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Layer formation

Stem layer adsorption was involved in the discussion of the effect of ions on f potentials (Section V-6), electrocapillary behavior (Section V-7), and electrode potentials (Section V-8) and enters into the effect of electrolytes on charged monolayers (Section XV-6). More speciflcally, this type of behavior occurs in the adsorption of electrolytes by ionic crystals. A large amount of wotk of this type has been done, partly because of the importance of such effects on the purity of precipitates of analytical interest and partly because of the role of such adsorption in coagulation and other colloid chemical processes. Early studies include those by Weiser [157], by Paneth, Hahn, and Fajans [158], and by Kolthoff and co-workers [159], A recent calorimetric study of proton adsorption by Lyklema and co-workers [160] supports a new thermodynamic analysis of double-layer formation. A recent example of this is found in a study... [Pg.412]

For many electronic and electrical appHcations, electrically conductive resias are required. Most polymeric resias exhibit high levels of electrical resistivity. Conductivity can be improved, however, by the judicious use of fillers eg, in epoxy, silver (in either flake or powdered form) is used as a filler. Sometimes other fillers such as copper are also used, but result in reduced efficiency. The popularity of silver is due to the absence of the oxide layer formation, which imparts electrical insulating characteristics. Consequently, metallic fibers such as aluminum are rarely considered for this appHcation. [Pg.531]

Figure 8-16. Boundary-layer formation in a radial-flow impeller. Figure 8-16. Boundary-layer formation in a radial-flow impeller.
It is clear that such a surface offers a wide range of sorption and displacement processes that can take place between the solute and the stationary phase surface. Due to the bi-layer formation there are three different surfaces on which a molecule can interact by sorption and three different surfaces from which molecules of solvent can be displaced and allow the solute molecule to penetrate to the next layer. During a chromatographic separation under these circumstances, all the alternatives are possible. Nevertheless, depending on the magnitude of the forces between the solute molecule and the molecules in each layer, it is likely that one particular type of interaction will dominate. The various types of interaction are included in Figure 11. [Pg.100]

Cake layer formation builds on the membrane surface and extends outward into the feed channel. The constituents of the foulant layer may be smaller than the pores of the membrane. A gel layer can result from denaturation of some proteins. Internal pore fouling occurs inside the membrane. The size of the pore is reduced and pore flow is constricted. Internal pore fouling is usually difficult to clean. [Pg.352]

Hitzig et al. have produced a simplified model of the aluminium oxide layer(s) to explain impedance data of specimens prepared under different layer formation and sealing conditionsThe model also gives consideration to the formation of active and passive pits in the oxide layer. Shaw et al. have shown that it is possible to electrochemically incorporate molybdenum into the passive film which, as previously noted, improves the pitting resistance. [Pg.677]

It should be noted that for polymerization-modified perlite the strength parameters of the composition algo go up with the increasing initial particle size. [164]. In some studies it has been shown that the filler modification effect on the mechanical properties of composites is maximum when only a portion of the filler surface is given the polymerophilic properties (cf., e.g. [166-168]). The reason lies in the specifics of the boundary layer formation in the polymer-filler systems and formation of a secondary filler network . In principle, the patchy polymerophilic behavior of the filler in relation to the matrix should also have place in the failing polymerization-modified perlite. [Pg.25]

J6. Jiji, L. M Incipient boiling and the bubble boundary layer formation over a heated plate for forced convection flow in a pressurized rectangular channel, Ph.D. Thesis, Univ. of Michigan, Ann Arbor, 1962. [Pg.290]

Barrier layer formation Diffusion across barrier control (reaction deceleratory)... [Pg.13]

The telluride halides crystallize in monoclinic lattices, but only In-TeBr and InTel are isotypic 162). InTeCl forms a layer type of structure, as do InSCl and its analogs, but, owing to the size of the Te atom and the enhanced covalency of the In-Te bond, only a coordination number of 4 for indium is realized. The structure is built up of strongly distorted, InTesraCli/j tetrahedra that share the corners and edges occupied by Te atoms. The Cl atoms are coordinated to one tetrahedron each, and do not take part in the layer formation 324, 325). [Pg.388]

Hartl, M., Kfupka, I., and LiSka, M., Experimental Study of Boundary Layers Formation by Thin Film Colorimetric Interferometry," Sci. China, Ser. A Math., Phys., Astron. Technol. Sci.,Vol. 44(supp), 2001,pp. 412-417. [Pg.36]

Comparative study of LB films of cytochrome P450 wild type and recombinant revealed similar surface-active properties of the samples. CD spectra have shown that the secondary structure of these proteins is practically identical. Improved thermal stability is also similar for LB films built up from these proteins. Marked differences for LB films of wild type and recombinant protein were observed in surface density and the thickness of the deposited layer. These differences can be explained by improved purity of the recombinant sample. In fact, impurity can disturb layer formation, preventing closest packing and diminishing the surface density and the average monolayer thickness. Decreased purity of... [Pg.173]

The observed complexity of the Se(IV) electrochemistry due to adsorption layers, formation of surface compounds, coupled chemical reactions, lack of electroactivity of reduction products, and other interrelated factors has been discussed extensively. Zuman and Somer [31] have provided a thorough literature-based review with almost 170 references on the complex polarographic and voltammetric behavior of Se(-i-IV) (selenous acid), including the acid-base properties, salt and complex formation, chemical reduction and reaction with organic and inorganic... [Pg.70]

Considering the major importance of catalysts, especially for gas-phase reactions, a separate section was allocated to the description of techniques for catalyst layer formation in micro channels and the respective analytical characterization (see Section 3.1). [Pg.258]

The first step of oxide-layer formation is oxygen adsorption (chemisorption). In the case of platinum, the process stops at this stage, and depending on the conditions, an incomplete or complete monolayer of adsorbed oxygen is present on the platinum surface. In the case of other metals, layer formation continues. When its thickness 5 has attained two to three atomic diameters, the layer is converted to an individual surface phase that is crystalline (more seldom, amorphous) and has properties analogous to those of the corresponding bulk oxides. [Pg.301]

Climent V, Coles BA, Compton RG. 2002c. Laser-induced potential transients on a Au(lll) single-crystal electrode. Determination of the potential of maximum entropy of double layer formation. J Phys Chem B 106 5258-5265. [Pg.240]

Addition of an alkali metal oxide as a "network modifier to the "network former causes pH sensitivity, i.e., small amounts of alkali metal induce superficial gel layer formation as a merely local chemical attack and so with limited alkali error larger amounts will result in more pronounced dissolving properties of the glass up to complete dissolution, e.g., water-glass with large amounts of sodium oxide. Simultaneous addition of an alkaline earth metal oxide, however, diminishes the dissolution rate. Substitution of lithium for sodium in pH-sensitive glass markedly reduces the alkali error. [Pg.75]

Fig. 2.21 Prandtl and Nernst layer formation at the boundary between a solid plate and flowing liquid (c = 0)... [Pg.146]

The capacitance determined from the initial slopes of the charging curve is about 10/a F/cm2. Taking the dielectric permittivity as 9.0, one could calculate that initially (at the OCP) an oxide layer of the barrier type existed, which was about 0.6 nm thick. A Tafelian dependence of the extrapolated initial potential on current density, with slopes of the order of 700-1000 mV/decade, indicates transport control in the oxide film. The subsequent rise of potential resembles that of barrier-layer formation. Indeed, the inverse field, calculated as the ratio between the change of oxide film thickness (calculated from Faraday s law) and the change of potential, was found to be about 1.3 nm/V, which is in the usual range. The maximum and the subsequent decay to a steady state resemble the behavior associated with pore nucleation and growth. Hence, one could conclude that the same inhomogeneity which leads to pore formation results in the localized attack in halide solutions. [Pg.437]

Accidental addition of 6500 1 of cone, hydrochloric acid to a bulk sulfuric acid storage tank released sufficient hydrogen chloride gas by dehydration to cause the tank to burst violently [1], Complete dehydration of hydrochloric acid solution releases some 250 volumes of gas. A laboratory apparatus for effecting this safely has been described [2], which avoids the possibility of layer formation in unstirred flask generators [3],... [Pg.1349]

In a continuous operation to bleach a fat-derived acid, the latter was stirred and treated at 80°C with a slow stream of 50 wt% hydrogen peroxide. Un-noticed failure of the agitator led to peroxide build-up, layer formation and eventual formation of an explosive mixture. When this passed into a centrifugal pump, it detonated. [Pg.1633]


See other pages where Layer formation is mentioned: [Pg.143]    [Pg.72]    [Pg.75]    [Pg.2041]    [Pg.131]    [Pg.444]    [Pg.977]    [Pg.109]    [Pg.79]    [Pg.184]    [Pg.24]    [Pg.52]    [Pg.285]    [Pg.450]    [Pg.461]    [Pg.107]    [Pg.301]    [Pg.303]    [Pg.21]    [Pg.195]    [Pg.229]    [Pg.47]    [Pg.195]    [Pg.388]    [Pg.76]    [Pg.662]   
See also in sourсe #XX -- [ Pg.5 , Pg.11 ]




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