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The effect of equivalence ratio on the soot onset chemistry in one-dimensional, atmospheric-pressure, premixed ethylbenzene flames

机译:一维大气压预混乙苯火焰中当量比对烟灰开始化学的影响

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An investigation was conducted on the evolution of products of incomplete combustion (PIC) emitted from one-dimensional, laminar, atmospheric-pressure ethylbenzene flames in the vicinity of the soot onset threshold. The objective of this study was to identify the role of the fuel-to-air equivalence ratio in the evolution of polycyclic aromatic hydrocarbons (PAH) and other PIC as soot precursors, just prior to and subsequent to soot onset in premixed flames. Liquid ethylbenzene was prevaporized in nitrogen and blended with an oxygen-nitrogen mixture. Upon ignition, premixed flat flames were stabilized over a burner at atmospheric pressure. Temperature measurements and product sampling were conducted at various heights above the burner. Collected samples were analyzed for soot, PAH, oxygenated species, fixed gases, and light hydrocarbons. Three flames were investigated in the vicinity of the observed soot onset threshold, at equivalence ratios of φ_1 = 1.68, φ_2 = 1.74, and φ_3 = 1.83. By adjusting the amounts of oxygen, nitrogen, and fuel, both the maximum measured flame temperature and the spatial profile of the temperature were kept nearly constant as the equivalence ratio was varied. The cold gas velocity through the burner was also kept nearly constant. Changes in species concentration profiles prior to, at and beyond the sooting limit were evaluated. The results indicated that the soot onset limit is not a function of flame temperature alone; i.e., while the maximum measured flame temperatures was kept fairly constant, the flame could be either sooting, at the sooting limit or nonsooting depending on the equivalence ratio. A detailed chemical kinetic model, previously tested against sooting premixed benzene and ethylbenzene flames, was used to gain insight in chemical processes involved in soot formation. A reaction flux analysis was conducted to determine the pathways for ethylbenzene consumption, as well as for benzene and naphthalene formation. Examination of experimental measurements of species along the axis of the flame, in view of the theoretical predictions, showed a rather direct correlation of acetylene to soot formation. Moreover, a correlation between the consumption of ethylbenzene pyrolyzates, such as styrene, and soot formation at the soot onset was also apparent. Whereas the model's results were very encouraging, additional development is deemed necessary to improve its predictive capability in the challenging regime of soot inception.
机译:对烟灰开始阈值附近一维,层状,大气压力的乙苯火焰散发出的不完全燃烧产物的演变进行了研究。这项研究的目的是确定燃料/空气当量比在预混合火焰中烟尘发作之前和之后,在烟尘前体多环芳烃(PAH)和其他PIC演变中的作用。将液态乙苯在氮气中预蒸发,并与氧气-氮气混合物混合。点燃后,预混合的平焰在燃烧器上稳定在大气压下。在燃烧器上方的不同高度进行温度测量和产品采样。分析收集的样品中的烟灰,多环芳烃,含氧物质,固定气体和轻烃。在观察到的烟灰起始阈值附近研究了三个火焰,当量比为φ_1= 1.68,φ_2= 1.74和φ_3= 1.83。通过调节氧气,氮气和燃料的量,当当量比变化时,最大测得的火焰温度和温度的空间分布几乎保持恒定。通过燃烧器的冷气速度也保持几乎恒定。评价了在烟so极限之前,在和超过烟so极限时物种浓度分布的变化。结果表明,烟灰起燃极限不仅是火焰温度的函数,还取决于火焰温度。即,虽然最高测得的火焰温度保持相当恒定,但根据当量比,火焰可能会在烟limit极限处so烟或不or烟。使用详细的化学动力学模型(先前已针对烟灰预混合的苯和乙苯火焰进行了测试)来深入了解烟灰形成所涉及的化学过程。进行了反应通量分析,以确定乙苯消耗以及苯和萘形成的途径。根据理论预测,沿火焰轴对物种进行实验测量的结果表明,乙炔与烟灰的形成有相当直接的关系。此外,乙苯热解产物(如苯乙烯)的消耗与烟so开始时烟so形成之间的相关性也很明显。尽管该模型的结果非常令人鼓舞,但仍认为有必要进行进一步开发以提高其在具有挑战性的烟灰起始状态下的预测能力。

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