Oxidation of methyl and ethyl butanoates
This paper describes an experimental and modeling study of the oxidation of methyl and ethyl butanoates in a shock tube. The ignition delays of these two esters mixed with oxygen and argon for equivalence ratios from 0.25 to 2 and ester concentrations of 0.5% and 1% were measured behind a reflected...
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| Veröffentlicht in: | International journal of chemical kinetics 2010-04, Vol.42 (4), p.226-252 |
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| container_title | International journal of chemical kinetics |
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| creator | Hakka, M. H. Bennadji, H. Biet, J. Yahyaoui, M. Sirjean, B. Warth, V. Coniglio, L. Herbinet, O. Glaude, P. A. Billaud, F. Battin-Leclerc, F. |
| description | This paper describes an experimental and modeling study of the oxidation of methyl and ethyl butanoates in a shock tube. The ignition delays of these two esters mixed with oxygen and argon for equivalence ratios from 0.25 to 2 and ester concentrations of 0.5% and 1% were measured behind a reflected shock wave for temperatures from 1250 to 2000 K and pressures around 8 atm. To extend the range of studied temperatures in the case of methyl butanoate, two sets of measurements were also made in a jet‐stirred reactor at 800 and 850 K, at atmospheric pressure, at residence times varying between 1.5 and 9 s and for equivalence ratios of 0.5 and 1. Detailed mechanisms for the combustion of methyl and ethyl butanoates have been automatically generated using a version of EXGAS software improved to take into account these oxygenated reactants. These mechanisms have been validated through comparison of simulated and experimental results in both types of reactor. The main reaction pathways have been derived from reaction flux and sensitivity analyses performed at different temperatures. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 226–252, 2010 |
| doi_str_mv | 10.1002/kin.20473 |
| format | Article |
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H. ; Bennadji, H. ; Biet, J. ; Yahyaoui, M. ; Sirjean, B. ; Warth, V. ; Coniglio, L. ; Herbinet, O. ; Glaude, P. A. ; Billaud, F. ; Battin-Leclerc, F.</creator><creatorcontrib>Hakka, M. H. ; Bennadji, H. ; Biet, J. ; Yahyaoui, M. ; Sirjean, B. ; Warth, V. ; Coniglio, L. ; Herbinet, O. ; Glaude, P. A. ; Billaud, F. ; Battin-Leclerc, F.</creatorcontrib><description>This paper describes an experimental and modeling study of the oxidation of methyl and ethyl butanoates in a shock tube. The ignition delays of these two esters mixed with oxygen and argon for equivalence ratios from 0.25 to 2 and ester concentrations of 0.5% and 1% were measured behind a reflected shock wave for temperatures from 1250 to 2000 K and pressures around 8 atm. To extend the range of studied temperatures in the case of methyl butanoate, two sets of measurements were also made in a jet‐stirred reactor at 800 and 850 K, at atmospheric pressure, at residence times varying between 1.5 and 9 s and for equivalence ratios of 0.5 and 1. Detailed mechanisms for the combustion of methyl and ethyl butanoates have been automatically generated using a version of EXGAS software improved to take into account these oxygenated reactants. These mechanisms have been validated through comparison of simulated and experimental results in both types of reactor. The main reaction pathways have been derived from reaction flux and sensitivity analyses performed at different temperatures. © 2010 Wiley Periodicals, Inc. 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The ignition delays of these two esters mixed with oxygen and argon for equivalence ratios from 0.25 to 2 and ester concentrations of 0.5% and 1% were measured behind a reflected shock wave for temperatures from 1250 to 2000 K and pressures around 8 atm. To extend the range of studied temperatures in the case of methyl butanoate, two sets of measurements were also made in a jet‐stirred reactor at 800 and 850 K, at atmospheric pressure, at residence times varying between 1.5 and 9 s and for equivalence ratios of 0.5 and 1. Detailed mechanisms for the combustion of methyl and ethyl butanoates have been automatically generated using a version of EXGAS software improved to take into account these oxygenated reactants. These mechanisms have been validated through comparison of simulated and experimental results in both types of reactor. 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| title | Oxidation of methyl and ethyl butanoates |
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