Solute chemistry

The kinetics of crystal growth has been much studied Refs. 98-102 are representative. Often there is a time lag before crystallization starts, whose parametric dependence may be indicative of the nucleation mechanism. The crystal growth that follows may be controlled by diffusion or by surface or solution chemistry (see also Section XVI-2C). 

This interface is critically important in many applications, as well as in biological systems. For example, the movement of pollutants tln-ough the enviromnent involves a series of chemical reactions of aqueous groundwater solutions with mineral surfaces. Although the liquid-solid interface has been studied for many years, it is only recently that the tools have been developed for interrogating this interface at the atomic level. This interface is particularly complex, as the interactions of ions dissolved in solution with a surface are affected not only by the surface structure, but also by the solution chemistry and by the effects of the electrical double layer [31]. It has been found, for example, that some surface reconstructions present in UHV persist under solution, while others do not. 

The percolation argument is based on the idea that with an increasing Cr content an insoluble interlinked cliromium oxide network can fonn which is also protective by embedding the otherwise soluble iron oxide species. As the tlireshold composition for a high stability of the oxide film is strongly influenced by solution chemistry and is different for different dissolution reactions [73], a comprehensive model, however, cannot be based solely on geometrical considerations but has in addition to consider the dissolution chemistry in a concrete way. 

Decomposition of potassium ferratefVI) at 1000 K gives a ferrate V), K3Fe04, and several types of ferrate(IV), for example FeOj", Fe04 are known these ferrates(IV) have no solution chemistry and are probably best regarded as mixed oxides, since the FeOl" ion has no identifiable structure. 

The example clearly demonstrates the main advantages of solution chemistry over the solid-phase approach ... 

Synthesis. In contrast to pituitary hormones, which usually can be obtained in pure form only after extraction from animal tissues, brain oligopeptides are readily available because of their small size. The synthetic repHca represents the most economical and readily accessible source for the oligopeptides. Two techniques are available for laboratory synthesis of oligopeptides, ie, solution chemistry and soHd-phase peptide synthesis (SPPS). 

Citrates. Iron citrate [2338-05-8] is a compound that contains citric acid and iron(II) and iron(III) in indefinite ratios. Iron(II) citrate [23383-11-1] and iron(III) citrate [28633-45-6] are also of indefinite stoichiometry, although iron(III) citrate which contains Fe and citric acid in a 1 1 ratio [3522-50-7] is known. These compounds dissolve slowly in water and are more readily soluble in hot water. The solution chemistry of these compounds is comphcated by formation of a number of monomeric and oligomeric species. All of the iron citrate compounds are used as supplements to soils and animal diets. 

First Carbonation. The process stream OH is raised to 3.0 with carbon dioxide. Juice is recycled either internally or in a separate vessel to provide seed for calcium carbonate growth. Retention time is 15—20 min at 80—85°C. OH of the juice purification process streams is more descriptive than pH for two reasons first, all of the important solution chemistry depends on reactions of the hydroxyl ion rather than of the hydrogen ion and second, the nature of the C0 2 U20-Ca " equiUbria results in a OH which is independent of the temperature of the solution. AH of the temperature effects on the dissociation constant of water are reflected by the pH. 

PZN-PT, and YBa2Cug02 g. For the preparation of PZT thin films, the most frequently used precursors have been lead acetate and 2irconium and titanium alkoxides, especially the propoxides. Short-chain alcohols, such as methanol and propanol, have been used most often as solvents, although there have been several successful investigations of the preparation of PZT films from the methoxyethanol solvent system. The use of acetic acid as a solvent and chemical modifier has also been reported. Whereas PZT thin films with exceUent ferroelectric properties have been prepared by sol-gel deposition, there has been relatively Httle effort directed toward understanding solution chemistry effects on thin-film properties. 

K. L. Mittal, ed.. Solution Chemistry of Sufactants, Vol. 2, Plenum Press, New York, 1979. 

Physical-Chemical Phenomena. Several physical-chemical phenomena occur when chemical reagents are added to an air-water solid system due to the interaction of the reagents with the air-water, water-sohd, and air-solid interfaces. This causes changes in the solution chemistry in which the particles are suspended. Some of the... 

Ohtaki, H., 1998. Crystallization Processes, Wiley Series in Solution Chemistry, Vol. 3. West Sussex John Wiley Sons. 

The central role of the concept of polarity in chemistry arises from the electrical nature of matter. In the context of solution chemistry, solvent polarity is the ability of a solvent to stabilize (by solvation) charges or dipoles. " We have already seen that the physical quantities e (dielectric constant) and p (dipole moment) are quantitative measures of properties that must be related to the qualitative concept of... 

The interaction between a solute species and solvent molecules is called solvation, or hydration in aqueous solution. This phenomenon stabilizes separated charges and makes possible heterolytic reactions in solution. Solvation is, therefore, an important subject in solution chemistry. The solvation of ions has been most thoroughly studied. 

This approach to solution chemistry was largely developed by Hildebrand in his regular solution theory. A regular solution is one whose entropy of mixing is ideal and whose enthalpy of mixing is nonideal. Consider a binary solvent of components 1 and 2. Let i and 2 be numbers of moles of 1 and 2, 4>, and 4>2 their volume fractions in the mixture, and Vi, V2 their molar volumes. This treatment follows Shinoda. ... 

Many books on chemical kinetics have been published, but few of these are devoted solely or even primarily to solution phase chemical kinetics. Textbooks of physical organic chemistry must deal with solution chemistry, but kinetics is only one part of their subject. From my teaching experience I have concluded that there is no current text that meets the needs, as I interpret them, of the student and practitioner of solution chemical kinetics. 

The aqueous solution chemistry of Al and the other group 13 metals is rather complicated. The aquo ions are acidic with... 

M = Al, Ga, In, Tl). The solution chemistry of Al in particular has been extensively investigated because of its industrial importance in water treatment plants, its use in many toiletry formulations, its possible implication in both Altzheimer s disease and the deleterious effects of acid rain, and the ubiquity of Al cooking utensils.For example, hydrated aluminium sulphate (10-30 gm ) can be added to turbid water supplies at pH 6.5-7.5 to flocculate the colloids, some 3 million tonnes per annum being used worldwide for this application alone. Likewise kilotonne amounts of A1(OH)2.5C1o.5 in concentrated (6m) aqueous solution are used in the manufacture of deodorants and antiperspirants. 

The solution chemistry of nitric acid is extremely varied. Redox data are summarized in Table 11.4 and Fig. 11.9 (pp. 434-8). In... 

In addition to simple dissolution, ionic dissociation and solvolysis, two further classes of reaction are of pre-eminent importance in aqueous solution chemistry, namely acid-base reactions (p. 48) and oxidation-reduction reactions. In water, the oxygen atom is in its lowest oxidation state (—2). Standard reduction potentials (p. 435) of oxygen in acid and alkaline solution are listed in Table 14.10- and shown diagramatically in the scheme opposite. It is important to remember that if or OH appear in the electrode half-reaction, then the electrode potential will change markedly with the pH. Thus for the first reaction in Table 14.10 O2 -I-4H+ -I- 4e 2H2O, although E° = 1.229 V,... 

Acidification of solutions of disulfites regenerates HSO3 and SO2 again, and the solution chemistry of S205 is essentially that of the normal sulfites and hydrogen sulfites, despite the formal presence of S and S (rather than S ) in the solid state. 

G. Gordon, R. G. Kieffer and D. H. Rosenblatt, Progr. Inorg. Chem. 15, 201-86 (1972). The first half of this review deals with the aqueous solution chemistry of chlorous acid and chlorites. 

Sandoz, G., Fujii, C. T. and Brown, B. F., Solution Chemistry Within Stress-corrosion Cracks in Alloy Steels , Corros. Sci., 10, 839 (1970)... 

The Gibbs-Duhem equation is extremely important in solution chemistry and it can be seen from equation 20.171 that it provides a means of determining the activity of one component in a binary solution providing the activity of the other is known. 

The I——12 half-reaction has many applications in aqueous solution chemistry. The use of I- as a reducing agent and I2 as an oxidizing agent, particularly for quantitative purposes, is called iodimetry. 

Under certain condition, however, reactions are still preferably conducted in solution. This is the case e.g., for heterogeneous reactions and for conversions, which deliver complex product mixtures. In the latter case, further conversion of this mixture on the solid support is not desirable. In these instances, the combination of solution chemistry with polymer-assisted conversions can be an advantageous solution. Polymer-assisted synthesis in solution employs the polymer matrix either as a scavenger or for polymeric reagents. In both cases the virtues of solution phase and solid supported chemistry are ideally combined allowing for the preparation of pure products by filtration of the reactive resin. If several reactive polymers are used sequentially, multi-step syntheses can be conducted in a polymer-supported manner in solution as well. As a further advantage, many reactive polymers can be recycled for multiple use. 

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