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Experimental and modeling study of the oxidation of natural gas in a premixed flame, shock tube, and jet-stirred reactor

机译:预混火焰,激波管和射流搅拌反应器中天然气氧化的实验和模型研究

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摘要

New experimental results have been obtained for the oxidation of a stoichiometric premixed synthetic natural gas flame at low pressure (10.6 kPa). Mole fraction profiles of stable and reactive species and temperature were measured using molecular beam/mass spectrometry, gas chromatography, and thermocouple techniques. A detailed reaction mechanism has been evaluated by comparison of computed and measured species mole fraction profiles. Good agreement was obtained for most molecular species (reactants, intermediate species, and final products). The proposed mechanism was also validated by modeling the laminar flame speeds of methane/air, ethane/air, and propane/air flames reported in the literature over a wide range of equivalence ratios. The model reproduces correctly the experimental values. The model was also used to simulate new experimental results ob-lained in a jet-stirred reactor (JSR) at atmospheric pressure and variable equivalence ratio (Φ = 0.75 : 1.0 : 1.5) for the oxidation of methane-ethane mixtures representative of natural gas. The ignition delays of methane-oxygen-argon and methane-ethane-oxygen were modeled. Sensitivity analyses and reaction path analyses, based on species rates of reaction, were used to interpret the results, especially the effect of higher alkanes on the oxidation of natural gas.
机译:在低压(10.6 kPa)下化学计量的预混合合成天然气火焰的氧化获得了新的实验结果。使用分子束/质谱,气相色谱和热电偶技术测量了稳定和反应性物种及温度的摩尔分数分布。通过比较计算出的物种摩尔分数和测得的物种摩尔分数,评估了详细的反应机理。大多数分子物种(反应物,中间物种和最终产品)均获得了良好的一致性。通过对文献中报道的甲烷/空气,乙烷/空气和丙烷/空气火焰的层流火焰速度进行建模,并在较宽的当量比范围内对所提出的机理进行了验证。该模型正确地再现了实验值。该模型还用于模拟在大气压和可变当量比(Φ= 0.75:1.0:1.5)的喷射搅拌反应器(JSR)中用于代表天然气的甲烷-乙烷混合物氧化的新实验结果。对甲烷-氧气-氩气和甲烷-乙烷-氧气的点火延迟进行了建模。基于反应的物种速率进行敏感性分析和反应路径分析,以解释结果,尤其是高级烷烃对天然气氧化的影响。

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