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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 33 (1994), S. 2151-2156 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-9729
    Keywords: sulfur dioxide ; sulfate-reducing bacteria ; sewage digest ; immobilization ; flue gas desulfurization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Sulfur dioxide (SO2) is one of the major pollutantsin the atmosphere that cause acid rain. Microbialprocesses for reducing SO2 to hydrogen sulfide(H2S) have previously been demonstrated byutilizing mixed cultures of sulfate-reducing bacteria(SRB) with municipal sewage digest as the carbon andenergy source. To maximize the productivity of theSO2-reducing bioreactor in this study, variousimmobilized cell bioreactors were investigated: a stirredtank with SRB flocs and columnar reactors with cellsimmobilized in either κ-carrageenan gel matrix orpolymeric porous BIO-SEPTM beads. Themaximum volumetric productivity for SO2reduction in the continuous stirred-tank reactor (CSTR)with SRB flocs was 2.1 mmol SO2/h·l. Theκ-carrageenan gel matrix used for cellimmobilization was not durable at feed sulfiteconcentrations greater than 2000 mg/l or at sulfite feedrate of 1.7 mmol/h·l. A columnar reactor withmixed SRB cells that had been allowed to grow intohighly stable BIO-SEP polymeric beads exhibited thehighest sulfite conversion rates, in the range of16.5 mmol/h·l (with 100% conversion) to20 mmol/h·l (with 95% conversion). In addition toflue gas desulfurization, potential applications of thismicrobial process include the treatment ofsulfate/sulfite-laden wastewater from the pulp and paper,petroleum, mining, and chemical industries.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 52 (1996), S. 423-428 
    ISSN: 0006-3592
    Keywords: hydrogenase ; organic biocatalysis ; polyethylene glycol ; modified enzymes ; sulfur ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Naturally occurring enzymes may be modified by covalently attaching hydrophobic groups that render the enzyme soluble and active in organic solvents, and have the potential to greatly expand applications of enzymatic catalysis. The reduction of elemental sulfur to hydrogen sulfide by a hydrogenase isolated from Pyrococcus furiosus has been investigated as a model system for organic biocatalysis. While the native hydrogenase catalyzed the reduction of sulfur to H2S in aqueous solution, no activity was observed when the aqueous solvent was replaced with anhydrous toluene. Hydrogenase modified with PEG p-nitrophenyl carbonate demonstrated its native biocatalytic ability in toluene when the reducing dye, benzyl viologen, was also present. Neither benzyl viologen nor PEG p-nitrophenyl carbonate alone demonstrated reducing capability. PEG modified cellulase and benzyl viologen were also incapable of reducing sulfur to H2S, indicating that the enzyme itself, and not the modification procedure, is responsible for the conversion in the nonpolar organic solvent. Sulfide production in toluene was tenfold higher than that produced in an aqueous system with equal enzyme activity, demonstrating the advantages of organic biocatalysis. Applications of bio-processing in nonaqueous media are expected to provide significant advances in the areas of fossil fuels, renewable feedstocks, organic synthesis, and environmental control technology. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 66 (1996), S. 365-374 
    ISSN: 0268-2575
    Keywords: gypsum sludge ; sulfate-reducing bacteria ; sulfur ; calcium carbonate ; flue gas desulfurization ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A combined chemical and biological process for the recycling of flue gas desulfurization (FGD) gypsum into calcium carbonate and elemental sulfur is demonstrated. In this process, a mixed culture of sulfate-reducing bacteria (SRB) utilizes sewage digest as its carbon source to reduce FGD gypsum to hydrogen sulfide. The sulfide is then oxidized to elemental sulfur via reaction with ferric sulfate, and accumulating calcium ions are precipitated to calcium carbonate using carbon dioxide. Employing anaerobically digested-municipal sewage sludge (AD-MSS) medium as a carbon source, SRB in serum bottles demonstrated an FGD gypsum reduction rate of 8 mg dm-3 h-1 (109 cells)-1. A chemostat with continuous addition of both AD-MSS medium and gypsum exhibited sulfate reduction rates as high as 1·3kg FGD gypsumm-3 day-1. The increased biocatalyst density afforded by cell immobilization in a columnar reactor allowed a productivity of 152 mg SO4 dm-3 h-1 or 6·6kg FGD gypsum m-3 day-1. Both reactors demonstrated 100% conversion of sulfate, with 75-100% recovery of elemental sulfur and as high as 70% COD utilization. Calcium carbonate was recovered from the reactor effluent upon precipitation using carbon dioxide. The formation of two marketable products - elemental sulfur and calcium carbonate - from FGD gypsum sludge, combined with the use of a low-cost carbon source and further improvements in reactor design, promises to offer an attractive alternative to the landfilling of FGD gypsum.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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