乙炔
化学
激进的
苯
亚甲基
光化学
基本反应
炔丙基
反应机理
计算化学
有机化学
动力学
催化作用
量子力学
物理
作者
R.P. Lindstedt,G. Skevis
标识
DOI:10.1080/00102209708935656
摘要
Abstract Acetylene constitutes one of the major intermediates in hydrocarbon flames and is important through its links to soot inception and mass growth processes. In the present study a detailed kinetic mechanism is developed and tested against experimental data for six lean (φ = 0.12) to sooting (φ = 2.50) laminar, premixed, low-pressure acetylene flames. Generally the agreement between computations and experiments is acceptable. It is suggested that OH attack competes with O attack as the major acetylene breakdown path in rich flames. It is further shown that the balancing of the ketyl radical destruction chemistry to a significant extent determines important flame features such as CO/C02 ratio and H radical concentrations. The balancing of the methylene and methyne radical chemistry in both lean and rich environments is discussed in detail and the importance of molecular oxygen attack on 3CH2 is outlined. It is further shown that the present mechanism accurately predicts the qualitative evolution of methylene and methyne radical levels as a fucntion of stoichiometry. The present study incorporates the benzene oxidation mechanism by Lindstedt and Skevis (1994) and the benzene formation steps, involving isometri-zation reactions between linear and cyclic C6 intermediates, reported by Leung and Lindstedt (1995). The results obtained show that for rich acetylene flames the primary path for benzene formation passes via propargyl radical recombination and that benzene levels are generally satisfactorily predicted. However, computations also indicate that for leaner flames paths involving acetylene addition to n-C4H3 and 1,3-C3H5 radicals become increasingly important. This study also identifies reactions where further experimental investigations are required. Keywords: Acetylene oxidationbenzene formationsoot formationreburn chemistrydetailed kineticslaminar flames
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