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Lead ionic strength dependence

For practical purposes, within the NN frame the ionic strength dependence can be taken into account in the estimate of the free energy and of the melting temperature by using empirical equations with numerical prefactors. Such equations display a leading logarithmic dependence on salt concentration which reproduces the experimental observations well and allows simple and reliable calculations [3, 15]. [Pg.234]

Unsymmetrical inert electrolyte binding leads to semantic problems even at pristine conditions PZC becomes ionic strength dependent, the surface potential is not equal to zero at the PZC. etc., cf. Eqs. (3.2) and (3.3). Fortunately such problems are encountered in modeling exercises with unsymmetrical electrolyte binding, but not in reality. Anyway, this modification is not recommended. Ultimately a TLM with seven adjustable parameters (equilibrium constants of reactions (5.32), (5.33), (5.46), and (5.47) are unrelated) can be used to model raw titration data (the charging curves were not shifted to produce PZC = CIP) [66], but physical meaning of such model exercises is questionable. [Pg.664]

In perchloric acid solution, oxidation of [Mo(CN)g] by VO2 is biphasic, consisting of parallel cyanide-bridged inner-sphere and outer-sphere pathways. Both pathways are catalyzed by [H ] which is presumed to coordinate to the molybdenum complex and ionic-strength dependencies indicate that [HNa2Mo(CN)g] and [HNaMo(CN)g] are the reactive species. Photoexcitation of the intervalence transfer band in the [Mo(CN)g] , CUaq ion pair leads to electron transfer and allows determination of the dark reaction rate. The oxidation of Mn04 by [Mo(CN)g] has also been examined, in alkaline media. The reaction is outer sphere as are the corresponding reactions of [W(CN)g] and... [Pg.53]

Precipitation is affected by pH, solubiUty product of the precipitant, ionic strength and temperature of the aqueous stream, and the presence of metal complexes. For each metal precipitant, there is an optimum pH where its solubiUty is lowest and hence, the highest removals may be achieved. When an aqueous stream contains various metals, the precipitation process caimot be optimized for each metal, sometimes making it difficult to achieve effluent targets for each. SolubiUty products depend on the form of the metal compound and ate lowest for metal sulfides, reflecting the relative insolubiUty of these compounds. For example, the solubiUty product for lead sulfide [1314-87-0] is on the order of compared to 10 for lead carbonate. Metal... [Pg.164]

At a finite distance, where the surface does not come into molecular contact, equilibrium is reached between electrodynamic attractive and electrostatic repulsive forces (secondary minimum). At smaller distance there is a net energy barrier. Once overcome, the combination of strong short-range electrostatic repulsive forces and van der Waals attractive forces leads to a deep primary minimum. Both the height of the barrier and secondary minimum depend on the ionic strength and electrostatic charges. The energy barrier is decreased in the presence of electrolytes (monovalent < divalent [Pg.355]


See other pages where Lead ionic strength dependence is mentioned: [Pg.121]    [Pg.457]    [Pg.241]    [Pg.241]    [Pg.2593]    [Pg.332]    [Pg.245]    [Pg.159]    [Pg.437]    [Pg.572]    [Pg.161]    [Pg.179]    [Pg.195]    [Pg.1194]    [Pg.72]    [Pg.6359]    [Pg.673]    [Pg.277]    [Pg.554]    [Pg.145]    [Pg.224]    [Pg.740]    [Pg.327]    [Pg.449]    [Pg.10]    [Pg.253]    [Pg.72]    [Pg.363]    [Pg.592]    [Pg.644]    [Pg.110]    [Pg.545]    [Pg.193]    [Pg.170]    [Pg.277]    [Pg.84]    [Pg.472]    [Pg.78]    [Pg.88]    [Pg.178]    [Pg.349]    [Pg.197]    [Pg.111]    [Pg.397]    [Pg.555]    [Pg.138]   
See also in sourсe #XX -- [ Pg.846 ]




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Ionic strength

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