4.7 Article

Temporal trends of polychlorinated biphenyls in precipitation in Beijing, China

期刊

ATMOSPHERIC ENVIRONMENT
卷 56, 期 -, 页码 222-227

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.atmosenv.2012.03.070

关键词

Polychlorinated biphenyls; Precipitation; Flux; Beijing

资金

  1. National Natural Science Foundation of China [11075171, 10505023, 10905061]
  2. Innovation Program of Institute of High Energy Physics
  3. Chinese Academy of Sciences (CAS)
  4. State Key Lab of Research Center for Eco-Environmental Sciences, CAS [KF 2009-07]

向作者/读者索取更多资源

Temporal trend of polychlorinated biphenyls (PCBs) was determined in precipitation and monthly depositional fluxes were calculated in Beijing for the first time from February 2009 to March 2011. Total PCBs concentrations ranged from 7.00 to 993 ng L-1 in dissolved phase and from 1.00 to 133 ng L-1 in particulate phase, with a two orders of magnitude variation. Concentrations of PCBs were dominated by dissolved phase, which accounted for 82.5% of the total PCBs in precipitation, implying PCBs enrichment in rainwater due to efficient scavenging of highly contaminated gas phase and nonfilterable submicron particles which easily adsorbed organic contaminants in urban atmosphere. Highest concentrations of PCBs were measured in snow, which were about two times higher than those in rainwater, demonstrating more efficient scavenging of PCBs by snow. The sum of bi-, tri- and tetrachlorinated congeners accounted for 70.5% of total PCBs in precipitation, suggesting that PCBs mainly come from the historical usage of domestic PCB product, e.g., trichlorobiphenyl. PCBs concentrations in both dissolved and particulate phases showed slow rate of decline, with a half-life of 16.9 years in precipitation, suggesting that the atmospheric concentrations of PCBs were decreasing slowly in Beijing. The wet deposition flux of Sigma PCBs ranged from 0.240 to 6.55 mu g m(-2) month(-1) (mean: 1.41 mu g m(-2) month(-1)), indicating a relatively high level of PCBs contamination in Beijing atmosphere. (C) 2012 Elsevier Ltd. All rights reserved.

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