The oxidation of methane-based fuels was studied experimentally in a fused silica jet-stirred reactor (JSR) operating at 1–10 atm, over the temperature range 900-1400 K, from fuel-lean to fuel-rich conditions. Similar experiments were performed in presence of carbon dioxide or syngas (CO/H2). A previously proposed kinetic reaction mechanism updated for modeling the oxidation of hydrogen, CO, methane, methanol, formaldehyde, and natural gas over a wide range of conditions including JSR, flame, shock tube, and plug flow reactor was used. A detailed chemical kinetic modeling of the present experiments was performed yielding a good agreement between the data and the modeling. Literature burning velocities and ignition delays were also modeled. Reaction paths analyses were used to delineate the important reactions influencing the kinetic of oxidation of the fuels in presence of variable amounts of CO2. The kinetic reaction scheme proposed helps determining the effect of the additives on the oxidation of methane.
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ASME Turbo Expo 2007: Power for Land, Sea, and Air
May 14–17, 2007
Montreal, Canada
Conference Sponsors:
- International Gas Turbine Institute
ISBN:
0-7918-4790-X
PROCEEDINGS PAPER
Kinetics of Natural Gas, Natural Gas/Syngas Mixtures Oxidation and Effect of Burnt Gas Recirculation: Experimental and Detailed Modeling
Philippe Dagaut
Philippe Dagaut
CNRS, Orle´ans, France
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Tanh Le Cong
CNRS, Orle´ans, France
Philippe Dagaut
CNRS, Orle´ans, France
Paper No:
GT2007-27146, pp. 387-395; 9 pages
Published Online:
March 10, 2009
Citation
Le Cong, T, & Dagaut, P. "Kinetics of Natural Gas, Natural Gas/Syngas Mixtures Oxidation and Effect of Burnt Gas Recirculation: Experimental and Detailed Modeling." Proceedings of the ASME Turbo Expo 2007: Power for Land, Sea, and Air. Volume 1: Turbo Expo 2007. Montreal, Canada. May 14–17, 2007. pp. 387-395. ASME. https://doi.org/10.1115/GT2007-27146
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