Kinetic coupling effects on the extinction limits of diffusion flames of hydrocarbons blended with ammonia

Chemical kinetic coupling effects between NH 3 and liquid hydrocarbon fuels on extinction limits of diffusion flames are experimentally and numerically investigated. Three n-alkanes (n-heptane, n-decane, and n-dodecane), isooctane as a representative fully branched isoalkane, and toluene as a representative mono-aromatic are each tested, along with their blends with NH 3 . The measured extinction strain rates are analyzed, employing transport-weighted enthalpy and radical index to demonstrate relative changes of chemical kinetic potentials for each fuel evaluated. The results show a significantly lower chemical kinetic potential for NH 3 , compared to hydrocarbon fuels. Comparison of extinction limits as a function of transport-weighted enthalpy multiplied by radical index for fuel/NH 3 mixtures shows potential promotive effects for n-alkanes and no significant coupling for isooctane and toluene. Planar laser-induced fluorescence is applied to quantify OH concentrations for n-heptane, isooctane, and their mixtures with NH 3 , and data are modeled to test the fidelity of chemical kinetic model predictions. It is found that including interaction reactions of n-alkyl and isoalkyl fragments with NH 2 , and the reactions involving methylamine and cyanide are critical to predicting OH production rates, as well as extinction limits for hydrocarbon/NH 3 blends. Promotive effects of NH 3 blending on n-alkanes diffusion flame extinction limits are primarily from higher flame temperatures due to the reduced fraction of CO 2 found in the flame products. In the case of isooctane blended with NH 3 , the formation of two main isoalkyl fragments, CH 3 and C 3 H 6 , are found to interact with NH 2 , resulting in the suppression of the reactive radical pool population and kinetic inhibition. A significantly weaker reactive radical pool in toluene oxidation leads to more significant inhibitive kinetic coupling from NH 3 -related reactions.

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Publication Details

Journal
Proceedings of the Combustion Institute
Published
2025-01-01
DOI
https://doi.org/10.1016/j.proci.2025.105801
Primary Topic
Advanced Combustion Engine Technologies
Type
article
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article

Kinetic coupling effects on the extinction limits of diffusion flames of hydrocarbons blended with ammonia

Frederick L. Dryer, Michael P. Burke, Sang Hee Won, M. Yoon
Proceedings of the Combustion Institute
Advanced Combustion Engine Technologies
article

Kinetic coupling effects on the extinction limits of diffusion flames of hydrocarbons blended with ammonia

Frederick L. Dryer, Michael P. Burke, Sang Hee Won, M. Yoon
article en

Abstract

Chemical kinetic coupling effects between NH 3 and liquid hydrocarbon fuels on extinction limits of diffusion flames are experimentally and numerically investigated. Three n-alkanes (n-heptane, n-decane, and n-dodecane), isooctane as a representative fully branched isoalkane, and toluene as a representative mono-aromatic are each tested, along with their blends with NH 3 . The measured extinction strain rates are analyzed, employing transport-weighted enthalpy and radical index to demonstrate relative changes of chemical kinetic potentials for each fuel evaluated. The results show a significantly lower chemical kinetic potential for NH 3 , compared to hydrocarbon fuels. Comparison of extinction limits as a function of transport-weighted enthalpy multiplied by radical index for fuel/NH 3 mixtures shows potential promotive effects for n-alkanes and no significant coupling for isooctane and toluene. Planar laser-induced fluorescence is applied to quantify OH concentrations for n-heptane, isooctane, and their mixtures with NH 3 , and data are modeled to test the fidelity of chemical kinetic model predictions. It is found that including interaction reactions of n-alkyl and isoalkyl fragments with NH 2 , and the reactions involving methylamine and cyanide are critical to predicting OH production rates, as well as extinction limits for hydrocarbon/NH 3 blends. Promotive effects of NH 3 blending on n-alkanes diffusion flame extinction limits are primarily from higher flame temperatures due to the reduced fraction of CO 2 found in the flame products. In the case of isooctane blended with NH 3 , the formation of two main isoalkyl fragments, CH 3 and C 3 H 6 , are found to interact with NH 2 , resulting in the suppression of the reactive radical pool population and kinetic inhibition. A significantly weaker reactive radical pool in toluene oxidation leads to more significant inhibitive kinetic coupling from NH 3 -related reactions.

Proceedings of the Combustion InstituteVol. 41
University of South Carolina (US), Columbia University (US)
Openalex Percentile: Top 84%
Advanced Combustion Engine Technologies
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