Atmospheric chemistry of cyclohexanone: UV spectrum and kinetics of reaction with chlorine atoms |
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Authors: | E Iwasaki Y Matsumi K Takahashi T J Wallington MD Hurley J J Orlando E W Kaiser J G Calvert |
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Institution: | 1. Solar‐Terrestrial Environment Laboratory and Graduate School of Science, Nagoya University, Furo‐cho, Chikusa‐ku, Nagoya 464‐8601, Japan;2. Kyoto University Pioneering Research Unit for Next Generation, Kyoto University Gokasho, Uji, Kyoto 611‐0011, Japan;3. Ford Motor Company, Mail Drop RIC‐2122, P.O. Box 2053, Dearborn, MI 48121‐2053;4. Atmospheric Chemistry Division, Earth and Sun Systems Laboratory, National Center for Atmospheric Research, PO Box 3000, Boulder, CO 80307‐3000;5. Department of Natural Sciences, 4901 Evergreen Road, University of Michigan–Dearborn, Dearborn, MI 48128;6. Environmental Sciences Division, Oak Ridge National Laboratory, Building 1505, Room 368, Oak Ridge, TN 37831‐6036 |
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Abstract: | Absolute and relative rate techniques were used to study the reactivity of Cl atoms with cyclohexanone in 6 Torr of argon or 800–950 Torr of N2 at 295 ± 2 K. The absolute rate experiments gave k(Cl + cyclohexanone) = (1.88 ± 0.38) × 10?10, whereas the relative rate experiments gave k(Cl + cyclohexanone) = (1.66 ± 0.26) × 10?10 cm3 molecule?1 s?1. Cyclohexanone has a broad UV absorption band with a maximum cross section of (4.0 ± 0.3) × 10?20 cm2 molecule?1 near 285 nm. The results are discussed with respect to the literature data. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 40: 223–229, 2008 |
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