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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 21 (1982), S. 298-305 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 42 (1996), S. 10-22 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Formation of asphalt aggregates and their deposition on the pore surfaces of a porous medium, which alter the structure of the medium and its effective properties, is a critical problem to catalytic and oil recovery and refinery processes. Extensive new experimental data for the amount of precipitated asphalt formed with crude oil and various solvents are presented. Results indicate that, contrary to the previous assumptions, asphalt formation is at best partially reversible. A thermodynamic model based on the Flory-Huggins theory of polymer solutions is used, together with the Soave equation of state, to predict the data. Critical evaluation of the model shows that its predictions do not agree well with our data. As an alternative, we propose a new model that employs a scaling equation, somewhat similar to those encountered in aggregation and gelation phenomena. The scaling function takes on a very simple form, and its predictions are in very good agreement with the data. It also predicts that the onset of precipitation may obey a simple universal equation.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Chemical Technology AND Biotechnology 67 (1996), S. 15-20 
    ISSN: 0268-2575
    Keywords: oxidative coupling reactions ; differential reactors ; catalytic reactions mechanism ; reaction kinetics ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Kinetic studies on the oxidative coupling of methane at 760, 770 and 780°C have been conducted in a differential tubular flow reactor, using perovskite titanate as the reaction catalyst. Correlation of the kinetic data has been performed with the mechanisms proposed. At low oxygen partial pressure, the experimental results best fitted the Mars-Van Krevelen type mechanism, whereas at higher partial pressure of oxygen, a Langmuir-Hinshelwood type model provided the best fit to the data. A model for the rate of reaction has been derived assuming methyl radical as the intermediate.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 14 (1991), S. 96-100 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Oxidation of methanol to formaldehyde, using a mixture of ferric and molybdenum oxides as catalyst, has been studied in a fixed bed integral reactor, 150 mm long, 25 mm o.d. and 10 mm i.d. The catalyst was prepared by reaction between aqueous solutions of ammonium heptamolybdate and ferric chloride. It has been shown that, under experimental conditions similar to those employed in industry, neither external nor internal diffusion had been effective in the process and isothermal conditions prevailed in both gas and solid phases. A two-step mechanism has been put forward for the oxidation of methanol. According to such a mechanism, methanol is first oxidized to formaldehyde, accepting an oxygen molecule from the catalyst and changing the latter into a reduced form. In the second step, the reduced catalyst is transformed into the original form on obtaining an oxygen molecule from the gas phase. Based on this scheme, a rate model has been derived and verified by experimental results.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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