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Oxidation of m-Xylene in a JSR: Experimental Study and Detailed Chemical Kinetic Modeling

机译:JSR中间二甲苯的氧化:实验研究和详细的化学动力学建模

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New experimental results were obtained for the oxidation of meta-xylene studied in a jet-stirred reactor at atmospheric pressure in dilute conditions over the temperature range 900-1400 K, and variable equivalence ratio (0.5 ≤φ ≤ 1.5). They consisted of concentration profiles of the reactants, stable intermediates and final products, measured by sonic probe sampling followed by on-line GC-MS analyses and off-line GC-TCD-F1D and GC-MS analyses. The oxidation of meta-xyIene in these conditions was modeled using a detailed chemical kinetic reaction mechanism (189 species and 1359 reactions, most of them reversible) deriving from a previous scheme proposed for the ignition, oxidation, and combustion of simple aromatics (benzene, toluene, styrene, n-propyl-benzene, and para-xylene). Sensitivity analyses and reaction path analyses, based on rates of reaction, were used to interpret the results. This study showed the reactivity of m-xylene is quite similar to that of p-xylene under the present conditions: m-xylene reacts slightly slower than p-xylene.
机译:在900-1400 K的温度范围和稀当量比(0.5≤φ≤1.5)的稀薄条件下,在大气压下在喷气搅拌反应器中研究间二甲苯的氧化获得了新的实验结果。它们由反应物,稳定的中间体和最终产物的浓度分布图组成,这些分布图是通过声波探针采样,在线GC-MS分析以及离线GC-TCD-F1D和GC-MS分析来测量的。在这种条件下,间二甲苯的氧化反应是根据详细的化学动力学反应机理(189种和1359种反应,其中大多数是可逆的)建立的,该机理源自先前提出的用于点燃,氧化和燃烧简单芳族化合物(苯,甲苯,苯乙烯,正丙基苯和对二甲苯)。基于反应速率的敏感性分析和反应路径分析被用来解释结果。这项研究表明,在当前条件下,间二甲苯的反应性与对二甲苯非常相似:间二甲苯的反应比对二甲苯的反应稍慢。

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