Source Attribution of Submicron Organic Aerosols during Wintertime Inversions by Advanced Factor Analysis of Aerosol Mass Spectra

Real-time measurements of submicrometer aerosol were performed using an Aerodyne aerosol mass spectrometer (AMS) during three weeks at an urban background site in Zurich (Switzerland) in January 2006. A hybrid receptor model which incorporates a priori known source composition was applied to the AMS...

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Veröffentlicht in:Environmental science & technology 2008-01, Vol.42 (1), p.214-220
Hauptverfasser: Lanz, Valentin A, Alfarra, M. Rami, Baltensperger, Urs, Buchmann, Brigitte, Hueglin, Christoph, Szidat, Sönke, Wehrli, Miriam N, Wacker, Lukas, Weimer, Silke, Caseiro, Alexandre, Puxbaum, Hans, Prevot, Andre S. H
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Sprache:eng
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Zusammenfassung:Real-time measurements of submicrometer aerosol were performed using an Aerodyne aerosol mass spectrometer (AMS) during three weeks at an urban background site in Zurich (Switzerland) in January 2006. A hybrid receptor model which incorporates a priori known source composition was applied to the AMS highly time-resolved organic aerosol mass spectra. Three sources and components of submicrometer organic aerosols were identified: the major component was oxygenated organic aerosol (OOA), mostly representing secondary organic aerosol and accounting on average for 52–57% of the particulate organic mass. Radiocarbon (14C) measurements of organic carbon (OC) indicated that ∼31 and ∼69% of OOA originated from fossil and nonfossil sources, respectively. OOA estimates were strongly correlated with measured particulate ammonium. Particles from wood combustion (35–40%) and 3–13% traffic-related hydrocarbon-like organic aerosol (HOA) accounted for the other half of measured organic matter (OM). Emission ratios of modeled HOA to measured nitrogen oxides (NO x ) and OM from wood burning to levoglucosan from filter analyses were found to be consistent with literature values.
ISSN:0013-936X
1520-5851
DOI:10.1021/es0707207