Atmospheric Gas-Phase Formation of Methanesulfonic Acid

被引:17
作者
Chen, Jing [1 ]
Lane, Joseph R. [2 ]
Bates, Kelvin H. [3 ,4 ]
Kjaergaard, Henrik G. [1 ]
机构
[1] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen O, Denmark
[2] Univ Waikato, Sch Sci, Hamilton 3240, New Zealand
[3] Univ Colorado, NOAA, Chem Sci Lab, Earth Syst Res Labs, Boulder, CO 80305 USA
[4] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80305 USA
关键词
dimethyl sulfide oxidation; mechanism; sulfuricacid; quantum chemical computation; global modeling; PEROXY RADICAL ISOMERIZATION; METHANE SULFINIC ACID; DIMETHYL SULFIDE; OH RADICALS; INITIATED OXIDATION; AEROSOL FORMATION; DMS OXIDATION; SO2; FORMATION; RO2; RADICALS; CL ATOMS;
D O I
10.1021/acs.est.3c07120
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Despite its impact on the climate, the mechanism of methanesulfonic acid (MSA) formation in the oxidation of dimethyl sulfide (DMS) remains unclear. The DMS + OH reaction is known to form methanesulfinic acid (MSIA), methane sulfenic acid (MSEA), the methylthio radical (CH3S), and hydroperoxymethyl thioformate (HPMTF). Among them, HPMTF reacts further to form SO2 and OCS, while the other three form the CH3SO2 radical. Based on theoretical calculations, we find that the CH3SO2 radical can add O-2 to form CH3S-(O)(2)OO, which can react further to form MSA. The branching ratio is highly temperature sensitive, and the MSA yield increases with decreasing temperature. In warmer regions, SO2 is the dominant product of DMS oxidation, while in colder regions, large amounts of MSA can form. Global modeling indicates that the proposed temperature-sensitive MSA formation mechanism leads to a substantial increase in the simulated global atmospheric MSA formation and burden.
引用
收藏
页码:21168 / 21177
页数:10
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