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Diffusion average diffusivities

The diesel engine operates, inherently by its concept, at variable fuel-air ratio. One easily sees that it is not possible to attain the stoichiometric ratio because the fuel never diffuses in an ideal manner into the air for an average equivalence ratio of 1.00, the combustion chamber will contain zones that are too rich leading to incomplete combustion accompanied by smoke and soot formation. Finally, at full load, the overall equivalence ratio... [Pg.212]

IHP) (the Helmholtz condenser formula is used in connection with it), located at the surface of the layer of Stem adsorbed ions, and an outer Helmholtz plane (OHP), located on the plane of centers of the next layer of ions marking the beginning of the diffuse layer. These planes, marked IHP and OHP in Fig. V-3 are merely planes of average electrical property the actual local potentials, if they could be measured, must vary wildly between locations where there is an adsorbed ion and places where only water resides on the surface. For liquid surfaces, discussed in Section V-7C, the interface will not be smooth due to thermal waves (Section IV-3). Sweeney and co-workers applied gradient theory (see Chapter III) to model the electric double layer and interfacial tension of a hydrocarbon-aqueous electrolyte interface [27]. [Pg.179]

It is known that even condensed films must have surface diffusional mobility Rideal and Tadayon [64] found that stearic acid films transferred from one surface to another by a process that seemed to involve surface diffusion to the occasional points of contact between the solids. Such transfer, of course, is observed in actual friction experiments in that an uncoated rider quickly acquires a layer of boundary lubricant from the surface over which it is passed [46]. However, there is little quantitative information available about actual surface diffusion coefficients. One value that may be relevant is that of Ross and Good [65] for butane on Spheron 6, which, for a monolayer, was about 5 x 10 cm /sec. If the average junction is about 10 cm in size, this would also be about the average distance that a film molecule would have to migrate, and the time required would be about 10 sec. This rate of Junctions passing each other corresponds to a sliding speed of 100 cm/sec so that the usual speeds of 0.01 cm/sec should not be too fast for pressurized film formation. See Ref. 62 for a study of another mechanism for surface mobility, that of evaporative hopping. [Pg.450]

Two applications of the flucUiathig diffusion equation are made here to illustrate tlie additional infonnation the flucUiations provide over and beyond the detenninistic behaviour. Consider an infinite volume with an initial concentration, c, that is constant, Cq, everywhere. The solution to the averaged diffusion equation is then simply (c) = Cq for all t. However, the two-time correlation fiinction may be shown [26] to be... [Pg.704]

This example illustrates how the Onsager theory may be applied at the macroscopic level in a self-consistent maimer. The ingredients are the averaged regression equations and the entropy. Together, these quantities pennit the calculation of the fluctuating force correlation matrix, Q. Diffusion is used here to illustrate the procedure in detail because diffiision is the simplest known case exlribiting continuous variables. [Pg.705]

AE at the n-p heterointerface which prevents their injection into the n region. The result is that the injected minority carriers are confined to the thin narrow-bandgap region. If this region is thinner than the average diffusion... [Pg.2893]

Ifihe Bath relaxation con start t, t, is greater than 0.1 ps. yon should be able Lo calculate dyriani ic p roperlies, like time correlation fun c-tioris and diffusion constants, from data in the SNP and/or C.SV files (sec "Collecting Averages from Simulations"... [Pg.72]

Now encounters between molecules, or between a molecule and the wall are accompanied by momentuin transfer. Thus if the wall acts as a diffuse reflector, molecules colliding wlch it lose all their axial momentum on average, so such encounters directly change the axial momentum of each species. In an intermolecuLar collision there is a lateral transfer of momentum to a different location in the cross-section, but there is also a net change in total momentum for species r if the molecule encountered belongs to a different species. Furthermore, chough the total momentum of a particular species is conserved in collisions between pairs of molecules of this same species, the successive lateral transfers of momentum associated with a sequence of collisions may terminate in momentum transfer to the wall. Thus there are three mechanisms by which a given species may lose momentum in the axial direction ... [Pg.7]

Now consider Che cross-sectional average N of the total molar flux and the cross-sectional average diffusion fluxes J, defined by... [Pg.31]

The shear viscosity is a tensor quantity, with components T] y, t],cz, T)yx> Vyz> Vzx> Vzy If property of the whole sample rather than of individual atoms and so cannot be calculat< with the same accuracy as the self-diffusion coefficient. For a homogeneous fluid the cor ponents of the shear viscosity should all be equal and so the statistical error can be reducf by averaging over the six components. An estimate of the precision of the calculation c then be determined by evaluating the standard deviation of these components from tl average. Unfortunately, Equation (7.89) cannot be directly used in periodic systems, evi if the positions have been unfolded, because the unfolded distance between two particl may not correspond to the distance of the minimum image that is used to calculate the fore For this reason alternative approaches are required. [Pg.397]

Other Models for Mass Transfer. In contrast to the film theory, other approaches assume that transfer of material does not occur by steady-state diffusion. Rather there are large fluid motions which constantiy bring fresh masses of bulk material into direct contact with the interface. According to the penetration theory (33), diffusion proceeds from the interface into the particular element of fluid in contact with the interface. This is an unsteady state, transient process where the rate decreases with time. After a while, the element is replaced by a fresh one brought to the interface by the relative movements of gas and Uquid, and the process is repeated. In order to evaluate a constant average contact time T for the individual fluid elements is assumed (33). This leads to relations such as... [Pg.23]

The effective saturation depth,, represents the depth of water under which the total pressure (hydrostatic plus atmospheric) would produce a saturation concentration equal to for water ia contact with air at 100% relative humidity. This can be calculated usiag the above equation, based on a spatial average value of T, measured by a clean water test. For design purposes,, can be estimated from clean water test results on similar systems, and it can range from 5 to 50% of tank Hquid depth. Effective depth values for coarse bubble diffused air, fine bubble diffused air, and low speed surface aerators are 26 to 34%, 21 to 44%, and 5 to 7%, of the Hquid depth, respectively. [Pg.342]

Rotating vanes are provided in the rooms to ensure diffuse sound fields. Sound is introduced into the source room, the average sound pressure level is measured in one-third octave bands in both rooms, and the sound-transmission loss is calculated as follows, where and die average sound... [Pg.316]

Charge carriers in a semiconductor are always in random thermal motion with an average thermal speed, given by the equipartion relation of classical thermodynamics as m v /2 = 3KT/2. As a result of this random thermal motion, carriers diffuse from regions of higher concentration. Applying an electric field superposes a drift of carriers on this random thermal motion. Carriers are accelerated by the electric field but lose momentum to collisions with impurities or phonons, ie, quantized lattice vibrations. This results in a drift speed, which is proportional to the electric field = p E where E is the electric field in volts per cm and is the electron s mobility in units of cm /Vs. [Pg.346]

Unlike solar thermal systems or PV concentrator systems, the PV flat plate systems work well in cloudy locations because these latter convert diffuse as well as direct sunlight to electricity. On an aimualized basis, the energy produced by a photovoltaic array varies by only about 25% from an average value for the contiguous 48 states of the United States. As a result, it is practical to use photovoltaic systems in normally cloudy locations such as Seattle or northern Maine. [Pg.236]

Emulsion Polymerization. Emulsion polymerization takes place in a soap micelle where a small amount of monomer dissolves in the micelle. The initiator is water-soluble. Polymerization takes place when the radical enters the monomer-swollen micelle (91,92). Additional monomer is supphed by diffusion through the water phase. Termination takes place in the growing micelle by the usual radical-radical interactions. A theory for tme emulsion polymerization postulates that the rate is proportional to the number of particles [N. N depends on the 0.6 power of the soap concentration [S] and the 0.4 power of initiator concentration [i] the average number of radicals per particle is 0.5 (93). [Pg.502]


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See also in sourсe #XX -- [ Pg.253 ]




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Average diffusion coefficient

Averaged diffusion equation

Diffusion coefficient mixture averaged

Turbulent flux of a scalar quantity averaged diffusion equation

Z-average diffusion coefficient

Z-average translational diffusion

Z-average translational diffusion coefficient

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