Carbon kinetic isotope effects in the gas-phase reactions of aromatic hydrocarbons with the OH radical at 296 ± 4 K

dc.contributor.authorAnderson, Rebecca S.
dc.contributor.authorIannone, Richard
dc.contributor.authorThompson, Alexandra E.
dc.contributor.authorRudolph, Jochen
dc.contributor.authorHuang, Lin
dc.date.accessioned2010-05-10T19:32:00Z
dc.date.available2010-05-10T19:32:00Z
dc.date.issued2004
dc.description.abstractThe carbon kinetic isotope effects (KIEs) of the room temperature reactions of benzene and several light alkyl benzenes with OH radicals were studied in a reaction chamber at ambient pressure using gas chromatography coupled with online combustion and isotope ratio mass spectrometry (GCC‐IRMS). The KIEs are reported in per mil according to $\varepsilon$ (‰) = (KIE − 1) × 1000, where KIE = k12/k13. The following average KIEs were obtained, (all in ‰): benzene 7.53 ± 0.50; toluene 5.95 ± 0.28; ethylbenzene 4.34 ± 0.28; o‐xylene 4.27 ± 0.05, p‐xylene 4.83 ± 0.81; o‐ethyltoluene 4.71 ± 0.12 and 1,2,4‐trimethylbenzene 3.18 ± 0.09. Our KIE value for benzene + OH agrees with the only reported value known to us [Rudolph et al., 2000]. It is shown that measurements of the stable carbon isotope ratios of light aromatic compounds should be extremely useful to study atmospheric processing by the OH radical.en
dc.identifier.urihttp://hdl.handle.net/10315/4083
dc.language.isoenen
dc.publisherAGUen
dc.rights.journalhttp://www.agu.org/journals/jd/en
dc.titleCarbon kinetic isotope effects in the gas-phase reactions of aromatic hydrocarbons with the OH radical at 296 ± 4 Ken
dc.typeArticleen

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