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dc.contributor.authorChao, Wenen_US
dc.contributor.authorHsieh, Jun-Tingen_US
dc.contributor.authorChang, Chun-Hungen_US
dc.contributor.authorLin, Jim Jr-Minen_US
dc.date.accessioned2015-07-21T08:29:08Z-
dc.date.available2015-07-21T08:29:08Z-
dc.date.issued2015-02-13en_US
dc.identifier.issn0036-8075en_US
dc.identifier.urihttp://dx.doi.org/10.1126/science.1261549en_US
dc.identifier.urihttp://hdl.handle.net/11536/124327-
dc.description.abstractCarbonyl oxides, or Criegee intermediates, are important transient species formed in the reactions of unsaturated hydrocarbons with ozone. Although direct detection of Criegee intermediates has recently been realized, the main atmospheric sink of Criegee intermediates remains unclear. We report ultraviolet absorption spectroscopic measurements of the lifetime of the simplest Criegee intermediate, CH2OO, at various relative humidity levels up to 85% at 298 kelvin. An extremely fast decay rate of CH2OO was observed at high humidity. The observed quadratic dependence of the decay rate on water concentration implied a predominant reaction with water dimer. On the basis of the water dimer equilibrium constant, the effective rate coefficient of the CH2OO + (H2O)(2) reaction was determined to be 6.5 (+/-0.8) x 10(-12) cubic centimeters per second. This work would help modelers to better constrain the atmospheric concentrations of CH2OO.en_US
dc.language.isoen_USen_US
dc.titleDirect kinetic measurement of the reaction of the simplest Criegee intermediate with water vaporen_US
dc.typeArticleen_US
dc.identifier.doi10.1126/science.1261549en_US
dc.identifier.journalSCIENCEen_US
dc.citation.volume347en_US
dc.citation.issue6223en_US
dc.citation.spage751en_US
dc.citation.epage754en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000349221300043en_US
dc.citation.woscount3en_US
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