Single Droplet Tweezer Revealing the Reaction Mechanism of Mn(II)-Catalyzed SO2 Oxidation

被引:1
|
作者
Cao, Xue [1 ]
Liu, Yu-Xin [1 ]
Huang, Qishen [1 ]
Chen, Zhe [1 ]
Sun, Jiuyi [1 ]
Sun, Jian [1 ]
Pang, Shu-Feng [1 ]
Liu, Pai [1 ]
Wang, Weigang [2 ]
Zhang, Yun-Hong [1 ]
Ge, Maofa [2 ]
机构
[1] Beijing Inst Technol, Inst Chem Phys, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
[2] Chinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Res Educ Ctr Excellence Mol Sci,Inst Chem, State Key Lab Struct Chem Unstable & Stable Specie, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
aerosol optical tweezer; sulfate aerosol; Mn(II)-catalysis; SO2; oxidation; fine particulate matter; SECONDARY INORGANIC AEROSOL; SULFUR-DIOXIDE; CATALYZED OXIDATION; HETEROGENEOUS REACTION; SULFATE AEROSOLS; TRACE-ELEMENTS; CHEMISTRY; SURFACES; KINETICS; PATHWAY;
D O I
10.1021/acs.est.4c00309
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Sulfate aerosol is one of the major components of secondary fine particulate matter in urban haze that has crucial impacts on the social economy and public health. Among the atmospheric sulfate sources, Mn(II)-catalyzed SO2 oxidation on aerosol surfaces has been regarded as a dominating one. In this work, we measured the reaction kinetics of Mn(II)-catalyzed SO2 oxidation in single droplets using an aerosol optical tweezer. We show that the SO2 oxidation occurs at the Mn(II)-active sites on the aerosol surface, per a piecewise kinetic formulation, one that is characterized by a threshold surface Mn(II) concentration and gaseous SO2 concentration. When the surface Mn(II) concentration is lower than the threshold value, the reaction rate is first order with respect to both Mn(II) and SO2, agreeing with our traditional knowledge. But when surface Mn(II) concentration is above the threshold, the reaction rate becomes independent of Mn(II) concentration, and the reaction order with respect to SO2 becomes greater than unity. The measured reaction rate can serve as a tool to estimate sulfate formation based on field observation, and our established parametrization corrects these calculations. This framework for reaction kinetics and parametrization holds promising potential for generalization to various heterogeneous reaction pathways. [GRAPHICS]
引用
收藏
页码:5068 / 5078
页数:11
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