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dc.contributor.authorLuo, Pei-Lingen_US
dc.contributor.authorChung, Chen-Anen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.date.accessioned2019-10-05T00:08:38Z-
dc.date.available2019-10-05T00:08:38Z-
dc.date.issued2019-08-28en_US
dc.identifier.issn1463-9076en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c9cp03333een_US
dc.identifier.urihttp://hdl.handle.net/11536/152789-
dc.description.abstractThe reaction of the simplest Criegee intermediate CH2OO with NO2 is considered to be important in atmospheric chemistry because of its prospective contribution to the decay of CH2OO and the additional source of NO3, hence its effects on the NOx and HOx cycles. The reported rate coefficients of this reaction varied by a factor of 5. Employing a cw quantum-cascade laser with wavelength near 11 mu m coupled with Herriott mirrors to probe CH2OO sensitively, we investigated in detail the reaction CH2OO + NO2 under total pressure 5.9-9.7 Torr at 298 K and reported a rate coefficient k(NO2) = (1.0 +/- 0.2) x 10(-12) cm(3) molecule(-1) s(-1), about one-seventh the value determined with direct measurements of CH2OO by Weltz et al. This smaller rate coefficient implies that the title reaction contributes to the atmospheric source of NO3 and the decay of CH2OO much less than previously conceived.en_US
dc.language.isoen_USen_US
dc.titleRate coefficient of the reaction CH2OO + NO2 probed with a quantum-cascade laser near 11 mu men_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c9cp03333een_US
dc.identifier.journalPHYSICAL CHEMISTRY CHEMICAL PHYSICSen_US
dc.citation.volume21en_US
dc.citation.issue32en_US
dc.citation.spage17578en_US
dc.citation.epage17583en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000481777100007en_US
dc.citation.woscount0en_US
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