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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 26 (1992), S. 1165-1173 
    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
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 109 (1987), S. 6004-6010 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 103-125 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of experiments have been performed to study the ozone-isoprene reaction in a smog chamber by adding externally produced O3 to the hydrocarbon in the dark. A chemical tracer, methyl cyclohexane, was added to probe the OH formation in the system. O(3P) formation was also examined using the known distribution of products that are unique to the O(3P)-isoprene reaction (part I). The results provide clear evidence that both OH and O(3P) are produced by the O3-isoprene reaction directly in large quantities; about 0.68 ± 0.15 and 0.45 ± 0.20 per O3-isoprene reaction, respectively. These additional radicals severely complicate the analysis of the O3 reaction, hence, computer kinetic modeling was necessary to ascertain the products of the O3 reaction itself, corrected for OH and O(3P) reactions. The product distribution, which differs dramatically from that published previously, is: 67 ± 9% methacrolein, 26 ± 6% methyl vinyl ketone, and 7 ± 3% propene, accounting for 100 ± 10% of the reacted isoprene. Applicability of these results to the gas-phase O3 reaction with other unsaturated hydrocarbons is briefly discussed.
    Additional Material: 8 Ill.
    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. 997-1008 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficients for the reaction of O(3P) with the biogenic hydrocarbons Δ3-carene, α-pinene, and isoprene have been measured using a direct method for the first time. O(3P) was generated from the pulsed photolysis of NO2 or O3 at 308 nm, and measured by resonance fluorescence at 131 nm. Rate coefficients at room temperature for the biogenics are similar: (3.4 ± 0.6) × 10-11, (3.7 ± 0.6) × 10-11, and (3.5 ± 0.6) × 10-11 cm3 molec-1 s-1, for Δ3-carene, α-pinene, and isoprene, respectively. The rate coefficients for the reaction of O(3P) with NO2 and ethene were also measured with the same method, and these values are within 4% and 10% of the currently recommended values, respectively. The correlation between OH and O(3P)-alkene reaction rate coefficients is updated and discussed. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 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 24 (1992), S. 79-101 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The OH reaction with isoprene is studied. Methyl nitrite photolysis experiments were carried out in an outdoor smog chamber in an attempt to identify as completely as possible OH-isoprene product distribution. Emphasis was placed on identification and quantification of oxygenated products. A Tenax-based cryo-trap thermal desorber used to trap, concentrate, and dry chamber samples for identification on a GC/MS is described. Analysis of the products revealed that O(3P) can form in reaction systems designed to study OH reactions that include high concentrations of NO, and consequently NO2, hence, this reaction is also examined. The yields of methacrolein and methyl vinyl ketone are determined as 25 ± 3 and 35.5 ± 4%, respectively, with an additional 4 ± 2% as 3-methyl furan, totaling 65 ± 4%. These results, combined with those of previous studies allow 80% of isoprene's products to be explicitly identified, and the general structure of the remaining products to be ascertained. The O(3P) reaction produces 84 ± 8% epoxides, and 8 ± 3% species which result in production of HO2, and subsequently, OH. A heretofore unidentified product of the O(3P) reaction, 2-methyl 2-butenal, is identified. The rate constant of the NO2-isoprene reaction is measured.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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