Scavenging ratios of polycyclic aromatic compounds in rain and snow in the Athabasca oil sands region

• Main Authors: L. Zhang, I. Cheng, D. Muir, J.-P. Charland
• Format: Article
• Language: English
• Published: Copernicus Publications 2015-02-01
• Series: Atmospheric Chemistry and Physics
• Online Access: http://www.atmos-chem-phys.net/15/1421/2015/acp-15-1421-2015.pdf

The Athabasca oil sands industry in northern Alberta, Canada, is a possible source of polycyclic aromatic compounds (PACs). Monitored PACs, including polycyclic aromatic hydrocarbons (PAHs), alkylated PAHs, and dibenzothiophenes (DBTs), in precipitation and in air at three near-source sites in the Fort MacKay and Fort McMurray area during January 2011 to May 2012, were used to generate a database of scavenging ratios (<i>W</i>_t) for PACs scavenged by both snow and rain. Higher concentrations in precipitation and air were observed for alkylated PAHs and DBTs compared to the other PACs. The sums of the median precipitation concentrations over the period of data analyzed were 0.48 μ g L⁻¹ for the 18 PAHs, 3.38 μ g L⁻¹ for the 20 alkylated PAHs, and 0.94 μ g L⁻¹ for the 5 DBTs. The sums of the median air concentrations for parent PAHs, alkylated PAHs, and DBTs were 8.37, 67.26, and 11.83 ng m⁻³, respectively. <br><br> Median <i>W</i>_t over the measurement period were 6100 &ndash; 1.1 &times; 10⁶ from snow scavenging and 350 &ndash; 2.3 &times; 10⁵ from rain scavenging depending on the PAC species. Median <i>W</i>_t for parent PAHs were within the range of those observed at other urban and suburban locations, but <i>W</i>_t for acenaphthylene in snow samples were 2–7 times higher compared to other urban and suburban locations. <i>W</i>_t for some individual snow and rain samples exceeded literature values by a factor of 10. <i>W</i>_t for benzo(<i>a</i>)pyrene, dibenz(<i>a,h</i>)anthracene, and benzo(<i>g,h,i</i>)perylene in snow samples had reached 10⁷, which is the maximum for PAH snow scavenging ratios reported in the literature. From the analysis of data subsets, <i>W</i>_t for particulate-phase dominant PACs were 14–20 times greater than gas-phase dominant PACs in snow samples and 7–20 times greater than gas-phase dominant PACs in rain samples. <i>W</i>_t from snow scavenging were ~ 9 times greater than from rain scavenging for particulate-phase dominant PACs and 4–9.6 times greater than from rain scavenging for gas-phase dominant PACs. Gas-particle fractions of each PAC, particle size distributions of particulate-phase dominant PACs, and the Henry's law constant of gas-phase dominant PACs explained, to a large extent, the different <i>W</i>_t values among the different PACs and precipitation types. The trend in <i>W</i>_t with increasing alkyl substitutions may be attributed to their physico-chemical properties, such as octanol–air and particle partition coefficients and subcooled vapor pressure, which increases gas-particle partitioning and, subsequently, the particulate mass fraction. This study verified findings from a previous study of Wang et al. (2014) that suggested that snow scavenging is more efficient than rain scavenging of particles for equivalent precipitation amounts, and also provided new knowledge of the scavenging of gas-phase PACs and alkylated PACs by snow and rain.