Promoting Effect of Syngas Addition on Ammonia Consumption and NO x Emission at High Pressure
Abstract
Understanding the microspecies behavior of ammonia–syngas mixtures is crucial for cutting NO x emissions in engine applications of ammonia. Experiments were carried out at 5.0 MPa, with the mixture volume fraction varying from 0–50%. Concentrations of reactants, key intermediate species, and products were measured during the oxidation of ammonia–syngas mixtures. A detailed reaction mechanism was fully validated against the measured data. Experimental data indicated that the onset temperature of NH 3, H 2, and CO decreased with more syngas addition as well as the consumption temperature window, indicating an apparent improvement in the overall reactivity. An N-shape trend can be observed in NO concentration profiles under higher syngas blending ratios and fuel-lean conditions. The model in this paper can accurately predict the measured concentration data. Kinetic analysis showed that ammonia oxidation is first sensitive to NH 2 -involved reactions and the increase in radicals due to the blending of syngas enhances the sensitivity of these reactions. Then, ammonia oxidation is more sensitive to reaction NH 2 + H 2 = NH 3 + H and reactions related to H 2 O 2 at a higher syngas blending ratio. Third, reaction H + O 2 (+M) = HO 2 (+M) exhibits a strong promoting effect on NH 3 consumption at 10% syngas addition but instead shows an inhibiting effect at 50% syngas addition. As to NO formation, the chemical kinetic effect of syngas addition is more dominant than the dilution effect. Meanwhile, the reduction of NO is not significant. It eventually results in a significant rise of NO concentration. As for N 2 O, the dilution effect and chemical kinetic effect of syngas are comparable, resulting in a slight increase in the peak concentration of N 2 O with more syngas blending.
Fields of Study & Subjects
Advanced Combustion Engine Technologies
Combustion and flame dynamics
Catalytic Processes in Materials Science
Publication details
- Journal / source
- Energy & Fuels
- Volume
- 40
- Issue
- 4
- Pages
- 2213–2227
- Publication date
- 15 January 2026
- Language
- EN