Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/84685
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dc.titleThe exchange of SVOCs across the air-sea interface in Singapore's coastal environment
dc.contributor.authorHe, J.
dc.contributor.authorBalasubramanian, R.
dc.date.accessioned2014-10-07T06:28:01Z
dc.date.available2014-10-07T06:28:01Z
dc.date.issued2010
dc.identifier.citationHe, J., Balasubramanian, R. (2010). The exchange of SVOCs across the air-sea interface in Singapore's coastal environment. Atmospheric Chemistry and Physics 10 (4) : 1837-1852. ScholarBank@NUS Repository.
dc.identifier.issn16807316
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/84685
dc.description.abstractCoastal areas are vulnerable to the accumulation of semivolatile organic compounds, such as PAHs, OCPs and PCBs from atmospheric inputs. Dry particulate and wet depositions, and air-water diffusive exchange in the Singapore's south coastal area, where most of chemical and oil refinery industries are situated in, were estimated. Based on a yearly dataset, the mean annual dry particulate deposition fluxes of σ16-PAHs, σ7OCPs and σ21 PCBs were 1328.8±961.1 μg m-2y -1, 5421.4±3426.7 ng m-2 y-1 and 811.8±578.3 ng m-2y-1, and the wet deposition of ∑16-PAHs and σ7 OCPs were 6667.1±1745.2 and 115.4±98.3 μg m-2 y-1, respectively. Seasonal variation of atmospheric depositions was influenced by meteorological conditions. Air-water gas exchange fluxes were shown to be negative values for PAHs, HCHs and DDXs, indicating Singapore's south coast as a sink for the above-mentioned SVOCs. The relative contribution of each depositional process to the total atmospheric input was assessed by annual fluxes. The profile of dry particulate deposition, wet deposition and gas exchange fluxes seemed to be correlated with individual pollutant's properties such as molecular weight and Henry's law constant, etc. For the water column partitioning, the organic carbon-normalized partition coefficients between particulate and dissolved phases (K/iOC) for both PAHs and OCPs were obtained. The relationships between iK/iOC of PAHs and OCPs and their respective octanol-water partition coefficient (iK/iOW) were examined. In addition, both adsorption onto combustion-derived soot carbon and absorption into natural organic matter for PAHs in marine water column were investigated. Enrichment factors in the sea-surface microlayer (SML) of the particulate phase were 1.2-7.1 and 3.0-4.9 for PAHs and OCPs, and those of dissolved phase were 1.1-4.9 and 1.6-4.2 for PAHs and OCPs, respectively. These enrichment factors are relatively higher than those reported for nearby coastal areas, which are most likely due to more organic surfactants floating in the south coastal surface of Singapore.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCIVIL ENGINEERING
dc.contributor.departmentDIVISION OF ENVIRONMENTAL SCIENCE & ENGG
dc.description.sourcetitleAtmospheric Chemistry and Physics
dc.description.volume10
dc.description.issue4
dc.description.page1837-1852
dc.identifier.isiutNOT_IN_WOS
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