TY - JOUR
T1 - Anthropogenic Pollutants Induce Changes in Peroxyacetyl Nitrate Formation Intensity and Pathways in a Mountainous Background Atmosphere in Southern China
AU - Wang, Yu
AU - Liu, Tao
AU - Gong, Daocheng
AU - Wang, Hao
AU - Guo, Hai
AU - Liao, Minping
AU - Deng, Shuo
AU - Cai, Huang
AU - Wang, Boguang
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (42121004, 42077190, and 42005080), Science and Technology Project of Guangdong Province of China (2019B121202002), Science and Technology Project of Shaoguan (210811164532141), the fellowship of China Postdoctoral Science Foundation (2020M673059), the research support scheme of Research Institute for Land and Space at The Hong Kong Polytechnic University (1-CD79), and the Start-up Fund for RAPs under the Strategic Hiring Scheme of the Hong Kong Polytechnic University (1-BD3T). The authors thank Dr. Xiaopu Lyu from Hong Kong Baptist University for constructive discussions on model usage. They also thank Jie Ou and Yu Zheng of Shaoguan Environmental Monitoring Central Station, for their help during the sampling campaign. They also thank Guangdong Tianjing Shan Forest Farm for their great support in the field sampling.
Publisher Copyright:
© 2023 American Chemical Society
PY - 2023/4/18
Y1 - 2023/4/18
N2 - Mountainous background areas are typically considered to have a clean atmosphere where peroxyacetyl nitrate (PAN) can be decomposed. This study demonstrated that PAN was photochemically formed with a simulated production rate of 0.28 ± 0.06 ppbv h-1 in the Nanling mountains (1690 m a.s.l.) of South China and that net PAN formation was dependent on both volatile organic compounds (VOCs) and NOx precursors (transition regime). In contrast to dominated acetaldehyde oxidation in previous urban and rural research, PAN at Nanling was primarily formed by methylglyoxal (38%), acetaldehyde (28%), radicals (20%), and other oxygenated volatile organic compounds (OVOCs) (13%). Moreover, when polluted air masses invaded the Nanling mountains, the PAN production rate was altered, primarily because anthropogenic aromatics intensified PAN formation via the oxidized pathways of methylglyoxal, other OVOCs, and radicals. Finally, net PAN formation at Nanling reduced the hydroxyl radical level by consuming NOx, impaired local radical cycling, and thereby suppressed local O3 production. This suppressing effect was exacerbated on polluted days. The findings of this study deepen our understanding of PAN photochemistry and the impact of anthropogenic intrusions on the background atmosphere of mountainous regions.
AB - Mountainous background areas are typically considered to have a clean atmosphere where peroxyacetyl nitrate (PAN) can be decomposed. This study demonstrated that PAN was photochemically formed with a simulated production rate of 0.28 ± 0.06 ppbv h-1 in the Nanling mountains (1690 m a.s.l.) of South China and that net PAN formation was dependent on both volatile organic compounds (VOCs) and NOx precursors (transition regime). In contrast to dominated acetaldehyde oxidation in previous urban and rural research, PAN at Nanling was primarily formed by methylglyoxal (38%), acetaldehyde (28%), radicals (20%), and other oxygenated volatile organic compounds (OVOCs) (13%). Moreover, when polluted air masses invaded the Nanling mountains, the PAN production rate was altered, primarily because anthropogenic aromatics intensified PAN formation via the oxidized pathways of methylglyoxal, other OVOCs, and radicals. Finally, net PAN formation at Nanling reduced the hydroxyl radical level by consuming NOx, impaired local radical cycling, and thereby suppressed local O3 production. This suppressing effect was exacerbated on polluted days. The findings of this study deepen our understanding of PAN photochemistry and the impact of anthropogenic intrusions on the background atmosphere of mountainous regions.
KW - aldehydes
KW - master chemical mechanism
KW - ozone
KW - radical cycling
KW - volatile organic compounds
UR - http://www.scopus.com/inward/record.url?scp=85152134493&partnerID=8YFLogxK
U2 - 10.1021/acs.est.2c02845
DO - 10.1021/acs.est.2c02845
M3 - Journal article
C2 - 37017935
AN - SCOPUS:85152134493
SN - 0013-936X
VL - 57
SP - 6253
EP - 6262
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 15
ER -