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Fluid theory for

When a spherical particle exists in a stagnant, suspending gas, its velocity can be predicted from viscous fluid theory for the transfer of momentum to the particle. Perhaps no other result has had such wide application to aerosol mechanics as Stokes (1851) theory for the motion of a solid particle in a stagnant medium. The model estimates that the drag force 2) acting on the sphere is... [Pg.60]

The contribution "Application of Meso-Scale Field-based Models to Predict Stability of Particle Dispersions in Polymer Melts" by Prasanna Jog, Valeriy Ginzburg, Rakesh Srivastava, Jeffrey Weinhold, Shekhar Jain, and Walter Chapman examines and compares Self Consistent Field Theory and interfacial Statistical Associating Fluid Theory for use in predicting the thermodynamic phase behavior of dispersions in polymer melts. Such dispersions are of quite some technological importance in the... [Pg.227]

The results obtained encourage future study and illustrate the power of conformal solution methods. It is reasonable to expect that the excellent accuracy obtained by Mollerup (16,17,18) with the VDW one-fluid theory for natural gas mixtures can be expected with the HSE theory for polar mixtures and other systems in which there are large dissimilarities between the components and the reference fluid. [Pg.100]

Comparison of experirnental pressures with those calculated from perfect-fluid theory for a streamlined body. [From H. Muttray, Die experimentalen Tatsachen des Widerstandes ohne Auftrieb (The experimental data of drag without lift), in Handbuch der Experimentalphysik Hydro- und Aero-Dynamik, Leipzig, 1932, p. 316 based on data by Fuhrmann.]... [Pg.382]

FEN Feng, W., Wen, H., Xu, Z., and Wang, W., Comparison of perturbed hard-sphere-chain theory with statistical associating fluid theory for square-well fluids, Ind. Eng. Chem. Res., 39, 2559, 2000. [Pg.114]

Gil-Villegas A, Galindo A, Whitehead PJ, Mills SJ, Jackson G, Burgess AN (1997) Statistical associating fluid theory for chain molecules with attractive potentials of variable range. J Chem Phys 106 4168-4186... [Pg.773]

The van der Waals one-fluid theory for mixtures assumes the properties of a mixture can be represented by a hypothetical pure fluid. Thus the thermodynamic behaviour of a mixture of constant composition is assumed to be isomorphic to that of a one-component fluid this assumption is not true near the critical point where the thermodynamic behaviour of a mixture at constant thermodynamic potential is isomorphic with that of a one-component fluid and this is discussed further in Chapter 10. [Pg.88]

Papaioaimou, V., Lafitte, T, Avendano, C., Adjiman, C.S., Jackson, G., Muller, E.A., and Galindo, A., 2014. Group contribution methodology based on the statistical associating fluid theory for heteronuclear molecules formed from Mie segments. J. Chem. Phys., 140 054107. [Pg.246]

A.M. Sonnet, E.G. Virga, The Dissipative Ordered Fluids, Theories for Liquid Crystals (Springer, New York, 2012)... [Pg.205]

Gloor, G.J. Jackson, G. Bias, F.J. del Rio, E.M. de Miguel, E. (2004). An accurate density functional theory for the vapor-liquid interface of associating chain molecules based on the statistical associating fluid theory for potentials of variable range. ]. Chem. Phys. 121,12740-12759. [Pg.324]


See other pages where Fluid theory for is mentioned: [Pg.133]    [Pg.387]    [Pg.2441]    [Pg.8082]    [Pg.1480]    [Pg.1132]   
See also in sourсe #XX -- [ Pg.11 ]




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