An experimental and modeling study of ammonia oxidation in a jet stirred reactor

• Published in: Combustion and flame 2022-06, Vol.240, p.112007, Article 112007
• Main Authors: Tang, Ruoyue, Xu, Qiang, Pan, Jiaying, Gao, Jian, Wang, Zhandong, Wei, Haiqiao, Shu, Gequn
• Format: Article
• Language: English
• Subjects: Ammonia; Ammonia oxidation; Chemical kinetic model; Dehydrogenation; Equivalence ratio; Gas chromatography; Jet-stirred reactor; Mass spectrometry; Modelling; Nitrogen dioxide; Nitrous oxide; Oxidation; Oxygen concentration; Photoionization; Rate constants; Sensitivity analysis; Synchrotrons
• ISSN: 0010-2180; 1556-2921
• DOI: 10.1016/j.combustflame.2022.112007

Ammonia is a promising carbon-free fuel and has attracted massive attention nowadays. However, there are still large uncertainties in the mechanism of ammonia oxidation that motivate further fundamental investigations. In this work, oxidation experiments of ammonia were carried out in a jet-stirred reactor (JSR) equipped with synchrotron vacuum ultraviolet (SVUV) photoionization mass spectrometry and gas chromatography. Ammonia/O2/Ar mixtures were tested under wide-range operating conditions covering an oxidation temperature of 700–1200 K and an equivalence ratio of ϕ = 0.1–1.0. Important intermediates and products (e.g., NO, NO2, N2O, N2, H2, and H2O) were detected and quantified. A chemical kinetic model for ammonia oxidation was proposed by integrating the rate constants of critical reactions from different models. The results show that ammonia oxidation reactivity is quite strong at ultra-lean conditions, manifesting lower oxidization temperatures and greater oxidization rates. However, this behavior becomes weakened rapidly with the elevation of equivalence ratio, such that ammonia oxidation characteristics are highly similar between ϕ = 0.5 and 1.0. Meanwhile, important intermediates like NO2 and N2O are only detected under ultra-lean conditions. Reaction pathway analysis for equivalence ratios shows that high oxygen concentration is beneficial to the formation of HO2, which leads to a huge amount of OH and promotes the dehydrogenation of ammonia. With the elevation of equivalence ratio, the dehydrogenation of ammonia becomes difficult and reactions NO+HO2=NO2+OH and NH2+NO2=N2O+H2O are suppressed, which answers for the vanishing of NO2 and N2O at ϕ = 0.5 and 1.0. Reaction pathway analysis for oxidation temperatures also emphasizes the significance of HO2 and its conversion pathway to OH, but they are also strongly influenced by equivalence ratios. The current work provides useful insights into ammonia oxidation and a reliable experimental database for modeling.