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Adsorbed additives

Currently, the most frequently used technology for SO reduction in the flue gas is a SO adsorbing additive. With such an additive, the following steps occur.Oxidation of SO to SO in the regenerator. [Pg.214]

Adsorbed additives also tend to undergo reduction during the electroless process, and become incorporated as impurities into deposits, most likely via a mechanism similar to that involved in ternary alloy deposition. In a manner similar to that discussed below in greater detail for dissolved 02, electroless deposition rates will be lower for features smaller than the stabilizer diffusion layer thickness. The edges of larger features, which experience higher stabilizer levels due to enhanced nonplanar... [Pg.264]

Sorptive reactions of LNAPLs and dissolved organic compounds moving through soil are almost always reversible equilibrium reactions. A concentration equilibrium is established between the concentration of chemical dissolved in water and that which is attached to the soil particles. When concentrations change, the soil may adsorb additional organic molecules or release them to reestablish the equilibrium. [Pg.144]

In the experimental analysis the SW potential scan is preceded by a certain delay period (/delay) to allow the reactant to adsorb on the electrode surface. Besides, the reactant adsorbs additionally in the course of the voltammetric scan starting from the initial (Es) to the peak potential (fp). Thus, the total accumulation period (face)... [Pg.98]

Adsorbed additives affect both of these mechanisms by changing the concentration of growth sites Cg on the surface [n Jcm (where is the number of growth sites)],... [Pg.189]

Nucleation. In the presence of adsorbed additives, the mean free path for lateral diffusion of adions is shortened, which is equivalent to a decrease in the diffusion coefficient D (diffusivity) of adions. This decrease in D can result in an increase in adion concentration at steady state and thus an increase in the frequency of the two-dimensional nucleation between diffusing adions. [Pg.190]

They may accelerate or retard the process. Additives may act in solution (via com-plexation), but more often adsorb on the oxide and either raise or lower the energy of attachment between the surface ions and those of the interior. In extreme cases, adsorbed additives may inhibit dissolution. pH has a strong influence on the dissolution of iron oxides. At atmospheric pressure, dissolution of well crystalline Fe " oxides requires a pH of <1 even at 70 °C. The high affinity of protons with structural 0 assists the release of iron particularly at low pH. It is the release of the cation, rather than the anions which is likely to be rate limiting. pH also influences the electrochemical surface potential and hence redox processes. The surface potential is determined largely by surface charge, which in turn, depends upon pH (see Chap. 10). [Pg.299]

Use Adsorbant additive for the chromatographic separation of 3 -terminal polynucleotides from RNA. [Pg.62]

The NOx removal process was studied experimentally in a pulsed corona discharge combined with the Ti02 photocatalytic reaction [387]. N02 was found to adsorb easily on the photocatalyst surface, whereas NO was hardly adsorbed. Addition of water vapor enhanced the N02 adsorption. It was concluded that the main role of the plasma-chemical reaction in this system is the oxidation of NO into N02. A considerable part of N02 is adsorbed on the photocatalyst surface, and is transformed to HN03 through photocatalytic reaction with OH. [Pg.21]

These equations form a system of partial differential equations of the second order. Examples of two complete systems are given in Table 2.1 (a binary mixture and a pure mobile phase or a mobile phase containing only weakly adsorbed additives, a two-component system) and Table 2.2 (a binary mixture and a binary mobile phase with a strongly adsorbed additive, a three-component system). For the sake of simplicity, the equilibrium-dispersive model (see Section 2.2.2) has been used in both cases. The problem of the choice of the isotherm model will be discussed in the next two chapters. [Pg.43]

Chemical modification of filler surface reduces the surface area available for interaction. This reduces bound rubber (Figure 7.26). The quantity of adsorbing additives on the filler surface must be strictly controlled because these additives compete with the reinforcing effect of the bound rubber. Thermal treatment of rubber increased the quantity of bound rubber but only when rubber was added prior to the addition of low molecular processing additives. " This shows that there was competition between the low molecular additive and the rubber for adsorption sites. [Pg.379]

Hydrolytic species of iron are also able to adsorb humic substances on their surfaces and the negatively charged humic substances can adsorb additional Fe cations. From our results we can at least conclude that iron forms negatively charged complexes with humic substances and that humic substances solubilize iron when they are present in diluted seawater. If we compare the quantity of Fe in the anionic zones depending on the humic substance used, we get the following sequence of the humic substances FAC > HAC > HAM > HAN. [Pg.408]

Wang, H. Y., G. F. Payne, and F. M. Robinson. Enhanced Cycloheximide Production through Neutral Adsorbant Addition. Presented at the XIII International Congress of Microbiology, Boston, Mass. 1982. [Pg.135]

The critical temperature of lubricated friction has been related to the physical chemistry of adsorption by interpreting the transition from smooth sliding with a low coefficient of friction to high values of friction with scuffing as the critical depletion of the adsorbed lubricant film. The critical transition temperature is identified with the critical temperature of desorption. Frewing [31] developed the following relation for the stable existence of a film of adsorbed additive in equilibrium with its oil solution ... [Pg.226]

Dilution by an inert non-adsorbable additive is equivalent to reducing the reactant pressure without changing the feed ratio. Although there may be reasons why a dilute reactant stream has to be used, the purely kinetic effects of diluents are simple. The novel issues that are raised by the addition of a diluent concern changes in space velocity, the heat capacity of the feed stream, and possibly heat transfer between the reactants and the surroundings. Some of these effects may be advantageous but, since dilution increases the space velocity based on total feed rate, it results in a lower throughput of the reactants at a fixed space velocity. [Pg.274]

Additives for dump sealing materials and cements used for waste consolidation Pollutant-adsorbing additive to cements used for consolidation of industrial waste and for barrier systems... [Pg.176]

Bisulfites, as adsorbent additives, 177 Borates and boric acid, as adsorbent additives, 175... [Pg.208]

Cobalt oxide, as adsorbent additive, 177 Column chromatography, see Elution Column length, effect on N, 115-117 Column packing, see HETP values Column pressure, effect on TV, 115-117 Coluisns, for liquid chromatography, 347-348... [Pg.208]

Concave isotherm. 23 Configuration of adsorbate, 54 alkyl groups, 201-202 aromatic hydrocarbons, 289-290 azaaromatics, 290 determination of. 205, 288-291 phenols on alumina. 306 Continuous development, 32 Convex isotherm, 23 Copper ion, as adsorbent additive, 177 Copper sulfate, as adsorbent, 177 Coupled columns, effect on bed efficiency. [Pg.208]


See other pages where Adsorbed additives is mentioned: [Pg.167]    [Pg.289]    [Pg.579]    [Pg.310]    [Pg.319]    [Pg.25]    [Pg.95]    [Pg.231]    [Pg.337]    [Pg.30]    [Pg.177]    [Pg.289]    [Pg.410]    [Pg.148]    [Pg.196]    [Pg.114]    [Pg.167]    [Pg.363]    [Pg.1168]    [Pg.110]    [Pg.116]    [Pg.615]    [Pg.640]    [Pg.6]    [Pg.975]    [Pg.497]    [Pg.208]   
See also in sourсe #XX -- [ Pg.66 , Pg.67 , Pg.68 ]




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