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Transition diffusion

In addition to the adsorption and desorption explained in Sec. II A, we can also include the diffusion process within our master-equation formahsm (10) [47]. For this purpose, we must only include the supplementary channel of the diffusive transition into the right-hand side of Eq. (10). A diffusion jump... [Pg.881]

The first paper that was devoted to the escape problem in the context of the kinetics of chemical reactions and that presented approximate, but complete, analytic results was the paper by Kramers [11]. Kramers considered the mechanism of the transition process as noise-assisted reaction and used the Fokker-Planck equation for the probability density of Brownian particles to obtain several approximate expressions for the desired transition rates. The main approach of the Kramers method is the assumption that the probability current over a potential barrier is small and thus constant. This condition is valid only if a potential barrier is sufficiently high in comparison with the noise intensity. For obtaining exact timescales and probability densities, it is necessary to solve the Fokker-Planck equation, which is the main difficulty of the problem of investigating diffusion transition processes. [Pg.358]

For styrene-crosslinked unsaturated polyesters and vinyl esters, v is considerably higher v (20 5)10 4 KT1 and v/G —3. It is noteworthy that in such networks (Tg 100°C) the temperature interval between ambient temperature and Tg is a diffuse transition region in which tan 8 increases almost continuously with temperature. [Pg.344]

Solvents are selected such that some will escape relatively quickly from paint films to prevent excessive flow, while others will escape slowly to provide film leveling and adhesion. With typical alkyd coatings, the first 30% of solvent has been observed to evaporate as quickly as the neat solvents, essentially at a constant rate which is dependent on volatility. Later stage evaporation occurred several times more slowly and was rate-controlled by solvent diffusion to the surface of the paint film. The transition point between this behavior was defined as the resin solids content at which the evaporation rate due to volatility equaled that due to diffusion. Transition points have been observed to typically occur at a resin solids content of 40-50% v/v. Thus alkyd paints, normally formulated at 27-40% v/v resin solids, generally exhibit rapid initial solvent-release driven by volatility while high solids coatings (usually 65-75% v/v resin solids) dry solely by a diffusion-controlled process with negligible influence by solvent volatility (Ellis, 1983). [Pg.384]

An explanation of the observed relaxation transition of the permittivity in carbon black filled composites above the percolation threshold is again provided by percolation theory. Two different polarization mechanisms can be considered (i) polarization of the filler clusters that are assumed to be located in a non polar medium, and (ii) polarization of the polymer matrix between conducting filler clusters. Both concepts predict a critical behavior of the characteristic frequency R similar to Eq. (18). In case (i) it holds that R= , since both transitions are related to the diffusion behavior of the charge carriers on fractal clusters and are controlled by the correlation length of the clusters. Hence, R corresponds to the anomalous diffusion transition, i.e., the cross-over frequency of the conductivity as observed in Fig. 30a. In case (ii), also referred to as random resistor-capacitor model, the polarization transition is affected by the polarization behavior of the polymer matrix and it holds that [128, 136,137]... [Pg.43]

Schofield [49] has shown that in DCMD applications, the net flux of air across the membrane is extremely small relative to the flux of water, and viscous flux can be neglected (unless the process solutions have been degassed). With these assumptions Equations 19.36 and 19.37 reduce to the Knudsen-molecular diffusion transition form and can be written as [43]... [Pg.524]

Gas diffusion in a porous structure is of particular interest to this book as many porous fibre preforms are densified by CVI. The diffusion of gases in porous media can be classified into three regimes according to the ratio of the free mean path to the pore diameter within the structure. As shown in Figure 2.15, they are Fick gas diffusion, transition gas diffusion and Knudsen gas diffusion. [Pg.59]

Welch, G. R. Easterby, J. S. (1994). Metabolite channeling versus free diffusion Transition-time analysis. Trends Biochem. Sci. 19,193-197. [Pg.92]

The fuel and air mixture leaves the vaporizer and is fed to the combustor assembly, which consists of a diffuser, plenum with flow conditioning, nozzle, and combustor test section. The diffuser transits the flow from a 50.8-millimeter circular duct to a 160 X 120 mm rectangular-shaped plenum. The flow conditioning consists of two perforated plates, which enhance the flow uniformity and serve as effective flame arresters. The two-dimensional nozzle is constructed from sectors of a large-radius pipe and has an area ratio of 6 1. Pitot probe surveys showed that this setup produced a uniform top-hat velocity distribution across the area of the nozzle exit [2],... [Pg.77]

The relationship between the strength of an aromatic central group and the reaction rate is given approximately by Hammett s equation. Normally, for a basic reaction p is positive, but with a diffuse transition state p is negative. Hammett cites sixteen cases of basic reactions in which the central group is aromatic and has been varied by... [Pg.428]


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See also in sourсe #XX -- [ Pg.361 ]




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