Shon Zang-Ho, Kim Ki-Hyun
Department of Environmental Engineering, College of Engineering, Dong-Eui University, 995 Eomgwangno, Busanjin-gu, Gayadong San 24, Busan 614-714, Republic of Korea.
Chemosphere. 2006 Jun;63(11):1859-69. doi: 10.1016/j.chemosphere.2005.10.021. Epub 2005 Dec 1.
This study examines the oxidation of reduced sulfur compounds (RSCs) in urban ambient air. The photochemical conversions of RSC (such as DMS, CS2, H2S, DMDS, and CH3SH) to a further oxidized form (e.g., SO2, MSA, and H2SO4) were assessed using a photochemical box model. For our model simulation of RSC oxidation, measurements were taken at an urban monitoring station in Seoul, Korea (37.6 degrees N, 127 degrees E) during three separate time periods (e.g., Sept. 17-18, Oct. 23, and Oct. 27-28, 2003). The results indicate that DMS and H2S were the dominant RSCs with concentrations of 370 +/- 140 and 110 +/- 60 pptv, respectively. The photochemical conversion of DMDS to SO2 was found to occur more efficiently than other RSCs. The overall results of our study suggest that photochemical conversion of RSCs accounted for less than 15% of the observed SO2 during the measurement period. The SO2 production from DMS oxidation (mainly by the reaction with OH) was found to be affected primarily by the abstraction channel due to high NOx levels during the experimental conditions.
本研究考察了城市环境空气中还原态硫化合物(RSCs)的氧化情况。使用光化学箱模型评估了RSC(如二甲基硫醚、二硫化碳、硫化氢、二甲基二硫醚和甲硫醇)向进一步氧化形式(如二氧化硫、甲基磺酸和硫酸)的光化学转化。对于我们对RSC氧化的模型模拟,在韩国首尔一个城市监测站(北纬37.6度,东经127度)于三个不同时间段(例如,2003年9月17 - 18日、10月23日以及10月27 - 28日)进行了测量。结果表明,二甲基硫醚和硫化氢是主要的RSC,其浓度分别为370±140和110±60 pptv。发现二甲基二硫醚向二氧化硫的光化学转化比其他RSC更高效。我们研究的总体结果表明,在测量期间,RSC的光化学转化占观测到的二氧化硫的比例不到15%。由于实验条件下氮氧化物水平较高,二甲基硫醚氧化(主要通过与OH反应)产生的二氧化硫主要受提取通道影响。