Impact of aftertreatment devices on primary emissions and secondary organic aerosol formation potential from in-use diesel vehicles: results from smog chamber experiments

dc.contributor.authorChirico, Roberto
dc.contributor.authorDeCarlo, Peter F.
dc.contributor.authorHeringa, Maarten F.
dc.contributor.authorTritscher, Torsten
dc.contributor.authorRichter, René
dc.contributor.authorPrévôt, André S. H.
dc.contributor.authorDommen, Josef
dc.contributor.authorWeingartner, Ernest
dc.contributor.authorWehrle, Günther
dc.contributor.authorGysel, Martin
dc.contributor.authorLaborde, Marie
dc.contributor.authorBaltensperger, Urs
dc.date.accessioned2024-08-13T13:44:23Z
dc.date.available2024-08-13T13:44:23Z
dc.date.issued2010-12-06
dc.description.abstractDiesel particulate matter (DPM) is a significant source of aerosol in urban areas and has been linked to adverse health effects. Although newer European directives have introduced increasingly stringent standards for primary PM emissions, gaseous organics emitted from diesel cars can still lead to large amounts of secondary organic aerosol (SOA) in the atmosphere. Here we present results from smog chamber investigations characterizing the primary organic aerosol (POA) and the corresponding SOA formation at atmospherically relevant concentrations for three in-use diesel vehicles with different exhaust aftertreatment systems. One vehicle lacked exhaust aftertreatment devices, one vehicle was equipped with a diesel oxidation catalyst (DOC) and the third vehicle used both a DOC and diesel particulate filter (DPF). The experiments presented here were obtained from the vehicles at conditions representative of idle mode, and for one car in addition at a speed of 60 km/h. An Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was used to measure the organic aerosol (OA) concentration and to obtain information on the chemical composition. For the conditions explored in this paper, primary aerosols from vehicles without a particulate filter consisted mainly of black carbon (BC) with a low fraction of organic matter (OM, OM/BC < 0.5), while the subsequent aging by photooxidation resulted in a consistent production of SOA only for the vehicles without a DOC and with a deactivated DOC. After 5 h of aging ~80% of the total organic aerosol was on average secondary and the estimated "emission factor" for SOA was 0.23–0.56 g/kg fuel burned. In presence of both a DOC and a DPF, only 0.01 g SOA per kg fuel burned was produced within 5 h after lights on. The mass spectra indicate that POA was mostly a non-oxidized OA with an oxygen to carbon atomic ratio (O/C) ranging from 0.10 to 0.19. Five hours of oxidation led to a more oxidized OA with an O/C range of 0.21 to 0.37.
dc.identifier.doi10.5194/acp-10-11545-2010
dc.identifier.issn1680-7324
dc.identifier.issn1680-7316
dc.identifier.urihttps://irf.fhnw.ch/handle/11654/46614
dc.identifier.urihttps://doi.org/10.26041/fhnw-9672
dc.issue23
dc.language.isoen
dc.publisherCopernicus
dc.relation.ispartofAtmospheric Chemistry and Physics
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.spatialGöttingen
dc.subject.ddc550 - Geowissenschaften
dc.titleImpact of aftertreatment devices on primary emissions and secondary organic aerosol formation potential from in-use diesel vehicles: results from smog chamber experiments
dc.type01A - Beitrag in wissenschaftlicher Zeitschrift
dc.volume10
dspace.entity.typePublication
fhnw.InventedHereNo
fhnw.ReviewTypeAnonymous ex ante peer review of a complete publication
fhnw.affiliation.hochschuleHochschule für Technik und Umwelt FHNWde_CH
fhnw.affiliation.institutlnstitut für Sensorik und Elektronikde_CH
fhnw.openAccessCategoryGold
fhnw.pagination11545-11563
fhnw.publicationStatePublished
relation.isAuthorOfPublication05dd9a19-7a24-4325-805a-2d121483b168
relation.isAuthorOfPublication54997bb8-cf4a-4120-b0c7-f8e731e8eea1
relation.isAuthorOfPublication.latestForDiscovery05dd9a19-7a24-4325-805a-2d121483b168
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