A comprehensive kinetic mechanism for CO, CH2O, and CH3OH combustion

化学 动能 反应速率常数 燃烧 层流 甲醇 甲醛 热力学 氧气 物理化学 分析化学(期刊) 动力学 有机化学 物理 量子力学
作者
Juan Li,Zhenwei Zhao,Andrei F. Kazakov,Marcos Chaos,Frederick L. Dryer,James J. Scire
出处
期刊:International Journal of Chemical Kinetics [Wiley]
卷期号:39 (3): 109-136 被引量:817
标识
DOI:10.1002/kin.20218
摘要

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/H 2 O/H 2 /O 2 , CH 2 O, and CH 3 OH 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 = CO 2 + 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 k 23 = 2.23 × 10 5 T 1.89 exp(583/ T ) cm 3 /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 k 24 = 4.75 × 10 11 T 0.66 exp(−7485/ T ) cm 3 /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 C 1 /O 2 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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