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Recovery systems, sulfur

Uranium ores are leached with dilute sulfuric acid or an alkaline carbonate [3812-32-6] solution. Hexavalent uranium forms anionic complexes, such as uranyl sulfate [56959-61-6], U02(S0 3, which are more selectively adsorbed by strong base anion exchangers than are other anions in the leach Hquors. Sulfate complexes are eluted with an acidified NaCl or ammonium nitrate [6484-52-2], NH NO, solution. Carbonate complexes are eluted with a neutral brine solution. Uranium is precipitated from the eluent and shipped to other locations for enrichment. Columnar recovery systems were popular in South Africa and Canada. Continuous resin-in-pulp (RIP) systems gained popularity in the United States since they eliminated a difficult and cosdy ore particle/leach hquor separation step. [Pg.387]

Other Specialty Chemicals. In fuel-ceU technology, nickel oxide cathodes have been demonstrated for the conversion of synthesis gas and the generation of electricity (199) (see Fuel cells). Nickel salts have been proposed as additions to water-flood tertiary cmde-oil recovery systems (see Petroleum, ENHANCED oil recovery). The salt forms nickel sulfide, which is an oxidation catalyst for H2S, and provides corrosion protection for downweU equipment. Sulfur-containing nickel complexes have been used to limit the oxidative deterioration of solvent-refined mineral oils (200). [Pg.15]

The 1990 Amendments to the U.S. Clean Air Act require a 50% reduction of sulfur dioxide emissions by the year 2000. Electric power stations are beheved to be the source of 70% of all sulfur dioxide emissions (see Power generation). As of the mid-1990s, no utiUties were recovering commercial quantities of elemental sulfur ia the United States. Two projects had been aimounced Tampa Electric Company s plan to recover 75,000—90,000 metric tons of sulfuric acid (25,000—30,000 metric tons sulfur equivalent) aimuaHy at its power plant ia Polk County, Elorida, and a full-scale sulfur recovery system to be iastaHed at PSl Energy s Wabash River generating station ia Terre Haute, Indiana. Completed ia 1995, the Terre Haute plant should recover about 14,000 t/yr of elemental sulfur. [Pg.123]

The H2S comes out with the reactor products, goes through the product-recovery system of the FCCU, and eventually goes to a Claus plant for sulfur recovery. The metal oxide adsorbent recirculates with the spent cracking catalyst back to the regenerator for the next SO adsorption cycle. [Pg.215]

Plant operators should aim at using fuel with less than 0.5% sulfur (or an emissions level corresponding to 0.5% sulfur in fuel). High-sulfur fuels should be directed to units equipped with SO, controls. Fuel blending is another option. A sulfur recovery system that achieves at least 97% (but preferably... [Pg.107]

Sulfide ores usually contain small amounts of mercury, arsenic, selenium, and tellurium, and these impurities volatilize during the ore treatment. All the volatilized impurities, with the exception of mercury, are collected in the dust recovery systems. On account of its being present in low concentrations, mercury is not removed by such a system and passes out with the exit gases. The problem of mercury contamination is particularly pertinent to zinc plants since the sulfidic ores of zinc contain traces of mercury (20-300 ppm). The mercury traces in zinc sulfide concentrates volatilize during roasting and contaminate the sulfuric acid that is made from the sulfur dioxide produced. If the acid is then used to produce phosphatic fertilizers, this may lead to mercury entering the food chain as a contaminant. Several processes have been developed for the removal of mercury, but these are not yet widely adopted. [Pg.772]

Numerous sulfite chemical pulping recovery systems are in use today. Heat and sulfur can be recovered from all liquors generated however, the base chemical can only be recovered from magnesium and sodium base processes. See Smook s Handbook12 for more information. [Pg.870]

Sodium hydrosulfite is produced through the Formate process where sodium formate solution, sodium hydroxide, and liquid sulfur dioxide reacted in the presence of a recycled stream of methanol solvent. Other products are sodium sulfite, sodium bicarbonate, and carbon monoxide. In the reactor, sodium hydrosulfite is precipitated to form a slurry of sodium hydrosulfite in the solution of methanol, methyl formate, and other coproducts. The mixture is sent to a pressurized filter system to recover sodium hydrosulfite crystals that are dried in a steam-heated rotary drier before being packaged. Heat supply in this process is highly monitored in order not to decompose sodium hydrosulfite to sulfite. Purging is periodically carried out on the recycle stream, particularly those involving methanol, to avoid excessive buildup of impurities. Also, vaporized methanol from the drying process and liquors from the filtration process are recycled to the solvent recovery system to improve the efficiency of the plant. [Pg.944]

The direct-oxidation processes for recovery of sulfur from raw gases are also applicable on acid-gas streams. Usually, a direct oxidation process would be applied when a nonselective acid-gas removal system had been employed and the sulfur concentration in the acid gas is relatively low. At higher H2S concentrations, as achieved through selective acid-gas removal, the conventional Claus process appears to be more economic. [Pg.30]

Smith, R. M., Sheputis, J., Kim, U. B., and Chin, Y. B., Sulfuric Acid Heat Recovery System (HRS) Operations at Namhae Chemical Corporation, Korea, paper read at Sulphur 88, Vienna, Austria, Nov. 6-9, 1988. [Pg.1182]

Fig. 24.7. Schematic of acid heat to steam energy recovery system, after Puricelli et al., 1998. It is for intermediate H2S04 making, Fig. 9.6. Note (i) the double packed bed H2S04 making tower and (ii) boiler. Industrial acid heat recovery H2S04 making towers are 25m high and 10 m diameter. They produce 2000 to 4000 tonnes of H2S04 per day. For photographs see Sulfur, 2004.--------- large flows. small flows. Fig. 24.7. Schematic of acid heat to steam energy recovery system, after Puricelli et al., 1998. It is for intermediate H2S04 making, Fig. 9.6. Note (i) the double packed bed H2S04 making tower and (ii) boiler. Industrial acid heat recovery H2S04 making towers are 25m high and 10 m diameter. They produce 2000 to 4000 tonnes of H2S04 per day. For photographs see Sulfur, 2004.--------- large flows. small flows.
Acid plants (especially sulfur burning plants) are now often built with acid heat to steam energy recovery systems. These significantly increase acidmaking energy efficiency. [Pg.284]

Outokumpu (2005) HEROS, the Outokumpu Technology Heat Recovery System in Sulfuric Acid Plants, brochure distributed at 29th Annual Clearwater Conference, Clearwater, Florida, June 3 and 4, 2005. www.outokumpu.com... [Pg.284]

Design of Rotary Filter for Sulfur Dioxide Recovery System 835... [Pg.817]


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See also in sourсe #XX -- [ Pg.21 , Pg.22 , Pg.23 , Pg.24 , Pg.25 , Pg.26 , Pg.27 , Pg.28 , Pg.29 , Pg.30 , Pg.31 , Pg.32 , Pg.33 , Pg.34 ]




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