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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 71 (1998), S. 57-60 
    ISSN: 0268-2575
    Keywords: diesel soot ; carbon gasification ; NOx ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The reactions of soot particulates and carbons with three oxidising agents expected in the exhaust gases from a diesel engine have been studied. Nitrogen dioxide has been found to be an efficient gasifying agent for carbons, carbon oxides and nitric oxide being produced. The reaction with diesel particulates commences above c. 150°C: with graphite, gasification became significant only above c. 550°C. The presence of oil on the particulates does not affect gasification. © 1998 SCI.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 68 (1997), S. 411-416 
    ISSN: 0268-2575
    Keywords: hydrogen sulphide ; adsorption ; oxidation ; carbon ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The use of porous materials for the removal of traces of hydrogen sulphide from gas streams was investigated in this study. It was found that microporous carbons had the highest removal efficiency. This was due to the fact that carbons have extra potential for the oxidation of hydrogen sulphide while other sorbents remove the gas only by adsorption. The oxidative removal efficiency of microporous carbons was found to be a function of water vapour pressure, oxygen concentration and temperature. The mechanism of the reaction is discussed. © 1997 SCI.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 72 (1998), S. 19-22 
    ISSN: 0268-2575
    Keywords: oxidative dehydrogenation ; catalyst ; vanadia ; molybdena ; niobia ; ethane ; propane ; n-butane ; isobutane ; isopropylbenzene ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The oxidative dehydrogenation of ethane, propane and n-butane over a vanadia-molybdena-niobia catalyst has been compared with propane substituted in the 2 position with a methyl (isobutane) or a benzyl (isopropylbenzene) group. In the normal paraffins, selectivity to the olefin was found to decrease as the chain length increased. Substitution at the propane 2 position increased selectivity, particularly in the case of isopropylbenzene. The results are explained partially in terms of over oxidation of the product olefin and partially in terms of structural effects in the parent hydrocarbon influencing the olefin-producing oxidative dehydrogenation reaction. © 1998 SCI
    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. 381-386 
    ISSN: 0268-2575
    Keywords: liquid phase oxidation ; trihydroxy aluminium ; gibbsite ; precipitation ; poisoning ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Organic compounds are known to interfere with the precipitation of trihydroxy aluminium (gibbsite) in the Bayer process. Studies have been carried out of the effect of 3,4-dihydroxybenzoic acid on precipitation and of the beneficial effect that can be achieved by oxidising the acid. Measurements of precipitate yields both in the presence of the acid and of products obtained by oxidising the acid were made. Oxidation in the presence of various metal ions was also examined. The yield of precipitate was found to decrease in the order Cu2+ (1·9 mM) 〉 Fe3+ (2·2 mM) 〉 blank (no added organics) 〉 Mn4+ (44·3 and 2·3 mM) 〉 Mn2+ (2·3 mM) 〉 Mn2+ (44·3 mM) ≈ uncatalyset oxidation 〉 Fe3+ (43·5 mM) 〉 Cu2+ (38·2 mM) 〉 untreated sample. This relative ordering was generally unaffected by reaction temperature or oxygen partial pressure. Soluble manganese salts were formed by partial dissolution of MnO2 in the alkaline solutions. These salts were required for oxidation of the 3,4-dihydroxybenzoic acid to products which, collectively, did not poison the trihydroxy aluminium precipitation process.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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