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Reducing agents sulfites

Removal of brine contaminants accounts for a significant portion of overall chlor—alkali production cost, especially for the membrane process. Moreover, part or all of the depleted brine from mercury and membrane cells must first be dechlorinated to recover the dissolved chlorine and to prevent corrosion during further processing. In a typical membrane plant, HCl is added to Hberate chlorine, then a vacuum is appHed to recover it. A reducing agent such as sodium sulfite is added to remove the final traces because chlorine would adversely react with the ion-exchange resins used later in the process. Dechlorinated brine is then resaturated with soHd salt for further use. [Pg.502]

Reductions. Hydrazine is a very strong reducing agent. In the presence of oxygen and peroxides, it yields primarily nitrogen and water with more or less ammonia and hydrazoic acid [7782-79-8]. Based on standard electrode potentials, hydrazine in alkaline solution is a stronger reductant than sulfite but weaker than hypophosphite in acid solution, it falls between and Ti ( 7). [Pg.277]

Photography. Sodium sulfite is useful as a reducing agent in certain photographic fixing baths, developers, hardeners, and intensifiers (334). However, the principal use is as a film preservative and discoloration preventative (see Photography). [Pg.149]

Dithionite is a stronger reducing agent than sulfite. Many metal ions, eg, Cu", Ag", Pb ", Sb ", and Bi ", are reduced to the metal, whereas TiO " is reduced to (346). Dithionite readily reduces iodine, peroxides, ferric salts, and oxygen. Some of the decolorizing appHcations of dithionite, eg, in clay bleaching, are based on the reduction of ferric iron. [Pg.150]

The reducing agents generally used in bleaching include sulfur dioxide, sulfurous acid, bisulfites, sulfites, hydrosulfites (dithionites), sodium sulfoxylate formaldehyde, and sodium borohydride. These materials are used mainly in pulp and textile bleaching (see Sulfur compounds Boron compounds). [Pg.149]

Dithionites. Although the free-dithionous acid, H2S2O4, has never been isolated, the salts of the acid, in particular zinc [7779-86-4] and sodium dithionite [7775-14-6] have been prepared and are widely used as industrial reducing agents. The dithionite salts can be prepared by the reaction of sodium formate with sodium hydroxide and sulfur dioxide or by the reduction of sulfites, bisulfites, and sulfur dioxide with metallic substances such as zinc, iron, or zinc or sodium amalgams, or by electrolytic reduction (147). [Pg.149]

Chromium Removal System. Chlorate manufacturers must remove chromium from the chlorate solution as a result of environmental regulations. During crystallization of sodium chlorate, essentially all of the sodium dichromate is recycled back to the electrolyzer. Alternatively, hexavalent chromium, Cr, can be reduced and coprecipitated in an agitated reactor using a choice of reducing agents, eg, sodium sulfide, sulfite, thiosulfate, hydrosulfite, hydrazine, etc. The product is chromium(III) oxide [1333-82-0] (98—106). Ion exchange and solvent extraction techniques have also... [Pg.499]

A dichromate or chromate solution is reduced under pressure to produce a hydrous oxide, which is filtered, washed, and calcined at 1000°C. The calcined oxide is washed to remove sodium chromate, dried, and ground. Sulfur, glucose, sulfite, and reducing gases may be used as reducing agent, and temperatures may reach 210°C and pressures 4—5 MPa (600—700 psi). [Pg.145]

Conversely, sulfites can act as oxidants in the presence of strong reducing agents e.g. sodium amalgam yields dithionite, and formates (in being oxidized to oxalates) yield thiosulfate ... [Pg.719]

The parent acid has no independent existence and has not been detected in aqueous solution either. Sodium dithionite is widely used as an industrial reducing agent and can be prepared by reduction of sulfite using Zn dust, Na/Hg or electrolytically, e.g. ... [Pg.720]

Various multicomponent systems have also been described. Three component systems in which a second reducing agent (eg. sulfite) acts to recycle the transition metal salt, have the advantage that less metal is used (Scheme 3.43). [Pg.95]

NOTE Sulfite, bisulfite, and metabisulfite are commonly used as a reducing agent for chromate in industrial water and chlorine in potable water. [Pg.487]

The oxidation number of sulfur in sulfur dioxide and the sulfites is +4, an intermediate value in sulfur s range from —2 to +6. Hence, these compounds can act as either oxidizing agents or reducing agents. By far the most important reaction of sulfur dioxide is its slow oxidation to sulfur trioxide, S03 (13), in which sulfur has the oxidation number +6 ... [Pg.757]

Sulfinic acids can be prepared by reduction of sulfonyl chlorides. Though mostly done on aromatic sulfonyl chlorides, the reaction has also been applied to alkyl compounds. Besides zinc, sodium sulfite, hydrazine, sodium sulfide, and other reducing agents have been used. For reduction of sulfonyl chlorides to thiols, see 19-57. [Pg.577]

Many of the modifications of the pyrazolone antiinflammatory agents are intended to increase the limited hydrophilicity of the parent molecules. Reaction of aminopyrine (157) with formaldehyde and sodium hydrogen sulfite affords dipyrone (158). The first step can be rationalized as an Eschweiler-Clark type N-methylation reaction, with bisulfite acting as the reducing agent. The resulting mono N-methyl analogue of 157 then apparently forms the sulfite adduct of the carbinolamine of formaldehyde. [Pg.262]

Citrate, C20)-, 2,3-dimercaptopropanol, EDTA, F-, I-, OH-, oxidation with bromine water, phosphate(3—), tartrate, triethanolamine, thioglycolic acid Citrate, jV.jV-dihydroxyethylglycine, EDTA, F-, SO)-, tartrate Citrate, F-, H202, OH-, oxalate, tartrate Citrate, F-, I-, reducing agents, S2-, sulfite, tartrate... [Pg.1445]


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See also in sourсe #XX -- [ Pg.457 ]




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