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Atmospheric chemistry of cyclohexanone: UV spectrum and kinetics of reaction with chlorine atoms

dc.contributor.authorIwasaki, E.en_US
dc.contributor.authorMatsumi, Y.en_US
dc.contributor.authorTakahashi, K.en_US
dc.contributor.authorWallington, Timothy J.en_US
dc.contributor.authorHurley, M. D.en_US
dc.contributor.authorOrlando, J. J.en_US
dc.contributor.authorKaiser, E. W.en_US
dc.contributor.authorCalvert, J. G.en_US
dc.date.accessioned2008-03-31T18:39:54Z
dc.date.available2009-05-04T19:09:21Zen_US
dc.date.issued2008-05en_US
dc.identifier.citationIwasaki, E.; Matsumi, Y.; Takahashi, K.; Wallington, T. J.; Hurley, M.D.; Orlando, J. J.; Kaiser, E. W.; Calvert, J. G. (2008). "Atmospheric chemistry of cyclohexanone: UV spectrum and kinetics of reaction with chlorine atoms." International Journal of Chemical Kinetics 40(5): 223-229. <http://hdl.handle.net/2027.42/58072>en_US
dc.identifier.issn0538-8066en_US
dc.identifier.issn1097-4601en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58072
dc.description.abstractAbsolute 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 N 2 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 cm 3 molecule −1 s −1 . Cyclohexanone has a broad UV absorption band with a maximum cross section of (4.0 ± 0.3) × 10 −20 cm 2 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, 2008en_US
dc.format.extent220713 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherTheoretical, Physical and Computational Chemistryen_US
dc.titleAtmospheric chemistry of cyclohexanone: UV spectrum and kinetics of reaction with chlorine atomsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Natural Sciences, 4901 Evergreen Road, University of Michigan–Dearborn, Dearborn, MI 48128en_US
dc.contributor.affiliationotherSolar-Terrestrial Environment Laboratory and Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japanen_US
dc.contributor.affiliationotherSolar-Terrestrial Environment Laboratory and Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japanen_US
dc.contributor.affiliationotherKyoto University Pioneering Research Unit for Next Generation, Kyoto University Gokasho, Uji, Kyoto 611-0011, Japanen_US
dc.contributor.affiliationotherFord Motor Company, Mail Drop RIC-2122, P.O. Box 2053, Dearborn, MI 48121-2053 ; Ford Motor Company, Mail Drop RIC-2122, P.O. Box 2053, Dearborn, MI 48121-2053en_US
dc.contributor.affiliationotherFord Motor Company, Mail Drop RIC-2122, P.O. Box 2053, Dearborn, MI 48121-2053en_US
dc.contributor.affiliationotherAtmospheric Chemistry Division, Earth and Sun Systems Laboratory, National Center for Atmospheric Research, PO Box 3000, Boulder, CO 80307-3000en_US
dc.contributor.affiliationotherEnvironmental Sciences Division, Oak Ridge National Laboratory, Building 1505, Room 368, Oak Ridge, TN 37831-6036en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58072/1/20291_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/kin.20291en_US
dc.identifier.sourceInternational Journal of Chemical Kineticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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