Research Article
A comprehensive kinetic mechanism for CO, CH2O, and CH3OH combustion
Article first published online: 5 JAN 2007
DOI: 10.1002/kin.20218
Copyright © 2007 Wiley Periodicals, Inc.
Additional Information
How to Cite
Li, J., Zhao, Z., Kazakov, A., Chaos, M., Dryer, F. L. and Scire, J. J. (2007), A comprehensive kinetic mechanism for CO, CH2O, and CH3OH combustion. Int. J. Chem. Kinet., 39: 109–136. doi: 10.1002/kin.20218
Publication History
- Issue published online: 5 JAN 2007
- Article first published online: 5 JAN 2007
- Manuscript Accepted: 3 OCT 2006
- Manuscript Revised: 18 SEP 2006
- Manuscript Received: 27 MAY 2006
Funded by
- Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy. Grant Number: DE-FG02-86ER13503
- Abstract
- Article
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- Cited By
Abstract
New experimental profiles of stable species concentrations are reported for formaldehyde oxidation in a variable pressure flow reactor at initial temperatures of 850–950 K and at constant pressures ranging from 1.5 to 6.0 atm. These data, along with other data published in the literature and a previous comprehensive chemical kinetic model for methanol oxidation, are used to hierarchically develop an updated mechanism for CO/H2O/H2/O2, CH2O, and CH3OH oxidation. Important modifications include recent revisions for the hydrogen–oxygen submechanism (Li et al., Int J Chem Kinet 2004, 36, 565), an updated submechanism for methanol reactions, and kinetic and thermochemical parameter modifications based upon recently published information. New rate constant correlations are recommended for CO + OH = CO2 + H (R23) and HCO + M = H + CO + M (R24), motivated by a new identification of the temperatures over which these rate constants most affect laminar flame speed predictions (Zhao et al., Int J Chem Kinet 2005, 37, 282). The new weighted least-squares fit of literature experimental data for (R23) yields k23 = 2.23 × 105T1.89exp(583/T) cm3/mol/s and reflects significantly lower rate constant values at low and intermediate temperatures in comparison to another recently recommended correlation and theoretical predictions. The weighted least-squares fit of literature results for (R24) yields k24 = 4.75 × 1011T0.66exp(−7485/T) cm3/mol/s, which predicts values within uncertainties of both prior and new (Friedrichs et al., Phys Chem Chem Phys 2002, 4, 5778; DeSain et al., Chem Phys Lett 2001, 347, 79) measurements. Use of either of the data correlations reported in Friedrichs et al. (2002) and DeSain et al. (2001) for this reaction significantly degrades laminar flame speed predictions for oxygenated fuels as well as for other hydrocarbons. The present C1/O2 mechanism compares favorably against a wide range of experimental conditions for laminar premixed flame speed, shock tube ignition delay, and flow reactor species time history data at each level of hierarchical development. Very good agreement of the model predictions with all of the experimental measurements is demonstrated. © 2007 Wiley Periodicals, Inc. 39: 109–136, 2007

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