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Proc Natl Acad Sci U S A


Title:Response of an aerosol mass spectrometer to organonitrates and organosulfates and implications for atmospheric chemistry
Author(s):Farmer DK; Matsunaga A; Docherty KS; Surratt JD; Seinfeld JH; Ziemann PJ; Jimenez JL;
Address:"Cooperative Institute for Research in Environmental Sciences and Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA"
Journal Title:Proc Natl Acad Sci U S A
Year:2010
Volume:20100301
Issue:15
Page Number:6670 - 6675
DOI: 10.1073/pnas.0912340107
ISSN/ISBN:1091-6490 (Electronic) 0027-8424 (Print) 0027-8424 (Linking)
Abstract:"Organonitrates (ON) are important products of gas-phase oxidation of volatile organic compounds in the troposphere; some models predict, and laboratory studies show, the formation of large, multifunctional ON with vapor pressures low enough to partition to the particle phase. Organosulfates (OS) have also been recently detected in secondary organic aerosol. Despite their potential importance, ON and OS remain a nearly unexplored aspect of atmospheric chemistry because few studies have quantified particulate ON or OS in ambient air. We report the response of a high-resolution time-of-flight aerosol mass spectrometer (AMS) to aerosol ON and OS standards and mixtures. We quantify the potentially substantial underestimation of organic aerosol O/C, commonly used as a metric for aging, and N/C. Most of the ON-nitrogen appears as NO(x)+ ions in the AMS, which are typically dominated by inorganic nitrate. Minor organonitrogen ions are observed although their identity and intensity vary between standards. We evaluate the potential for using NO(x)+ fragment ratios, organonitrogen ions, HNO(3)+ ions, the ammonium balance of the nominally inorganic ions, and comparison to ion-chromatography instruments to constrain the concentrations of ON for ambient datasets, and apply these techniques to a field study in Riverside, CA. OS manifests as separate organic and sulfate components in the AMS with minimal organosulfur fragments and little difference in fragmentation from inorganic sulfate. The low thermal stability of ON and OS likely causes similar detection difficulties for other aerosol mass spectrometers using vaporization and/or ionization techniques with similar or larger energy, which has likely led to an underappreciation of these species"
Keywords:"*Aerosols Air Pollutants/analysis/chemistry Ammonia/chemistry Chemistry/*methods Chemistry, Organic/*instrumentation/*methods Chromatography, Ion Exchange/methods Ions Mass Spectrometry/*instrumentation/*methods Nitrates/*chemistry Nitrogen/chemistry Olei;"
Notes:"MedlineFarmer, D K Matsunaga, A Docherty, K S Surratt, J D Seinfeld, J H Ziemann, P J Jimenez, J L eng Research Support, U.S. Gov't, Non-P.H.S. 2010/03/03 Proc Natl Acad Sci U S A. 2010 Apr 13; 107(15):6670-5. doi: 10.1073/pnas.0912340107. Epub 2010 Mar 1"

 
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