Glyoxal Oxidation Mechanism: Implications for the Reactions HCO + O-2 and OCHCHO + HO2.

Fassheber, Nancy, Friedrichs, Gernot, Marshall, Paul and Glarborg, Peter (2015) Glyoxal Oxidation Mechanism: Implications for the Reactions HCO + O-2 and OCHCHO + HO2. Journal of Physical Chemistry A, 119 (28). pp. 7305-7315. DOI 10.1021/jp512432q.

Full text not available from this repository.

Supplementary data:

Abstract

A detailed mechanism for the thermal decomposition and oxidation of the flame intermediate glyoxal (OCHCHO), has been assembled from available theoretical and experimental literature data. The modeling capabilities of this extensive mechanism have been tested by simulating experimental HCO profiles measured at intermediate and high temperatures in previous glyoxal photolysis and pyrolysis studies. Additionally, new experiments on glyoxal pyrolysis and oxidation have been performed with glyoxal and glyoxal/oxygen mixtures in Ar behind shock waves at temperatures of 1285-1760 K at two different total density ranges. HCO concentration time profiles have been detected by frequency modulation spectroscopy at a wavelength of lambda = 614.752 urn. The temperature range of available direct rate constant data of the high-temperature key reaction HCO + 02 -> CO + HO2 has been extended up to 1705 K and confirms a temperature dependence consistent with a dominating direct abstraction channel. Taking into account available literature data obtained at lower temperatures, the following rate constant expression is recommended over the temperature range 295 K < T < 1705 K: k(1)/(cm(3) mol(-1) s(-1)) = 6.92 X 106 X T-1.09 X exp(+5.73 kJ/mol/RT). At intermediate temperatures, the reaction OCHCHO + HO2 becomes more important. A detailed reanalysis of previous experimental data as well as more recent theoretical predictions favor the formation of a recombination product in contrast to the formerly assumed dominating and fast OH-forming channel. Modeling results of the present study support the formation of HOCH(OO)CHO and provide a 2 orders of magnitude lower rate constant estimate for the OH channel. Hence, low-temperature generation of chain carriers has to be attributed to secondary reactions of HOCH(OO)CHO.

Document Type: Article
Additional Information: Times Cited: 0
Research affiliation: Kiel University > Kiel Marine Science
OceanRep > The Future Ocean - Cluster of Excellence
Kiel University
Refereed: Yes
Open Access Journal?: No
DOI etc.: 10.1021/jp512432q
ISSN: 1089-5639
Projects: Future Ocean
Date Deposited: 20 Oct 2016 10:53
Last Modified: 22 Aug 2019 12:35
URI: http://oceanrep.geomar.de/id/eprint/32468

Actions (login required)

View Item View Item