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dc.contributor.authorHohaus, T.
dc.contributor.authorTrimborn, D.
dc.contributor.authorKiendler-Scharr, A.
dc.contributor.authorGensch, I.
dc.contributor.authorLaumer, W.
dc.contributor.authorKammer, B.
dc.contributor.authorAndres, S.
dc.contributor.authorBoudries, H.
dc.contributor.authorSmith, Kenneth A.
dc.contributor.authorWorsnop, D. R.
dc.contributor.authorJayne, John T.
dc.date.accessioned2011-08-11T14:37:28Z
dc.date.available2011-08-11T14:37:28Z
dc.date.issued2010-10
dc.date.submitted2010-07
dc.identifier.issn1867-1381
dc.identifier.issn1867-8548
dc.identifier.urihttp://hdl.handle.net/1721.1/65105
dc.description.abstractIn many environments organic matter significantly contributes to the composition of atmospheric aerosol particles influencing its properties. Detailed chemical characterization of ambient aerosols is critical in order to understand the formation process, composition, and properties of aerosols and facilitates source identification and relative contributions from different types of sources to ambient aerosols in the atmosphere. However, current analytical methods are far from full speciation of organic aerosols and often require sampling times of up to one week. Offline methods are also subjected to artifacts during aerosol collection and storage. In the present work a new technique for quasi on-line compound specific measurements of organic aerosol particles was developed. The Aerosol Collection Module (ACM) focuses particles into a beam which is directed to a cooled sampling surface. The sampling takes place in a high vacuum environment where the gas phase from the sample volume is removed. After collection is completed volatile and semi-volatile compounds are evaporated from the collection surface through heating and transferred to a detector. For laboratory characterization the ACM was interfaced with a Gas Chromatograph Mass Spectrometer, Flame Ionization Detector system (GC/MS-FID), abbreviated as ACM GC-MS. The particle collection efficiency, gas phase transfer efficiency, and linearity of the ACM GC-MS were determined using laboratory generated octadecane aerosols. The ACM GC-MS is linear over the investigated mass range of 10 to 100 ng and a recovery rate of 100% was found for octadecane particles. The ACM GC-MS was applied to investigate secondary organic aerosol (SOA) formed from β-pinene oxidation. Nopinone, myrtanal, myrtenol, 1-hydroxynopinone, 3-oxonopinone, 3,7-dihydroxynopinone, and bicyclo[3,1,1]hept-3-ene-2-one were found as products in the SOA. The ACM GC-MS results are compared to quartz filter samples taken in parallel to the ACM GC-MS measurements. First measurements of ambient atmospheric aerosols are presented.en_US
dc.description.sponsorshipUnited States. Environmental Protection Agency (grant number RD-83107701-0)en_US
dc.description.sponsorshipUnited States. Dept. of Energy (grant number DE-FG02-05ER84269)en_US
dc.language.isoen_US
dc.publisherCopernicus Publications on behalf of the European Geosciences Unionen_US
dc.relation.isversionofhttp://dx.doi.org/10.5194/amt-3-1423-2010en_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0en_US
dc.sourceCopernicusen_US
dc.titleA new aerosol collector for quasi on-line analysis of particulate organic matter: the Aerosol Collection Module (ACM) and first applications with a GC/MS-FIDen_US
dc.typeArticleen_US
dc.identifier.citationHohaus, T. et al. “A New Aerosol Collector for Quasi On-line Analysis of Particulate Organic Matter: The Aerosol Collection Module (ACM) and First Applications with a GC/MS-FID.” Atmospheric Measurement Techniques 3.5 (2010) : 1423-1436.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.approverSmith, Kenneth A.
dc.contributor.mitauthorBoudries, H.
dc.contributor.mitauthorSmith, Kenneth A.
dc.relation.journalAtmospheric Measurement Techniquesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHohaus, T.; Trimborn, D.; Kiendler-Scharr, A.; Gensch, I.; Laumer, W.; Kammer, B.; Andres, S.; Boudries, H.; Smith, K. A.; Worsnop, D. R.; Jayne, J. T.en
dc.identifier.orcidhttps://orcid.org/0000-0001-7002-1681
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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