Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9458764 | Atmospheric Environment | 2005 | 9 Pages |
Abstract
The size-fractionated particulate mercury in ambient air was collected at the top of a university campus building in Shanghai from March 2002 to September 2003. Wet digestion followed by cold vapor atom adsorption spectroscopy (CVAAS) was employed to analyze total particulate mercury concentration. Two-step extraction was performed to differentiate volatile particle-phase mercury (VPM), reactive particle-phase mercury (RPM) and inert particle-phase mercury (IPM). The average concentrations of mercury in PM1.6, PM8 and total suspended particle (TSP) were 0.058-0.252, 0.148-0.398 and 0.233-0.529 ng mâ3, respectively. About 50%-60% of mercury in PM8 was in PM1.6, and about 60%-70% of mercury in TSP was in PM8. Particulate mercury was mainly concentrated on fine particles. The mercury fraction in fine particulate matters (<1.6 μm) was over 4 μg gâ1 while 1-2 μg gâ1 in TSP. Both were much higher than background values, suggesting that anthropogenic sources are the predominant emission contributors. Seasonal variation indicated that the mercury in TSP in spring was higher than that in summer; however, the mercury in fine particles (<1.6 μm) varied little. The fact that fine particulate mercury (<1.6 μm) was well correlated with sulfate and elemental carbon, but not with fluoride, chloride, nitrate and organic carbon, demonstrates that fine particulate mercury is closely associated with stationary sources and gas-particle transformation. Speciation analysis of mercury showed that VPM fraction decreased with the decrease of particle size, while IPM fraction increased and occupied over 50% in particle <1.6 μm. The detailed species in VPM, RPM and IPM were discussed. Coal burning was estimated to contribute approximately 80% of total atmospheric mercury.
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Authors
Guangli L. Xiu, Qingxi Jin, Danian Zhang, Shuangyan Shi, Xuejuan Huang, Wenying Zhang, Liang Bao, Pengtao Gao, Bo Chen,