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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 658-666 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A general, statistical mechanical theory which relates the properties of mixtures of different compositions is presented. It is developed within a semigrand canonical framework, and thus the mixtures are formally described by species chemical potential differences, rather than directly by composition. The introduction of a set of n-particle composition distribution functions leads to a composition-space superposition approximation (CSSA), which forms the only approximate part of the treatment. A functional expansion of the canonical partition function in terms of the composition density is used to develop systematic corrections to the CSSA. Infinitely polydisperse mixtures [D. A. Kofke and E. D. Glandt, J. Chem. Phys. 90, 439 (1989)] are shown to be the composition-space analogs of homogeneous pure fluids, and the scaling properties of these mixtures make them ideal as a reference in the theory. The required input is the density-invariant composition of the infinitely polydisperse reference. The validity of the method is demonstrated on hard-particle fluids using accurate equations of state from the literature. Although based on a polydisperse reference, the treatment is equally applicable to discrete, i.e., conventional mixtures. In its most stringent test—the prediction of pure-fluid properties—the theory based on an infinitely polydisperse reference displays quantitative agreement with known behavior.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 1055-1063 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The complete description of a homogeneous, multiphase dispersion is contained within the infinite set of n-body density distribution functions g(rn) which have been used to calculate macroscopic properties such as interfacial area and specific volume. Certain quantities of interest, however, must take the connectedness of the individual phases into account. This requires the introduction of a complete set of n-body connectedness functions g+n(rn). Until now, only the pair-connectedness function g+2(r2) has been computed. Here, a formalism for the estimation of higher-order connectedness functions from lower order ones is presented. Results are given for the average volume and interfacial area per cluster for a dispersion of randomly placed spheres.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 1932-1936 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A previously derived expression for the specific surface area of a dispersion of mutually penetrable spheres or pores is generalized for the calculation of the length of sphere–sphere intersections (lines common to two pores) and the number of cusps (points common to three pores). The results are in the form of alternating series involving correlation functions of successively higher order. Closed-form expressions are obtained for the case of randomly centered spheres. For a porous material with number density ρ of spherical pores of radius a, the length of pore–pore intersections per unit volume is 2π3a4ρ2 exp(−4πa3ρ/3) and the number of cusps per unit volume is (4)/(3) π4a6ρ3 exp(−4πa3ρ/3). The analysis is also extended to the general case of dispersions of hyperspheres in d dimensions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 8365-8373 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Wertheim's dual density formalism is applied to study the percolation behavior of dimerizing permeable spheres. The model is that of permeable spheres introduced by Blum and Stell as a generalized potential having ideal-gas (randomly centered) spheres as one limit and Percus–Yevick hard spheres as the other. Both thermodynamic results (pressure and site–site pair-correlation functions) and connectivity results (percolation threshold and site–site pair-connectedness functions) are determined for mixtures of dumbbells and spheres as a function of the penetrability factor ε, the bond length L and the fraction x1 of spheres forming dumbbells. A critical bond length L=0.553 was found for which the percolation threshold is independent of the amount of dimerization.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 4417-4425 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A theory recently proposed by the authors [Kofke and Glandt, J. Chem. Phys. 92, 658 (1990)] is applied to the study of freezing in hard spheres and hard sphere mixtures. The theory, which expresses the free energy of an arbitrary mixture as a functional of the composition density of an infinitely polydisperse (IP) reference, is used to evaluate the properties of mixtures of hard spheres constrained to the Wigner–Seitz cells of an fcc lattice. Semigrand Monte Carlo simulations are used to determine the properties of the IP reference mixture, which is also constrained to an fcc lattice. Freezing is determined by comparing the predicted properties of the Wigner–Seitz crystal with the known properties of the fluid phase. A freezing transition is found for monodisperse hard spheres; the estimated solid-phase density and the transition pressure differ from the accepted values by 2% and 8%, respectively. The treatment is also used to study freezing in polydisperse mixtures with Gaussian distributions of diameters. In accordance with the findings of others, an upper bound is found to the variance of the distribution, beyond which freezing no longer occurs. However, the maximum variance predicted here is approximately one order of magnitude less than that previously found. Discrepancies here and in the pure-fluid results are attributed largely to ergodic difficulties in the simulations of the IP reference. Finally, the possibility of a phase transition in IP mixtures is demonstrated through a calculation of the freezing point of IP hard spheres.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 439-447 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A generalized semigrand formalism for polydisperse fluids is presented and is used to derive a thermodynamic consistency equation. In the infinitely polydisperse limit—corresponding to a flat distribution of chemical potential differences—a characteristic parameter is eliminated, and the description of the mixture is greatly simplified. In the case of infinitely polydisperse hard spheres, the absence of a characteristic diameter implies that all quantities must scale to the density, which provides the only length. This leads to an exact equation of state which, remarkably, is PV/NkBT=4/3 at all densities. The treatment is generalized, to show that there exists a whole family of stationary composition distributions which have invariant compressibility factors. Monte Carlo simulation is used to verify these results, and applications to other potentials are discussed. Infinitely polydisperse fluids provide a convenient starting point for new mixture theories.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 4316-4325 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Wertheim's dual density formalism is applied to study the thermodynamics and gelation behavior of dimerizing adhesive spheres. Both the thermodynamic results (critical points and site–site correlation functions) and connectivity results (gelation threshold and site–site connectedness functions) are determined for mixtures of dumbbells and spheres as a function of the fraction x1 of spheres forming dumbbells, the bond length, and the degree of adhesiveness.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5945-5953 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Ornstein–Zernike equations previously introduced by two of the authors for a fluid in equilibrium within a quenched disordered matrix are solved numerically within the Percus–Yevick approximation. The structure of a fluid of hard spheres is reported for two types of microporous matrices: a sintered-type structure of mutually penetrable (randomly placed) obstacles or sites, and a packed bed of quenched hard spheres. The integral-equation results agree well with Monte Carlo simulation data also reported here. For the case of point obstacles, when both models coincide, the structure of the fluid is found to be insensitive to obstacle concentration. The structure of a hard-sphere fluid in a bed of other quenched hard spheres is found to be significantly different from that of the equilibrium binary mixture of the two types of particles. Pressures and bulk-pore partition coefficients are reported for beds of randomly placed obstacles. A sparse-matrix approximation is presented and compared with the full solution. These are the first results for the equilibrium properties of fluids in disordered substrates.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 8325-8329 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The behavior of molecular and polymeric fluids adsorbed within microporous solids plays an important role in many technologies. We apply a recently proposed statistical mechanical model which combines ideas found in two different formalisms: The polymer RISM theory of Curro and Schweizer, and the integral equations of Madden and Glandt for a simple fluid adsorbed within a random porous solid. These approaches yield a detailed systematic microscopic model for the structure of flexible polymers in microporous materials. We have obtained numerical results for the structural properties of ideal polymer melts confined within a matrix of hard-sphere obstacles.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 4257-4264 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Using the Gibbs Ensemble Monte Carlo (GEMC) simulation technique, we examine the liquid–liquid phase behavior for a symmetric binary LJ fluid confined in a disordered solid matrix. Increasing the matrix packing fraction and adsorption strength, and lowering the ratio of adsorbent to adsorbate particle size reduces the magnitude of the miscibility gap. We also employ Voronoi tessellations to analyze the distribution of cavity sizes in mono- and polydisperse matrices to help explain the observed phase behavior. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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