Molecular composition of biogenic secondary organic aerosols using ultrahigh resolution mass spectrometry: comparing laboratory and field studies


Autoria(s): Kourtchev, Ivan; Fuller, S. J.; Giorio, C.; Healy, Robert M.; Wilson, Eoin; O'Connor, Ian P.; Wenger, John C.; McLeod, M.; Aalto, Juho; Ruuskanen, T. M.; Maenhaut, W.; Jones, R. L.; Venables, Dean S.; Sodeau, John R.; Kulmala, M.; Kalberer, M.; Kalberer, M.
Contribuinte(s)

European Commission

European Research Council

Suomen Akatemia, Finland

Data(s)

03/03/2014

03/03/2014

01/11/2013

13/11/2013

Resumo

Numerous laboratory experiments have been performed in an attempt to mimic atmospheric secondary organic aerosol (SOA) formation. However, it is still unclear how close the aerosol particles generated in laboratory experiments resemble atmospheric SOA with respect to their detailed chemical composition. In this study, we generated SOA in a simulation chamber from the ozonolysis of α-pinene and a biogenic volatile organic compound (BVOC) mixture containing α- and β-pinene, Δ3-carene, and isoprene. The detailed molecular composition of laboratory-generated SOA was compared with that of background ambient aerosol collected at a boreal forest site (Hyytiälä, Finland) and an urban location (Cork, Ireland) using direct infusion nanoelectrospray ultrahigh resolution mass spectrometry. Kendrick Mass Defect and Van Krevelen approaches were used to identify and compare compound classes and distributions of the detected species. The laboratory-generated SOA contained a distinguishable group of dimers that was not observed in the ambient samples. The presence of dimers was found to be less pronounced in the SOA from the VOC mixtures when compared to the one component precursor system. The elemental composition of the compounds identified in the monomeric region from the ozonolysis of both α-pinene and VOC mixtures represented the ambient organic composition of particles collected at the boreal forest site reasonably well, with about 70% of common molecular formulae. In contrast, large differences were found between the laboratory-generated BVOC samples and the ambient urban sample. To our knowledge this is the first direct comparison of molecular composition of laboratory-generated SOA from BVOC mixtures and ambient samples.

European Commission (Marie Curie Intra-European fellowship (project # 254319)); European Commission (project EUROCHAMP-2, contract number 228335); European Research Council (ERC starting grant 279405); Suomen Akatemia, Finland (Center of Excellence Program (project number 1118615))

Published Version

Not peer reviewed

Formato

application/pdf

Identificador

KOURTCHEV, I., FULLER, S. J., GIORIO, C., HEALY, R. M., WILSON, E., O'CONNOR, I. P., WENGER, J. C., MCLEOD, M., AALTO, J., RUUSKANEN, T. M., MAENHAUT, W., JONES, R., VENABLES, D. S., SODEAU, J. R., KULMALA, M. & KALBERER, M. 2013. Molecular composition of biogenic secondary organic aerosols using ultrahigh resolution mass spectrometry: comparing laboratory and field studies. Atmospheric Chemistry and Physics Discussions. 13, 29593-29627.

13

29593

29627

1680-7375

http://hdl.handle.net/10468/1422

10.5194/acpd-13-29593-2013

Atmospheric Chemistry and Physics Discussions

Idioma(s)

en

Publicador

Copernicus Publications

Relação

http://www.atmos-chem-phys-discuss.net/13/29593/2013/

Direitos

© Author(s) 2013. CC Attribution 3.0 License.

http://creativecommons.org/licenses/by/3.0/

Palavras-Chave #Atmospheric secondary organic aerosol #Biogenic volatile organic compound
Tipo

Article (non peer-reviewed)