The impact of hydrogen substitution by ammonia on low- and high-temperature combustion

被引:6
作者
Greenblatt, D. [1 ]
Tian, L. [1 ,2 ]
Lindstedt, R. P. [1 ]
机构
[1] Imperial Coll, Dept Mech Engn, Exhibit Rd, London SW7 2AZ, England
[2] Loughborough Univ, Dept Aeronaut & Automot Engn, Loughborough LE11 3TU, England
关键词
Ammonia chemistry; Ammonia -hydrogen fuel blends; SNCR; Auto; -ignition; Laminar flames; Turbulent combustion; LAMINAR BURNING VELOCITY; PROBABILITY DENSITY-FUNCTION; EVALUATED KINETIC-DATA; RATE CONSTANTS; PRESSURE-DEPENDENCE; NITROGEN CHEMISTRY; MARKSTEIN LENGTH; DIFFUSION FLAMES; PREMIXED FLAMES; AUTO-IGNITION;
D O I
10.1016/j.combustflame.2023.112733
中图分类号
O414.1 [热力学];
学科分类号
摘要
The combustion behaviour of ammonia has attracted intermittent interest with the original patent by Lyon (US3900554A) relating to its use for nitric oxide reduction through selective non-catalytic reduction (SNCR) a focal point. The recent interest in ammonia stems from its use as a hydrogen rich energy carrier with practical use requiring a much wider parameter space. The corresponding challenges (e.g. Kobayashi et al., Proc. Combust. Inst. 37 (2019) 109-133) include different flame dynamics and high emissions of oxides of nitrogen. The current paper explores the complex nature of ammonia oxidation and provides a reduced size reaction mechanism that enables application, without approximation, to the computation of turbulent flames through a joint-scalar transported probability density function (JPDF) method. Comprehensive validation suggests similar accuracy to a reference mechanism (Glarborg et al., Prog. Energy Combust. Sci. 67 (2018) 31-68) and highlights some uncertainties. The selected turbulent flame configuration features auto-ignition stabilised flames supported by a coflow of hot combustion products. The base case features a H 2 / N 2 fuel jet that permits flame stabilisation at 1045 K corresponding to the onset of the SNCR temperature window. The impact of a gradual substitution of hydrogen by ammonia on flame stabilisation, emissions of oxides of nitrogen and the flame structure is quantified. It is shown that ammonia substitution leads to more prevalent local extinction, a more distributed flame structure and requires substantially increased coflow temperatures to achieve a similar flame stabilisation point. A lowering of the coflow temperature to operate within the SNCR regime substantially reduces NO x and leads towards a homogeneous/distributed reaction mode. The reduced fuel reactivity highlights the importance of turbulence-chemistry interactions leading to complexities in the design of practical devices. (c) 2023 The Author(s). Published by Elsevier Inc. on behalf of The Combustion Institute. This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ )
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页数:17
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