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Mass transport transfer

Ruby, C. L. and Elgin, J. C. Mass transfer—Transport properties. Chem. Eng. Prog. Symp. Series No. 16, 51 (1955) 17. Mass transfer between liquid drops and a continuous liquid phase in a countercurrent fluidized system. Liquid-liquid extraction in a spray tower. [Pg.768]

J. Lipzinski, G. Tragardh, 2001, Modelling of Pervaporation, Models to analyze and prediet the mass transfer transport in Pervaporation, Separation and Purifieation Methods, vol. 30(1), 49-25. [Pg.78]

Brasser, R, (2009), Modeling The Relation Between Comfort And Rrotection Of CBRN-Suits , ia Porous Media Heat and Mass Transfer, Transport and Mechanics, Aco a, J. L. and Camacho, A. F. (Eds), New York Nova Science Rublishers. [Pg.258]

This leads to rate equations with constant mass transfer coefficients, whereas the effect of net transport through the film is reflected separately in thej/gj and Y factors. For unidirectional mass transfer through a stagnant gas the rate equation becomes... [Pg.22]

For weU-defined reaction zones and irreversible, first-order reactions, the relative reaction and transport rates are expressed as the Hatta number, Ha (16). Ha equals (k- / l ) where k- = reaction rate constant, = molecular diffusivity of reactant, and k- = mass-transfer coefficient. Reaction... [Pg.509]

Using this simplified model, CP simulations can be performed easily as a function of solution and such operating variables as pressure, temperature, and flow rate, usiag software packages such as Mathcad. Solution of the CP equation (eq. 8) along with the solution—diffusion transport equations (eqs. 5 and 6) allow the prediction of CP, rejection, and permeate flux as a function of the Reynolds number, Ke. To faciUtate these calculations, the foUowiag data and correlations can be used (/) for mass-transfer correlation, the Sherwood number, Sb, is defined as Sh = 0.04 S c , where Sc is the Schmidt... [Pg.148]

In considering the effect of mass transfer on the boiling of a multicomponent mixture, both the boiling mechanism and the driving force for transport must be examined (17—20). Moreover, the process is strongly influenced by the effects of convective flow on the boundary layer. In Reference 20 both effects have been taken into consideration to obtain a general correlation based on mechanistic reasoning that fits all available data within 15%. [Pg.96]

In engineering appHcations, the transport processes involving heat and mass transfer usually occur in process equipment involving vapor—gas mixtures where the vapor undergoes a phase transformation, such as condensation to or evaporation from a Hquid phase. In the simplest case, the Hquid phase is pure, consisting of the vapor component alone. [Pg.96]

Mass Transport. Probably the most iavestigated physical phenomenon ia an electrode process is mass transfer ia the form of a limiting current. A limiting current density is that which is controlled by reactant supply to the electrode surface and not the appHed electrode potential (42). For a simple analysis usiag the limiting current characteristics of various correlations for flow conditions ia a parallel plate cell, see Reference 43. [Pg.88]

Eddy diffusion as a transport mechanism dominates turbulent flow at a planar electrode ia a duct. Close to the electrode, however, transport is by diffusion across a laminar sublayer. Because this sublayer is much thinner than the layer under laminar flow, higher mass-transfer rates under turbulent conditions result. Assuming an essentially constant reactant concentration, the limiting current under turbulent flow is expected to be iadependent of distance ia the direction of electrolyte flow. [Pg.88]

CO conversion is a function of both temperature and catalyst volume, and increases rapidly beginning at just under 100°C until it reaches a plateau at about 150°C. But, unlike NO catalysts, above 150°C there is Htde benefit to further increasing the temperature (44). Above 150°C, the CO conversion is controUed by the bulk phase gas mass transfer of CO to the honeycomb surface. That is, the catalyst is highly active, and its intrinsic CO removal rate is exceedingly greater than the actual gas transport rate (21). When the activity falls to such an extent that the conversion is no longer controUed by gas mass transfer, a decline of CO conversion occurs, and a suitable regeneration technique is needed (21). [Pg.512]


See other pages where Mass transport transfer is mentioned: [Pg.2449]    [Pg.147]    [Pg.306]    [Pg.318]    [Pg.50]    [Pg.6]    [Pg.93]    [Pg.2449]    [Pg.147]    [Pg.306]    [Pg.318]    [Pg.50]    [Pg.6]    [Pg.93]    [Pg.1939]    [Pg.22]    [Pg.332]    [Pg.16]    [Pg.342]    [Pg.342]    [Pg.52]    [Pg.510]    [Pg.156]    [Pg.95]    [Pg.480]    [Pg.512]    [Pg.170]    [Pg.343]    [Pg.31]    [Pg.32]    [Pg.234]    [Pg.53]    [Pg.90]    [Pg.504]   
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See also in sourсe #XX -- [ Pg.96 , Pg.122 ]




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