scholarly journals Effects of radiation on the uncertainty of flame speed determination using spherically propagating flames with CO/CO2/H2O dilutions at elevated pressures

Author(s):  
Chae Hoon Sohn ◽  
Zheng Chen ◽  
Yiguang Ju
Author(s):  
William Lowry ◽  
Jaap de Vries ◽  
Michael Krejci ◽  
Eric Petersen ◽  
Zeynep Serinyel ◽  
...  

Alkanes such as methane, ethane, and propane make up a large portion of most natural gas fuels. Natural gas is the primary fuel used in industrial gas turbines for power generation. Because of this, a fundamental understanding of the physical characteristics such as the laminar flame speed is necessary. Most importantly, this information is needed at elevated pressures to have the most relevance to the gas turbine industry for engine design. This study includes experiments performed at elevated pressures, up to 10 atm initial pressure, and investigates the fuels in a pure form as well as in binary blends. Flame speed modeling was done using an improved version of the kinetics model that the authors have been developing over the past few years. Modeling was performed for a wide range of conditions, including elevated pressures. Experimental conditions include pure methane, pure ethane, 80/20 mixtures of methane/ethane, and 60/40 mixtures of methane/ethane at initial pressures of 1 atm, 5 atm, and 10 atm. Also included in this study are pure propane and 80/20 methane/propane mixtures at 1 atm and 5 atm. The laminar flame speed and Markstein length measurements were obtained from a high-pressure flame speed facility using a constant-volume vessel. The facility includes optical access, a high-speed camera, a schlieren optical setup, a mixing manifold, and an isolated control room. The experiments were performed at room temperature, and the resulting images were analyzed using linear regression. The experimental and modeling results are presented and compared with previously published data. The data herein agree well with the published data. In addition, a hybrid correlation was created to perform a rigorous uncertainty analysis. This correlation gives the total uncertainty of the experiment with respect to the true value rather than reporting the standard deviation of a repeated experiment. Included in the data set are high-pressure results at conditions where in many cases for the single-component fuels few data existed and for the binary blends no data existed prior to this study. Overall, the agreement between the model and data is excellent.


Author(s):  
Michael C. Krejci ◽  
Olivier Mathieu ◽  
Andrew J. Vissotski ◽  
Sankaranarayanan Ravi ◽  
Travis G. Sikes ◽  
...  

Laminar flame speeds and ignition delay times have been measured for hydrogen and various compositions of H2/CO (syngas) at elevated pressures and elevated temperatures. Two constant-volume cylindrical vessels were used to visualize the spherical growth of the flame through the use of a schlieren optical setup to measure the laminar flame speed of the mixture. Hydrogen experiments were performed at initial pressures up to 10 atm and initial temperatures up to 443 K. A syngas composition of 50/50 by volume was chosen to demonstrate the effect of carbon monoxide on H2-O2 chemical kinetics at standard temperature and pressures up to 10 atm. All atmospheric mixtures were diluted with standard air, while all elevated-pressure experiments were diluted with a He:O2 ratio of 7:1 to minimize instabilities. The laminar flame speed measurements of hydrogen and syngas are compared to available literature data over a wide range of equivalence ratios, where good agreement can be seen with several data sets. Additionally, an improved chemical kinetics model is shown for all conditions within the current study. The model and the data presented herein agree well, which demonstrates the continual, improved accuracy of the chemical kinetics model. A high-pressure shock tube was used to measure ignition delay times for several baseline compositions of syngas at three pressures across a wide range of temperatures. The compositions of syngas (H2/CO) by volume presented in this study included 80/20, 50/50, 40/60, 20/80, and 10/90, all of which are compared to previously published ignition delay times from a hydrogen-oxygen mixture to demonstrate the effect of carbon monoxide addition. Generally, an increase in carbon monoxide increases the ignition delay time, but there does seem to be a pressure dependency. At low temperatures and pressures higher than about 12 atm, the ignition delay times appear to be indistinguishable with an increase in carbon monoxide. However, at high temperatures the relative composition of H2 and CO has a strong influence on ignition delay times. Model agreement is good across the range of the study, particularly at the elevated pressures.


Author(s):  
David Beerer ◽  
Vincent McDonell ◽  
Peter Therkelsen ◽  
Robert K. Cheng

This paper reports flashback limits and turbulent flame local displacement speed measurements in flames stabilized by a low swirl injector operated at elevated pressures and inlet temperatures with hydrogen and methane blended fuels. The goal of this study is to understand the physics that relate turbulent flame speed to flashback events at conditions relevant to gas turbine engines. Testing was conducted in an optically accessible single nozzle combustor rig at pressures ranging from 1 to 8 atm, inlet temperatures from 290 to 600 K, and inlet bulk velocities between 20 and 60 m/s for natural gas and a 90%/10% (by volume) hydrogen/methane blend. The propensity of flashback is dependent upon the proximity of the lifted flame to the nozzle that is itself dependent upon pressure, inlet temperature, and bulk velocity. Flashback occurs when the leading edge of the flame in the core of the flow ingresses within the nozzle, even in cases when the flame is attached to the burner rim. In general the adiabatic flame temperature at flashback is proportional to the bulk velocity and inlet temperature and inversely proportional to the pressure. The unburned reactant velocity field approaching the flame was measured using a laser Doppler velocimeter with water seeding. Turbulent displacement flame speeds were found to be linearly proportional to the root mean square of the velocity fluctuations about the mean velocity. For identical inlet conditions, high-hydrogen flames had a turbulent flame local displacement speed roughly twice that of natural gas flames. Pressure, inlet temperature, and flame temperature had surprisingly little effect on the local displacement turbulent flame speed. However, the flow field is affected by changes in inlet conditions and is the link between turbulent flame speed, flame position, and flashback propensity.


Fuel ◽  
2020 ◽  
Vol 266 ◽  
pp. 117061 ◽  
Author(s):  
Shu Zheng ◽  
Wenkai Liang ◽  
Huaqiang Chu ◽  
Huaichun Zhou

Author(s):  
Yash Kochar ◽  
Jerry Seitzman ◽  
Timothy Lieuwen ◽  
Wayne Metcalfe ◽  
Sine´ad Burke ◽  
...  

Laminar flame speeds at elevated pressure for methane-based fuel blends are important for refining the chemical kinetics that are relevant at engine conditions. The present paper builds on earlier measurements and modeling by the authors by extending the validity of a chemical kinetics mechanism to laminar flame speed measurements obtained in mixtures containing significant levels of helium. Such mixtures increase the stability of the experimental flames at elevated pressures and extend the range of laminar flame speeds. Two experimental techniques were utilized, namely a Bunsen burner method and an expanding spherical flame method. Pressures up to 10 atm were studied, and the mixtures ranged from pure methane to binary blends of CH4/C2H6 and CH4/C3H8. In the Bunsen flames, the data include elevated initial temperatures up to 650 K. There is generally good agreement between model and experiment, although some discrepancies still exist with respect to equivalence ratio for certain cases. A significant result of the present study is that the effect of mixture composition on flame speed is well captured by the mechanism over the extreme ranges of initial pressure and temperature covered herein. Similarly, the mechanism does an excellent job at modeling the effect of initial temperature for methane-based mixtures up to at least 650 K.


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