Characterizations of volatile organic compounds during high ozone episodes in Beijing, China

被引:53
作者
An Jun-lin [1 ,2 ]
Wang Yue-si [1 ]
Wu Fang-kun [1 ]
Zhu Bin [2 ]
机构
[1] Chinese Acad Sci, Inst Atmospher Phys, LAPC, Beijing 100029, Peoples R China
[2] Nanjing Univ Informat Sci & Technol, Key Lab Meteorol Disaster, Minist Educ, Sch Atmospher Phys, Nanjing 210044, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Volatile organic compounds; Beijing; PCA/APCS; PEARL RIVER-DELTA; SOURCE APPORTIONMENT; AMBIENT AIR; HONG-KONG; NONMETHANE HYDROCARBONS; COMPOUNDS VOCS; ATMOSPHERE; POLLUTION; CITIES; REGION;
D O I
10.1007/s10661-011-2086-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Air samples were collected in Beijing from June through August 2008, and concentrations of volatile organic compounds (VOCs) in those samples are here discussed. This sampling was performed to increase understanding of the distributions of their compositions, illustrate the overall characteristics of different classes of VOCs, assess the ages of air masses, and apportion sources of VOCs using principal compound analysis/absolute principal component scores (PCA/APCS). During the sampling periods, the relative abundance of the four classes of VOCs as determined by the concentration-based method was different from that determined by the reactivity approach. Alkanes were found to be most abundant (44.3-50.1%) by the concentration-based method, but aromatic compounds were most abundant (38.2-44.5%) by the reactivity approach. Aromatics and alkenes contributed most (73-84%) to the ozone formation potential. Toluene was the most abundant compound (11.8-12.7%) during every sampling period. When the maximum incremental reactivity approach was used, propene, toluene, m,p-xylene, 1-butene, and 1,2,4-trimethylbenzene were the five most abundant compounds during two sampling periods. X/B, T/B, and E/B ratios in this study were lower than those found in other cities, possibly due to the aging of the air mass at this site. Four components were extracted from application of PCA to the data. It was found that the contribution of vehicle exhaust to total VOCs accounted for 53% of VOCs, while emissions due to the solvent use contributed 33% of the total VOCs. Industrial sources contributed 3% and biogenic sources contributed 11%. The results showed that vehicle exhausts (i.e., unburned vehicle emissions + vehicle internal engine combustion) were dominant in VOC emissions during the experimental period. The solvent use made the second most significant contribution to ambient VOCs.
引用
收藏
页码:1879 / 1889
页数:11
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