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Activation diffusion

For adsorption from the vapor phase, Kmay be very large (sometimes as high as 10 ) and then clearly the effective diffusivity is very much smaller than the pore diffusivity. Furthermore, the temperature dependence of K follows equation 2, giving the appearance of an activated diffusion process with... [Pg.260]

Activated diffusion of the adsorbate is of interest in many cases. As the size of the diffusing molecule approaches that of the zeohte channels, the interaction energy becomes increasingly important. If the aperture is small relative to the molecular size, then the repulsive interaction is dominant and the diffusing species needs a specific activation energy to pass through the aperture. Similar shape-selective effects are shown in both catalysis and ion exchange, two important appHcations of these materials (21). [Pg.447]

Atoms move by thermally activated diffusion from site to site. [Pg.82]

When using the microporous zeolite membrane (curve 3) the N2 permeance decreases when the pressure increases such a behaviour can be accounted for by activated diffusion mechanisms [21], which are typical of zeolite microporous systems. In such systems the difflisivity depends on the nature and on the concentration of the diffusing molecule which interacts with the surface of the pore. For gases with low activation energies of diffusion, a decrease of the permeability can be observed [22]. [Pg.135]

As the pore size is reduced to 1 nm or less, gas permeation may exhibit a thermally activated diffusion phenomena. For example, in studies at Oak Ridge National Laboratory, for a certain proprietary membrane material and configuration, permeation of helium appeared to increase much faster than other gases resulting in an increase in Helium to C02 selectivity from 5 at 25°C to about 48.3 at 250°C (Bischoff and Judkins, 2006). Hydrothermal stability of this membrane in the presence of steam, however, was not reported. [Pg.308]

Castilla y Leon, and Castilla la Mancha. This part is also the most significant for industrial plants such as biomass crops and oilseed rape. In the southernmost regions of Castilla La Mancha and Catalunya, dry fruit trees and vineyards increase in significance, while the Ebro River delta supports a well-developed rice farming activity. Diffuse pollution originated by pesticides application in the basin has been widely studied [1-3]. A historical pollution from chemical plants manufacturing solvents and chlorinated pesticides in the southern part of the river basin is also well known [4]. Automobile, textile, food, and wood industry as well as mining activities are important in the northern part. [Pg.334]

The second method of minimizing the junction potential is to employ a swamping electrolyte S. We saw in Section 4.1 how diffusion occurs in response to entropy effects, themselves due to differences in activity. Diffusion may be minimized by decreasing the differences in activity, achieved by adding a high concentration of ionic electrolyte to both half-cells. Such an addition increases their ionic strengths I, and decreases all activity coefficients y to quite a small value. [Pg.343]

The shape of the relaxation spectrum predicted by Eq. (22) does indeed fit rheological data on pure star melts better than the quadratic expression calculated for stars in permanent networks [27], except at high frequencies where the assumption of activated diffusion breaks down (it may easily be verified that Ugff(s)[Pg.218]

Some aspects of thermally activated diffusion were discussed in section 5.9.1 in regard to intracrystalline exchange geothermometry. Concerning more precisely isotope diffusion, there are two main aspects that may be relevant in geochemistry ... [Pg.735]

Results were then interpreted in terms of the usual form for thermally activated diffusion ... [Pg.737]

Assuming that Ti(IV) is distributed statistically in all tetrahedral positions, it can be easily seen that even for crystallite sizes of 0,2 m the great majority of T1(IV) is located inside the pore structure. Assuming that every Ti(IV) is a catalytic centre with equal activity, diffusion limitations for molecules of different sizes should be observed. This is in fact the case. It has been shown [27] that the rate of oxidation of primary alcohols decreases regularly as the chain length increases, while for iso-butyl alcohol a sudden drop in the rate is observed. Also the reactivity order of olefins on TS-1 is different from the order observed with homogeneous electrophilic catalysts, while as already indicated very bulky molecules are unreactive when TS-1 is used as the catalyst. All these facts can only be interpreted as due to diffusion limitations of the larger molecules, which means that the catalytic sites are located inside the pore structure of the solid. [Pg.351]

The transport process within the zeolite pore system involves the passage of sorbate molecules through the windows between adjacent cavities. For molecules with critical diameters similar to the free aperture of the window ( 4.2 A for type A zeolites), an activated diffusion process is to be expected, and a molecule at the center of the window may be identified as the transition state. For the A-type lattice the following expression for the limiting diffusivity may be derived from absolute rate theory (14)... [Pg.340]

Small solute atoms in the interstices between the larger host atoms in a relaxed metallic glass diffuse by the direct interstitial mechanism (see Section 8.1.4). The host atoms can be regarded as immobile. A classic example is the diffusion of H solute atoms in glassy Pd8oSi2o- For this system, a simplified model that retains the essential physics of a thermally activated diffusion process in disordered systems is used to interpret experimental measurements [20-22]. [Pg.234]

A 64-year-old African-American man developed worsening renal insufficiency, raised creatine kinase activity, diffuse muscle pain, and severe muscle weakness. He had been taking simvastatin for about 6 months and clarithromycin for sinusitis for about 3 weeks. He was treated aggressively with intravenous hydration, sodium bicarbonate, and hemodialysis. A muscle biopsy showed necrotizing myopathy secondary to a toxin. He continued to receive intermittent hemodialysis until he died from infectious complications 3 months after admission. [Pg.569]


See other pages where Activation diffusion is mentioned: [Pg.448]    [Pg.109]    [Pg.858]    [Pg.72]    [Pg.311]    [Pg.437]    [Pg.454]    [Pg.455]    [Pg.109]    [Pg.281]    [Pg.275]    [Pg.423]    [Pg.146]    [Pg.147]    [Pg.215]    [Pg.217]    [Pg.249]    [Pg.50]    [Pg.118]    [Pg.412]    [Pg.159]    [Pg.23]    [Pg.87]    [Pg.238]    [Pg.674]    [Pg.675]    [Pg.54]    [Pg.55]    [Pg.23]    [Pg.385]    [Pg.589]    [Pg.191]    [Pg.101]    [Pg.101]    [Pg.422]    [Pg.439]   
See also in sourсe #XX -- [ Pg.8 , Pg.11 , Pg.12 , Pg.15 , Pg.27 , Pg.28 , Pg.29 , Pg.30 , Pg.31 , Pg.32 , Pg.33 , Pg.38 , Pg.50 , Pg.54 , Pg.83 , Pg.157 , Pg.284 , Pg.296 ]

See also in sourсe #XX -- [ Pg.208 ]




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Activated diffusion healing

Activated diffusion through polymers

Activated gaseous diffusion

Activated state during diffusion

Activation bulk diffusion through

Activation energies for diffusion

Activation energy and diffusion

Activation energy bulk diffusion

Activation energy diffusion into solution

Activation energy diffusion, sorption, permeation

Activation energy diffusion-limited

Activation energy dislocation diffusion

Activation energy for oxygen diffusion

Activation energy for surface diffusion

Activation energy from diffusion

Activation energy grain-boundary diffusion

Activation energy of diffusion

Activation energy self-diffusion

Activation energy surface diffusion

Activation for diffusion

Activation grain boundary diffusion

Activation hydrogen diffusion

Activation ionic diffusion

Activation of diffusion

Activation self-diffusion

Activation-diffusion control

Activation-diffusion kinetics

Active diffusion

Activity coefficient, diffusion kinetics

Analogy between activated diffusion

Antibacterial activity disc diffusion agar method

Apparent activation energy diffusion

Apparent activation energy of diffusion

Carbon diffusion, activation

Carbon diffusion, activation energies

Diffusant activity

Diffusion Activated process

Diffusion Activated zone

Diffusion activated

Diffusion activated

Diffusion activated rate process

Diffusion activation energy

Diffusion activation energy, total

Diffusion active electrode

Diffusion coefficients activated state theories

Diffusion multi-activation process

Diffusion thermally activated

Diffusion-controlled reactions, activation

Diffusion-controlled reactions, activation definition

Diffusivity activation volume

Diffusivity measured activation energy

Diffusivity real activation energy

Electron transfer, activation control diffusion limit

Facilitated Diffusion and Active Transport

Hydrogen diffusion activation energy

Membrane diffusion active

Mixed activation-diffusion

Multicomponent diffusivity matrix (activity-based)

Passive diffusion active/carrier-mediated transport

Pharmacokinetics active diffusion

Polymer oxygen diffusion, activation energy

Solution-diffusion mechanism activated process

Surface and bulk diffusion of active particles

Thermal activation surface diffusion

Thermally Activated Motion of Diffuse Interfaces by Self-Diffusion

Tracer diffusion activation energy

Transport mechanisms activated diffusion

Water diffusion, activation energy

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