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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 8 (1974), S. 43-46 
    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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  • 2
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Novel modeling and sensitivity analysis techniques are used with experimental data obtained from discharge flow–resonance fluorescence experiments to evaluate the product branching ratio of OH+H2CO. Two channels are considered: the H-atom abstraction reaction (R2) to form HCO and H2O; and the addition reaction (R17) followed by rearrangement and decomposition to form HCOOH and H. The rate constant values obtained at 298 K are kR2 =(7.75±1.24)×10−12 cm3/molecule s and kR17=(0.2+0.8−0.2) ×10−12 cm3/molecule s. The results demonstrate that the reaction proceeds almost exclusively via the H-atom abstraction pathway.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 1497-1507 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 883-909 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction experiments on mixtures of N2O/H2O/N2 were performed in a variable pressure flow reactor over temperature, pressure, and residence time ranges of 1103-1173 K, 1.5-10.5 atm, and 0.2-0.8 s, respectively. Mixtures of approximately 1% N2O in N2 were studied with the addition of varying amounts of water vapor, from background to 3580 ppm. Experimentally measured profiles of N2O, O2, NO, NO2, H2O, and temperature were compared with predictions from detailed kinetic modeling calculations to assess the validity of a reaction mechanism developed from currently available literature thermochemical and rate constant parameters. Sensitivity and reaction flux analyses were performed to determine key elementary reaction path processes and rates.Reaction rate constants for the uni-molecular reaction, N2O → N2 + O, were determined at various pressures in order to match overall experimental and numerical decomposition rates of N2O. The numerical model included a newly determined rate constant for N2O + OH → HO2 + N2 with an upper limit of 5.66 × 108 cm3 mol-1 sec-1 at 1123 K. This is considerably smaller than presently reported in the literature. The experimentally observed rate of N2O decomposition was found to be slightly dependent on added water concentration. The rate constant determined for the elementary decomposition is strongly dependent on the choice of rate constants for the N2O + O ⇔ N2 + O2 and N2O + O ⇔ NO + NO reactions. In the absence of accurate data at the temperatures of this work, and based on these and other experiments in this laboratory, we presently recommend rate constants from the review of Baulch et al. The basis for this recommendation is discussed, including the impact on the rate constants derived for elementary nitrous oxide decomposition. The uncertainties in the rate constants as reported here are ±30%.The present mechanism was applied to previously reported high-pressure shock tube data and yields a high-pressure limit rate constant a factor of three larger than previously reported at these temperatures. The following expressions for the elementary decomposition reaction are recommended: k0, N2 = 9.13 × 1014 exp (-57, 690/RT) cm3 mol-1 s-1 and k∞ = 7.91 × 1010 exp(-56020/RT) s-1. Simple Lindemann fits utilizing these parameters reproduce the pressure dependent rate constants measured here within ±25%. © 1995 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 805-830 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A comprehensive detailed chemical kinetic mechanism for methanol oxidation has been developed and validated against multiple experimental data sets. The data are from static-reactor, flow-reactor, shock-tube, and laminar-flame experiments, and cover conditions of temperature from 633-2050 K, pressure from 0.26-20 atm, and equivalence ratio from 0.05-2.6. Methanol oxidation is found to be highly sensitive to the kinetics of the hydroperoxyl radical through a chain-branching reaction sequence involving hydrogen peroxide at low temperatures, and a chain-terminating path at high temperatures. The sensitivity persists at unusually high temperatures due to the fast reaction of CH2OH+O2=CH2O+HO2 compared to CH2OH+M=CH2O+H+M. The branching ratio of CH3OH+OH=CH2OH/CH3O+H2O was found to be a more important parameter under the higher temperature conditions, due to the rate-controlling nature of the branching reaction of the H-atom formed through CH3O thermal decomposition. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 805-830, 1998
    Additional Material: 25 Ill.
    Type of Medium: Electronic Resource
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