Atmospheric particulate mercury: Concentrations and size distributions

被引:75
|
作者
Kim, Pyung-Rae [1 ]
Han, Young-Ji [1 ]
Holsen, Thomas M. [2 ]
Yi, Seung-Muk [3 ]
机构
[1] Kangwon Natl Univ, Coll Nat Sci, Dept Environm Sci, Chunchon 200701, Kangwon Do, South Korea
[2] Clarkson Univ, Dept Civil & Environm Engn, Potsdam, NY 13699 USA
[3] Seoul Natl Univ, Grad Sch Publ Hlth, Dept Environm Hlth, Seoul 151742, South Korea
基金
新加坡国家研究基金会;
关键词
Particulate mercury; Size distribution; Urban; Rural; Oxidation; GASEOUS ELEMENTAL MERCURY; POLYCYCLIC AROMATIC-HYDROCARBONS; SEMIVOLATILE ORGANIC-COMPOUNDS; LONG-TERM MEASUREMENTS; SPECIATED MERCURY; DRY-DEPOSITION; WET DEPOSITION; HG-P; URBAN; GAS;
D O I
10.1016/j.atmosenv.2012.07.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, the size distributions of atmospheric particulate mercury (PHg) were measured in both urban and rural areas during the summer, fall, and winter. Both PHg concentrations and the contribution of PHg to total PM aerosol were higher at the urban (PHg = 6.8 +/- 6.5 pg m(-3), PHg/total PM = 0.18 pg mu g(-1)) than at the rural site (PHg = 4.6 +/- 2.7 pg m(-3), PHg/total PM = 0.06 pg mu g(-1)). Based on size-distribution measurements, the fine mode was the dominant size at both sites in winter while the coarse mode became more important during summer. In winter PHg concentrations in the fine mode increased because of the effective adsorption of gaseous Hg onto the fine particles at the low temperature and increased Hg oxidation reactions in the presence of high particles concentrations. During winter elevated concentrations of total PHg were measured when the prevailing winds were northwesterly originating in China. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 102
页数:9
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