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Barker theory

A simphfied lattice theory put forward by Barker [43] is applied to obtain expressions for G . In addition to the well-known assumptions of Barkers theory, it is assumed that... [Pg.67]

Barker J and Henderson D 1967 Perturbation theory and equation of state for a fluids II. A successful theory of liquids J. Chem. Phys. 47 4714... [Pg.555]

J. A. Barker, Lattice Theories of the Liquid State Pergamon, New York (1963). [Pg.305]

The vapour-pressure equation (22) has been verified for brom-and iodo-naphthalene by L. Rollo(7) (1909), and for toluene, naphthalene, and benzene by J. T. Barker (1910). The latter finds that the solid and liquid states give the same chemical constant, which is in agreement with Nemst s theory. [Pg.497]

As we have already pointed out, the theoretical basis of free energy calculations were laid a long time ago [1,4,5], but, quite understandably, had to wait for sufficient computational capabilities to be applied to molecular systems of interest to the chemist, the physicist, and the biologist. In the meantime, these calculations were the domain of analytical theories. The most useful in practice were perturbation theories of dense liquids. In the Barker-Henderson theory [13], the reference state was chosen to be a hard-sphere fluid. The subsequent Weeks-Chandler-Andersen theory [14] differed from the Barker-Henderson approach by dividing the intermolecular potential such that its unperturbed and perturbed parts were associated with repulsive and attractive forces, respectively. This division yields slower variation of the perturbation term with intermolecular separation and, consequently, faster convergence of the perturbation series than the division employed by Barker and Henderson. [Pg.4]

Woods Hutchinson declined to apologize for mounting yet another attack on the uric acid theory because, he warned, "if we do not take it, it will take us." (43) The fact that other medical celebrities, including Lafayette Mendel, (44) Lewellys Barker, (45) and J. J. R. Macleod, (46) took the time to second... [Pg.168]

Lind J, Shen X, Merenyi G, Jonsson B (1989) Determination of the rate constant of self-exchange of theCVCV- couple in water by 180/160 isotope marking. J Am Chem Soc 111 7654-7655 Liu Y, Pimentel AS, Antoku Y, Barker JR (2002) Temperature-dependent rate and equilibrium constants for Br (aq) + Br(aq) <=> Br2- (aq). J Phys Chem A 106 11075-11082 Marcus RA (1993) Elektronentransferreaktionen in der Chemie - Theorie und Experiment (Nobel Vortrag). Angew Chem 105 1161-1172... [Pg.98]

Reisler, H. and Wittig, C. (1992). State-resolved simple bond-fission reactions Experiment and theory, in Advances in Chemical Kinetics and Dynamics, ed. J.A. Barker (JAI Press, Greenwich). [Pg.402]

There are three clear divisions in the photoelectrochemical field. In the first, one shines light upon a metal electrode. Here, the theory is well worked out (Barker, 1974 Khan and Uosaki, 1976), but metals absorb light very poorly compared with semiconductors, and this makes the photocurrents obtained by irradiating them extremely small. The second division concerns the absorption of light by molecules in solution and electron transfer from or to these photoactivated species and to or from a conveniently placed electrode (Albery, 1989). Such phenomena are of interest to photochemists, but here the electrode is the handmaiden of the photochemistry and so we regretfully forgo a description of the material. [Pg.38]

MATRICES AND LINEAR ALGEBRA. Hans Schneider and George Phillip Barker. Basic textbook covers theory of matrices and its applications to systems of linear equations and related topics such as determinants, eigenvalues and differential equations. Numerous exercises. 432pp. 5X x 8X. 66014-1 Pa. 8.95... [Pg.116]

A well-known approximate molecular theory of a fluid at a planar interface is originally due to Helfand, Frisch and Lebowitz [76] and later to Henderson, Abraham and Barker [77] and Perram and White [78]. Consider a binary mixture (A,B) in which one of the species (A) becomes extremely dilute and infinitely large. S.E. [52] show that if the size of species A tends to infinity while the concentration of A tends toward zero, then a consequence of the OZ equation, coupled with the PY equation, is the relation... [Pg.634]

Barker AS, Loudon R. Response functions in the theory of Raman scattering by vibrational and polariton modes in dielectric crystals. Rev Modern Phys 1972 44 18. [Pg.549]

Band gap -> semiconductor Band-pass filter -> signal filtering Band-stop filter -> signal filtering Bardeen-Cooper-Schrieffer theory -> BCS theory Barker, Geoffrey Cecil... [Pg.40]

The theory of simple liquids achieved a mature state in the era 1965-1975 (Barker and Henderson, 1976 Hansen and McDonald, 1976). As this mature theory was extended towards molecular liquids, simple molecular cases such as liquid N2 or liquid CCI4 were treated first. But the molecular liquids that were brought within the perimeter of the successful theory were remote extremities compared with the liquids synthesized, poured from bottles or pipes, and used. In addition, the results traditionally sought from molecular theories (Rowlinson and Swinton, 1982) often appear to have shifted to accommodate the limitations of the available theories. Overlooking molecular simulation techniques... [Pg.3]

Henderson, D. and Barker, J. A., Perturbation theories. In D. Henderson (ed.). Physical Chemistry. An Advanced Treatise, pp. 377 12. New York Academic Press (1971). [Pg.219]

There have been several approaches to the expression of thermodynamic quantities of solutions. Scatchard published a series of papers (see 1801 and previous papers, especially 1802) based on the classical approach via chemical potentizil. Barker (130, 128, 131) applied the theory of conformal solutions (1254) to some H bonding systems after modifying it to allow for dipole attractions or, more generally, molecular orientations. The curves are similar in both cases. [Pg.222]

J. A. Barker. J. Chem. Phys. 20, 1526-32 (1952). Theory cooperative orientation effects in solution. [Pg.390]

The density profile pi z) for the uncharged surface has three different terms according to the contact theorem (73) and according to the expression (28) for the pressure. The first two of them describe the hard-sphere and ion-pairing contributions, respectively. They can be obtained in the framework of the associative version of the Henderson-Abraham-Barker (HAB) theory [53, 54], According to the obtained results [54],... [Pg.67]

C. M. Barker, D. Gleeson, N. Kaltsoyannis, C. R. A. Catlow, G. Sankar, J. M. Thomas, On the structure and coordination of the oxygen-donating species in TiMCM-41/TBHP oxidation catalysts A density functional theory and EXAFS study, Phys. Chem. Chem. Phys. 4 (2002) 1228. [Pg.91]


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See also in sourсe #XX -- [ Pg.67 , Pg.68 ]




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