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Volume 15, issue 13
Atmos. Chem. Phys., 15, 7735–7752, 2015
https://doi.org/10.5194/acp-15-7735-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 15, 7735–7752, 2015
https://doi.org/10.5194/acp-15-7735-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 15 Jul 2015

Research article | 15 Jul 2015

Particle size-resolved source apportionment of primary and secondary organic tracer compounds at urban and rural locations in Spain

B. L. van Drooge and J. O. Grimalt B. L. van Drooge and J. O. Grimalt
  • Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18–26, 08034 Barcelona, Catalonia, Spain

Abstract. Atmospheric particulate matter (PM) was fractionated in six aerodynamic sizes, > 7.2, 7.2–3, 3–1.5, 1.5–1, 1–0.5 and < 0.5 μm, using a cascade impactor. These fractions were collected at urban and rural sites during warm and cold seasons. Organic tracer compounds, such as levoglucosan, isoprene, pinene oxidation products, polycyclic aromatic hydrocarbons and quinones, were analyzed by gas chromatography coupled with mass spectrometry. These analyses showed that the composition in the smallest size fractions (< 0.5 μm) was more uniform than in the larger sizes (7.2> PM > 0.5 μm). Thus, markers of photochemically synthesized organic compounds or combustion sources, either biomass burning or traffic emissions, were predominantly observed in the fraction < 0.5 μm, whereas the larger particles were composed of mixed sources from combustion processes, vegetation emissions, soil resuspension, road dust, urban lifestyle activities and photochemically synthesized organic compounds.

Important seasonal differences were observed at the rural site. In the < 0.5 μm fraction these were related to a strong predominance of biomass burning in the cold period and photochemically transformed biogenic organic compounds in the warm period. In the 7.2 > PM > 0.5 μm fractions the differences involved predominantly soil-sourced compounds in the warm period and mixed combustion sources, photochemical products and vegetation emissions in the cold. Multivariate curve resolution/alternating least squares showed that these organic aerosols essentially originated from six source components. Four of them reflected primary emissions related to either natural products, e.g., vegetation emissions and upwhirled soil dust, or anthropogenic contributions, e.g., combustion products and compounds related to urban lifestyle activities like vehicular exhaust and tobacco smoking. Two secondary organic aerosol components were identified. They accumulated in the smallest (< 0.5 μm) or in the larger fractions (> 0.5 μm) and involved strong or mild photochemical transformations of vegetation precursor molecules, respectively. Toxicologically relevant information was also disclosed with the present approach. Thus, the strong predominance of biomass burning residues at the rural site during the cold period involved atmospheric concentrations of polycyclic aromatic hydrocarbons that were 3 times higher than at the urban sites and benzo[a]pyrene concentrations above legal recommendations.

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Molecular organic tracer compounds were analyzed in six particle sizes in an urban background site (Barcelona) and in a rural site in Spain. The results improve considerably our current understanding on the composition and particle-size distribution of organic air pollution in traffic intensive urban areas and rural sites where combustion of biomass plays an important role on the local and regional air quality, either by emissions from open fires or from domestic heating.
Molecular organic tracer compounds were analyzed in six particle sizes in an urban background...
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