Articles | Volume 26, issue 3
https://doi.org/10.5194/acp-26-2103-2026
© Author(s) 2026. 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-26-2103-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Elucidation of the myrcene ozonolysis mechanism from a Criegee Chemistry perspective
Meifang Chen
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
University of Chinese Academy of Sciences, Beijing 100049, P.R. China
Shengrui Tong
CORRESPONDING AUTHOR
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
Shanshan Yu
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
Xiaofan Lv
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
University of Chinese Academy of Sciences, Beijing 100049, P.R. China
Yanyong Xu
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
University of Chinese Academy of Sciences, Beijing 100049, P.R. China
Hailiang Zhang
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, P.R. China
University of Chinese Academy of Sciences, Beijing 100049, P.R. China
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This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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This study examines NH3 effects on photochemical oxidation of mixed AVOC and BVOC under high-NOx conditions. NH3 promotes nucleation and accelerates SOA formation, though its impact on particle size is limited by the VOC/NOx ratio. NH3 enhances carbonyl production, strengthens SOA formation through acid-base and radical reactions, and suppresses OOMs. The results improve understanding of SOA formation in complex emission environments and support more accurate air quality forecasting.
Mingzhu Zhai, Shengrui Tong, Wenqian Zhang, Hailiang Zhang, Xin Li, Xiaoqi Wang, and Maofa Ge
Atmos. Chem. Phys., 25, 16679–16695, https://doi.org/10.5194/acp-25-16679-2025, https://doi.org/10.5194/acp-25-16679-2025, 2025
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To explore how anthropogenic activities affect HONO formation, we conducted comprehensive observations in Beijing. During clean periods with a 53 % drop in Traffic Performance Index, HONO, CO, and NO2 levels decreased by 2–3 times compared to polluted periods. Emission reduction simulations showed that a 50 % NOx reduction could lower HONO by up to 46.3 %, indicating that reducing anthropogenic activities significantly suppresses HONO formation and provides direct evidence for pollution control.
Narcisse Tsona Tchinda, Xiaofan Lv, Stanley Numbonui Tasheh, Julius Numbonui Ghogomu, and Lin Du
Atmos. Chem. Phys., 25, 8575–8590, https://doi.org/10.5194/acp-25-8575-2025, https://doi.org/10.5194/acp-25-8575-2025, 2025
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This study examines the transformation of organosulfates through reaction with HO• radicals. The results show that the nature of substituents on the carbon chain can effectively affect the decomposition rate of organosulfates, and ozone is unveiled as a complementary oxidant in the intermediate steps of this decomposition. The primary products from these reactions include carbonyl compounds and inorganic sulfate, which highlights the role of organosulfates in altering aerosol chemical composition.
Junling Li, Chaofan Lian, Mingyuan Liu, Hao Zhang, Yongxin Yan, Yufei Song, Chun Chen, Jiaqi Wang, Haijie Zhang, Yanqin Ren, Yucong Guo, Weigang Wang, Yisheng Xu, Hong Li, Jian Gao, and Maofa Ge
Atmos. Chem. Phys., 25, 2551–2568, https://doi.org/10.5194/acp-25-2551-2025, https://doi.org/10.5194/acp-25-2551-2025, 2025
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As a key source of hydroxyl (OH) radical, nitrous acid (HONO) has attracted much attention for its important role in the atmospheric oxidant capacity (AOC) increase. In this study, we made a comparison of the ambient levels, variation patterns, sources, and formation pathway in the warm season on the basis of continuous intensive observations at an urban site of Beijing. This work highlights the importance of HONO for the AOC in the warm season.
Junling Li, Kun Li, Hao Zhang, Xin Zhang, Yuanyuan Ji, Wanghui Chu, Yuxue Kong, Yangxi Chu, Yanqin Ren, Yujie Zhang, Haijie Zhang, Rui Gao, Zhenhai Wu, Fang Bi, Xuan Chen, Xuezhong Wang, Weigang Wang, Hong Li, and Maofa Ge
Atmos. Chem. Phys., 22, 10489–10504, https://doi.org/10.5194/acp-22-10489-2022, https://doi.org/10.5194/acp-22-10489-2022, 2022
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Ozone formation is enhanced by higher OH concentration and higher temperature but is influenced little by SO2. SO2 can largely enhance the particle formation. Organo-sulfates and organo-nitrates are detected in the formed particles, and the presence of SO2 can promote the formation of organo-sulfates. The results provide a scientific basis for systematically evaluating the effects of SO2, OH concentration, and temperature on the oxidation of mixed organic gases in the atmosphere.
Jingwei Zhang, Chaofan Lian, Weigang Wang, Maofa Ge, Yitian Guo, Haiyan Ran, Yusheng Zhang, Feixue Zheng, Xiaolong Fan, Chao Yan, Kaspar R. Daellenbach, Yongchun Liu, Markku Kulmala, and Junling An
Atmos. Chem. Phys., 22, 3275–3302, https://doi.org/10.5194/acp-22-3275-2022, https://doi.org/10.5194/acp-22-3275-2022, 2022
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This study added six potential HONO sources to the WRF-Chem model, evaluated their impact on HONO and O3 concentrations, including surface and vertical concentrations. The simulations extend our knowledge on atmospheric HONO sources, especially for nitrate photolysis. The study also explains the HONO difference in O3 formation on clean and hazy days, and reveals key potential HONO sources to O3 enhancements in haze-aggravating processes with a co-occurrence of high PM2.5 and O3 concentrations.
Junling Li, Hong Li, Kun Li, Yan Chen, Hao Zhang, Xin Zhang, Zhenhai Wu, Yongchun Liu, Xuezhong Wang, Weigang Wang, and Maofa Ge
Atmos. Chem. Phys., 21, 7773–7789, https://doi.org/10.5194/acp-21-7773-2021, https://doi.org/10.5194/acp-21-7773-2021, 2021
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SOA formation from the mixed anthropogenic volatile organic compounds was enhanced compared to the predicted SOA mass concentration based on the SOA yield of single species; interaction occurred between intermediate products from the two precursors. Interactions between the intermediate products from the mixtures and the effect on SOA formation give us a further understanding of the SOA formed in the atmosphere.
Chao Peng, Patricia N. Razafindrambinina, Kotiba A. Malek, Lanxiadi Chen, Weigang Wang, Ru-Jin Huang, Yuqing Zhang, Xiang Ding, Maofa Ge, Xinming Wang, Akua A. Asa-Awuku, and Mingjin Tang
Atmos. Chem. Phys., 21, 7135–7148, https://doi.org/10.5194/acp-21-7135-2021, https://doi.org/10.5194/acp-21-7135-2021, 2021
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Organosulfates are important constituents in tropospheric aerosol particles, but their hygroscopic properties and cloud condensation nuclei activities are not well understood. In our work, three complementary techniques were employed to investigate the interactions of 11 organosulfates with water vapor under sub- and supersaturated conditions.
Weigang Wang, Ting Lei, Andreas Zuend, Hang Su, Yafang Cheng, Yajun Shi, Maofa Ge, and Mingyuan Liu
Atmos. Chem. Phys., 21, 2179–2190, https://doi.org/10.5194/acp-21-2179-2021, https://doi.org/10.5194/acp-21-2179-2021, 2021
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Aerosol mixing state regulates the interactions between water molecules and particles and thus controls aerosol activation and hygroscopic growth, which thereby influences visibility degradation, cloud formation, and its radiative forcing. However, there are few studies attempting to investigate their interactions with water molecules. Here, we investigated the effect of organic coatings on the hygroscopic behavior of the inorganic core.
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Short summary
The critical role of Criegee intermediates (CIs) in the myrcene ozonolysis was elucidated through the combined approach of matrix isolation Fourier transform infrared spectroscopy and smog chamber experiments. Distinct mechanisms of different-sized CIs in secondary organic aerosol formation were proposed, and a synergistic effect between RO2 autoxidation and CIs oligomerization was identified. This study provided new insights into the ozonolysis process from the Criegee chemistry perspective.
The critical role of Criegee intermediates (CIs) in the myrcene ozonolysis was elucidated...
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