4.6 Article

Quantitative Kinetics of the Reaction between CH2OO and H2O2 in the Atmosphere

期刊

JOURNAL OF PHYSICAL CHEMISTRY A
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.2c04408

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资金

  1. National Natural Science Foundation of China [42120104007, 41775125, 91961123]
  2. Science and Technology Foundation of Guizhou Province, China [[2019] 5648]
  3. Science and Technology Foundation of Guizhou Provincial Department of Q4 Education, China [[2021] 014]

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This study investigates the mechanism and quantitative kinetics of the CH2OO + H2O2 reaction, showing that the rate constant of the reaction changes with temperature and can impact the distribution of H2O2 under certain atmospheric conditions.
Criegee intermediates (CIs) are generated from the ozonolysis of unsaturated hydrocarbons in the atmosphere. They have an important role in determining the implications of atmospheric bimolecular reactions with other atmospheric species. The reaction between CH2OO and H2O2 plays a crucial role in understanding how CIs impact the HOx budget in the atmosphere. The reaction mechanism and kinetics are critical to atmospheric modeling, which is a prominent challenge in present-day climate change modeling. This is particularly true for bimolecular reactions that involve complex reaction sequences. Here, we report the mechanism and quantitative kinetics of the CH2OO + H2O2 reaction by using a novel dual-level strategy that contains W3X-L//CCSD(T)-F12a/cc-pVTZ-F12 for the transition state theory and M11-L/MG3S functional method for direct dynamics calculations using canonical variational transition state theory with small-curvature tunneling to obtain both recrossing effects and tunneling. The present work shows that the CH2OO + H2O2 reaction has a negative temperature dependency with the decrease in the rate constant of CH2OO + H2O2 from 1.31 x 10-13 cm3 molecule-1 s-1 to 3.80 x 10(-14) cm3 molecule-1 s-1 between 200 and 350 K. The calculated results also show that the CH2OO + H2O2 reaction can have an impact on the H2O2 profile under certain atmospheric conditions. The present findings should have implications for the quantitative kinetics of Criegee intermediates with other hydroperoxides.

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