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Diffusion Reference equation

Since in most situations the perturbation quantities (V and c() are not explicitly resolved, it is not possible to evaluate the turbulent flux term directly. Instead, it must be related to the distribution of averaged quantities - a process referred to as parameterization. A common assumption is to relate the turbulent flux vector to the gradient of the averaged tracer distribution, which is analogous with the molecular diffusion expression. Equation (35). [Pg.78]

The diffusion-reaction equations are solved using finite-difference techniques employing a multilayer spatial grid to account for the corrosion product deposits present on the fuel and carbon steel surfaces, Fig. 21. For further details the reader is referred to more extensive discussions published elsewhere (6,23). [Pg.233]

The mass flux a the sum of the diffusive flux 7a > which accounts for the movement of A due to concentration gradients, and the quantity o)a( a + B) which accounts for the movement of A due to bulk motion of the fluid. Equation 3-20 is the appropriate form of the diffusive flux equation to use for most engineering problems, since quantities are usually measured with respect to some fixed frame of reference. For many of the problems considered here, A is a dilute species in water, in which case coa 0 and the bulk motion term can be neglected. [Pg.30]

Although these authors did not indicate a method for estimating ag, other than from diffusion data, equation (1.18) is one of the most widely used and referred to in the literature. [Pg.87]

If we use the one internal collocation point approximation for the diffusion reaction equation inside the floe as shown in the next section, then the left-hand side of Eq. (6.133) can be approximated using the orthogonal collocation formula (refer to Appendix E for orthogonal collocation method), and, thus, Eq. (6.133) becomes... [Pg.518]

Figure 1.7 Analysis of the water diffusion according to the ECM (Eq. 1.18). Dependence of the function (1 - U)I 1 + UI2) on the effective mi(xUe volume fraction (O, )- U was calculated from the water diffusion using Equation 1.17 and the micellar volume fraction from the AOT and bmim+ diffusion using Equations 1.9 and 1.10. Closed symbols refer to the NaAOT/W/ bmimBF system open symbols refer to the NaAOT/W/bmimBEyp-xylene system (in this last case, the miceUar volume fraction also accounts for thep-xylene volume fraction). Reproduced from Murgia et al. [26] with permission from American Chemical Society. Figure 1.7 Analysis of the water diffusion according to the ECM (Eq. 1.18). Dependence of the function (1 - U)I 1 + UI2) on the effective mi(xUe volume fraction (O, )- U was calculated from the water diffusion using Equation 1.17 and the micellar volume fraction from the AOT and bmim+ diffusion using Equations 1.9 and 1.10. Closed symbols refer to the NaAOT/W/ bmimBF system open symbols refer to the NaAOT/W/bmimBEyp-xylene system (in this last case, the miceUar volume fraction also accounts for thep-xylene volume fraction). Reproduced from Murgia et al. [26] with permission from American Chemical Society.
As the resulting amplitude equations. Equation (15), have a lower dimension they are simpler to analyze than the original reaction-diffusion systems [Equation (1)] remembering however that they are only valid in some neighbourhood of the point where the reference state linearly looses its stability. Because of this relative simplicity they allow to scrutinize the key nonlinear effects that govern the structure of the bifurcation diagram. In the first place however they allow one to obtain the bifurcated solutions and to discuss their stability. [Pg.330]

Thermal Diffusivity. Referring to the defining equation, equation 4b, it would appear that thermal diffusivity is a more easily measured quantity than thermal conductivity, and from the experimental point of view this is often true. This is mainly so because it is not necessary to measure a heat flux with the attendant problems of guarding against heat losses, and it is not necessary to achieve a steady-state condition. Hence the measurement can be very rapid. [Pg.1166]

The species continuity equation (CE) is an expression of the Lavoisier general law of conservation of mass. Equation 2.1 presents the CE in vector form and provides the proper context for the various types of chemical mass transport processes needed for chemical modeling and fate analysis. In Section 2.2.2, the mass accumulation portion of the CE is highlighted as the principal term for assessing chemical fate in the media compartments. This term includes reaction, advection, diffusion, and turbulent transport and dispersion processes. Because the magnitude and direction of this term reflect the sum total of all processes, this term uniquely defines chemical fate. In Equation 2.2, the steady-state CE minus the reaction term is commonly referred to as the advective-diffusive (AD) equation. It provides the appropriate starting point for addressing the various transport processes associated with the mobile phases in near-surface soils. [Pg.187]

Reference 115 gives the diffusion coefficient of DTAB (dodecyltrimethylammo-nium bromide) as 1.07 x 10" cm /sec. Estimate the micelle radius (use the Einstein equation relating diffusion coefficient and friction factor and the Stokes equation for the friction factor of a sphere) and compare with the value given in the reference. Estimate also the number of monomer units in the micelle. Assume 25°C. [Pg.490]

These three terms represent contributions to the flux from migration, diffusion, and convection, respectively. The bulk fluid velocity is determined from the equations of motion. Equation 25, with the convection term neglected, is frequently referred to as the Nemst-Planck equation. In systems containing charged species, ions experience a force from the electric field. This effect is called migration. The charge number of the ion is Eis Faraday s constant, is the ionic mobiUty, and O is the electric potential. The ionic mobiUty and the diffusion coefficient are related ... [Pg.65]

Values for many properties can be determined using reference substances, including density, surface tension, viscosity, partition coefficient, solubihty, diffusion coefficient, vapor pressure, latent heat, critical properties, entropies of vaporization, heats of solution, coUigative properties, and activity coefficients. Table 1 Hsts the equations needed for determining these properties. [Pg.242]

Diffusivity correfations for gases are outhned in Table 5-14. Specific parameters for individual eqiiations are defined in the specific text regarding each equation. References are given after Table 5-19. The errors reported for Eq. (5-194) through (5-197) were compiled by Reid et al., who compared the predictions with 68 experimental values of D g. Errors cited for Eqs. (5-198) to (5-202) were reported by the authors. [Pg.594]

Equations (12-31), (12-32), and (12-33) hold only for a slab-sheet solid whose thickness is small relative to the other two dimensions. For other shapes, reference should be made to Crank The Mathematics of Diffusion, Oxford, London, 1956). [Pg.1181]

To apply Equation (3), it is necessary to determine the diffusion coefficients Oy and o. The diffusion coefficients can be related to the deviation in the wind direction, given by o, in the azimuth angle (azimuth refers to the lateral or cross-wind direction), and o in the deviation angle (deviation refers to... [Pg.286]


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See also in sourсe #XX -- [ Pg.172 ]




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