An experimental and kinetic modeling study of premixed nitroethane flames at low pressure

被引:32
作者
Zhang, Kuiwen [1 ]
Zhang, Lidong [1 ]
Xie, Mingfeng [1 ]
Ye, Lili [1 ]
Zhang, Feng [1 ]
Glarborg, Peter [2 ]
Qi, Fei [1 ,3 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
[2] Tech Univ Denmark, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[3] Univ Sci & Technol China, State Key Lab Fire Sci, Hefei 230026, Anhui, Peoples R China
基金
中国博士后科学基金;
关键词
Nitroethane; Premixed flame; Kinetic modeling; Synchrotron VUV photoionization mass spectrometry; GAS-PHASE REACTIONS; THERMAL-DECOMPOSITION; NITROMETHANE FLAME; OXIDATION; DISSOCIATION; RADICALS;
D O I
10.1016/j.proci.2012.06.010
中图分类号
O414.1 [热力学];
学科分类号
摘要
An experimental and kinetic modeling study is reported on three premixed nitroethane/oxygen/argon flames at low pressure (4.655 kPa) with the equivalence ratios (Phi) of 1.0, 1.5 and 2.0. Over 30 flame species were identified with tunable synchrotron vacuum ultraviolet photoionization mass spectrometry, with their mole fractions quantified as the function of the height above burner. The flame temperature profiles were measured with a Pt-6%Rh/Pt-30%Rh thermocouple. A detailed kinetic mechanism with 115 species and 730 reactions was proposed and validated against experimental results. The computed predictions have shown satisfactory agreement with the experimental results. Basing on the rate-of-production analysis, the reaction pathways that feature the combustion of nitroethane were revealed, including the primary decomposition of C-N bond fission, the oxidation of C2 and C1 hydrocarbons and the formation of nitrogenous species. The presence of NO2 and NO has been proved to be important for these processes. (C) 2012 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:617 / 624
页数:8
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