walls, choosing both species as hard spheres of unit diameter... [Pg.331]

Finally, the closure relations for the inhomogeneous pair functions must be chosen. The PY approximation for the fluid-fluid direct correlation function presumes that its blocking part vanishes. This implies that c, ii(/,y) = 0, and... [Pg.332]

Equation 3 is exact for fluids obeying Equations 1 and 2. However, in order to compute the density n(r) from the YBG equation one must know the relationship between density distribution and the pair correlation function of Inhomogeneous fluid. Such a relationship Is not available in general. However, an approximation introduced by Fischer and Methfessel (1.) has been shown to give fairly accurate predictions of the density... [Pg.258]

Local Average Density Model (LADM) of Transt)ort. In the spirit of the Flscher-Methfessel local average density model. Equation 4, for the pair correlation function of Inhomogeneous fluid, a local average density model (LADM) of transport coefficients has been proposed ( ) whereby the local value of the transport coefficient, X(r), Is approximated by... [Pg.261]

It was Ziman [77] who has noted that there is little hope, at least at present, to develop an experimental technique permitting the direct measurement of these correlation functions. The only exception are the joint densities x / (r> ) information about which could be learned from the diffraction structural factors of inhomogeneous systems. On the other hand, optical spectroscopy allows estimation of concentrations of such aggregate defects in alkali halide crystals as Fn (n = 1,2,3,4) centres, i.e., n nearest anion vacancies trapped n electrons [80]. That is, we can find x mK m = 1 to 4, but at small r only. Along with the difficulties known in interpretating structure factors of binary equilibrium systems (gases or liquids), obvious specific complications arise for a system of recombining particles in condensed media which, in its turn, are characterized by their own structure factors. [Pg.114]

The space correlation function has been extensively used by Kratky and Pored148 149) for monodisperse particles and was also introduced by Pekeris150 and by Debye151 for a description of spatial inhomogeneities in condensed matter. y(r) always has the properties... [Pg.55]

An alternative, already implicit in van der Waals theory of the surface tension [237], exploits an interconnection between the coefficient Co and the pair correlation function g(ra, rp) of the inhomogeneous system. As the local density distribution determining g(ra, rp) is unknown, one has to resort to a... [Pg.35]

The traditional apparatus of statistical physics employed to construct models of physico-chemical processes is the method of calculating the partition function [17,19,26]. The alternative method of correlation functions or distribution functions [75] is more flexible. It is now the main method in the theory of the condensed state both for solid and liquid phases [76,77]. This method has also found an application for lattice systems [78,79]. A new variant of the method of correlation functions - the cluster approach was treated in the book [80]. The cluster approach provides a procedure for the self-consistent calculation of the complete set of probabilities of particle configurations on a cluster being considered. This makes it possible to take account of the local inhomogeneities of a lattice in the equilibrium and non-equilibrium states of a system of interacting particles. In this section the kinetic equations for wide atomic-molecular processes within the gas-solid systems were constructed. [Pg.370]


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