Acetaldehyde oxidation at elevated pressure |
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Authors: | Hamid Hashemi Jakob M Christensen Paul Marshall Peter Glarborg |
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Institution: | 1. DTU Chemical Engineering, Technical University of Denmark, Lyngby DK-2800, Denmark;2. Department of Chemistry and Center for Advanced Scientific Computing and Modeling, University of North Texas, 1155 Union Circle #305070, Denton, TX 76203-5017, USA |
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Abstract: | A detailed chemical kinetic model for oxidation of CH3CHO at intermediate to high temperature and elevated pressure has been developed and evaluated by comparing predictions to novel high-pressure flow reactor experiments as well as shock tube ignition delay measurements and jet-stirred reactor data from literature. The flow reactor experiments were conducted with a slightly lean CH3CHO/O2 mixture highly diluted in N2 at 600–900 K and pressures of 25 and 100 bar. At the highest pressure, the oxidation of CH3CHO was in the NTC regime, controlled to a large extent by the thermal stability and reactions of peroxide species such as HO2, CH3OO, and CH3C(O)OO. Model predictions were generally in good agreement with the experimental data, even though the predicted temperature for onset of reaction was overpredicted at 100 bar. This discrepancy was attributed mainly to uncertainties in the CH3C(O)OO reaction subset. Predictions of ignition delays in shock tubes and species profiles in JSR experiments were also satisfactory. At temperatures above the NTC regime, acetaldehyde ignition and oxidation is affected mainly by the competition between dissociation of CH3CHO and reaction with the radical pool, and by reactions in the methane subset. |
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