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dc.contributor.authorAmelynck, C.
dc.contributor.authorStépien, C.
dc.contributor.authorSchoon, N.
dc.contributor.authorCatoire, V.
dc.contributor.authorLabonnette, D.
dc.contributor.authorArijs, E.
dc.contributor.authorPoulet, G.
dc.date2001
dc.date.accessioned2017-05-04T09:31:05Z
dc.date.available2017-05-04T09:31:05Z
dc.identifier.urihttps://orfeo.belnet.be/handle/internal/5255
dc.descriptionThe reactions of the halide anions (F-, Cl-, Br-, and I-), NO2-, SF6-, CO3- and CO4- with ClONO2 have been studied at room temperature in a flowing afterglow apparatus. All these reactions are found to proceed at the collision limit and the experimental data are compared with literature values. The reaction of I- with ClONO2 was studied at stratospheric pressures and temperatures in view of its use as a possible precursor ion for the measurement of stratospheric N2O5+ClONO2 mixing ratio height profiles by chemical ionization mass spectrometry. No pressure or temperature dependence of the rate constant has been observed. In order to correct the observed rate constants for HNO3 impurities, the reaction rate constants of F-, Br-, and NO2- with HNO3 have also been determined. In addition, the apparent second-order clustering rate constant of NO3- with ClONO2 in Ar/N2 and Ar/He mixtures has been measured.
dc.languageeng
dc.titleGas phase reactions of negative ions with ClONO2
dc.typeArticle
dc.subject.frascatiPhysical sciences
dc.audienceScientific
dc.subject.freeanion
dc.subject.freebromide
dc.subject.freecarbonic acid
dc.subject.freechloride
dc.subject.freechlorine nitrate
dc.subject.freefluoride
dc.subject.freehalide
dc.subject.freeiodide
dc.subject.freenitrate
dc.subject.freenitric acid derivative
dc.subject.freenitric oxide
dc.subject.freeunclassified drug
dc.subject.freeapparatus
dc.subject.freearticle
dc.subject.freegas analysis
dc.subject.freeionization
dc.subject.freemass spectrometry
dc.subject.freeprecursor
dc.subject.freepressure
dc.subject.freereaction analysis
dc.subject.freestratosphere
dc.subject.freetemperature
dc.source.titleInternational Journal of Mass Spectrometry
dc.source.volume207
dc.source.issue3
dc.source.page205-215
Orfeo.peerreviewedYes
dc.identifier.doi10.1016/S1387-3806(01)00373-6
dc.identifier.scopus2-s2.0-0035897562


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