Journal
ACS EARTH AND SPACE CHEMISTRY
Volume 3, Issue 10, Pages 2363-2371Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsearthspacechem.9b00213
Keywords
Criegee intermediates; acetone; atmospheric chemistry; global modelling; reaction rates
Funding
- Natural Environment Research Council (NERC) [NE/K004905/1, NE/P013104/1]
- National Aeronautics and Space Administration (NASA)
- Upper Atmosphere Research and Tropospheric Chemistry program
- NERC [NE/I014381/1, NE/P013104/1, NE/J009008/1, NE/K004905/1] Funding Source: UKRI
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Mounting evidence suggests that Criegee intermediates are important tropospheric oxidants of both organic and inorganic gases, supplementing the oxidation chemistry initiated by OH radicals. Here, the rate coefficient for the reaction of the simplest Criegee intermediate CH2OO with acetone, k(CH2OO + (CH3)(2)CO), was measured using laser flash photolysis and cavity ring-down spectroscopy methods under tropospherically relevant conditions of pressure and temperature. The pressure dependence of k(CH2OO + (CH3)(2)CO) = (4.7 +/- 0.1) x 10(-13) [N-2]/((3.7 +/- 1.4) x 10(16) + [N-2]) cm(3) molecule(-1) s(-1) was measured in the 5-100 Torr range, returning a high-pressure limit value of (4.7 +/- 0.1) x 10(-13) cm(3) molecule(-1) s(-1) at 293 K. A temperature dependence of k(CH2OO + (CH3)(2)CO) = (1.4 +/- 0.2) x 10(-21) T-2 exp(2421 +/- 40/T) cm(3) molecule(-1) s(-1) was observed in the 250-310 K range. The global chemical transport model (STOCHEM-CRI) was used to model the speciated Criegee intermediate field using the recently reported temperature-dependent rate coefficient values for various reactions of Criegee intermediates. The incorporation of the Criegee intermediate reaction with acetone in the model predicts decreases in acetone concentration of as much as 10-40 ppt in various regions of the world.
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