Study of Extinction Limits of Diluted Hydrogen-Air Counter-Flow Diffusion Flames with the Redim Method

2014 ◽  
Vol 186 (10-11) ◽  
pp. 1502-1516 ◽  
Author(s):  
A. Neagos ◽  
V. Bykov ◽  
U. Maas
2021 ◽  
Vol 46 ◽  
pp. 101263
Author(s):  
Shahin Akbari ◽  
Moein Farmahini Farahani ◽  
Sadegh Sadeghi ◽  
Masoud Hajivand ◽  
Fei Xu ◽  
...  

2017 ◽  
Vol 42 (49) ◽  
pp. 29532-29544 ◽  
Author(s):  
Khadidja Safer ◽  
Ahmed Ouadha ◽  
Fouzi Tabet

2018 ◽  
Vol 22 (Suppl. 2) ◽  
pp. 769-776
Author(s):  
Fei Ren ◽  
Longkai Xiang ◽  
Huaqiang Chu ◽  
Weiwei Han

The reduction of nitrogen oxides in the high temperature flame is the key factor affecting the oxygen-enriched combustion performance. A numerical study using an OPPDIF code with detailed chemistry mechanism GRI 3.0 was carried out to focus on the effect of strain rate (25-130 s?1) and CO2 addition (0-0.59) on the oxidizer side on NO emission in CH4 / N2 / O2 counter-flow diffusion flame. The mole fraction profiles of flame structures, NO, NO2 and some selected radicals (H, O, OH) and the sensitivity of the dominant reactions contributing to NO formation in the counter-flow diffusion flames of CH4\/ N2 /O2 and CH4 / N2 / O2 / CO2 were obtained. The results indicated that the flame temperature and the amount of NO were reduced while the sensitivity of reactions to the prompt NO formation was gradually increased with the increasing strain rate. Furthermore, it is shown that with the increasing CO2 concentration in oxidizer, CO2 was directly involved in the reaction of NO consumption. The flame temperature and NO production were decreased dramatically and the mechanism of NO production was transformed from the thermal to prompt route.


2015 ◽  
Vol 40 (33) ◽  
pp. 10662-10672 ◽  
Author(s):  
Aman Satija ◽  
Xianan Huang ◽  
Pratikash P. Panda ◽  
Robert P. Lucht

It is shown that the establishment of a large flat diffusion flame in the counter-flow régime of opposed jets of two gaseous reactants could very considerably extend the range of applicability of flame-kinetics studies by structure analysis. Suitable flames are stabilized and their characteristics and behaviour described. The flow patterns, spectrum , refractive index fields, temperature distributions and gas composition at a few selected points are studied for ethylene flames by methods including the use of thermocouples, sodium line reversal, illuminated particle tracks, interferometry and gas chromatography. The aerodynamic and thermal structures are analyzed to yield the distribution of the rate of heat release per unit volume. The following are among the conclusions: two stagnation points and two planes which particles cannot cross occur when the centres of the reaction and aerodynamic systems are made to coincide—this can be prevented by displacing the plane of stoichiometry from that of aerodynamic symmetry; the radial component of flow velocity is proportional to radial distance in the central parts. Isotherms are parallel to each other and to the flame, away from the edges, but maximum temperatures occur at the periphery, at least for some flames. The heat release profile shows regions where small amounts of heat are absorbed; C 2 H 6 and H 2 appear on the oxidant side of the flame. The most significant observation is that the zone of heat release is about ten times wider than would be expected of the equivalent pre-mixed flame and this makes the method applicable to the study of faster flame reactions.


Author(s):  
A. G. Kyne ◽  
M. Pourkashanian ◽  
C. W. Wilson ◽  
A. Williams

As emission regulations become more stringent there is increasing interest in the formation of NO2 in combustion products where it is in higher concentration than if slowly formed from NO in the atmosphere. It is common knowledge that NO2 is significantly more toxic than NO. The chemistry of NO2 formation in combustion processes is simple in comparison to that of NO. Indeed, all NO2 is formed from oxidation of NO mainly by reaction with HO2 radicals with its conversion back to NO resulting from reactions involving O and H atoms. Since consumption and formation of NO2 always occur simultaneously, although with unbalanced kinetic rates leading to local super-equilibrium concentrations, parameters such as temperature, velocity and species concentrations fields can drastically affect the degree of conversion of NO to NO2 in combustion applications. It is not well known what these conditions are and in certain circumstances, such as aircraft engine reheat systems, the emission of NO2 is clearly visible under the form of brown fumes. A comprehensive numerical simulation was undertaken to investigate the NO-NO2 relationship in a counter-flow diffusion flame. The CHEMKIN II suite of software (Kee et al., 1989) in conjunction with the opposed diffusion flame code OPPDIF (Lutz et al, 1997) was run using the Gas Research Institute’s (GRI’s) methane reaction mechanism v.3.0. A number of different strain rates using boundary conditions typical in a gas turbine exhaust were investigated. A rate of production and sensitivity analysis was made in determining which reactions were important in the NO-NO2 conversion process.


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