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The water-soluble ionic composition of PM2.5 in Shanghai and Beijing, China

Authors :
Yao, Xiaohong
Chan, Chak K.
Fang, Ming
Cadle, Steven
Chan, Tai
Mulawa, Patricia
He, Kebin
Ye, Boming
Source :
Atmospheric Environment. 2002, Vol. 36 Issue 26, p4223. 12p.
Publication Year :
2002

Abstract

A year-long field study to characterize the ionic species in PM2.5 was carried out in Shanghai and Beijing, China, in 1999–2000. Weekly samples of PM2.5 were collected using a special low flow rate (0.4 l min−1) sampler. In Shanghai, SO42− NO3− and NH4+ were the dominant ionic species, which accounted for 46%, 18% and 17% of the total mass of ions, respectively. Local SO2 emissions were an important source of SO42− in PM2.5 because the SO42− concentration was correlated with the SO2 concentration (<f>r=0.66</f>). The relatively stable SO42−/SO2 mass ratio over a large range of temperatures suggests that gas-phase oxidation of SO2 played a minor role in the formation of SO42−. The sum of SO42− and NO3− was highly correlated with NH4+ (<f>r=0.96</f>), but insufficient ammonium was present to totally neutralize the aerosol. In Beijing, SO42−, NO3− and NH4+ were also the dominant ionic species, constituting 44%, 25% and 16% of the total mass of water-soluble ions, respectively. Local SO2 emissions were an important source of SO42− in the winter since SO42− was correlated with SO2 (<f>r=0.83</f>). The low-mass SO42−/SO2 ratio (0.27) during winter, which had low humidity, suggests that gas-phase oxidation of SO2 was a major route of sulfate formation. In the summer, however, much higher mass ratios of SO42−/SO2 (5.6) were observed and were ascribed to in-cloud sulfate formation. The annual average ratio of NO3−/SO42− was 0.4 and 0.6 in Shanghai and in Beijing, respectively, suggesting that stationary emissions were still a dominant source in these two cities. [Copyright &y& Elsevier]

Subjects

Subjects :
*SULFATES
*CARBOXYLIC acids

Details

Language :
English
ISSN :
13522310
Volume :
36
Issue :
26
Database :
Academic Search Index
Journal :
Atmospheric Environment
Publication Type :
Academic Journal
Accession number :
8844143
Full Text :
https://doi.org/10.1016/S1352-2310(02)00342-4