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Reduction of the gas-phase reaction mechanism of iso-octane for the catalytic oxidation and non-catalytic applications

机译:还原异辛烷的气相反应机理,用于催化氧化和非催化应用

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In this study, catalytic oxidation of iso-octane is investigated for a very fuel-rich and for a fuel-lean condition in a batch reactor. For this purpose, skeletal mechanisms are derived and their results are compared with detailed reaction mechanism results. It is shown that skeletal mechanisms, which have 61-62% less species and 57-59% less reactions than the detailed reaction mechanism, allow an accurate prediction of species distributions in the batch reactor. Hydrogen selectivity decrease and soot precursors increase at fuel-rich condition. Further, the behavior of a gas composition downstream a catalyst is investigated for fuel-rich conditions in a plug-flow reactor. Skeletal mechanism yields similar results to the detailed reaction mechanism and experiment in plug-flow reactor. The results show that iso-octane is completely converted in the beginning of the reactor (0.01-0.05 m) for fuel-rich conditions, while other hydrocarbon species like methane, ethylene, propylene and acetylene are produced within 0.05 m.
机译:在这项研究中,研究了在间歇反应器中,对于非常富燃料和贫燃料条件的异辛烷催化氧化。为此,推导了骨骼机制,并将其结果与详细的反应机制结果进行了比较。结果表明,与详细的反应机理相比,骨架机理的物种减少了61-62%,反应减少了57-59%,可以准确预测间歇反应器中的物种分布。在富燃料条件下,氢的选择性降低,烟灰前驱物增加。此外,针对活塞流反应器中的富燃料条件,研究了催化剂下游气体成分的行为。骨架机理产生的结果与详细的反应机理和活塞流反应器中的实验相似。结果表明,在富含燃料的条件下,异辛烷在反应器开始时(0.01-0.05 m)完全转化,而其他烃类(如甲烷,乙烯,丙烯和乙炔)在0.05 m内产生。

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