Laminar Flame Speed Measurements of Kerosene-Based Fuels Accounting for Uncertainties in Mixture Average Molecular Weight

2021 ◽  
Author(s):  
Charles Keesee ◽  
Bing Guo ◽  
Eric Petersen
Keyword(s):  
Molecular Weight ◽  
Laminar Flame ◽  
Average Molecular Weight ◽  
Flame Speed ◽  
Laminar Flame Speed

Laminar Flame Speed Measurements of Kerosene-Based Fuels Accounting for Uncertainties in Mixture Average Molecular Weight

2020 ◽  
Author(s):  
Charles L. Keesee ◽  
Bing Guo ◽  
Eric L. Petersen
Keyword(s):  
Molecular Weight ◽  
Equivalence Ratio ◽  
Laminar Flame ◽  
Initial Conditions ◽  
Average Molecular Weight ◽  
Flame Speed ◽  
Liquid Fuels ◽  
Laminar Flame Speed ◽  
Noticeable Effect ◽  
Data Points

Abstract New laminar flame speed experiments have been collected for some kerosene-based liquid fuels: Jet-A, RP-1, and Diesel Fuel #2. Accurately understanding the combustion characteristics of these, and all kerosene-based fuels in general, is an important step in developing new chemical kinetics mechanisms that can be applied to these fuels. It is well known that the precise composition of these fuels changes from one production batch to the next, leading to significant uncertainty in the mixture average properties. For example, uncertainty in a fuel blend’s molecular weight can have a noticeable effect on defining an equivalence ratio for a typical fuel-air mixture, on the order of 15%. Because of these uncertainties, fuel mole fraction, Xfuel, is shown to be a more appropriate parameter for comparison between different batches of fuel. Additionally, a strong linear correlation was detected between the burned-gas Markstein length and the equivalence ratio. This correlation is shown to be useful in determining the acceptability and accuracy of individual data points. Spherically expanding flames were measured over a range of fuel mole fractions corresponding to equivalence ratios of 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. These new results are compared with the limited set of laminar flame speed data currently available in the literature for this fuel.

Laminar Flame Speed Measurements of Kerosene-Based Fuels Accounting for Uncertainties in Mixture Average Molecular Weight

2021 ◽  
Vol 143 (4) ◽  
Author(s):  
Charles L. Keesee ◽  
Bing Guo ◽  
Eric L. Petersen
Keyword(s):  
Molecular Weight ◽  
Equivalence Ratio ◽  
Laminar Flame ◽  
Initial Conditions ◽  
Average Molecular Weight ◽  
Flame Speed ◽  
Liquid Fuels ◽  
Laminar Flame Speed ◽  
Noticeable Effect ◽  
Data Points

Abstract New laminar flame speed experiments have been collected for some kerosene-based liquid fuels: Jet-A, RP-1, and diesel fuel #2. Accurately understanding the combustion characteristics of these, and all kerosene-based fuels in general, is an important step in developing new chemical kinetics mechanisms that can be applied to these fuels. It is well known that the precise composition of these fuels changes from one production batch to the next, leading to significant uncertainty in the mixture average properties. For example, uncertainty in a fuel blend's molecular weight can have a noticeable effect on defining an equivalence ratio for a typical fuel–air mixture, of the order of 15%. Because of these uncertainties, fuel mole fraction, XFUEL, is shown to be a more appropriate parameter for comparison between different batches of fuel. Additionally, a strong linear correlation was detected between the burned-gas Markstein length and the equivalence ratio. This correlation is shown to be useful in determining the acceptability and accuracy of individual data points. Spherically expanding flames were measured over a range of fuel mole fractions corresponding to equivalence ratios of 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. These new results are compared with the limited set of laminar flame speed data currently available in the literature for this fuel.

A Numerical Study on the Reactivity of Biogas/Reformed-Gas/Air and Methane/Reformed-Gas/Air Mixtures at Gas Turbine Relevant Conditions

2016 ◽  
Author(s):  
Pablo Diaz Gomez Maqueo ◽  
Philippe Versailles ◽  
Gilles Bourque ◽  
Jeffrey M. Bergthorson
Keyword(s):  
Gas Turbine ◽  
Laminar Flame ◽  
Numerical Study ◽  
Flame Temperature ◽  
Flame Speed ◽  
Flame Stability ◽  
Laminar Flame Speed ◽  
Fuel Reforming ◽  
Numerical Work ◽  
Chemical Effects

This study investigates the increase in methane and biogas flame reactivity enabled by the addition of syngas produced through fuel reforming. To isolate thermodynamic and chemical effects on the reactivity of the mixture, the burner simulations are performed with a constant adiabatic flame temperature of 1800 K. Compositions and temperatures are calculated with the chemical equilibrium solver of CANTERA® and the reactivity of the mixture is quantified using the adiabatic, freely-propagating premixed flame, and perfectly-stirred reactors of the CHEMKIN-Pro® software package. The results show that the produced syngas has a content of up to 30 % H2 with a temperature up to 950 K. When added to the fuel, it increases the laminar flame speed while maintaining a burning temperature of 1800 K. Even when cooled to 300 K, the laminar flame speed increases up to 30 % from the baseline of pure biogas. Hence, a system can be developed that controls and improves biogas flame stability under low reactivity conditions by varying the fraction of added syngas to the mixture. This motivates future experimental work on reforming technologies coupled with gas turbine exhausts to validate this numerical work.

An experimental and reduced modeling study of the laminar flame speed of jet fuel surrogate components

Fuel ◽  
2013 ◽  
Vol 113 ◽  
pp. 586-597 ◽  
Author(s):  
J.D. Munzar ◽  
B. Akih-Kumgeh ◽  
B.M. Denman ◽  
A. Zia ◽  
J.M. Bergthorson
Keyword(s):  
Laminar Flame ◽  
Jet Fuel ◽  
Flame Speed ◽  
Laminar Flame Speed ◽  
Reduced Modeling ◽  
Fuel Surrogate ◽  
Modeling Study

Laminar flame speed measurements of dimethyl ether in air at pressures up to 10atm

Fuel ◽  
2011 ◽  
Vol 90 (1) ◽  
pp. 331-338 ◽  
Author(s):  
Jaap de Vries ◽  
William B. Lowry ◽  
Zeynep Serinyel ◽  
Henry J. Curran ◽  
Eric L. Petersen
Keyword(s):  
Dimethyl Ether ◽  
Laminar Flame ◽  
Flame Speed ◽  
Laminar Flame Speed

Laminar flame speed correlations for methane, ethane, propane and their mixtures, and natural gas and gasoline for spark-ignition engine simulations

2017 ◽  
Vol 18 (9) ◽  
pp. 951-970 ◽  
Author(s):  
Riccardo Amirante ◽  
Elia Distaso ◽  
Paolo Tamburrano ◽  
Rolf D Reitz
Keyword(s):  
Natural Gas ◽  
Laminar Flame ◽  
Spark Ignition ◽  
Flame Speed ◽  
Operating Conditions ◽  
Spark Ignition Engine ◽  
Computational Time ◽  
Laminar Flame Speed ◽  
Spark Ignition Engines ◽  
Empirical Correlations

The laminar flame speed plays an important role in spark-ignition engines, as well as in many other combustion applications, such as in designing burners and predicting explosions. For this reason, it has been object of extensive research. Analytical correlations that allow it to be calculated have been developed and are used in engine simulations. They are usually preferred to detailed chemical kinetic models for saving computational time. Therefore, an accurate as possible formulation for such expressions is needed for successful simulations. However, many previous empirical correlations have been based on a limited set of experimental measurements, which have been often carried out over a limited range of operating conditions. Thus, it can result in low accuracy and usability. In this study, measurements of laminar flame speeds obtained by several workers are collected, compared and critically analyzed with the aim to develop more accurate empirical correlations for laminar flame speeds as a function of equivalence ratio and unburned mixture temperature and pressure over a wide range of operating conditions, namely [Formula: see text], [Formula: see text] and [Formula: see text]. The purpose is to provide simple and workable expressions for modeling the laminar flame speed of practical fuels used in spark-ignition engines. Pure compounds, such as methane and propane and binary mixtures of methane/ethane and methane/propane, as well as more complex fuels including natural gas and gasoline, are considered. A comparison with available empirical correlations in the literature is also provided.

Measurement of Laminar Flame Speed and Flammability Limits of a Biodiesel Surrogate

2016 ◽  
Vol 30 (10) ◽  
pp. 8737-8745 ◽  
Author(s):  
Carlos A. Gomez Casanova ◽  
Edwin Othen ◽  
John L. Sorensen ◽  
David B. Levin ◽  
Madjid Birouk
Keyword(s):  
Laminar Flame ◽  
Flame Speed ◽  
Laminar Flame Speed ◽  
Flammability Limits

Influence of water vapour and tar compound on laminar flame speed of gasified biomass gas

2012 ◽  
Vol 98 ◽  
pp. 114-121 ◽  
Author(s):  
Nur Farizan Munajat ◽  
Catharina Erlich ◽  
Reza Fakhrai ◽  
Torsten H. Fransson
Keyword(s):  
Water Vapour ◽  
Laminar Flame ◽  
Flame Speed ◽  
Laminar Flame Speed ◽  
Influence Of Water
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