
Journal of the Chemical Society - Faraday Transactions p. 2983 - 2991 (1993)
Update date:2022-08-11
Topics:
Jenkin, Michael E.
Cox, Richard A.
Emrich, Martin
Moortgat, Geert K.
The products of the Cl-atom-initiated oxidation of acetone and hydroxyacetone (CH3COCH2OH) in O2-N2 mixtures at 700 Torr and 298 K have been identified using long-path-length FTIR spectroscopy and long-path-length UV-visible diode array spectroscopy.The oxidation of acetone yields methyl glyoxal (CH3COCHO), HCHO, CO, CO2, CH3COOH, CH3OH, HCOOH and O3 as identifiable products.The data have been analysed, utilising the results of a kinetic study of the oxidation of acetone in air.The mechanism of the oxidation proceeds initially via the production of acetonylperoxy radicals (CH3COCH2O2) which are removed by their self-reaction (3), and reaction with other peroxy radicals a yield of (100 +/- 5)percent by the following reaction sequence: Cl + CH3COCH2OH --> HCl + CH3COCHOH (4), CH3COCHOH + O2 --> CH3COCHO + HO2 (5).The concentration-time dependence of a range of secondary organic products, formed in the system was also measured.Identifiable products are CO, CO2, CH3COOH, HCHO, CH3OH, HCOOH and pyruvic acid (CH3COCOOH).These results are consistent with the presence of the CH3COCH(OH)O2 radical, formed as an intermediate in reaction (5): CH3COCH(OH)O2 <--> CH3COCHO +HO2 (5 ).
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