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dc.contributor.authorFortner, E. C.
dc.contributor.authorZheng, J.
dc.contributor.authorZhang, R.
dc.contributor.authorKnighton, W. Berk
dc.contributor.authorMolina, Luisa Tan
dc.contributor.authorAndré, M.
dc.contributor.authorVolkamer, R. A.
dc.contributor.authorSheehy, P. M.
dc.date.accessioned2011-12-19T18:34:00Z
dc.date.available2011-12-19T18:34:00Z
dc.date.issued2009-01
dc.identifier.issn1680-7324
dc.identifier.issn1680-7316
dc.identifier.urihttp://hdl.handle.net/1721.1/67724
dc.description.abstractVolatile organic compounds (VOCs) were measured by proton transfer reaction – mass spectrometry (PTR-MS) on a rooftop in the urban mixed residential and industrial area North Northeast of downtown Mexico City as part of the Megacity Initiative – Local and Global Research Observations (MILAGRO) 2006 field campaign. Thirty eight individual masses were monitored during the campaign and many species were quantified including methanol, acetaldehyde, toluene, the sum of C2 benzenes, the sum of C3 benzenes, acetone, isoprene, benzene, and ethyl acetate. The VOC measurements were analyzed to gain a better understanding of the type of VOCs present in the MCMA, their diurnal patterns, and their origins. Diurnal profiles of weekday and weekend/holiday aromatic VOC concentrations showed the influence of vehicular traffic during the morning rush hours and during the afternoon hours. Plumes including elevated toluene as high as 216 parts per billion (ppb) and ethyl acetate as high as 183 ppb were frequently observed during the late night and early morning hours, indicating the possibility of significant industrial sources of the two compounds in the region. Wind fields during those peak episodes revealed no specific direction for the majority of the toluene plumes but the ethyl acetate plumes arrived at the site when winds were from the Southwest or West. The PTR-MS measurements combined with other VOC measuring techniques at the field site as well as VOC measurements conducted in other areas of the Mexico City Metropolitan Area (MCMA) will help to develop a better understanding of the spatial pattern of VOCs and its variability in the MCMA. Atmos. Chem. Phys., 9, 467–481, 2009.en_US
dc.description.sponsorshipRobert A. Welch Foundation (Grant A-1417)en_US
dc.description.sponsorshipTexas A & M University. Center for Atmospheric Chemistry and Environmenten_US
dc.description.sponsorshipNational Science Foundation (U.S.) (ATM-0528227)en_US
dc.language.isoen_US
dc.publisherEuropean Geosciences Unionen_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0en_US
dc.sourceCopernicusen_US
dc.titleMeasurements of Volatile Organic Compounds Using Proton Transfer Reaction - Mass Spectrometry during the MILAGRO 2006 Campaignen_US
dc.typeArticleen_US
dc.identifier.citationFortner, E.C. et al. "Measurements of Volatile Organic Compounds Using Proton Transfer Reaction – Mass Spectrometry during the MILAGRO 2006 Campaign." Atmos. Chem. Phys., 9, 467-481 (2009).en_US
dc.contributor.departmentmove to dc.description.sponsorshipen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.approverMolina, Luisa Tan
dc.contributor.mitauthorMolina, Luisa Tan
dc.contributor.mitauthorVolkamer, R. M.
dc.contributor.mitauthorSheehy, P.
dc.relation.journalAtmospheric Chemistry and Physicsen_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.orderedauthorsFortner, E. C.; Zheng, J.; Zhang, R.; Berk Knighton, W.; Volkamer, R. M.; Sheehy, P.; Molina, L.; André, M.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3596-5334
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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