TY - JOUR
T1 - Role of Ammonia on the Feedback Between AWC and Inorganic Aerosol Formation During Heavy Pollution in the North China Plain
AU - Ge, Baozhu
AU - Xu, Xiaobin
AU - Ma, Zhiqiang
AU - Pan, Xiaole
AU - Wang, Zhe
AU - Lin, Weili
AU - Ouyang, Bin
AU - Xu, Danhui
AU - Lee, James
AU - Zheng, Mei
AU - Ji, Dongsheng
AU - Sun, Yele
AU - Dong, Huabin
AU - Squires, Freya Anne
AU - Fu, Pingqing
AU - Wang, Zifa
N1 - Funding Information:
This study was financially supported by the National Natural Science Foundation of China (grants 41877313, 41571130024, 91744206 and 41575123) and Basic Research Fund of CAMS (2016Z001). The data used in this paper are available in https://www.pangaea.de/ .
Publisher Copyright:
© 2019. The Authors.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Atmospheric NH3 plays a vital role not only in the environmental ecosystem but also in atmosphere chemistry. To further understand the effects of NH3 on the formation of haze pollution in Beijing, ambient NH3 and related species were measured and simulated at high resolutions during the wintertime Air Pollution and Human Health-Beijing (APHH-Beijing) campaign in 2016. We found that the total NHx (gaseous NH3+particle NH4 +) was mostly in excess of the SO4 2−-NO3 −-NH4 +-water equilibrium system during our campaign. This NHx excess made medium aerosol acidity, with the median pH value being 3.6 and 4.5 for polluted and nonpolluted conditions, respectively, and enhanced the formation of particle phase nitrate. Our analysis suggests that NH4NO3 is the most important factor driving the increasing of aerosol water content with NO3 − controlling the prior pollution stage and NH4 + the most polluted stage. Increased formation of NH4NO3 under excess NHx, especially during the nighttime, may trigger the decreasing of aerosol deliquescence relative humidity even down to less than 50% and hence lead to hygroscopic growth even under RH conditions lower than 50% and the wet aerosol particles become better medium for rapid heterogeneous reactions. A further increase of RH promotes the positive feedback “aerosol water content-heterogeneous reactions” and ultimately leads to the formation of severe haze. Modeling results by Nested Air Quality Prediction Monitor System (NAQPMS) show the control of 20% NH3 emission may affect 5–11% of particulate matter PM2.5 formation under current emissions conditions in the North China Plain.
AB - Atmospheric NH3 plays a vital role not only in the environmental ecosystem but also in atmosphere chemistry. To further understand the effects of NH3 on the formation of haze pollution in Beijing, ambient NH3 and related species were measured and simulated at high resolutions during the wintertime Air Pollution and Human Health-Beijing (APHH-Beijing) campaign in 2016. We found that the total NHx (gaseous NH3+particle NH4 +) was mostly in excess of the SO4 2−-NO3 −-NH4 +-water equilibrium system during our campaign. This NHx excess made medium aerosol acidity, with the median pH value being 3.6 and 4.5 for polluted and nonpolluted conditions, respectively, and enhanced the formation of particle phase nitrate. Our analysis suggests that NH4NO3 is the most important factor driving the increasing of aerosol water content with NO3 − controlling the prior pollution stage and NH4 + the most polluted stage. Increased formation of NH4NO3 under excess NHx, especially during the nighttime, may trigger the decreasing of aerosol deliquescence relative humidity even down to less than 50% and hence lead to hygroscopic growth even under RH conditions lower than 50% and the wet aerosol particles become better medium for rapid heterogeneous reactions. A further increase of RH promotes the positive feedback “aerosol water content-heterogeneous reactions” and ultimately leads to the formation of severe haze. Modeling results by Nested Air Quality Prediction Monitor System (NAQPMS) show the control of 20% NH3 emission may affect 5–11% of particulate matter PM2.5 formation under current emissions conditions in the North China Plain.
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U2 - 10.1029/2019EA000799
DO - 10.1029/2019EA000799
M3 - Article
AN - SCOPUS:85073603213
SN - 2333-5084
VL - 6
SP - 1675
EP - 1693
JO - Earth and Space Science
JF - Earth and Space Science
IS - 9
ER -