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dc.rights.licenseopenen_US
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorTOMAZ, Sophie
hal.structure.identifierInstitut des Géosciences de l’Environnement [IGE]
dc.contributor.authorJAFFREZO, Jean-Luc
hal.structure.identifierInstitut National de l'Environnement Industriel et des Risques [INERIS]
dc.contributor.authorFAVEZ, Olivier
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorPERRAUDIN, Emilie
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorVILLENAVE, Eric
hal.structure.identifierInstitut National de l'Environnement Industriel et des Risques [INERIS]
dc.contributor.authorALBINET, Alexandre
dc.date.accessioned2024-10-07T09:35:16Z
dc.date.available2024-10-07T09:35:16Z
dc.date.issued2017-07
dc.identifier.issn1352-2310en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202276
dc.description.abstractEnTotal individual concentrations (in both gaseous and particulate phases) of 80 polycyclic aromatic compounds (PACs) including 32 nitro-PAHs, 27 oxy-PAHs (polycyclic aromatic hydrocarbons) and 21 parent PAHs have been investigated over a year in the ambient air of Grenoble (France) together with an extended aerosol chemical characterization. The results indicated that their concentrations were strongly affected by primary emissions in cold period, especially from residential heating (i.e. biomass burning). Besides, secondary processes occurred in summer but also in cold period under specific conditions such as during long thermal inversion layer periods and severe PM pollution events. Different secondary processes were involved during both PM pollution events observed in March–April and in December 2013. During the first one, long range transport of air masses, nitrate chemistry and secondary nitro-PAH formation seemed linked. During the second one, the accumulation of primary pollutants over several consecutive days enhanced secondary chemical processes notably highlighted by the dramatic increase of oxy-PAH concentrations. The study of the time trends of ratios of individual nitro- or oxy-PAHs to parent PAHs, in combination with key primary or secondary aerosol species and literature data, allowed the identification of potential molecular markers of PAH oxidation. Finally, 6H-dibenzo[b,d]pyran-6-one, biphenyl-2,2’-dicarboxaldehyde and 3-nitrophenanthrene have been selected to be the best candidates as markers of PAH oxidation processes in ambient air.
dc.language.isoENen_US
dc.subject.enPAH
dc.subject.enOPAH
dc.subject.enNPAH
dc.subject.enAEROSOL
dc.subject.enSOA
dc.subject.enREACTIVITY
dc.title.enSources and atmospheric chemistry of oxy- and nitro-PAHs in the ambient air of Grenoble (France)
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.atmosenv.2017.04.042en_US
dc.subject.halSciences de l'environnementen_US
bordeaux.journalAtmospheric Environmenten_US
bordeaux.page144-154en_US
bordeaux.volume161en_US
bordeaux.hal.laboratoriesEPOC : Environnements et Paléoenvironnements Océaniques et Continentaux - UMR 5805en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamLPTCen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierineris-01863155
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
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