Experimental Study on Laminar Flame Speeds and Markstein Length of Methane-Air Mixtures at Atmospheric Conditions

2014 ◽  
Vol 699 ◽  
pp. 714-719
Author(s):  
Alaeldeen Altag Yousif ◽  
Shaharin Anwar Sulaiman

Accurate value of laminar flame speed is an important parameter of combustible mixtures. In this respect, experimental data are very useful for modeling improvement and validating chemical kinetic mechanisms. To achieve this, an experimental characterization on spherically expanding flames propagation of methane-air mixtures were carried out. Tests were conducted in constant volume cylindrical combustion chamber to measure stretched, unstretched laminar flame speed, laminar burning velocity, and flame stretch effect as quantified by the associated Markstein lengths. The mixtures of methane-air were ignited at extensive ranges of lean-to-rich equivalence ratios, under ambient pressure and temperature. This is achieved by high speed schlieren cine-photography for flames observation in the vessel. The results showed that the unstretched laminar burning velocity increased and the peak value of the unstretched laminar burning velocity shifted to the richer mixture side with the increase of equivalence ratio. The flame propagation speed showed different trends at different equivalence ratio for tested mixtures. It was found that the Markstein length was increased with the increase of equivalence ratio.

Author(s):  
Sebastian Verhelst ◽  
Roger Sierens

During the development of a quasi-dimensional simulation programme for the combustion of hydrogen in spark-ignition engines, the lack of a suitable laminar flame speed formula for hydrogen/air mixtures became apparent. A literature survey shows that none of the existing correlations covers the entire temperature, pressure and mixture composition range as encountered in spark-ignition engines. Moreover, there is ambiguity concerning the pressure dependence of the laminar burning velocity of hydrogen/air mixtures. Finally, no data exists on the influence of residual gases. This paper looks at several reaction mechanisms found in the literature for the kinetics of hydrogen/oxygen mixtures, after which one is selected that corresponds best with available experimental data. An extensive set of simulations with a one-dimensional chemical kinetics code is performed to calculate the laminar flame speed of hydrogen/air mixtures, in a wide range of mixture compositions and initial pressures and temperatures. The use of a chemical kinetics code permits the calculation of any desired set of conditions and enables the estimation of interactions, e.g. between pressure and temperature effects. Finally, a laminar burning velocity correlation is presented, valid for air-to-fuel equivalence ratios λ between 1 and 3 (fuel-to-air equivalence ratio 0.33 < φ < 1), initial pressures between 1 bar and 16 bar, initial temperatures between 300 K and 800 K and residual gas fractions up to 30 vol%. These conditions are sufficient to cover the entire operating range of hydrogen fuelled spark-ignition engines.


Author(s):  
Charles L. Keesee ◽  
Bing Guo ◽  
Eric L. Petersen

Abstract New laminar flame speed experiments have been collected for multiple alternative liquid fuels. Understanding the combustion characteristics of these synthetic fuels is an important step in developing new chemical kinetics mechanisms that can be applied to real fuels. Included in this study are two synthetic Jet fuels: Syntroleum S-8 and Shell GTL. The precise composition of these fuels is known to change from sample to sample. Since these are low vapor pressure fuels, there are additional uncertainties in their introduction into gas-phase mixtures, leading to uncertainty in the mixture equivalence ratio. An in-situ laser absorption technique was implemented to verify the procedure for filling the vessel and to minimize and quantify the uncertainty in the experimental equivalence ratio. The diagnostic utilized a 3.39-μm HeNe laser in conjunction with Beer’s Law. The resulting spherically expanding flame experiments were conducted over a range of equivalence ratios from φ = 0.7 to φ = 1.5 at initial conditions of 1 atm and 403 K in the high-temperature, high-pressure constant-volume vessel at Texas A&M University. The experimental results show that both fuels have similar flame speeds with a peak value just under 60 cm/s. However, it is shown that when comparing the results from different data sets for these real fuels, equivalence ratio is not necessarily the best parameter to use. Fuel mole fraction may be a better parameter to use as it is independent of the average fuel molecule or fuel surrogate used to calculate equivalence ratio in these real fuel/air mixtures.


Author(s):  
Sandra Richter ◽  
Jörn Ermel ◽  
Thomas Kick ◽  
Marina Braun-Unkhoff ◽  
Clemens Naumann ◽  
...  

Currently, new concepts for power generation are discussed, as a response to combat global warming due to CO2 emissions stemming from the combustion of fossil fuels. These concepts include new, low-carbon fuels as well as centralized and decentralized solutions. Thus, a more diverse range of fuel supplies will be used, with (biogenic) low-caloric gases such as syngas and coke oven gas (COG) among them. Typical for theses low-caloric gases is the amount of hydrogen, with a share of 50% and even higher. However, hydrogen mixtures have a higher reactivity than natural gas (NG) mixtures, burned mostly in today's gas turbine combustors. Therefore, in the present work, a combined experimental and modeling study of nitrogen-enriched hydrogen–air mixtures, some of them with a share of methane, to be representative for COG, will be discussed focusing on laminar flame speed data as one of the major combustion properties. Measurements were performed in a burner test rig at ambient pressure and at a preheat temperature T0 of 373 K. Flames were stabilized at fuel–air ratios between about φ = 0.5–2.0 depending on the specific fuel–air mixture. This database was used for the validation of four chemical kinetic reaction models, including an in-house one, and by referring to hydrogen-enriched NG mixtures. The measured laminar flame speed data of nitrogen-enriched methane–hydrogen–air mixtures are much smaller than the ones of nitrogen-enriched hydrogen–air mixtures. The grade of agreement between measured and predicted data depends on the type of flames and the type of reaction model as well as of the fuel–air ratio: a good agreement was found in the fuel lean and slightly fuel-rich regime; a large underprediction of the measured data exists at very fuel-rich ratios (φ > 1.4). From the results of the present work, it is obvious that further investigations should focus on highly nitrogen-enriched methane–air mixtures, in particular for very high fuel–air ratio (φ > 1.4). This knowledge will contribute to a more efficient and a more reliable use of low-caloric gases for power generation.


Author(s):  
A. N. Mazas ◽  
D. A. Lacoste ◽  
T. Schuller

The effects of CO2 and H2O addition on premixed oxy-fuel combustion are investigated with experiments and numerical simulations on the laminar flame speed of CH4/O2/CO2/H2O(v) and CH4/O2/N2/H2O(v) mixtures, at atmospheric pressure and for a reactants inlet temperature Tu = 373 K. Experiments are conducted with steady laminar conical premixed flames over a range of operating conditions representative of oxy-fuel combustion with flue gas recirculation. The relative O2-to-CO2 and O2-to-N2 ratios, respectively defined as O2/(O2+CO2) (mol.) and O2/(O2+N2) (mol.), are varied from 0.21 to 1.0. The equivalence ratio of the mixtures ranges from 0.5 to 1.5, and the steam molar fraction in the reactive mixture is varied from 0 to 0.45. Laminar flame speeds are measured with the flame area method using a Schlieren apparatus. Experiments are completed by simulations with the PREMIX code using the detailed kinetic mechanism GRI-mech. 3.0. Numerical predictions are found in good agreement with experimental data for all cases explored. It is also shown that the laminar flame speed of CH4/O2/N2 mixtures diluted with steam H2O(v) features a quasi-linear decrease when increasing the diluent molar fraction, even at high dilution rates. Effects of N2 replacement by CO2 in wet reactive mixtures are then investigated. A similar quasi-linear decrease of the flame speed is observed for CH4/O2/CO2 H2O-diluted flames. For a similar flame speed in dry conditions, results show a larger reduction of the burning velocity for CH4/O2/N2/H2O mixtures than for CH4/O2/CO2/H2O mixtures, when the steam molar fraction is increased. Finally, it is observed that the laminar flame speed of weakly (CO2, H2O)-diluted CH4/O2 mixtures is underestimated by the GRI-mech 3.0 predictions.


2012 ◽  
Vol 4 (5) ◽  
pp. 75-83 ◽  
Author(s):  
Juan-Sebastián Gómez-Meyer ◽  
Subramanyam R Gollahalli ◽  
Ramkumar N. Parthasarathy ◽  
Jabid-Eduardo Quiroga

In this article, the flame speed values determined experimentally for laminar premixed flames of the vapors of two biofuels in air are presented. The laminar flame speed is a fundamental thermochemical property of fuels, and is essential for analyzing the flame propagation in practical devices, even those employing turbulent flames. The fuels obtained from transesterification of soy and canola oils are tested. Also, the diesel flames are studied to serve as a baseline for comparison. The experiments are performed with a tubular burner; pre-vaporized fuel is mixed with hot air and is ignited. The flame speed is determined at fuel-equivalence ratios of 1; 1,1 and 1,2 by recording the geometry of the flame. The experimental results show that the flame speed of biofuels is lower by about 15% than that of diesel. Also, the maximum value of flame speed is obtained at an equivalence ratio of approximately 1,1.


2019 ◽  
Vol 142 (1) ◽  
Author(s):  
Charles L. Keesee ◽  
Bing Guo ◽  
Eric L. Petersen

Abstract New laminar flame speed experiments have been collected for two alternative liquid fuels. Understanding the combustion characteristics of these synthetic fuels is an important step in developing new chemical kinetics mechanisms that can be applied to real fuels. Included in this study are two synthetic Jet fuels: Syntroleum S-8 and Shell GTL. The precise composition of these fuels is known to change from sample to sample. Since these are low-vapor pressure fuels, there are additional uncertainties in their introduction into gas-phase mixtures, leading to uncertainty in the mixture equivalence ratio. An in-situ laser absorption technique was implemented to verify the procedure for filling the vessel and to minimize and quantify the uncertainty in the experimental equivalence ratio. The diagnostic utilized a 3.39-μm HeNe laser in conjunction with Beer's law. The resulting spherically expanding, laminar flame experiments were conducted over a range of equivalence ratios from φ = 0.7 to φ = 1.5 at initial conditions of 1 atm and 403 K in the high-temperature, high-pressure (HTHP) constant-volume vessel at Texas A&M University. The experimental results show that both fuels have similar flame speeds with a peak value just under 60 cm/s. However, it is shown that when comparing the results from different datasets for these real fuels, equivalence ratio may not be the best parameter to use. Fuel mole fraction may be a better parameter to use as it is independent of the average fuel molecule or fuel surrogate used to calculate equivalence ratio in these real fuel/air mixtures.


Author(s):  
Mattias A. Turner ◽  
Tyler Paschal ◽  
Waruna D. Kulatilaka ◽  
Eric L. Petersen

Abstract The push for lower carbon emissions in power generation has driven interest in methods of carbon capture and sequestration. One such promising method involves the supercritical CO2 (sCO2) power cycle, a system which is powered by oxy-fuel combustion where supercritical carbon dioxide is used as the working fluid. The high CO2 concentration in the combustion products allows for relatively simple extraction of CO2 from the system. Although this is an active field of research, the design of such a combustor requires continued study of oxy-fuel combustion in high levels of CO2 diluent. With that objective in mind, laminar flame experiments were conducted for CH4-O2-CO2 mixtures at one atmosphere and room temperature, where the relative concentrations of O2 and CO2 in the oxidizer mixture were 34.0% and 66.0% by mole, respectively. These concentrations were chosen to ensure the flame would propagate quickly enough to overcome the effects of buoyancy, which were observed to become significant below laminar flame speeds of roughly 15 cm/s. A high-speed chemiluminescence imaging diagnostic was employed in place of the traditional schlieren technique. Laminar flame speed was measured from OH* emission at 306 nm for a full range of equivalence ratios, varying from 15.2 cm/s at 0.7 to 24.8 cm/s at stoichiometric. Additionally, images of OH* chemiluminescence of turbulent CH4-O2-CO2 flames and of quiescent, 5-atm CH4-O2-CO2 flames at stoichiometric concentration are also presented. These experiments provide useful data for validation of chemical kinetics models for oxy-methane combustion in a CO2 diluent, which can be applied to the modeling of oxy-methane combustion for supercritical CO2 power cycles.


2020 ◽  
Vol 214 ◽  
pp. 464-474 ◽  
Author(s):  
Hee J. Kim ◽  
Kyuho Van ◽  
Dae K. Lee ◽  
Chun S. Yoo ◽  
Jeong Park ◽  
...  

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