Atmos. Chem. Phys. Discuss., 12, 4831-4866, 2012
www.atmos-chem-phys-discuss.net/12/4831/2012/
doi:10.5194/acpd-12-4831-2012
© Author(s) 2012. This work is distributed
under the Creative Commons Attribution 3.0 License.
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This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Organic molecular markers and signature from wood combustion particles in winter ambient aerosols: aerosol mass spectrometer (AMS) and high time-resolved GC-MS measurements in Augsburg, Germany
M. Elsasser1,2, M. Crippa3, J. Orasche1,4, P. F. DeCarlo3,*, M. Oster1,2, M. Pitz5,6, T. L. Gustafson7, J. B. C. Pettersson7, J. Schnelle-Kreis1, A. S. H. Prévôt3, and R. Zimmermann1,2
1Joint Mass Spectrometry Centre, Cooperation Group Comprehensive Molecular Analytics, Helmholtz Zentrum München, Ingolstädter Landstr. 1, 85764 Neuherberg, Germany
2Joint Mass Spectrometry Centre, Universität Rostock, Institut für Chemie, Lehrstuhl für Analytische Chemie, Dr.-Lorenz-Weg 1, 18059 Rostock, Germany
3Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland
4Department of Sedimentology and Environmental Geology, Georg-August-University Göttingen, 37077 Göttingen, Germany
5Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Epidemiology II, 85764 Neuherberg, Germany
6University of Augsburg, Environment Science Center, 86159 Augsburg, Germany
7Department of Chemistry, University of Gothenburg, 412 96 Gothenburg, Sweden
*now at: Department of Civil Architectural and Environmental Engineering, Drexel University, 19104 Philadelphia, PA, USA

Abstract. The impact of wood combustion on ambient aerosols was investigated in Augsburg, Germany during a winter measurement campaign of a six-week period. Special attention was paid to the high time resolution observations of wood combustion with different mass spectrometric methods. Here we present and compare the results from an Aerodyne aerosol mass spectrometer (AMS) and gas chromatographic – mass spectrometric (GC-MS) analysed PM1 filters on an hourly basis. This includes source apportionment of the AMS derived organic mass by using positive matrix factorisation (PMF) and analysis of levoglucosan as wood combustion marker, respectively. In the measurement period nitrate and organics are the main contributors to the defined submicron particle mass with 28% and 35%, respectively. To the latter wood combustion organic aerosol (WCOA) contributes 23% on average and 27% in the evening and night-time. Conclusively, wood combustion has a strong influence on the organics and overall aerosol composition. Levoglucosan accounts for 14% of WCOA mass with a higher percentage in comparison to other studies. The ratio between the mass of levoglucosan and organic carbon amounts to 0.06. This study is unique in the one-hour time resolution comparison between the wood combustion results of the AMS and the GC-MS analysed filter method at a PM1 particle size range. This comparison of the concentration courses of the PMF WCOA factor, levoglucosan estimated by the AMS data and the levoglucosan measured by GC-MS is highly correlated, and a detailed discussion on the contributors to the wood combustion marker ion at mass-to-charge ratio 60 will be given. This offers a suitable application possibility for the description of the wood combustion course by the WCOA factor and the levoglucosan concentration estimated by AMS data. However, quantitative description of the levoglucosan concentration estimated by the AMS data is difficult due to the offset of latter compared to measured levoglucosan by the GC-MS.

Citation: Elsasser, M., Crippa, M., Orasche, J., DeCarlo, P. F., Oster, M., Pitz, M., Gustafson, T. L., Pettersson, J. B. C., Schnelle-Kreis, J., Prévôt, A. S. H., and Zimmermann, R.: Organic molecular markers and signature from wood combustion particles in winter ambient aerosols: aerosol mass spectrometer (AMS) and high time-resolved GC-MS measurements in Augsburg, Germany, Atmos. Chem. Phys. Discuss., 12, 4831-4866, doi:10.5194/acpd-12-4831-2012, 2012.
 
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