Heavy air pollution episodes in Beijing during January 2013: inorganic ion chemistry and source analysis using Highly Time-Resolved Measurements in an urban site
Item
Title (Dublin Core)
Heavy air pollution episodes in Beijing during January 2013: inorganic ion chemistry and source analysis using Highly Time-Resolved Measurements in an urban site
Description (Dublin Core)
Heavy air pollution episodes occurred in Beijing in January 2013 attracted intensively attention around the whole world. During this period, the authors conducted highly time-resolved measurements of water soluble ions associated with PM<sub>2.5</sub> at an urban site, and attempted to distinguish the ion chemistry and potential sources. In this study, hourly mean concentrations of Cl<sup>−</sup>, NO<sub>3</sub><sup>−</sup>, SO<sub>4</sub><sup>2−</sup>, Na<sup>+</sup>, NH<sub>4</sub><sup>+</sup>, K<sup>+</sup>, Mg<sup>2+</sup> and Ca<sup>2+</sup> were measured during the air pollution episode in January 2013, and the ions were found to exist mainly in the form of (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>, NH<sub>4</sub>NO<sub>3</sub>, NaCl and KCl in aerosol particles by correlation and linear analysis. SO<sub>4</sub><sup>2−</sup> and NO<sub>3</sub><sup>−</sup> were observed peak concentrations in 10–15, 18–20, 21–24, and 26–30 January during this monitoring campaign. The percentage of SO<sub>4</sub><sup>2−</sup> and NH<sub>4</sub><sup>+</sup> in total ions concentrations exhibited an increasing trend with the enhancement of PM<sub>2.5</sub> concentration, indicating high concentrations of SO<sub>4</sub><sup>2−</sup> and NH<sub>4</sub><sup>+</sup> had played important roles in the formation of air pollution episodes. Ratio of [NO<sub>3</sub><sup>−</sup>]/[SO<sub>4</sub><sup>2−</sup>] was calculated, finding the sources of SO<sub>4</sub><sup>2−</sup> would contribute more to the formation of PM<sub>2.5</sub> than mobile sources. Diurnal variations of SO<sub>4</sub><sup>2−</sup>, NO<sub>3</sub><sup>−</sup>, NH<sub>4</sub><sup>+</sup> were examined, and all of them exhibited similar pattern with high concentration in night and relative low level at daytime. Emission from coal combustion, remote transportation at night or impact of meteorological was likely to be responsible for the high level of SO<sub>4</sub><sup>2−</sup>, NH<sub>4</sub><sup>+</sup> andNO<sub>3</sub><sup>−</sup>. Potential sources were identified by applying PMF. Secondary nitrate, secondary sulfate, coal combustion and biomass burning, as well as fugitive dust were considered as the major contributors to total ions.
Creator (Dublin Core)
Han, B.
Zhang, R.
Yang, W.
Bai, Z.
Ma, Z.
Zhang, W.
Date (Dublin Core)
2018-08-10
Type (Dublin Core)
Text
Format (Dublin Core)
application/pdf
Identifier (Dublin Core)
10.5194/acpd-15-11111-2015
https://acp.copernicus.org/preprints/acp-2015-193/
Source (Dublin Core)
eISSN: 1680-7324
Language (Dublin Core)
eng



