Flow reactor studies and kinetic modeling of the H2/O2 reaction

Author(s):  
M. A. Mueller ◽  
T. J. Kim ◽  
R. A. Yetter ◽  
F. L. Dryer
Fuel ◽  
2019 ◽  
Vol 236 ◽  
pp. 437-444 ◽  
Author(s):  
Meirong Zeng ◽  
Yuyang Li ◽  
Wenhao Yuan ◽  
Yan Zhang ◽  
Jiuzhong Yang ◽  
...  

1992 ◽  
Vol 6 (2) ◽  
pp. 189-194 ◽  
Author(s):  
Corinne Bales-Gueret ◽  
Michel Cathonnet ◽  
Jean Claude Boettner ◽  
Francoise Gaillard

Fuel ◽  
2011 ◽  
Vol 90 (11) ◽  
pp. 3237-3253 ◽  
Author(s):  
H. Bennadji ◽  
P.A. Glaude ◽  
L. Coniglio ◽  
F. Billaud

2009 ◽  
Vol 26 (3) ◽  
pp. 840-844
Author(s):  
Shaozeng Sun ◽  
Huali Cao ◽  
Zhiqiang Wang ◽  
Lin Qian ◽  
Yukun Qin

2019 ◽  
Vol 37 (1) ◽  
pp. 727-734 ◽  
Author(s):  
J.M. Colom-Díaz ◽  
M. Abián ◽  
M.Y. Ballester ◽  
Á. Millera ◽  
R. Bilbao ◽  
...  

Author(s):  
T. Le Cong ◽  
P. Dagaut ◽  
G. Dayma

The oxidation of methane-based fuels was studied experimentally in a fused-silica jet-stirred reactor (JSR) operating at 1–10atm, over the temperature range of 900–1450K, from fuel-lean to fuel-rich conditions. Similar experiments were performed in the 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 modeling, the present data and literature burning velocities, and ignition data. Reaction path analyses were used to delineate the important reactions influencing the kinetic of oxidation of the fuels in the presence of variable amounts of CO2. The kinetic reaction scheme proposed helps understand the effect of the additives on the oxidation of methane.


Sign in / Sign up

Export Citation Format

Share Document