GSTDTAP  > 地球科学
DOI10.5194/acp-17-1689-2017
Deciphering potential chemical compounds of gaseous oxidized mercury in Florida, USA
Huang, Jiaoyan1; Miller, Matthieu B.2; Edgerton, Eric3; Gustin, Mae Sexauer2
2017-02-03
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2017
卷号17期号:3
文章类型Article
语种英语
国家USA
英文摘要

The highest mercury (Hg) wet deposition in the United States of America (USA) occurs along the Gulf of Mexico, and in the southern and central Mississippi River Valley. Gaseous oxidized Hg (GOM) is thought to be a major contributor due to high water solubility and reactivity. Therefore, it is critical to understand concentrations, potential for wet and dry deposition, and GOM compounds present in the air. Concentrations and dry-deposition fluxes of GOM were measured and calculated for Naval Air Station Pensacola Outlying Landing Field (OLF) in Florida using data collected by a Tekran (R) 2537/1130/1135, the University of Nevada Reno Reactive Mercury Active System (UNRRMAS) with cation exchange and nylon membranes, and the Aerohead samplers that use cation-exchange membranes to determine dry deposition. Relationships with Tekran (R) derived data must be interpreted with caution, since the GOM concentrations measured are biased low depending on the chemical compounds in air and interferences with water vapor and ozone.


Criteria air pollutants were concurrently measured. This allowed for comparison and better understanding of GOM. In addition to other methods previously applied at OLF, use of the UNRRMAS provided a platform for determination of the chemical compounds of GOM in the air. Results from nylon membranes with thermal desorption analyses indicated seven GOM compounds in this area, including HgBr2, HgCl2, HgO, Hg-nitrogen and sulfur compounds, and two unknown compounds. This indicates that the site is influenced by different gaseous phase reactions and sources. Using back-trajectory analysis during a high-GOM event related to high CO, but average SO2, indicated air parcels moved from the free troposphere and across Arkansas, Mississippi, and Alabama at low elevation (<300 m). This event was initially characterized by HgBr2, followed by a mixture of GOM compounds. Overall, GOM chemistry indicates oxidation reactions with local mobile source pollutants and long-range transport.


In order to develop methods to measure GOM concentrations and chemistry, and model dry-deposition processes, the actual GOM compounds need to be known, as well as their corresponding physicochemical properties, such as Henry's Law constants.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000395097100002
WOS关键词PASSIVE SAMPLING SYSTEMS ; WESTERN UNITED-STATES ; DRY-DEPOSITION ; ATMOSPHERIC MERCURY ; SPECIATED MERCURY ; OZONE ; SITES ; AIR ; NEVADA ; QUANTIFICATION
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/20616
专题地球科学
作者单位1.Univ N Carolina, Inst Environm, 100 Europa Dr,Suite 490, Chapel Hill, NC 27517 USA;
2.Univ Nevada, Dept Nat Resources & Environm Sci, 1664 N Virginia St, Reno, NV 89557 USA;
3.Atmospher Res & Anal Inc, 410 Midenhall Way, Cary, NC 27513 USA
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GB/T 7714
Huang, Jiaoyan,Miller, Matthieu B.,Edgerton, Eric,et al. Deciphering potential chemical compounds of gaseous oxidized mercury in Florida, USA[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2017,17(3).
APA Huang, Jiaoyan,Miller, Matthieu B.,Edgerton, Eric,&Gustin, Mae Sexauer.(2017).Deciphering potential chemical compounds of gaseous oxidized mercury in Florida, USA.ATMOSPHERIC CHEMISTRY AND PHYSICS,17(3).
MLA Huang, Jiaoyan,et al."Deciphering potential chemical compounds of gaseous oxidized mercury in Florida, USA".ATMOSPHERIC CHEMISTRY AND PHYSICS 17.3(2017).
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