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Titel Influence of aerosol acidity on the chemical composition of secondary organic aerosol from β-caryophyllene
VerfasserIn M. N. Chan, J. D. Surratt, A. W. H. Chan, K. Schilling, J. H. Offenberg, M. Lewandowski, E. O. Edney, T. E. Kleindienst, M. Jaoui, E. S. Edgerton, R. L. Tanner, S. L. Shaw, M. Zheng, E. M. Knipping, J. H. Seinfeld
Medientyp Artikel
Sprache Englisch
ISSN 1680-7316
Digitales Dokument URL
Erschienen In: Atmospheric Chemistry and Physics ; 11, no. 4 ; Nr. 11, no. 4 (2011-02-25), S.1735-1751
Datensatznummer 250009375
Publikation (Nr.) Volltext-Dokument vorhandencopernicus.org/acp-11-1735-2011.pdf
 
Zusammenfassung
The secondary organic aerosol (SOA) yield of β-caryophyllene photooxidation is enhanced by aerosol acidity. In the present study, the influence of aerosol acidity on the chemical composition of β-caryophyllene SOA is investigated using ultra performance liquid chromatography/electrospray ionization-time-of-flight mass spectrometry (UPLC/ESI-TOFMS). A number of first-, second- and higher-generation gas-phase products having carbonyl and carboxylic acid functional groups are detected in the particle phase. Particle-phase reaction products formed via hydration and organosulfate formation processes are also detected. Increased acidity leads to different effects on the abundance of individual products; significantly, abundances of organosulfates are correlated with aerosol acidity. To our knowledge, this is the first detection of organosulfates and nitrated organosulfates derived from a sesquiterpene. The increase of certain particle-phase reaction products with increased acidity provides chemical evidence to support the acid-enhanced SOA yields. Based on the agreement between the chromatographic retention times and accurate mass measurements of chamber and field samples, three β-caryophyllene products (i.e., β-nocaryophyllon aldehyde, β-hydroxynocaryophyllon aldehyde, and β-dihydroxynocaryophyllon aldehyde) are suggested as chemical tracers for β-caryophyllene SOA. These compounds are detected in both day and night ambient samples collected in downtown Atlanta, GA and rural Yorkville, GA during the 2008 August Mini-Intensive Gas and Aerosol Study (AMIGAS).
 
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