Diode laser absorption measurement and analysis of HCN in atmospheric-pressure, fuel-rich premixed methane/air flames

被引:24
作者
Gersen, S. [1 ]
Mokhov, A. V. [1 ]
Levinsky, H. B. [1 ,2 ]
机构
[1] Univ Groningen, Lab Fuel & Combust Sci, NL-9700 AB Groningen, Netherlands
[2] NV Nederlandse Gasunie, Gasunie Engn & Technol, Groningen, Netherlands
关键词
NO formation; HCN formation; Laminar flames; Diode laser absorption spectroscopy;
D O I
10.1016/j.combustflame.2008.04.006
中图分类号
O414.1 [热力学];
学科分类号
摘要
Measurements of HCN in flat, fuel-rich premixed methane/air flames at atmospheric pressure are reported. Quartz-microprobe sampling followed by wavelength modulation absorption spectroscopy with second harmonic detection was used to obtain an overall measurement uncertainty of better than 20% for mole fractions HCN oil the order of 10 ppm. The equivalence ratio, phi, was varied between 1.3 and 1.5, while the flame temperature was varied independently by changing the mass flux through the burner surface at constant equivalence ratio. Under the conditions of the experiments, the peak mole fractions vary little, in the range of 10-15 ppm. Increasing the flame temperature by increasing the mass flux had little influence on the peak mole fraction, but accelerated HCN burnout substantially. At high equivalence ratio and low flame temperature, HCN burnout is very slow: at phi = 1.5, similar to 10 ppm HCN is still present 7 mm above the burner surface. Substantial quantitative disagreement is observed between the experimental profiles and those obtained from calculations using GRI-Mech 3.0, with the calculations generally overpredicting the results significantly. Changing the rates of key formation and consumption reactions for HCN can improve the agreement, but only by making unreasonable changes in these rates. Inclusion of reactions describing NCN formation and consumption in the calculations improves the agreement with the measurements considerably. (c) 2008 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:267 / 276
页数:10
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