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

被引:711
作者
Li, Juan
Zhao, Zhenwei
Kazakov, Andrei
Chaos, Marcos
Dryer, Frederick L. [1 ]
Scire, James J., Jr.
机构
[1] Princeton Univ, Dept Mech & Aerosp Engn, Princeton, NJ 08544 USA
[2] Adv Fuel Res Inc, E Hartford, CT 06108 USA
关键词
D O I
10.1002/kin.20218
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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/H-2/O-2, CH2O, and CH3OH oxidation. Important modifications include recent revisions for the hydrogen-oxygen submechanism (Li et al., Int I 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 Hame speed predictions (Zhao et al., Int I Chem Kinet 2005, 37, 282). The new weighted least-squares fit of literature experimental data for (R23) yields k(23) = 2.23 X 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 x 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. (c) 2007 Wiley Periodicals, Inc.
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页码:109 / 136
页数:28
相关论文
共 136 条
[81]   Rate constants for H+O2+M→HO2+M in seven bath gases [J].
Michael, JV ;
Su, MC ;
Sutherland, JW ;
Carroll, JJ ;
Wagner, AF .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (21) :5297-5313
[82]   CHEMICAL-KINETICS AND COMBUSTION MODELING [J].
MILLER, JA ;
KEE, RJ ;
WESTBROOK, CK .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 :345-387
[83]   Significance of the HO2+CO reaction during the combustion of CO+H2 mixtures at high pressures [J].
Mittal, G. ;
Sung, C. J. ;
Fairweather, M. ;
Tomlin, A. S. ;
Griffiths, J. F. ;
Hughes, K. J. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2007, 31 (419-427) :419-427
[84]  
MITTAL G, IN PRESS COMBUST SCI
[85]   Autoignition of H2/CO at elevated pressures in a rapid compression machine [J].
Mittal, Gaurav ;
Sung, Chih-Jen ;
Yetter, Richard A. .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2006, 38 (08) :516-529
[86]  
Mueller M.A., 2000, THESIS PRINCETON U P
[87]  
Mueller MA, 1999, INT J CHEM KINET, V31, P113
[88]  
Mueller MA, 1999, INT J CHEM KINET, V31, P705, DOI 10.1002/(SICI)1097-4601(1999)31:10<705::AID-JCK4>3.0.CO
[89]  
2-#
[90]  
Mueller MA, 2000, INT J CHEM KINET, V32, P317, DOI 10.1002/(SICI)1097-4601(2000)32:6<317::AID-KIN1>3.0.CO