Campholenic aldehyde ozonolysis: A mechanism leading to specific biogenic secondary organic aerosol constituents

dc.bibliographicCitation.firstPage719eng
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.lastPage736eng
dc.bibliographicCitation.volume14
dc.contributor.authorKahnt, A.
dc.contributor.authorIinuma, Y.
dc.contributor.authorMutzel, A.
dc.contributor.authorBöge, O.
dc.contributor.authorClaeys, M.
dc.contributor.authorHerrmann, H.
dc.date.accessioned2017-12-01T03:35:17Z
dc.date.available2019-06-26T17:19:45Z
dc.date.issued2014
dc.description.abstractIn the present study, campholenic aldehyde ozonolysis was performed to investigate pathways leading to specific biogenic secondary organic aerosol (SOA) marker compounds. Campholenic aldehyde, a known α-pinene oxidation product, is suggested to be a key intermediate in the formation of terpenylic acid upon α-pinene ozonolysis. It was reacted with ozone in the presence and absence of an OH radical scavenger, leading to SOA formation with a yield of 0.75 and 0.8, respectively. The resulting oxidation products in the gas and particle phases were investigated employing a denuder/filter sampling combination. Gas-phase oxidation products bearing a carbonyl group, which were collected by the denuder, were derivatised by 2,4-dinitrophenylhydrazine (DNPH) followed by liquid chromatography/negative ion electrospray ionisation time-of-flight mass spectrometry analysis and were compared to the gas-phase compounds detected by online proton-transfer-reaction mass spectrometry. Particle-phase products were also analysed, directly or after DNPH derivatisation, to derive information about specific compounds leading to SOA formation. Among the detected compounds, the aldehydic precursor of terpenylic acid was identified and its presence was confirmed in ambient aerosol samples from the DNPH derivatisation, accurate mass data, and additional mass spectrometry (MS2 and MS3 fragmentation studies). Furthermore, the present investigation sheds light on a reaction pathway leading to the formation of terpenylic acid, involving α-pinene, α-pinene oxide, campholenic aldehyde, and terpenylic aldehyde. Additionally, the formation of diaterpenylic acid acetate could be connected to campholenic aldehyde oxidation. The present study also provides insights into the source of other highly functionalised oxidation products (e.g. m / z 201, C9H14O5 and m / z 215, C10H16O5), which have been observed in ambient aerosol samples and smog chamber-generated monoterpene SOA. The m / z 201 and 215 compounds were tentatively identified as a C9- and C10-carbonyl-dicarboxylic acid, respectively, based on reaction mechanisms of campholenic aldehyde and ozone, as well as detailed interpretation of mass spectral data, in conjunction with the formation of corresponding DNPH derivatives.eng
dc.description.versionpublishedVersioneng
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.identifier.urihttps://doi.org/10.34657/820
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/709
dc.language.isoengeng
dc.publisherMünchen : European Geopyhsical Unioneng
dc.relation.doihttps://doi.org/10.5194/acp-14-719-2014
dc.relation.ispartofseriesAtmospheric Chemistry and Physics, Volume 14, Issue 2, Page 719-736eng
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subjectaerosol formationaleng
dc.subjectdehydeeng
dc.subjecthydroxyl radicaleng
dc.subjectmonoterpeneeng
dc.subjectoxidationeng
dc.subjectozoneeng
dc.subject.ddc550eng
dc.titleCampholenic aldehyde ozonolysis: A mechanism leading to specific biogenic secondary organic aerosol constituentseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleAtmospheric Chemistry and Physicseng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectGeowissenschafteneng
wgl.typeZeitschriftenartikeleng
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