4.7 Article

Atmospheric concentrations, dry deposition and air-soil exchange of polycyclic aromatic hydrocarbons (PAHs) in an industrial region in Turkey

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 153, Issue 3, Pages 1093-1102

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2007.09.064

Keywords

atmospheric PAHs; dry deposition flux; deposition velocity; soil-air partitioning; fugacity ratio

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Concurrent ambient air and dry deposition samples were collected during two sampling periods at the Aliaga industrial region in Izmir, Turkey. Sigma(15)-PAH (particulate + gas) concentrations ranged between 7.3 and 44.8 ng m-3 (average +/- S.D., 25.2 +/- 8.8 ng m(-3)) and 10.2-71.9 ng m(-3) (44.1 +/- 16.6 ng m(-3)) in summer and winter, respectively. Winter/summer individual ambient PAH concentration ratios ranged between 0.8 (acenaphthene) and 6.6 (benz[a]anthracene) indicating that wintertime concentrations were affected by residential heating emissions. In contrast to the ambient concentrations, Sigma(15)-PAH particle dry deposition fluxes were higher in summer (5792 +/- 3516 ng m(-2) day(-1), average +/- S.D.) than in winter (2650 +/- 1829 ng m(-2) day(-1)), probably due to large particles from enhanced re-suspension of polluted soil particles and road dust. Average overall dry deposition velocity of PAHs calculated using the dry deposition fluxes and particle-phase concentrations was 2.9 +/- 3.5 cm s(-1). Sigma(15)-PAH concentrations in soils taken from 50 points in the area ranged between 11 and 4628 mu g kg(-1) in dry weight. The spatial distribution of these concentrations indicated that the urban Aliaga, steel plants, the petroleum refinery, and the petrochemical plant are the major Sigma(15)-PAH sources in the area. Fugacity calculations in air and soil showed that the soil acts as a secondary source to the atmosphere for low molecular weight PAHs in summer and as a sink for the higher molecular weight ones in summer and winter. (C) 2007 Elsevier B.V. All rights reserved.

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