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DOI10.5194/acp-20-4153-2020
Formation mechanisms of atmospheric nitrate and sulfate during the winter haze pollution periods in Beijing: gas-phase, heterogeneous and aqueous-phase chemistry
Liu, Pengfei1,2,3,5; Ye, Can1,3; Xue, Chaoyang1,3; Zhang, Chenglong1,2,3; Mu, Yujing1,2,3,4; Sun, Xu1,6
2020-04-07
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2020
卷号20期号:7页码:4153-4165
文章类型Article
语种英语
国家Peoples R China
英文摘要

A vast area in China is currently going through severe haze episodes with drastically elevated concentrations of PM2.5 in winter. Nitrate and sulfate are the main constituents of PM2.5, but their formations via NO2 and SO2 oxidation are still not comprehensively understood, especially under different pollution or atmospheric relative humidity (RH) conditions. To elucidate formation pathways of nitrate and sulfate in different polluted cases, hourly samples of PM2.5 were collected continuously in Beijing during the wintertime of 2016. Three serious pollution cases were identified reasonably during the sampling period, and the secondary formations of nitrate and sulfate were found to make a dominant contribution to atmospheric PM2.5 under the relatively high RH condition. The significant correlation between NOR, NOR = NO3-/ (NO3- + NO2), and [NO2](2) x [O-3] during the nighttime under the RH >= 60 % condition indicated that the heterogeneous hydrolysis of N2O5 involving aerosol liquid water was responsible for the nocturnal formation of nitrate at the extremely high RH levels. The more often coincident trend of NOR and [HONO] x [DR] (direct radiation) x [NO2] compared to its occurrence with [Dust] x [NO2] during the daytime under the 30 % < RH < 60 % condition provided convincing evidence that the gas-phase reaction of NO2 with OH played a pivotal role in the diurnal formation of nitrate at moderate RH levels. The extremely high mean values of SOR, SOR = SO42-/ (SO42- +SO2), during the whole day under the RH >= 60 % condition could be ascribed to the evident contribution of SO2 aqueous-phase oxidation to the formation of sulfate during the severe pollution episodes. Based on the parameters measured in this study and the known sulfate production rate calculation method, the oxidation pathway of H2O2 rather than NO2 was found to contribute greatly to the aqueous-phase formation of sulfate.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000525345100002
WOS关键词RESIDENTIAL COAL COMBUSTION ; WATER-SOLUBLE IONS ; NITROUS-ACID HONO ; N2O5 UPTAKE ; METEOROLOGICAL CONDITIONS ; PARTICULATE POLLUTION ; AEROSOL POLLUTION ; NORTHERN CHINA ; PARTICLE WATER ; TIANJIN-HEBEI
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
被引频次:135[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/278738
专题地球科学
作者单位1.Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China;
2.Chinese Acad Sci, Inst Urban Environm, Ctr Excellence Urban Atmospher Environm, Xiamen 361021, Peoples R China;
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China;
4.Univ Chinese Acad Sci, Natl Engn Lab VOCs Pollut Control Mat & Technol, Beijing 100049, Peoples R China;
5.China Meteorol Adm, Key Lab Atmospher Chem, Beijing 100081, Peoples R China;
6.Beijing Urban Ecosyst Res Stn, Beijing 100085, Peoples R China
推荐引用方式
GB/T 7714
Liu, Pengfei,Ye, Can,Xue, Chaoyang,et al. Formation mechanisms of atmospheric nitrate and sulfate during the winter haze pollution periods in Beijing: gas-phase, heterogeneous and aqueous-phase chemistry[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2020,20(7):4153-4165.
APA Liu, Pengfei,Ye, Can,Xue, Chaoyang,Zhang, Chenglong,Mu, Yujing,&Sun, Xu.(2020).Formation mechanisms of atmospheric nitrate and sulfate during the winter haze pollution periods in Beijing: gas-phase, heterogeneous and aqueous-phase chemistry.ATMOSPHERIC CHEMISTRY AND PHYSICS,20(7),4153-4165.
MLA Liu, Pengfei,et al."Formation mechanisms of atmospheric nitrate and sulfate during the winter haze pollution periods in Beijing: gas-phase, heterogeneous and aqueous-phase chemistry".ATMOSPHERIC CHEMISTRY AND PHYSICS 20.7(2020):4153-4165.
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