The NH3/NO2/O2 system: Constraining key steps in ammonia ignition and N2O formation

被引:82
作者
Glarborg, Peter [1 ]
机构
[1] Tech Univ Denmark, DTU Chem Engn, DK-2800 Lyngby, Denmark
基金
欧盟地平线“2020”;
关键词
NH3; NO2; N2O; Chemical kinetics; Flow reactor experiments; INITIO CHEMICAL-KINETICS; GAS-PHASE OXIDATION; RATE CONSTANTS; NITROGEN CHEMISTRY; FLOW REACTOR; DIODE-LASER; DELAY-TIME; SHOCK-TUBE; NO; OH;
D O I
10.1016/j.combustflame.2022.112311
中图分类号
O414.1 [热力学];
学科分类号
摘要
Amine/NO 2 interactions are important for ignition and N 2 O emissions in ammonia combustion. In the present work, reported results from batch reactors (580-690 K) and flow reactors (850-1350 K) for the NH 3 /NO 2 system were re-interpreted in terms of the present understanding of the amine chemistry. Furthermore, additional flow reactor results on the impact of O 2 on the NH 3 /NO 2 reaction were presented and analyzed. Based on the experimental results and the modeling analysis, it was possible to constrain the rate constants for reactions of NH 3 and NH 2 with NO 2 and for subsequent steps involving H 2 NO and HNO intermediates. The key reaction is NH 2 + NO 2 , forming H 2 NO + NO (R2) and N 2 O + H 2 O (R3). The results indicate that the yield of N 2 O in the NH 2 + NO 2 reaction decreases with temperature in the 850- 1350 K range, in agreement with the theoretical study by Klippenstein and coworkers. The fate of H 2 NO and HNO is important for the overall reactivity. In the absence of O 2 , formation of chain carriers is controlled by the sequence H 2 NO + NO 2 -> HNO + HONO, HNO + NO 2 -> NO + HONO, HONO (+M) -> NO + OH (+M). At higher temperatures, in the presence of O 2 , the sequence H 2 NO + O 2 -> HNO + HO 2 , HNO + O 2 -> NO + HO 2 , NO + HO 2 -> NO 2 + OH enhances radical formation and recycles NO 2 . The satisfactory agreement between experiments and modeling predictions, both without and with O 2 , supports the present rate constants for the reactions of H 2 NO and HNO with NO 2 and O 2 , respectively. (c) 2022 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:9
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共 76 条
[31]   Theoretical kinetics predictions for NH2 + HO2 [J].
Klippenstein, Stephen J. ;
Glarborg, Peter .
COMBUSTION AND FLAME, 2022, 236
[32]   Rate Constant and Branching Fraction for the NH2 + NO2 Reaction [J].
Klippenstein, Stephen J. ;
Harding, Lawrence B. ;
Glarborg, Peter ;
Gao, Yide ;
Hu, Huanzhen ;
Marshall, Paul .
JOURNAL OF PHYSICAL CHEMISTRY A, 2013, 117 (37) :9011-9022
[33]   The role of NNH in NO formation and control [J].
Klippenstein, Stephen J. ;
Harding, Lawrence B. ;
Glarborg, Peter ;
Miller, James A. .
COMBUSTION AND FLAME, 2011, 158 (04) :774-789
[34]   Science and technology of ammonia combustion [J].
Kobayashi, Hideaki ;
Hayakawa, Akihiro ;
Somarathne, K. D. Kunkuma A. ;
Okafor, Ekenechukwu C. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2019, 37 (01) :109-133
[35]   Nitrogen chemistry during burnout in fuel-staged combustion [J].
Kristensen, PG ;
Glarborg, P ;
DamJohansen, K .
COMBUSTION AND FLAME, 1996, 107 (03) :211-222
[36]   KINETICS OF THE REACTION OF NH2 WITH NO2 [J].
KURASAWA, H ;
LESCLAUX, R .
CHEMICAL PHYSICS LETTERS, 1979, 66 (03) :602-607
[37]   Numerical study on laminar burning velocity and ignition delay time of ammonia flame with hydrogen addition [J].
Li, Jun ;
Huang, Hongyu ;
Kobayashi, Noriyuki ;
Wang, Chenguang ;
Yuan, Haoran .
ENERGY, 2017, 126 :796-809
[38]   Product branching ratios of the NH2((XB1)-B-2)+NO2 reaction [J].
Lindholm, N ;
Hershberger, JF .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (27) :4991-4995
[39]   New reactions of diazene and related species for modelling combustion of amine fuels [J].
Marshall, Paul ;
Rawling, George ;
Glarborg, Peter .
MOLECULAR PHYSICS, 2021, 119 (17-18)
[40]   Experimental and modeling study on the high-temperature oxidation of Ammonia and related NOx chemistry [J].
Mathieu, Olivier ;
Petersen, Eric L. .
COMBUSTION AND FLAME, 2015, 162 (03) :554-570