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Sulfite aqueous solutions

Figure 11. Influence of solids fraction on k a in stirred tanks (a) sodium sulfite aqueous solution [89] (b) tap water [90] (c) NaCl aqueous solution [91],... Figure 11. Influence of solids fraction on k a in stirred tanks (a) sodium sulfite aqueous solution [89] (b) tap water [90] (c) NaCl aqueous solution [91],...
Huang, C., Adebiyi, 0., Muradov, N., and T-Raissi, A., UV Light Photolysis of Ammonium Sulfite Aqueous Solution for the Production of Hydrogen, Vroc.l6 World Hydrogen Energy Conf., Lyon, France, June 13-16, 2006. [Pg.45]

Another method employed is the treatment of aqueous solutions of aminophenols with activated carbon (81,82). During this procedure, sodium sulfite, sodium dithionite, or disodium ethylenediaminotetraacetate (82) is added to increase the quaUty and stabiUty of the products and to chelate heavy-metal ions that would catalyze oxidation. Addition of sodium dithionite, hydrazine (82), or sodium hydrosulfite (83) also is recommended during precipitation or crystallization of aminophenols. [Pg.311]

Xylose is obtained from sulfite Hquors, particularly from hardwoods, such as birch, by methanol extraction of concentrates or dried sulfite lyes, ultrafiltration (qv) and reverse osmosis (qv), ion exchange, ion exclusion, or combinations of these treatments (201). Hydrogenation of xylose is carried out in aqueous solution, usually at basic pH. The Raney nickel catalyst has a loading of 2% at 125°C and 3.5 MPa (515 psi) (202,203). [Pg.52]

Sulfur combines directly with hydrogen at 150—200°C to form hydrogen sulfide. Molten sulfur reacts with hydrogen to form hydrogen polysulfides. At red heat, sulfur and carbon unite to form carbon disulfide. This is a commercially important reaction in Europe, although natural gas is used to produce carbon disulfide in the United States. In aqueous solutions of alkaU carbonates and alkaU and alkaline-earth hydroxides, sulfur reacts to form sulfides, polysulfides, thiosulfates, and sulfites. [Pg.117]

The absorption of sulfur dioxide in alkaline (even weakly alkaline) aqueous solutions affords sulfites, bisulfites, and metabisulfites. The chemistry of the interaction of sulfur dioxide with alkaline substances, either in solution, slurry, or soHd form, is also of great technological importance in connection with air pollution control and sulfur recovery (25,227,235—241). Even weak bases such as 2inc oxide absorb sulfur dioxide. A slurry of 2inc oxide in a smelter can be used to remove sulfur dioxide and the resultant product can be recycled to the roaster (242). [Pg.144]

Aqueous solutions of sodium sulfite are alkaline and have a pH of ca 9.8 at 1 wt %. The solutions are oxidized readily by air. The redox potential is a function of pH, as would be expected from the foUowing equation ... [Pg.148]

Ma.nufa.cture. In a typical process, a solution of sodium carbonate is allowed to percolate downward through a series of absorption towers through which sulfur dioxide is passed countercurrently. The solution leaving the towers is chiefly sodium bisulfite of typically 27 wt % combined sulfur dioxide content. The solution is then mn into a stirred vessel where aqueous sodium carbonate or sodium hydroxide is added to the point where the bisulfite is fully converted to sulfite. The solution may be filtered if necessary to attain the required product grade. A pure grade of anhydrous sodium sulfite can then be crystallized above 40°C because the solubiUty decreases with increasing temperature. [Pg.149]

The deleterious effect of sulfur dioxide and sulfites in domestic water is increased corrosivity owing to the lowered pH. However, oxidation of sulfite to sulfate in aqueous solutions uses dissolved oxygen, and lliis may retard corrosion. While llte oxichition of sulfite and sulfiirous acid to sulfate and sulfuric acid in the atmosphere is an environmental concern, this reaction is too... [Pg.275]

In contrast to the free acid, stable thiosulfate salts can readily be prepared by reaction of HiS on aqueous solutions of sulfites ... [Pg.714]

Consistent with this, experiments using HS" labelled with radioactive (p. 661) show that acid hydrolysis of the 8203 produces elemental sulfur in which two-thirds of the activity is concentrated. Thiosulfates can also he made by boiling aqueous solutions of metal sulfites (or hydrogen sulfites) with elemental sulfur according to the stoichiometry... [Pg.714]

Crystalline dithionates are thermally stable above room temperature (e.g. K2S20technical scale aqueous. solutions of SO2 are oxidized by a suspension of hydrated Mn02 or FeiOv... [Pg.716]

The experimental finding was substantiated by high-level ab initio calculations. The unionized acid exists in only minute concentrations (if at all) in aqueous solutions of SOi- However, its salts, the sulfites, are quite stable and many are known... [Pg.718]

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]

Salts of nitridotrisulfuric acid, N(S03M )3, are readily obtained by the exothermic reaction of nitrites with sulfites or hydrogen sulfites in hot aqueous solution ... [Pg.743]

Reactions between A -(l-chloroalkyl)pyridinium chlorides 33 and amino acids in organic solvents have a low synthetic value because of the low solubility of the amine partner. A special protocol has been designed and tested in order to circumvent this drawback. Soon after the preparation of the salt, an aqueous solution of the amino acid was introduced in the reaction medium and the two-phase system obtained was heated under reflux for several hours. However, this was not too successful because sulfur dioxide, evolved during the preparation of the salt, was converted into sulfite that acted as an 5-nucleophile. As a result, A -(l-sulfonatoalkyl)pyridinium betaines such as 53 were obtained (Section IV,B,3) (97BSB383). To avoid the formation of such betaines, the salts 33 were isolated and reacted with an aqueous solution of L-cysteine (80) to afford thiazolidine-4-carboxylic acids hydrochlorides 81 (60-80% yields). [Pg.210]

Measurement of the absorption rate of carbon dioxide in aqueous solutions of sodium hydroxide has been used in some of the more recent work on mass-transfer rate in gas-liquid dispersions (D6, N3, R4, R5, V5, W2, W4, Y3). Although this absorption has a disadvantage because of the high solubility of C02 as compared to 02, it has several advantages over the sulfite-oxidation method. For example, it is relatively insensitive to impurities, and the physical properties of the liquid can be altered by the addition of other liquids without appreciably affecting the chemical kinetics. Yoshida and... [Pg.301]

Cooper et al. (C9) were the first to determine mass-transfer coefficients by measuring the oxidation rate of sodium sulfite in an aqueous solution catalyzed by cupric ions. Their data were taken for a vaned-disk agitator with 16 blades and for a flat paddle. The ratio of agitator-to-tank diameter was 0.4, and the ratio of paddle to tank diameter was 0.25. The tank was equipped with four baffles, with baffle-width to tank diameter ratio of 0.1. [Pg.303]

An aqueous solution of sodium sulfite, which was prepared at ambient temperature (or bisulfite, but free of thiosulfite) at a concentration of about 20%, is added to the reaction vessel. Usually 1.05-1.1 mol of the sulfite is required. The temperature is kept at 70-90°C with continuous stirring. The reaction can be finished when analytical data, e.g., content of free sulfite, are sufficient to fit the specification. Time required for the second step is around 30 min to 1 h. Finally the pH is adjusted to the desired level. [Pg.510]

The CuCl precipitate was obtained by mixing an aqueous solution of cupric sulfate and sodium sulfite to produce the reactions ... [Pg.326]

Frank SN, Bard AJ (1977) Heterogeneous photocatalytic oxidation of cyanide and sulfite in aqueous solutions at semiconductor powders. J Phys Chem 81 1484—1488... [Pg.302]

When S02 is added to a solution containing a sulfite, the S2052- ion is produced so the solution contains a salt of disulfurous acid (pyrosulfurous) acid. In aqueous solutions, these salts decompose when an acid is added. [Pg.540]

The checkers found that the procedure of Helberger and Lan-terman,2 which avoids the use of an ion-exchange resin, is also satisfactory in case it is regarded as inconvenient to set up the resin column. According to this procedure, after completion of the reaction with sodium sulfite, anhydrous hydrogen chloride is passed into the hot solution to liberate sulfur dioxide. After removal of sulfate as in the described procedure, the undiluted aqueous solution is saturated with hydrogen chloride gas at a temperature below 25°. The precipitated sodium chloride is removed by suction filtration, the filter cake is... [Pg.29]


See other pages where Sulfite aqueous solutions is mentioned: [Pg.348]    [Pg.349]    [Pg.348]    [Pg.349]    [Pg.271]    [Pg.49]    [Pg.85]    [Pg.148]    [Pg.172]    [Pg.216]    [Pg.217]    [Pg.155]    [Pg.263]    [Pg.263]    [Pg.706]    [Pg.716]    [Pg.719]    [Pg.679]    [Pg.98]    [Pg.300]    [Pg.688]    [Pg.201]    [Pg.63]    [Pg.91]    [Pg.277]    [Pg.267]    [Pg.915]    [Pg.166]    [Pg.605]    [Pg.255]   
See also in sourсe #XX -- [ Pg.137 , Pg.138 , Pg.139 , Pg.140 , Pg.141 , Pg.142 , Pg.143 ]




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