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  • Physical Chemistry  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 813-837 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Propane oxidation in jet-stirred reactor was modeled using a comprehensive kinetic reaction mechanism including the most recent findings concerning the kinetics of the reactions involved in the oxidation of C1—C4 hydrocarbons. The present detailed mechanism is able to reproduce experimental species concentration profiles obtained in our high-pressure jet-stirred reactor (900 ≤ T/K ≤ 1200; 1 ≤ P/atm ≤ 10; 0.15 ≤ φ ≤ 4) and in a turbulent flow reactor at 1 atm; ignition delay times measured in shock tube (1200 ≤ T/K ≤ 1700; 2 ≤ P/atm ≤ 15; 0.125 ≤ φ ≤ 2); H-atoms concentrations measured in shock tube during the pyrolysis of propane and burning velocities of freely propagating premixed propane-air laminar flames. The computed results are discussed in terms of pressure and equivalence ratio (φ) effects on propane oxidation. The same detailed kinetic reaction mechanism can also be used to model the oxidation of methane, ethylene, ethane, and propene in similar conditions. © John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 641-664 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethylene oxidation and pyrolysis was modeled using a comprehensive kinetic reaction mechanism. This mechanism is an updated version of one developed earlier. It includes the most recent findings concerning the kinetics of the reactions involved in the oxidation of ethylene. The proposed mechanism was tested against ethylene oxidation experimental data (molecular species concentration profiles) obtained in jet stirred reactors (1-10 atm, 880-1253 K), ignition delay times measured in shock tubes (0.2-12 atm, 1058-2200 K) and ethylene pyrolysis data in shock tube (2-6 atm, 1700-2200 K). The general prediction of concentration profiles of minor species formed during ethylene oxidation is improved in the present model by using more accurate kinetic data for several reactions (principally: HO2 + HO2 → H2O2 + O2, C2H4 + OH → C2H3 + H2O, C2H2 + OH → Products, C2H3 → C2H2 + H).
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 1303-1306 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 437-455 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethane oxidation in jet-stirred reactor has recently been investigated at high temperature (800-1200 K) in the pressure range 1-10 atm and molecular species (H2, CO, CO2, CH4, C2H2, C2H4, C2H6) concentration profiles were obtained by probe sampling and GC analysis. Ethane oxidation was modeled using a comprehensive kinetic reaction mechanism including the most recent findings concerning the kinetics of the reactions involved in the oxidation of C1—C4 hydrocarbons. The proposed mechanism is able to reproduce experimental data obtained in our high-pressure jet stirred reactor and ignition delay times measured in shock tube in the pressure range 1-13 atm, for temperatures extending from 800 to 2000 K and equivalence ratios of 0.1 to 2. It is also able to reproduce atoms concentrations (H,O) measured in shock tube at ≈2 atm. The same detailed kinetic mechanism can also be used to model the oxidation of methane, ethylene, propyne, and allene in similar conditions.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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