CO and H2O Time-Histories in Shock-Heated Blends of Methane and Ethane for Assessment of a Chemical Kinetics Model.

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Title: CO and H2O Time-Histories in Shock-Heated Blends of Methane and Ethane for Assessment of a Chemical Kinetics Model.
Authors: Mathieu, O.1 olivier.mathieu@tamu.edu, Mulvihill, C. R.1 cmulvihill@tamu.edu, Petersen, E. L.1 epetersen@tamu.edu, Zhang, Y.2 yjzhang_xjtu@xjtu.edu.cn, Curran, H. J.2 henry.curran@nuigalway.ie
Source: Journal of Engineering for Gas Turbines & Power. Dec2017, Vol. 139 Issue 12, p1-8. 8p.
Abstract: Methane and ethane are the two main components of natural gas and typically constitute more than 95% of it. In this study, a mixture of 90% CH4/10% C2H6 diluted in 99% Ar was studied at fuel lean (equiv. ratio = 0.5) conditions, for pressures around 1, 4, and 10 atm. Using laser absorption diagnostics, the time histories of CO and H2O were recorded between 1400 and 1800 K. Water is a final product from combustion, and its formation is a good marker of the completion of the combustion process. Carbon monoxide is an intermediate combustion species, a good marker of incomplete/inefficient combustion, as well as a regulated pollutant for the gas turbine industry. Measurements such as these species time histories are important for validating and assessing chemical kinetics models beyond just ignition delay times and laminar flame speeds. Time-history profiles for these two molecules were compared to a state-of-the-art detailed kinetics mechanism as well as to the well-established GRI 3.0 mechanism. Results show that the H2O profile is accurately reproduced by both models. However, discrepancies are observed for the CO profiles. Under the conditions of this study, the CO profiles typically increase rapidly after an induction time, reach a maximum, and then decrease. This maximum CO mole fraction is often largely over-predicted by the models, whereas the depletion rate of CO past this peak is often over-estimated for pressures above 1 atm. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Engineering for Gas Turbines & Power is the property of American Society of Mechanical Engineers and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: CO and H<subscript>2</subscript>O Time-Histories in Shock-Heated Blends of Methane and Ethane for Assessment of a Chemical Kinetics Model.
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  Data: <searchLink fieldCode="AR" term="%22Mathieu%2C+O%2E%22">Mathieu, O.</searchLink><relatesTo>1</relatesTo><i> olivier.mathieu@tamu.edu</i><br /><searchLink fieldCode="AR" term="%22Mulvihill%2C+C%2E+R%2E%22">Mulvihill, C. R.</searchLink><relatesTo>1</relatesTo><i> cmulvihill@tamu.edu</i><br /><searchLink fieldCode="AR" term="%22Petersen%2C+E%2E+L%2E%22">Petersen, E. L.</searchLink><relatesTo>1</relatesTo><i> epetersen@tamu.edu</i><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Y%2E%22">Zhang, Y.</searchLink><relatesTo>2</relatesTo><i> yjzhang_xjtu@xjtu.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Curran%2C+H%2E+J%2E%22">Curran, H. J.</searchLink><relatesTo>2</relatesTo><i> henry.curran@nuigalway.ie</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Engineering+for+Gas+Turbines+%26+Power%22">Journal of Engineering for Gas Turbines & Power</searchLink>. Dec2017, Vol. 139 Issue 12, p1-8. 8p.
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Methane and ethane are the two main components of natural gas and typically constitute more than 95% of it. In this study, a mixture of 90% CH4/10% C2H6 diluted in 99% Ar was studied at fuel lean (equiv. ratio = 0.5) conditions, for pressures around 1, 4, and 10 atm. Using laser absorption diagnostics, the time histories of CO and H2O were recorded between 1400 and 1800 K. Water is a final product from combustion, and its formation is a good marker of the completion of the combustion process. Carbon monoxide is an intermediate combustion species, a good marker of incomplete/inefficient combustion, as well as a regulated pollutant for the gas turbine industry. Measurements such as these species time histories are important for validating and assessing chemical kinetics models beyond just ignition delay times and laminar flame speeds. Time-history profiles for these two molecules were compared to a state-of-the-art detailed kinetics mechanism as well as to the well-established GRI 3.0 mechanism. Results show that the H2O profile is accurately reproduced by both models. However, discrepancies are observed for the CO profiles. Under the conditions of this study, the CO profiles typically increase rapidly after an induction time, reach a maximum, and then decrease. This maximum CO mole fraction is often largely over-predicted by the models, whereas the depletion rate of CO past this peak is often over-estimated for pressures above 1 atm. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Journal of Engineering for Gas Turbines & Power is the property of American Society of Mechanical Engineers and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1115/1.4037602
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        Text: English
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      – TitleFull: CO and H2O Time-Histories in Shock-Heated Blends of Methane and Ethane for Assessment of a Chemical Kinetics Model.
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              M: 12
              Text: Dec2017
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