An experimental study on the formation of polycyclic aromatic hydrocarbons in laminar coflow non-premixed methane/air flames doped with four isomeric butanols

被引:38
作者
Jin, Hanfeng [1 ]
Wang, Yizun [1 ]
Zhang, Kuiwen [2 ]
Guo, Hongsheng [3 ]
Qi, Fei [1 ,2 ]
机构
[1] Univ Sci & Technol China, State Key Lab Fire Sci, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
[3] Natl Res Council Canada, Ottawa, ON K1A 0R6, Canada
关键词
Laminar non-premixed coflow flame; Butanol; Synchrotron VUV photoionization mass spectrometry; Benzene and PAH formation; JET-STIRRED REACTOR; SHOCK-TUBE; N-BUTANOL; OXIDATION; PYROLYSIS; KINETICS; ACETYLENE; MIXTURES; PRESSURE;
D O I
10.1016/j.proci.2012.05.107
中图分类号
O414.1 [热力学];
学科分类号
摘要
Experimental measurements were conducted for temperatures and mole fractions of C1-C16 combustion intermediates in laminar coflow non-premixed methane/air flames doped with 3.9% (in volume) 1-butanol, 2-butanol, iso-butanol and tert-butanol, respectively. Synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) technique was utilized in the measurements of species mole fractions. The results show that the variant molecular structures of butyl alcohols have led to different efficiencies in the formation of polycyclic aromatic hydrocarbons (PAHs) that may cause the variations in sooting tendency. Detailed species information suggests that the presence of allene and propyne promotes benzene formation through the C3H3 + C3H4 reactions and consequently PAH formation through the additions of C2 and C3 species to benzyl or phenyl radicals. As a matter of fact, PAHs formed from the 1-butanol doped flame are the lowest among the four investigated flames, because 1-butanol mainly decomposes to ethylene and oxygenates rather than C3 hydrocarbon species. Meanwhile, the tert-butanol doped flame generates the largest quantities of allene and propyne among the four flames and therefore is the sootiest one. Crown (C) 2012 and Elsevier Inc. All rights reserved.
引用
收藏
页码:779 / 786
页数:8
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