Articles | Volume 25, issue 14
https://doi.org/10.5194/acp-25-7815-2025
https://doi.org/10.5194/acp-25-7815-2025
Research article
 | 
24 Jul 2025
Research article |  | 24 Jul 2025

Formation drivers and photochemical effects of ClNO2 in a coastal city of Southeast China

Gaojie Chen, Xiaolong Fan, Haichao Wang, Yee Jun Tham, Ziyi Lin, Xiaoting Ji, Lingling Xu, Baoye Hu, and Jinsheng Chen

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Cited articles

Atkinson, R., Baulch, D. L., Cox, R. A., Crowley, J. N., Hampson, R. F., Hynes, R. G., Jenkin, M. E., Rossi, M. J., Troe, J., and IUPAC Subcommittee: Evaluated kinetic and photochemical data for atmospheric chemistry: Volume II – gas phase reactions of organic species, Atmos. Chem. Phys., 6, 3625–4055, https://doi.org/10.5194/acp-6-3625-2006, 2006. 
Bannan, T. J., Bacak, A., Le Breton, M., Flynn, M., Ouyang, B., McLeod, M., Jones, R., Malkin, T. L., Whalley, L. K., Heard, D. E., Bandy, B., Khan, M. A. H., Shallcross, D. E., and Percival, C. J.: Ground and Airborne U. K. Measurements of Nitryl Chloride: An Investigation of the Role of Cl Atom Oxidation at Weybourne Atmospheric Observatory, J. Geophys. Res.-Atmos., 122, 11154–111165, https://doi.org/10.1002/2017jd026624, 2017. 
Bertram, T. H. and Thornton, J. A.: Toward a general parameterization of N2O5 reactivity on aqueous particles: the competing effects of particle liquid water, nitrate and chloride, Atmos. Chem. Phys., 9, 8351–8363, https://doi.org/10.5194/acp-9-8351-2009, 2009. 
Chen, G., Ji, X., Chen, J., Xu, L., Hu, B., Lin, Z., Fan, X., Li, M., Hong, Y., and Chen, J.: Photochemical pollution during summertime in a coastal city of Southeast China: Ozone formation and influencing factors, Atmos. Res., 301, 107270, https://doi.org/10.1016/j.atmosres.2024.107270, 2024. 
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Our study revealed that the nighttime heterogeneous dinitrogen pentoxide (N2O5) uptake process was the major contributor of nitryl chloride (ClNO2) sources, while nitrate photolysis may promote the elevation of daytime ClNO2 concentrations. The rates of alkane oxidation by chlorine (Cl) radical in the early morning exceeded those by OH radical, significantly promoted the formation of ROx and ozone (O3), and further enhanced the atmospheric oxidation capacity levels.
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