Oxidation of sulfur dioxide by nitrogen dioxide accelerated at the interface of deliquesced aerosol particles

被引:106
|
作者
Liu, Tengyu [1 ,2 ,3 ]
Abbatt, Jonathan P. D. [3 ]
机构
[1] Nanjing Univ, Sch Atmospher Sci, Joint Int Res Lab Atmospher & Earth Syst Sci, Nanjing, Peoples R China
[2] Jiangsu Prov Collaborat Innovat Ctr Climate Chang, Nanjing, Peoples R China
[3] Univ Toronto, Dept Chem, Toronto, ON, Canada
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会; 国家重点研发计划;
关键词
HAZE EVENTS; WINTER HAZE; AIR-QUALITY; SULFATE; NO2; PH; ABSORPTION; ISOTOPES; KINETICS; SULFITE;
D O I
10.1038/s41557-021-00777-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although the multiphase chemistry of SO2 in aerosol particles is of great importance to air quality under polluted haze conditions, a fundamental understanding of the pertinent mechanisms and kinetics is lacking. In particular, there is considerable debate on the importance of NO2 in the oxidation of SO2 in aerosol particles. Here experiments with atmospherically relevant deliquesced particles at buffered pH values of 4-5 show that the effective rate constant for the reaction of NO2 with SO32- ((1.4 +/- 0.5) x 10(10) M-1 s(-1)) is more than three orders of magnitude larger than the value in dilute solutions. An interfacial reaction at the surface of aerosol particles probably drives the very fast kinetics. Our results indicate that oxidation of SO2 by NO2 at aerosol surfaces may be an important source of sulfate aerosols under polluted haze conditions.
引用
收藏
页码:1173 / +
页数:12
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