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    Ignition of Lean Methane-Based Fuel Blends at Gas Turbine Pressures

    Source: Journal of Engineering for Gas Turbines and Power:;2007:;volume( 129 ):;issue: 004::page 937
    Author:
    Eric L. Petersen
    ,
    Anthony R. Amadio
    ,
    Mark W. Crofton
    ,
    Joel M. Hall
    ,
    Schuyler D. Smith
    ,
    Jaap de Vries
    DOI: 10.1115/1.2720543
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Shock-tube experiments and chemical kinetics modeling were performed to further understand the ignition and oxidation kinetics of lean methane-based fuel blends at gas turbine pressures. Such data are required because the likelihood of gas turbine engines operating on CH4-based fuel blends with significant (>10%) amounts of hydrogen, ethane, and other hydrocarbons is very high. Ignition delay times were obtained behind reflected shock waves for fuel mixtures consisting of CH4, CH4∕H2, CH4∕C2H6, and CH4∕C3H8 in ratios ranging from 90/10% to 60/40%. Lean fuel/air equivalence ratios (ϕ=0.5) were utilized, and the test pressures ranged from 0.54 to 30.0atm. The test temperatures were from 1090K to 2001K. Significant reductions in ignition delay time were seen with the fuel blends relative to the CH4-only mixtures at all conditions. However, the temperature dependence (i.e., activation energy) of the ignition times was little affected by the additives for the range of mixtures and temperatures of this study. In general, the activation energy of ignition for all mixtures except the CH4∕C3H8 one was smaller at temperatures below approximately1300K(∼27kcal∕mol) than at temperatures above this value (∼41kcal∕mol). A methane/hydrocarbon–oxidation chemical kinetics mechanism developed in a recent study was able to reproduce the high-pressure, fuel-lean data for the fuel/air mixtures. The results herein extend the ignition delay time database for lean methane blends to higher pressures (30atm) and lower temperatures (1100K) than considered previously and represent a major step toward understanding the oxidation chemistry of such mixtures at gas turbine pressures. Extrapolation of the results to gas turbine premixer conditions at temperatures less than 800K should be avoided however because the temperature dependence of the ignition time may change dramatically from that obtained herein.
    keyword(s): Fuels , Ignition , Methane , Mixtures , Temperature , Delays , Gas turbines AND Hydrogen ,
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      Ignition of Lean Methane-Based Fuel Blends at Gas Turbine Pressures

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    http://yetl.yabesh.ir/yetl1/handle/yetl/135659
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    • Journal of Engineering for Gas Turbines and Power

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    contributor authorEric L. Petersen
    contributor authorAnthony R. Amadio
    contributor authorMark W. Crofton
    contributor authorJoel M. Hall
    contributor authorSchuyler D. Smith
    contributor authorJaap de Vries
    date accessioned2017-05-09T00:23:34Z
    date available2017-05-09T00:23:34Z
    date copyrightOctober, 2007
    date issued2007
    identifier issn1528-8919
    identifier otherJETPEZ-26973#937_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/135659
    description abstractShock-tube experiments and chemical kinetics modeling were performed to further understand the ignition and oxidation kinetics of lean methane-based fuel blends at gas turbine pressures. Such data are required because the likelihood of gas turbine engines operating on CH4-based fuel blends with significant (>10%) amounts of hydrogen, ethane, and other hydrocarbons is very high. Ignition delay times were obtained behind reflected shock waves for fuel mixtures consisting of CH4, CH4∕H2, CH4∕C2H6, and CH4∕C3H8 in ratios ranging from 90/10% to 60/40%. Lean fuel/air equivalence ratios (ϕ=0.5) were utilized, and the test pressures ranged from 0.54 to 30.0atm. The test temperatures were from 1090K to 2001K. Significant reductions in ignition delay time were seen with the fuel blends relative to the CH4-only mixtures at all conditions. However, the temperature dependence (i.e., activation energy) of the ignition times was little affected by the additives for the range of mixtures and temperatures of this study. In general, the activation energy of ignition for all mixtures except the CH4∕C3H8 one was smaller at temperatures below approximately1300K(∼27kcal∕mol) than at temperatures above this value (∼41kcal∕mol). A methane/hydrocarbon–oxidation chemical kinetics mechanism developed in a recent study was able to reproduce the high-pressure, fuel-lean data for the fuel/air mixtures. The results herein extend the ignition delay time database for lean methane blends to higher pressures (30atm) and lower temperatures (1100K) than considered previously and represent a major step toward understanding the oxidation chemistry of such mixtures at gas turbine pressures. Extrapolation of the results to gas turbine premixer conditions at temperatures less than 800K should be avoided however because the temperature dependence of the ignition time may change dramatically from that obtained herein.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleIgnition of Lean Methane-Based Fuel Blends at Gas Turbine Pressures
    typeJournal Paper
    journal volume129
    journal issue4
    journal titleJournal of Engineering for Gas Turbines and Power
    identifier doi10.1115/1.2720543
    journal fristpage937
    journal lastpage944
    identifier eissn0742-4795
    keywordsFuels
    keywordsIgnition
    keywordsMethane
    keywordsMixtures
    keywordsTemperature
    keywordsDelays
    keywordsGas turbines AND Hydrogen
    treeJournal of Engineering for Gas Turbines and Power:;2007:;volume( 129 ):;issue: 004
    contenttypeFulltext
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