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dc.contributor.authorKroll, Jesse
dc.contributor.authorSmith, Jared D.
dc.contributor.authorWorsnop, Douglas R.
dc.contributor.authorWilson, Kevin R.
dc.date.accessioned2012-08-16T14:10:35Z
dc.date.available2012-08-16T14:10:35Z
dc.date.issued2012-06
dc.date.submitted2011-12
dc.identifier.issn1448-2517
dc.identifier.urihttp://hdl.handle.net/1721.1/72168
dc.description.abstractThe oxidative aging of the semivolatile fraction of diesel exhaust aerosol is studied in order to better understand the influence of oxidation reactions on particle chemical composition. Exhaust is sampled from an idling diesel truck, sent through a denuder to remove gas-phase species and oxidised by hydroxyl (OH•) radicals in a flow reactor. OH• concentrations are chosen to approximately match the OH• exposures a particle would experience over its atmospheric lifetime. Evolving particle composition is monitored using aerosol mass spectrometry in two different modes, electron impact ionisation (EI) for the measurement of elemental ratios and vacuum ultraviolet (VUV) photoionisation for the measurement of molecular components. Changes to mass spectra in both modes indicate major changes to particle composition over the range of OH• exposures studied. The product aerosol is only lightly oxidised (O/C < 0.3), suggesting an intermediate oxidation state between primary organics and the highly oxidised organic aerosol observed in the atmosphere. These lightly oxidised organics appear to be composed of secondary organic aerosol from semivolatile species, as well as from heterogeneously oxidised particle-phase organics. Key chemical characteristics (elemental ratios, oxidation kinetics and mass spectrometric features) of the reaction system are examined in detail. Similarities between this laboratory-generated aerosol and ‘hydrocarbon-like organic aerosol’ (HOA) reported in ambient studies suggest that HOA might not be entirely primary in origin, as is commonly assumed, but rather might include a significant secondary component.en_US
dc.description.sponsorshipUnited States. Dept. of Energy (Director, Office of Energy Research, Office of Basic Energy Sciences, and Chemical Sciences Division (contract number DE-AC02-05CH11231)en_US
dc.description.sponsorshipHenry & Camille Dreyfus Foundation (Postdoctral program in Environmental Chemistry)en_US
dc.language.isoen_US
dc.publisherCSIRO Publishingen_US
dc.relation.isversionofhttp://dx.doi.org/10.1071/EN11162en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceJesse Krollen_US
dc.titleCharacterisation of lightly oxidised organic aerosol formed from the photochemical aging of diesel exhaust particlesen_US
dc.typeArticleen_US
dc.identifier.citationKroll, Jesse H. et al. “Characterisation of Lightly Oxidised Organic Aerosol Formed from the Photochemical Aging of Diesel Exhaust Particles.” Environmental Chemistry 9.3 (2012): 211. Web.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
dc.contributor.approverKroll, Jesse H.
dc.contributor.mitauthorKroll, Jesse
dc.relation.journalEnvironmental Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKroll, Jesse H.; Smith, Jared D.; Worsnop, Douglas R.; Wilson, Kevin R.en
dc.identifier.orcidhttps://orcid.org/0000-0002-6275-521X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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