Cycle-resolved emission measurements of ammonia-hydrogen combustion in a spark-ignition engine

Ammonia–hydrogen mixtures are promising carbon-free fuels for internal combustion engines, but their unconventional combustion behavior complicates stable operation and emission control, particularly for NO, N 2 O, and unburned NH 3 . To characterize these emissions and their underlying formation pathways, diagnostics with high temporal resolution and strong species selectivity are required. This study employs high-speed, in-situ tunable diode laser absorption spectroscopy (TDLAS) to measure H 2 O, NH 3 , NO, and N 2 O at 1 kHz directly downstream of the exhaust valves of a single-cylinder spark-ignition engine. The technique resolves the temporal emission characteristic of individual cycles and provides insight into how cycle-to-cycle combustion behavior influences pollutant formation. Analysis across the tested operating points shows that increasing hydrogen content improves combustion stability and reduces NH 3 slip but elevates NO formation. NO correlates positively with mean in-cylinder pressure, whereas N 2 O exhibits an inverse trend, reflecting their distinct temperature-dependent production and decomposition pathways. During warm-up, the measurements capture a sudden advance in combustion phasing under otherwise constant boundary conditions. Zero-dimensional reactor simulations suggest a plausible explanation, indicating that temperature- and pressure-dependent NH 3 cracking can increase in-situ H 2 concentrations and thereby accelerate combustion. By combining cycle-resolved measurements with thermochemical simulations, this work clarifies how transient combustion dynamics, mixture reactivity, and boundary-temperature effects shape the formation of NO, N 2 O, and NH 3 in ammonia–hydrogen engines. The results support the development of stable and low-emission operating strategies and suggest that, under sufficiently high temperature, pressure and residence times, the cracking of NH 3 within the cylinder can provide enough H 2 to enable stable pure-ammonia combustion.

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Publication Details

Journal
International Journal of Engine Research
Published
2026-05-12
DOI
https://doi.org/10.1177/14680874261446628
Primary Topic
Advanced Combustion Engine Technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

Cycle-resolved emission measurements of ammonia-hydrogen combustion in a spark-ignition engine

Robin Schultheis, Jannick Erhard, Lars Illmann, Cooper Welch et al.
International Journal of Engine Research
Advanced Combustion Engine Technologies
article

Cycle-resolved emission measurements of ammonia-hydrogen combustion in a spark-ignition engine

Robin Schultheis, Jannick Erhard, Lars Illmann, Cooper Welch, Henrik Matero, Leon Schuhmann, Benjamin Böhm, Andreas Dreizler, Steven Wagner
article en

Abstract

Ammonia–hydrogen mixtures are promising carbon-free fuels for internal combustion engines, but their unconventional combustion behavior complicates stable operation and emission control, particularly for NO, N 2 O, and unburned NH 3 . To characterize these emissions and their underlying formation pathways, diagnostics with high temporal resolution and strong species selectivity are required. This study employs high-speed, in-situ tunable diode laser absorption spectroscopy (TDLAS) to measure H 2 O, NH 3 , NO, and N 2 O at 1 kHz directly downstream of the exhaust valves of a single-cylinder spark-ignition engine. The technique resolves the temporal emission characteristic of individual cycles and provides insight into how cycle-to-cycle combustion behavior influences pollutant formation. Analysis across the tested operating points shows that increasing hydrogen content improves combustion stability and reduces NH 3 slip but elevates NO formation. NO correlates positively with mean in-cylinder pressure, whereas N 2 O exhibits an inverse trend, reflecting their distinct temperature-dependent production and decomposition pathways. During warm-up, the measurements capture a sudden advance in combustion phasing under otherwise constant boundary conditions. Zero-dimensional reactor simulations suggest a plausible explanation, indicating that temperature- and pressure-dependent NH 3 cracking can increase in-situ H 2 concentrations and thereby accelerate combustion. By combining cycle-resolved measurements with thermochemical simulations, this work clarifies how transient combustion dynamics, mixture reactivity, and boundary-temperature effects shape the formation of NO, N 2 O, and NH 3 in ammonia–hydrogen engines. The results support the development of stable and low-emission operating strategies and suggest that, under sufficiently high temperature, pressure and residence times, the cracking of NH 3 within the cylinder can provide enough H 2 to enable stable pure-ammonia combustion.

International Journal of Engine Research
Technische Universität Darmstadt (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 8%
Advanced Combustion Engine Technologies
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