Articles | Volume 22, issue 17
https://doi.org/10.5194/acp-22-11239-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-22-11239-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Chemical evolution of secondary organic aerosol tracers during high-PM2.5 episodes at a suburban site in Hong Kong over 4 months of continuous measurement
Qiongqiong Wang
Department of Chemistry, The Hong Kong University of Science and
Technology, Hong Kong SAR, China
Shan Wang
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Yuk Ying Cheng
Department of Chemistry, The Hong Kong University of Science and
Technology, Hong Kong SAR, China
Hanzhe Chen
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Zijing Zhang
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Jinjian Li
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
Department of Chemistry, The Hong Kong University of Science and
Technology, Hong Kong SAR, China
Division of Environment and Sustainability, The Hong Kong University
of Science and Technology, Hong Kong SAR, China
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Men Xia, Xiang Peng, Weihao Wang, Chuan Yu, Zhe Wang, Yee Jun Tham, Jianmin Chen, Hui Chen, Yujing Mu, Chenglong Zhang, Pengfei Liu, Likun Xue, Xinfeng Wang, Jian Gao, Hong Li, and Tao Wang
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Mingshuai Zhang, Chun Zhao, Yuhan Yang, Qiuyan Du, Yonglin Shen, Shengfu Lin, Dasa Gu, Wenjing Su, and Cheng Liu
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Yuliang Liu, Wei Nie, Yuanyuan Li, Dafeng Ge, Chong Liu, Zhengning Xu, Liangduo Chen, Tianyi Wang, Lei Wang, Peng Sun, Ximeng Qi, Jiaping Wang, Zheng Xu, Jian Yuan, Chao Yan, Yanjun Zhang, Dandan Huang, Zhe Wang, Neil M. Donahue, Douglas Worsnop, Xuguang Chi, Mikael Ehn, and Aijun Ding
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Chao Peng, Yu Wang, Zhijun Wu, Lanxiadi Chen, Ru-Jin Huang, Weigang Wang, Zhe Wang, Weiwei Hu, Guohua Zhang, Maofa Ge, Min Hu, Xinming Wang, and Mingjin Tang
Atmos. Chem. Phys., 20, 13877–13903, https://doi.org/10.5194/acp-20-13877-2020, https://doi.org/10.5194/acp-20-13877-2020, 2020
Rui Li, Qiongqiong Wang, Xiao He, Shuhui Zhu, Kun Zhang, Yusen Duan, Qingyan Fu, Liping Qiao, Yangjun Wang, Ling Huang, Li Li, and Jian Zhen Yu
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Zhenhao Ling, Qianqian Xie, Min Shao, Zhe Wang, Tao Wang, Hai Guo, and Xuemei Wang
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Short summary
Secondary organic aerosol (SOA) is often enhanced during fine-particulate-matter (PM2.5) episodes. We examined bi-hourly measurements of SOA molecular tracers in suburban Hong Kong during 11 city-wide PM2.5 episodes. The tracers showed regional characteristics for both anthropogenic and biogenic SOA as well as biomass-burning-derived SOA. Multiple tracers of the same precursor revealed the dominance of low-NOx formation pathways for isoprene SOA and less-aged monoterpene SOA during winter.
Secondary organic aerosol (SOA) is often enhanced during fine-particulate-matter (PM2.5)...
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