975 resultados para potentials
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At head of title: Inquiry Reference Service.
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Mode of access: Internet.
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Transportation Department, Washington, D.C.
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Transportation Department, Washington, D.C.
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Mode of access: Internet.
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Bibliography: leaf at end.
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"Prepared under Contract AT(04-3)-413 for the San Francisco Operations Office, U.S. Atomic Energy Commission."
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"March 1, 1952."
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Mode of access: Internet.
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Mode of access: Internet.
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Running title: Electrode potentials.
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Mode of access: Internet.
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"First printing November, 1938."
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We present a new approach accounting for the nonadditivity of attractive parts of solid-fluid and fluidfluid potentials to improve the quality of the description of nitrogen and argon adsorption isotherms on graphitized carbon black in the framework of non-local density functional theory. We show that the strong solid-fluid interaction in the first monolayer decreases the fluid-fluid interaction, which prevents the twodimensional phase transition to occur. This results in smoother isotherm, which agrees much better with experimental data. In the region of multi-layer coverage the conventional non-local density functional theory and grand canonical Monte Carlo simulations are known to over-predict the amount adsorbed against experimental isotherms. Accounting for the non-additivity factor decreases the solid-fluid interaction with the increase of intermolecular interactions in the dense adsorbed fluid, preventing the over-prediction of loading in the region of multi-layer adsorption. Such an improvement of the non-local density functional theory allows us to describe experimental nitrogen and argon isotherms on carbon black quite accurately with mean error of 2.5 to 5.8% instead of 17 to 26% in the conventional technique. With this approach, the local isotherms of model pores can be derived, and consequently a more reliab * le pore size distribution can be obtained. We illustrate this by applying our theory against nitrogen and argon isotherms on a number of activated carbons. The fitting between our model and the data is much better than the conventional NLDFT, suggesting the more reliable PSD obtained with our approach.