Alkaline solution synthesis

There are several physical and chemical characteristics of these oxide pyrochlores which may contribute to their high electrocatalytic activity. The previously described alkaline solution synthesis technique (6,7) provided these materials with surface areas typically ranging from 50 to 200 m /g. Thus, one of the basic requirements for an effective electrocatalyst has been satisfied the electrocatalytic activity is not limited by the unavailability of catalytically active surface sites, as is so often the case with metal and mixed metal oxides. 

M.p. 190-192 C. The enolic form of 3-oxo-L-gulofuranolactone. It can be prepared by synthesis from glucose, or extracted from plant sources such as rose hips, blackcurrants or citrus fruits. Easily oxidized. It is essential for the formation of collagen and intercellular material, bone and teeth, and for the healing of wounds. It is used in the treatment of scurvy. Man is one of the few mammals unable to manufacture ascorbic acid in his liver. Used as a photographic developing agent in alkaline solution. 

The best synthesis is now by oxidation of alkaline solutions of Br03 using F2 gas under rather specific conditions " ... 

Isothiazolone dioxide rings are readily cleaved in diluted aqueous alkaline solution at r.t. and this feature allows their use, in some cases, as a protecting group (95TL(36)6227). An example is the efficient Fischer indole synthesis of 72. 

The formylation of a phenol 1 with chloroform in alkaline solution is called the Reimer-Tiemann reaction. It leads preferentially to formation of an ortho-formylated phenol—e.g. salicylic aldehyde 2 —while with other formylation reactions, e.g. the Gattermann reaction, the corresponding /jara-formyl derivative is obtained as a major product. The Reimer-Tiemann reaction is mainly used for the synthesis of o-hydroxy aromatic aldehydes. 

Another approach for the synthesis of enantiopure amino acids or amino alcohols is the enantioselective enzyme-catalyzed hydrolysis of hydantoins. As discussed above, hydantoins are very easily racemized in weak alkaline solutions via keto enol tautomerism. Sugai et al. have reported the DKR of the hydantoin prepared from DL-phenylalanine. DKR took place smoothly by the use of D-hydantoinase at a pH of 9 employing a borate buffer (Figure 4.17) [42]. 

A comprehensive work on the electrodeposition chemistry and characterization of anodically synthesized CdTe thin films has been presented by Ham et al. [98]. In this work, along with the electrolytic anodic synthesis of CdTe by using Cd anodes in alkaline solutions of sodium telluride, an electroless route of anodizing a Cd electrode held at open circuit in the same solution was also introduced. The anodic method was expected to produce CdTe with little contamination from Te on account of the thermodynamic properties of the system the open-circuit potential of Cd anodes in the Te electrolyte lies negative of the Te redox point, so... 

Nickel oxide anodes are another example for a relatively simple oxide electrocatalyst used rather widely in the oxidation of organic substances (alcohols, amines, etc.) in alkaline solutions at relatively low anodic potentials (about +0.6 V RHE). These processes, which occur at an oxidized nickel surface, are rather highly selective. As an example, we mention the industrial oxidation of diacetone-L-sorbose to the corresponding acid in vitamin C synthesis. This reaction occurs at nickel oxide electrodes with chemical yields close to 100%. 

In the chemical preparation of unprotected metal colloids, the metal concentration usually has a significant influence on the particle size of obtained metal nanoclusters. For example, when increasing Pd concentration from 0.1 to 1.0 mM in the preparation of Pd metal colloids by the thermal decomposition of Pd acetate in methyl isobutyl ketone, the average Pd particle size increased from 8 to 140nm [6,7]. However, in the alkaline EG synthesis method, the size of metal nanoclusters was only slightly dependent on the metal concentration of the colloidal solution. The colloidal Pt particles prepared with a metal concentration of 3.7 g/1 had an average diameter of... 

The alkaline EG synthesis method described in this chapter is highly efficient for preparing colloidal solutions of small and narrowly distributed unprotected noble metal or alloy nanoclusters with high metal concentration. 

The emphases of future investigation on these unprotected metal nanoclusters should be mainly placed on (1) further controlling the size, composition and shape of the unprotected metal or alloy nanoclusters (2) better understanding the stabilizing mechanism of the unprotected metal nanoclusters in colloidal solutions prepared by the alkaline EG synthesis method (3) developing novel catalytic and other functional systems for real applications. 

Tabushi et al. (1979) have shown that p-cyclodextrin in aqueous alkaline solution allows highly selective one-step synthesis of vitamin Kj (or K2) analogues here the key step is alkylation of 2-methyl hydronaphthoquinone with allyl, crotyl, methallyl, or prenyl bromide. 

Chitosan gels are chemically stable in alkaline solutions and are thermally stable until 200°C [5], These conditions are compatible with the synthesis field of most aluminium-rich zeolites and allow to prepare composite materials by several methods. 

A preformed chitosan-silica composite with 60% weight inorganic part [7] is used as the source of silica for the zeolite synthesis. An alkaline solution of sodium aluminate (Na 2.1 M, Al 1 M) was used in three methods of preparation (A) beads of the chitosan-silica composite were stirred overnight in the aluminate solution, extracted and submitted to a hydrothermal treatment at 80 °C during 48h (B) beads of the chitosan-silica composite were immersed in the aluminate solution and the system underwent a hydrothermal treatment at 80 °C for 48h (C) beads of the chitosan-silica composite were stirred overnight in the aluminate solution, extracted, dried at 80 °C and exposed to water vapour at 80°C during 48h. 

Zeolites are formed by crystallization at temperatures between 80 and 200 °C from aqueous alkaline solutions of silica and alumina gels in a process referred to as hydrothermal synthesis.15,19 A considerable amount is known about the mechanism of the crystallization process, however, no rational procedure, similar to organic synthetic procedures, to make a specifically designed zeolite topology is available. The products obtained are sensitive functions of the reaction conditions (composition of gel, reaction time, order of mixing, gel aging, etc.) and are kinetically controlled. Nevertheless, reproducible procedures have been devised to make bulk quantities of zeolites. Procedures for post-synthetic modifications have also been described.20 22... 

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