Roles of SO2 oxidation in new particle formation events

被引:8
|
作者
Meng, He [1 ]
Zhu, Yujiao [1 ]
Evans, Greg J. [2 ]
Jeong, Cheol-Heon [2 ]
Yao, Xiaohong [1 ,2 ]
机构
[1] Ocean Univ China, Minist Educ, Key Lab Marine Environm Sci & Ecol, Qingdao 266100, Peoples R China
[2] Univ Toronto, Southern Ontario Ctr Atmospher Aerosol Res, Toronto, ON M5S 3E5, Canada
来源
基金
中国国家自然科学基金;
关键词
Nucleation; Particle growth; Sulfuric acid; Photochemical oxidation; SO2; ATMOSPHERIC AEROSOL NUCLEATION; SULFURIC-ACID CONCENTRATION; SIZE DISTRIBUTION; NUMBER CONCENTRATIONS; BOREAL FOREST; VERTICAL EXTENT; MODE PARTICLES; HONG-KONG; GROWTH; NANOPARTICLES;
D O I
10.1016/j.jes.2014.12.002
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The oxidation of SO2 is commonly regarded as a major driver for new particle formation (NPF) in the atmosphere. In this study, we explored the connection between measured mixing ratio of SO2 and observed long-term (duration > 3 hr) and short-term (duration <1.5 hr) NPF events at a semi-urban site in Toronto. Apparent NPF rates (J(30)) showed a moderate correlation with the concentration of sulfuric acid ([H2SO4]) calculated from the measured mixing ratio of SO2 in long-term NPF events and some short-term NPF events (Category I) (R-2 = 0.66). The exponent in the fitting line of J(30) similar to [H2SO4](n) in these events was 1.6. It was also found that SO2 mixing ratios varied a lot during long-term NPF events, leading to a significant variation of new particle counts. In the SO2-unexplained short-term NPF events (Category II), analysis showed that new particles were formed aloft and then mixed down to the ground level. Further calculation results showed that sulfuric acid oxidized from SO2 probably made a negligible contribution to the growth of >10 nm new particles. (C) 2015 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
引用
收藏
页码:90 / 101
页数:12
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