Exploring the causes for co-pollution of O3 and PM2.5 in summer over North China

被引:12
|
作者
Ou, Shengju [1 ]
Wei, Wei [1 ]
Cai, Bin [1 ]
Yao, Shiyin [1 ]
Wang, Kai [1 ]
Cheng, Shuiyuan [1 ]
机构
[1] Beijing Univ Technol, Key Lab Beijing Reg Air Pollut Control, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
Co-pollution; Surface O-3 and PM2.5; Meteorology; Precursors; High level of oxidation products; URBAN OZONE POLLUTION; AIR-POLLUTION; METEOROLOGICAL DRIVERS; CHEMICAL-COMPOSITION; SOURCE APPORTIONMENT; HAZE POLLUTION; SURFACE OZONE; VISIBILITY; SUBMICRON; INSIGHTS;
D O I
10.1007/s10661-022-09951-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Co-pollution of surface O-3 and PM2.5 has become the most predominant type of air pollutions in Beijing-Tianjin-Hebei region in the hot season since 2017, particularly in May-July. Analysis based on observational data showed that co-pollution was always accompanied by high temperature, moderate relative humidity, extremely high SO2, and higher NO2. We also found that the meteorology and precursor dependence of O-3 was similar between co-pollution and O-3- single pollution. While PM2.5 in co-pollution was more related to temperature, relative humidity, and precursors, that in PM2.5-singe pollution were more related to small winds. These results indicate that co-pollution seemed to be more affected by atmospheric chemistry. According to the PM2.5 components, secondary inorganic aerosols (SIA) composed 44.3-48.7% of PM2.5 in co-pollution, while those accounting for 42.1-46.5% and 41.2 +1.3%, respectively, in O-3- and PM2.5-single pollution, which further confirmed the relatively stronger atmospheric chemistry processes in co-pollution. And the high proportion of SIA in co-pollution was mainly attributed to SO42-, which was observed to rapidly boom in non-refractory submicron aerosol (NR-PM1) on the condition of high level of O-3 at daytime. Additionally, we further explored the interactions of O-3 and PM2.5 in co-pollution. It was found that most (similar to 61.9%) co-pollution episodes were initiated by high O-3 at daytime; while for other episodes, high PM2.5 firstly occurred under the more stable meteorological conditions, and then accumulation of precursors further induced high O-3. A higher SIA concentration was observed in O-3-initiated co-pollution, indicating that the atmospheric oxidation in co-pollution caused by chemical processes was stronger than that by physical processes, which was further approved by the higher values of SOR and NOR in O-3-initiated co-pollution. This observational study revealed that controlling O-3 and precursor SO2 is the key to abating co-pollution in the hot season.
引用
收藏
页数:14
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