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dc.contributor.authorKessler, Sean Herbert
dc.contributor.authorNah, Theodora
dc.contributor.authorCarrasquillo, Anthony Joseph
dc.contributor.authorJayne, John T.
dc.contributor.authorWorsnop, Douglas R.
dc.contributor.authorWilson, Kevin R.
dc.contributor.authorKroll, Jesse
dc.date.accessioned2012-08-28T20:35:33Z
dc.date.available2012-08-28T20:35:33Z
dc.date.issued2011-05
dc.date.submitted2011-03
dc.identifier.issn1948-7185
dc.identifier.urihttp://hdl.handle.net/1721.1/72399
dc.description.abstractThe immense complexity inherent in the formation of secondary organic aerosol (SOA)—due primarily to the large number of oxidation steps and reaction pathways involved—has limited the detailed understanding of its underlying chemistry. As a means of simplifying such complexity, here we demonstrate the formation of SOA through the photolysis of gas-phase alkyl iodides, which generates organic peroxy radicals of known structure. In contrast to standard OH-initiated oxidation experiments, photolytically initiated oxidation forms a limited number of products via a single reactive step. As is typical for SOA, the yields of aerosol generated from the photolysis of alkyl iodides depend on aerosol loading, indicating the semivolatile nature of the particulate species. However, the aerosol was observed to be higher in volatility and less oxidized than in previous multigenerational studies of alkane oxidation, suggesting that additional oxidative steps are necessary to produce oxidized semivolatile material in the atmosphere. Despite the relative simplicity of this chemical system, the SOA mass spectra are still quite complex, underscoring the wide range of products present in SOA.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CHE-1012809)en_US
dc.description.sponsorshipAmerican Chemical Society Petroleum Research Fund (50341-DNI4)en_US
dc.description.sponsorshipUnited States. Dept. of Energy (Director, Office of Energy Research, Office of Basic Energy Sciences, and Chemical Sciences Division of the US DOE (contract no. DE-AC02-05CH11231))en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jz200432nen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceJesse Krollen_US
dc.titleFormation of Secondary Organic Aerosol from the Direct Photolytic Generation of Organic Radicalsen_US
dc.typeArticleen_US
dc.identifier.citationKessler, Sean H. et al. “Formation of Secondary Organic Aerosol from the Direct Photolytic Generation of Organic Radicals.” The Journal of Physical Chemistry Letters 2.11 (2011): 1295–1300. 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
dc.contributor.mitauthorKessler, Sean Herbert
dc.contributor.mitauthorCarrasquillo, Anthony Joseph
dc.contributor.mitauthorKroll, Jesse
dc.relation.journalJournal of Physical Chemistry Lettersen_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.orderedauthorsKessler, Sean H.; Nah, Theodora; Carrasquillo, Anthony J.; Jayne, John T.; Worsnop, Douglas R.; Wilson, Kevin R.; Kroll, Jesse H.en
dc.identifier.orcidhttps://orcid.org/0000-0002-6275-521X
dc.identifier.orcidhttps://orcid.org/0000-0003-1627-5618
dc.identifier.orcidhttps://orcid.org/0000-0002-9259-1869
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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