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  • 1990-1994  (5)
  • 1985-1989
  • 1990  (5)
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  • 1990-1994  (5)
  • 1985-1989
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 24 (1990), S. 1326-1332 
    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
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 59-67 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using a relative rate technique, rate constants for the gas-phase reactions of the OH radical with the three cresols and the six dimethylphenols have been determined at 296 ± 2 K and atmospheric pressure. The rate constants for the cresols, which range from 4.3 × 10-11 cm3molecule-1 s-1to 6.8 × 10-11 cm3molecule-1 s-1, are in good agreement with previous literature data. The rate constants for 2,3-, 2,4-, 2,5-, 2,6-, and 3,4-dimethylphenol are all in the range (6.6-8.1) × 10-11 cm3 molecule-1 s-1, with the rate constant for 3,5-dimethylphenol being somewhat higher at 1.13 × 10-10 cm3 molecule-1 s-1. Rate constants estimated from the number, identity, and positions of the substituent groups around the aromatic ring agree to within a factor of approximately 2 with these experimentally determined rate constants.
    Additional Material: 4 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. 981-998 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the gas-phase reactions of allyl chloride and benzyl chloride with the OH radical and O3 were investigated at 298 ± 2 K and atmospheric pressure. Direct measurements of the rate constants for reactions with ozone yielded values of k(O3 + allyl chloride) = (1.60 ± 0.18) × 10-18 cm3 molecule-1 s-1 and k(O3 + benzyl chloride) 〈 6 × 10-20 cm3 molecule-1 s-1. With the use of a relative rate technique and ethane as a scavenger of chlorine atoms produced in the OH radical reactions, rate constants of k(OH + allyl chloride) = (1.69 ± 0.07) × 10-11 cm3 molecule-1 s-1 and k(OH + benzyl chloride) = (2.80 ± 0.19) × 10-12 cm3 molecule-1 s-1 were measured. A study of the OH radical reaction with allyl chloride by long pathlength FT-IR absorption spectroscopy indicated that the co-products ClCH2CHO and HCHO account for ca. 44% of the reaction, and along with the other products HOCH2CHO, (ClCH2)2CO, and CH2 = CHCHO account for 84 ± 16% of the allyl chloride reacting. The data indicate that in one atmosphere of air in the presence of NO the chloroalkoxy radical formed following OH radical addition to the terminal carbon atom of the double bond decomposes to yield HOCH2CHO and the CH2Cl radical, which becomes a significant source of the Cl atoms involved in secondary reactions. A product study of the OH radical reaction with benzyl chloride identified only benzaldehyde and peroxybenzoyl nitrate in low yields (ca. 8% and ≤4%, respectively), with the remainder of the products being unidentified.
    Additional Material: 6 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 22 (1990), S. 871-887 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the gas-phase reactions of O3 with a series of monoterpenes and related compounds have been determined at 296 ± 2 K and 740 torr total pressure of air or O2 using a combination of absolute and relative rate techniques. Good agreement between the absolute and relative rate data was observed, and the rate constants obtained (in units of 10-17 cm3 molecule-1 s-1) were: α-pinene, 8.7; β-pinene, 1.5; Δ3-carene, 3.8; 2-carene, 24; sabinene, 8.8; d-limonene, 21; γ-terpinene, 14; terpinolene, 140; α-phellandrene, 190; α-terpinene, 870; myrcene, 49; trans-ocimene, 56; p-cymene, 〈0.005; and 1,8-cineole, 〈0.015. While these rate constants for α- and β-pinene and sabinene are in good agreement with recent absolute and relative rate determinations, those for the other monoterpenes are generally lower than the literature data by factors of ca. 2-10. The measured rate constants for the monoterpenes are reasonably consistent with predictions based upon the number and positions of the substituent groups around the 〉C=C〈 bond(s).
    Additional Material: 5 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 22 (1990), S. 999-1014 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and nitroarene product yields of the gas-phase reactions of naphthalene-d8, fluoranthene-d10, and pyrene with OH radicals in the presence of NOx and in N2O5—NO3—NO2—air mixtures have been investigated at 296 ± 2 K and atmospheric pressure of air. Using a relative rate method, naphthalene-d8 was shown to react in N2O5—NO3—NO2—air mixtures a factor of 1.22 ± 0.10 times faster than did naphthalene, with the 1- and 2-nitronaphthalene-d7 product yields being similar to those of 1- and 2-nitronaphthalene from naphthalene. From the measured PAH concentrations and the nitroarene product yields, formation yields of 2-, 7-, and 8-nitrofluoranthene-d9 and 2- and 4-nitropyrene of 0.03, 0.01, 0.003, 0.005, and 0.0006, respectively, were determined from the OH radical-initiated reactions. Effective rate constants for the reactions of fluoranthene-d10 and pyrene with N2O5 in N2O5—;NO3—NO2—air mixtures of ca. 1.8 × 10-17 cm3 molecule-1 s-1 and ca. 5.6 × 10-17 cm3 molecule-1 s-1, respectively, were derived. Formation yields of 2-nitrofluoranthene-d9 and 4-nitropyrene of ca. 0.24 and ca. 0.0006, respectively, were estimated for these reaction systems. 2-Nitropyrene was also observed to be formed in these N2O5—NO3—NO2 reactions, but was found to be a function of the NO2 concentration and, therefore, would be a negligible product under ambient NO2 concentrations. These product and kinetic data are consistent with ambient air measurements of the nitroarene concentrations.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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