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Dependence on Impurity Concentration

When an impurity is introduced into the liquid it dissociates to yield anions A and cations with subsequent recombination, according to the reaction [Pg.57]

For donor and acceptor impurities in mixture A a dependence cr oc is typical. This does not fit the simple model of dissociation with constant coefficients Kb and Kr. Apparently the ionization process in this system passes through an intermediate stage involving the formation of charge-transfer complexes [19]. [Pg.58]

The temperature dependence of conductivity (2.1) is controlled by the temperature dependence of ion mobilities and ionization-recombination constants and, in general, assumes an activation character [Pg.58]

The effect of dielectric relaxation on the frequency dependence of conductivity was already mentioned above. Its experimental confirmation is demonstrated in Fig. 2.8 [9]. The low-frequency conductivity of nematics measured at a relatively weak electric field a c is usually higher for the direction parallel to the director, a, CTx [18]. [Pg.58]


The Freezing Point Depends on Impurity Concentration and on Interface Curvature... [Pg.273]

When the feedstock contains constant proportions of reactive impurities, the rate of decline also may depend on the concentration of the main reactant, thus ... [Pg.2097]

Carbon steel Not below 60% concentration, depending on impurities... [Pg.59]

The corrosivity of a natural water depends on the concentration and type of impurity dissolved in it and especially on its oxygen content. Waters of similar oxygen content have generally similar corrosivities, e.g. well-aerated quiescent sea-water corrodes cast iron at ratesof 0 05-0-1 mm/y while most well-aerated quiescent fresh waters corrode iron at O Ol-O-1 mm/y. [Pg.589]

There is, however, one point where the different experiments do not agree Gougousi et al. found that the plasma decayed faster when the H2 concentration was increased. They concluded this from a large set of data over a significant range of H2 densities and they found the same to be true when Dj ions were studied in the presence of D2. Smith and Spanel carried out tests over a smaller range of H2 concentrations. Their data show the opposite dependence on H2 concentration, but unfortunately the authors discontinued this set of measurements since they became concerned about an increase in the concentration of impurity ions. [Pg.67]

If, however, the monomer contains as impurity the reagent F, then the DP will show a dependence on monomer concentration, the form of which will be determined by the nature of F, and hence its reactions. [Pg.403]

The usual picture here is that the foreign atom accepts an electron from an impurity level. The chemisorption is therefore depletive because the surface coverage depends on the concentration of impurity levels in the solid. The semiconductivity is, of course, reduced. We assume that the interaction problem is between the orbital on the foreign atom and the conduction band of the solid. The usual picture is then found in the A9 and AG C SL regions of Fig. 7, provided that the (P level lies below the impurity levels. An electron is lost from an impurity level for each foreign atom adsorbed, and if the (P level is anionic, the foreign atom is converted to an anion on the surface. [Pg.29]

In the case of a quasi-isolated surface, the bulk of the semiconductor (e.g., impurities inside the crystal) no longer influences its chemisorptive and catalytic properties, the latter depending only on the structure of the surface. This dependence is implicit in Equation (25), according to which the position of the Fermi level on the surface e.+ (and hence the chemisorptive and catalytic properties of the surface) depends on the concentration and nature of the chemisorbed particles and also on the concentration and nature of the structural defects on the surface. [Pg.230]

Soft crystalline solid rhombic crystal pure salt is white but color may vary the color of the mineral barite may vary among red, yellow, gray or green depending on impurities density 4.50 g/cm refractive index 1.64 melts around 1,580°C decomposes above 1,600°C hardness 4.3 to 4.6 Mohs insoluble in water (285 mg/L at 30°C) and alcohol Ksp 1.1 x 10-i° soluble in concentrated sulfuric acid. [Pg.92]

Some of these impurities have opposite effects on the catalytic activity and stereospecificity, depending on their concentration. [Pg.18]

The amount of adsorbate that can be held depends on the concentration or partial pressure and temperature, on the chemical nature of the fluid, and on the nature, specific surface, method of preparation, and regeneration history of the solid. For single adsorbable components of gases, the relations between amount adsorbed and the partial pressure have been classified into the six types shown in Figure 15.2. Many common systems conform to Type I, for example, some of the curves of Figure 15.3. Adsorption data are not highly reproducible because small contents of impurities and the history of the adsorbent have strong influences on their behavior. [Pg.495]

The triboluminescence of minerals has been studied visually (see the footnotes to Table I) but only a few minerals have been examined spectroscopically. There are a few clear examples of noncentric crystals, such as quartz, whose emission is lightning, sometimes with black body radiation. Most of the triboluminescent minerals appear to have activity and color which is dependent on impurities, as is the case for kunzite, fluorite, sphalerite and probably the alkali halides. Table I attempts to distinguish between fracto-luminescence and deformation luminescence, but the distinctions are not clear cut. A detailed analysis of the structural features of triboluminescent and nontriboluminescent minerals may make it possible to draw conclusions about the nature and concentration of trace impurities that are not obvious from the color or geological site of the crystals. Triboluminescence could be used as an additional method for characterizing minerals in the field, using only the standard rock hammer, with the sensitive human eye as a detector. [Pg.260]

The reaction is found to be zeroth order with respect to a-methylstyrene and approximately first order with respect to hydrogen in all solvents as shown in Table I. Reaction dependence on hydrogen in cyclohexane solvent is shown in Figure 2 and a typical Arrhenius plot is presented in Figure 3. Reaction rate is independent of Pd concentration (structure insensitive) in pure nonpolar solvents (cyclohexane, hexane (U.V.)) but becomes structure sensitive (i.e. dependent on Pd concentration) in solvents with impurities or which are more polar. The activation energy of 10.2 kcal/mol found in cyclohexane agreed well with the one determined by Germain et al. (6). [Pg.422]

Food-grade sodium metabisulfite that is free of impurities should be used in RO systems. The compound must not be cobalt-activated, as cobalt can catalyze the oxidation of the polyamide composite membrane in a manner similar to iron and manganese (see Chapter 7.6). Further, while the shelf life of solid sodium metabisulfite is 4-6 months, in solution, the shelf life depends on the concentration, as shown in Table 8.9.9... [Pg.181]

Fig. 14.5. Beryllium erosion rate depends both on impurity concentration in the incident plasma, as well as the sample temperature during the exposure. From [16]... Fig. 14.5. Beryllium erosion rate depends both on impurity concentration in the incident plasma, as well as the sample temperature during the exposure. From [16]...
Radiation Ionization of monomer Difunctional ion radicals and difunctional free radicals Termination of growing chains, of which mechanisms depends on the concentration of impurities... [Pg.58]

Since the previously measured rate of dissociation of N2 in Ar is lower than the observed rate by five orders of magnitude the production of N atoms followed by rapid radical reactions is ruled out. Furthermore, since oxygen is present as an impurity the reaction with N2 to form NO and N is indeed occurring. However, the exchange rate showed no dependence on oxygen concentration which verifies that nitrogen atom production is not rate controlling. [Pg.264]


See other pages where Dependence on Impurity Concentration is mentioned: [Pg.139]    [Pg.252]    [Pg.68]    [Pg.57]    [Pg.51]    [Pg.744]    [Pg.139]    [Pg.252]    [Pg.68]    [Pg.57]    [Pg.51]    [Pg.744]    [Pg.15]    [Pg.455]    [Pg.321]    [Pg.352]    [Pg.1305]    [Pg.115]    [Pg.89]    [Pg.441]    [Pg.101]    [Pg.139]    [Pg.28]    [Pg.39]    [Pg.1]    [Pg.67]    [Pg.377]    [Pg.274]    [Pg.495]    [Pg.106]   


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Concentration dependence

Concentration dependency

Dependence on concentration

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