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SURFACE MIGRATION

If we assume that the rates of adsorption and desorption are both large compared with the surface migration rate, the surface and bulk concentrations of each species will be almost in equlibriura, and hence will be... [Pg.59]

Surface Applied Surfactants. Antistat agents can be appHed direcdy to the surface of a plastic part. Usually the antistat is diluted in water or in a solvent. The antistat solution is appHed by spraying, dipping, or wiping on the surface. The water or solvent dries leaving a thin film that attracts moisture. Since it is appHed to the surface, migration through the resin is not a factor. In practice, the quaternary ammonium compounds find the most use. They are soluble in water and effective at low concentrations. [Pg.299]

While it is inherently probable that product formation will be most readily initiated at sites of effective contact between reactants (A IB), it is improbable that this process alone is capable of permitting continued product formation at low temperature for two related reasons. Firstly (as discussed in detail in Sect. 2.1.1) the area available for chemical contact in a mixture of particles is a very small fraction of the total surface (and, indeed, this total surface constitutes only a small proportion of the reactant present). Secondly, bulk diffusion across a barrier layer is usually an activated process, so that interposition of product between the points of initial contact reduces the ease, and therefore the rate, of interaction. On completion of the first step in the reaction, the restricted zones of direct contact have undergone chemical modification and the continuation of reaction necessitates a transport process to maintain the migration of material from one solid to a reactive surface of the other. On increasing the temperature, surface migration usually becomes appreciable at temperatures significantly below those required for the onset of bulk diffusion within a product phase. It is to be expected that components of the less refractory constituent will migrate onto the surfaces of the other solid present. These ions are chemisorbed as the first step in product formation and, in a subsequent process, penetrate the outer layers of the... [Pg.254]

The concept of a characteristic reaction temperature must, therefore, be accepted with considerable reservation and as being of doubtful value since the reactivity of a crystalline material cannot readily be related to other properties of the solid. Such behaviour may at best point towards the possible occurrence of common controlling factors in the reaction, perhaps related to the onset of mobility, e.g. melting of one component or eutectic formation, onset of surface migration or commencement of bulk migration in a barrier phase. These possibilities should be investigated in detail before a mechanism can be formulated for any particular chemical change. [Pg.260]

Bemabeu-Gonzalvez A., Pastor-Bias M.M., and Martm-Martmez J.M., 1998, Modified adhesion of rubber materials by surface migration of wax and zinc stearate, in Proceedings of the World Polymer Congress, 37th International Symposium on Macromolecules MACRO 98, Gold Coast, Australia, 705. Romero-Sanchez M.D., Pastor-Bias M.M., and Martm-Martmez J.M., 2001, Adhesion improvement of SBR rubber by treatment with trichloroisocyanuric acid solutions in different esters, Int. J. Adhes. Adhes., 21, 325-337. [Pg.772]

All of these results are consistent with the notion that surface migration of titanium oxide species Is an Important factor that contributes to the suppression of carbon monoxide chemisorption. The H2 chemisorption experiments on 1-2 ML of Ft, where no migration Is observed, strongly Indicate that electronic (bonding) Interactions are also occurring. Thus, for the tltanla system, both electronic Interactions and surface site blocking due to titanium oxide species must be considered In Interpreting SMSI effects. [Pg.86]

Anodic dissolution reactions of metals typically have rates that depend strongly on solution composition, particularly on the anion type and concentration (Kolotyrkin, 1959). The rates increase upon addition of surface-active anions. It follows that the first step in anodic metal dissolution reactions is that of adsorption of an anion and chemical bond formation with a metal atom. This bonding facilitates subsequent steps in which the metal atom (ion) is tom from the lattice and solvated. The adsorption step may be associated with simultaneous surface migration of the dissolving atom to a more favorable position (e.g., from position 3 to position 1 in Fig. 14.1 la), where the formation of adsorption and solvation bonds is facilitated. [Pg.299]

Fig.4.12. The sample construction 1 - polished quartz plate 2 — semiconductor sensor (ZnO) i - a strip of marblyte glass 4 - a layer of titanium (palladium) X = 0.027 cm ( the length of surface migration of H atoms h = 0.0025 cm ( the air gap between the quartz plate and the glass strip). Fig.4.12. The sample construction 1 - polished quartz plate 2 — semiconductor sensor (ZnO) i - a strip of marblyte glass 4 - a layer of titanium (palladium) X = 0.027 cm ( the length of surface migration of H atoms h = 0.0025 cm ( the air gap between the quartz plate and the glass strip).
As the working temperature of the substrate was increased, the induction period (the delay time) of increased conductivity decreased due to increased rate of lateral diffusion of hydrogen atoms towards the sensor. The activation energy for surface migration of particles along a Si02 substrate estimated from the tilt of the Arrhenius plot was found to be about 20 kj/mol. [Pg.241]

Klein, R. The surface migration of carbon on tungsten. Physic. Rev. [2]... [Pg.68]

Kruyer, S. Hopping molecules and surface migration. Proc. Acad. Sci. [Pg.68]

The surface processes may comprise adsorption, surface migration (across terraces or along steps), dehydration of ions, and integration in the growth sites which are assumed to be kinks in surface steps. Any of these processes may be rate controlling, either alone or several together (10-11). [Pg.604]

Fig. 16.3 Quantum yield (QY) for electron and hole transfer to solution redox acceptors/donors as a function of the reduced variables y (related to the surface properties of the catalyst, i.e., ratio between interfacial electron transfer rate and surface recombination rate) and w (related to the ratio between surface migration currents of hole and electrons to the rate of bulk recombination), according to the proposed kinetic model [23],... Fig. 16.3 Quantum yield (QY) for electron and hole transfer to solution redox acceptors/donors as a function of the reduced variables y (related to the surface properties of the catalyst, i.e., ratio between interfacial electron transfer rate and surface recombination rate) and w (related to the ratio between surface migration currents of hole and electrons to the rate of bulk recombination), according to the proposed kinetic model [23],...
Internal resistance relates to the diffusion of the molecules from the external surface of the catalyst into the pore volume where the major part of the catalyst s surface is found. To determine the diffusion coefficients inside a porous space is not an easy task since they depend not only on the molecules diffusivity but also on the pore shape. In addition, surface diffusion should be taken into account. Data on protein migration obtained by confocal microscopy [8] definitely demonstrate that surface migration of the molecules is possible, even though the mechanism is not yet well understood. All the above-mentioned effects are combined in a definition of the so-called effective diffusivity [7]. [Pg.170]

The nature of the surface migration provides the key to the differences between adsorption on liquid and solid surfaces. For liquid surfaces, it is, to a good approximation, possible to assume that the heat of adsorption (AH) is the same at all points on the surface. In other words, such a surface... [Pg.269]


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Adatom surface migration

Cell-surface interactions migration

Kinetics of Surface Migration

Migration of surface atoms

Migration on surfaces

Migration over the Clusters Surface

Oxide surface migration

Surface activation energy migration

Surface carbon atom migration

Surface character and oxygen migration

Surface migration and the influence of catalyst supports

Surface migration cell

Surface migration, high-temperature

Surface migration, high-temperature depositions

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