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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 14 (1975), S. 459-466 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 11 (1977), S. 471-475 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 1353-1371 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A novel technique for the control of continuous synthesis of addition polymers with precisely controlled average molecular weight and minimum polydispersity has been developed. A control system adjusts the concentration of chain-transfer agent in the reactor feed to compensate for all other upsets, in the reactor inputs: initiator and monomer concentrations, temperature and feed rate. The technique has been evaluated quantitatively on a digital computer using a kinetic model of homogeneous, free-radical solution polymerization. In computational tests, the modeled control system generally held the instantaneous number-average chain length within 1%, and quickly returned it to the desired value in response to a wide variety of upsets. By generalizing the Schulz distributions to include termination by disproportionation, combination and chain-transfer, it is shown that changes in the molecular-weight distribution resulting from the action of the control system are minor.
    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 60 (1994), S. 359-367 
    ISSN: 0268-2575
    Keywords: anearobic ; coal ; hydrogenation ; hydrogen uptake ; liquefaction ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Desulfovibrio desulfuricans and Acidianus brierleyi were used to study hydrogenation of coal, pretreated coal, asphaltenes, and model compounds [diphenyl methane (DPM) and fumarate] under anaerobic conditions. This study involved three primary aspects: (1) determination of net hydrogen-uptake, (2) identification of the biohydrogenated product of fumarate, and (3) testing the influence of hydrogen uptake/biohydrogenation of coal in terms of direct liquefaction yield. The net hydrogen uptake values (from Warburg and GC assays) by the coals or the model compounds (controls) were less than that of the biotreated samples. The greated hydrogen uptake (net, 1878 μmol g-1; coal control, 245; cell control, 127) occurred in untreated coal KCER No. 4677 in the presence of D. desulfuricans. The net hydrogen uptake by coals varied depending upon the coal type and the microorganism. Model compound DPM showed its highest hydrogen uptake rate when catalysed by D. desulfuricans (150 μmol g-1 h-1). D. desulfuricans also hydrogenated 36% of the fumarate to succinate in the presence of hydrogen.Biotrated coal KCER No. 4677 (with 1878 μmol H2 g-1) was subsequently subjected to direct liquefaction. It showed a net increase in liquefaction yield of 5·4% as a result of the biotreament.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 70 (1997), S. 316-322 
    ISSN: 0268-2575
    Keywords: Desulfovibrio desulfuricans ; fumarate ; dismutation ; sulphate ; reduction ; hydrogenation ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The biological hydrogenation of organic compounds using sulphate-reducing bacteria was investigated. A high pressure stainless steel bioreactor and an atmospheric pressure reactor were constructed so that identical reactions at different pressures could be compared. The mesophillic sulphate-reducing bacteria Desulfovibrio desulfuricans (ATCC 7757) were used. Qualitative tests showed that Desulfovibrio desulfuricans was able to retain its viability at hydrogen pressures up to 35 atmospheres at a temperature of 37°C when exposed to fumarate. Evidence of fumarate dismutation was observed since half of the fumarate was converted to succinate. The effect of bacterial cell concentration was also studied under hydrogen gas. For a doubling of the bacterial cell (reactivated) concentration, the conversion of fumarate doubled from 40% to 80% in 12 h. A first-order reaction rate model was fit to the fumarate concentration data. The first-order reaction rate constant was found to be a linear function of the bacterial cell concentration. ©1997 SCI
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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