EGU24-3795, updated on 08 Mar 2024
https://doi.org/10.5194/egusphere-egu24-3795
EGU General Assembly 2024
© Author(s) 2024. This work is distributed under
the Creative Commons Attribution 4.0 License.

Formation and reaction mechanisms of Criegee intermediates in the atmosphere

Shengrui Tong, Meifang Chen, Shanshan Yu, and Maofa Ge
Shengrui Tong et al.
  • Institute of Chemistry, Chinese Academy of Sciences, Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing, China (tongsr@iccas.ac.cn)

Criegee intermediates (CIs) can be generated by the ozonolysis of alkenes, and few amounts can come from radical-radical reactions. CIs are found to be the important oxidants, and can react with many gases in the atmosphere. The reaction rate of CIs with HCOOH is about 10-10 cm3molcule-1s-1, and the reaction rate of SO2 with CIs is much faster than with OH radical. A Matrix-isolate Vacuum FTIR method was constructed to capture CIs during the reaction of O3 with alkenes. Different kinds of Primary ozonides (POZs), CIs, and Secondary ozonides (SOZs) were detected, and the reaction processes were deduced. Combining of the experimental and quantum chemistry methods, the reactivity of different structure CIs were investigated. The contribution of these CIs to the formation of OH radicals and SOA were further discussed. Fundamental understanding on the structures and reactivity of CIs is crucial to deepen the understanding of Criegee chemistry and its impact on the atmospheric chemistry.

How to cite: Tong, S., Chen, M., Yu, S., and Ge, M.: Formation and reaction mechanisms of Criegee intermediates in the atmosphere, EGU General Assembly 2024, Vienna, Austria, 14–19 Apr 2024, EGU24-3795, https://doi.org/10.5194/egusphere-egu24-3795, 2024.