globalchange  > 气候变化事实与影响
DOI: 10.1016/j.atmosenv.2014.10.058
Scopus记录号: 2-s2.0-84909606519
论文题名:
Non-sulfate sulfur in fine aerosols across the United States: Insight for organosulfate prevalence
作者: Shakya K; M; , Peltier R; E
刊名: Atmospheric Environment
ISSN: 0168-2563
EISSN: 1573-515X
出版年: 2015
卷: 100
起始页码: 159
结束页码: 166
语种: 英语
Scopus关键词: Fine aerosols ; Sulfate sulfur ; organic carbon ; organosulfur derivative ; acidity ; aerosol composition ; atmospheric pollution ; geographical region ; ion chromatography ; long-term change ; particulate matter ; pollutant source ; seasonal variation ; size distribution ; speciation (chemistry) ; sulfur compound ; X-ray fluorescence ; acidity ; aerosol ; agriculture ; Article ; desert ; forest ; geography ; industrial area ; ion pair chromatography ; prevalence ; residential area ; seasonal variation ; United States ; X ray fluorescence ; United States
Scopus学科分类: Environmental Science: Water Science and Technology ; Earth and Planetary Sciences: Earth-Surface Processes ; Environmental Science: Environmental Chemistry
英文摘要: We investigated the discrepancies in long-term sulfur measurements from 2000 to 2012 by two separate speciation methods, X-ray fluorescence (XRF) spectroscopy and ion chromatography (IC) across the United States (334 sites). Overall, there was a good correlation between sulfur measurements by XRF spectroscopy and IC (R≥0.90 for most of the sites). However, the inorganic sulfate measured by ion chromatography was not sufficient to account for all the sulfur measured by XRF spectroscopy at many of the sites. Discrepancies were observed with the high ratios of sulfur measured by XRF spectroscopy to that by IC. Such high ratios also exhibited seasonal variation, and differed across land use types; significant differences occurred at locations classified as forest, agriculture, and mobile, but not in locations classified as commercial, desert, industrial, and residential. On average, the excess, or non-sulfate, sulfur (unmeasured organic sulfur or other inorganic species of sulfur) was variable and observed as high as ~13% of organic carbon and ~2% of PM2.5. The contribution of such assumed organosulfur was larger in the eastern region than other geographical locations in the United States. Besides the temporal and spatial trends, the additional sulfur was found to be related to other factors such as aerosol acidity and emission sources. The results suggest that these unmeasured sulfur species could have significant contribution to aerosol burden, and the understanding of these could help to control PM2.5 levels and to assess other effects of sulfur aerosols. © 2014 Elsevier Ltd.
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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/82100
Appears in Collections:气候变化事实与影响

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作者单位: Department of Environmental Health Sciences, University of Massachusetts, Amherst, United States

Recommended Citation:
Shakya K,M,, Peltier R,et al. Non-sulfate sulfur in fine aerosols across the United States: Insight for organosulfate prevalence[J]. Atmospheric Environment,2015-01-01,100
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