The role of naphthalene and its derivatives in the formation of secondary organic aerosol in the Yangtze River Delta region, China

被引:0
|
作者
Ye, Fei [1 ]
Li, Jingyi [1 ]
Gao, Yaqin [2 ]
Wang, Hongli [2 ]
An, Jingyu [2 ,3 ]
Huang, Cheng [2 ]
Guo, Song [4 ]
Lu, Keding [4 ]
Gong, Kangjia [1 ]
Zhang, Haowen [1 ]
Qin, Momei [1 ]
Hu, Jianlin [1 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Collaborat Innovat Ctr Atmospher Environm & Equipm, Sch Environm Sci & Engn, Jiangsu Key Lab Atmospher Environm Monitoring & Po, Nanjing 210044, Peoples R China
[2] Shanghai Acad Environm Sci, State Environm Protect Key Lab, Format & Prevent Urban Air Pollut Complex, Shanghai 200233, Peoples R China
[3] Fudan Univ, Dept Environm Sci & Engn, Shanghai Key Lab Atmospher Particle Pollut & Preve, Shanghai 200438, Peoples R China
[4] Peking Univ, Coll Environm Sci & Engn, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100871, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; SOURCE APPORTIONMENT; INITIATED OXIDATION; EMISSION INVENTORY; CHLORINE ATOMS; MODEL; PHOTOOXIDATION; SOA; SEMIVOLATILE;
D O I
10.5194/acp-24-7467-2024
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Naphthalene (Nap) and its derivatives, including 1-methylnaphthalene (1-MN) and 2-methylnaphthalene (2-MN), serve as prominent intermediate volatile organic compounds (IVOCs) and contribute to the formation of secondary organic aerosol (SOA). In this study, the Community Multiscale Air Quality (CMAQ) model coupled with detailed emissions and reactions of these compounds was utilized to examine their roles in the formation of SOA and other secondary pollutants in the Yangtze River Delta (YRD) region during summer. Significant underestimations of Nap and MN concentrations (by 79 % and 85 %) were observed at the Taizhou site based on the model results using the default emissions. Constrained by the observations, anthropogenic emissions of Nap and MN in the entire region were multiplied by 5 and 7, respectively, to better capture the evolution of pollutants. The average concentration of Nap reached 25 ppt (parts per trillion) in the YRD, with Nap contributing 4.1 % and 8.1 % (up to 12.6 %) of total aromatic emissions and aromatic-derived secondary organic carbon (SOC), respectively. The concentrations of 1-MN and 2-MN were relatively low, averaging 2 and 5 ppt, respectively. Together, they accounted for only 2.4 % of the aromatic-derived SOC. The impacts of Nap and MN oxidation on ozone and radicals were insignificant at regional scales but were not negligible when considering daily fluctuations in locations with high emissions of Nap and MN. This study highlights the significant roles of Nap and MN in the formation of SOA, which may pose environmental risks and result in adverse health effects.
引用
收藏
页码:7467 / 7479
页数:13
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