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Plasma flow reactor studies of H-2/O-2/Ar kinetics

机译:等离子流反应器对H-2 / O-2 / Ar动力学的研究

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In the present study, a plasma flow reactor (PFR) facility designed to perform both ex situ and in situ experiments of stable (H-2 and O-2) and intermediate (OH radicals) species detection was used to examine the plasma-assisted characteristics of hydrogen oxidation at I atm pressure for temperatures ranging from 420 K to 1100 K. Experiments were performed at nearly isothermal conditions, by heavily diluting reactive mixtures in argon, in an attempt to mitigate temperature changes from exothermic chemical reactions. This technique allows experimental results to be interpreted from a perspective that plasma and thermal (neutral) heat release effects are decoupled, essentially isolating the effects of the plasma-chemistry and its influence on the neutral-chemistry. Results showed no thermal reaction until 860 K at which point hydrogen was rapidly consumed within the flow residence time associated with the reactor. With the plasma discharge, the onset of oxidation was extended to lower temperatures (T < 860 K), while exhibiting a steady increase in the rate of oxidation starting from 470 K, and eventually consuming all the initial hydrogen by 800 K. Absolute measurements of OH mole fraction reveal that at conditions well below the dominance of the thermal chain branched chemistry (at T = 668 K), the plasma induced a chain-propagating effect on OH formation, which was entirely confined to the boundaries of the plasma discharge section of the reactor. Furthermore, temporal measurements were also performed, showing that the extent of OH formation and subsequently its global effect on the fuel consuming chemistry can be manipulated based on the plasma perturbation timescale the time scale at which the high-voltage pulses are administered to the reactive flow to generate the plasma discharge). Experimental results are compared to modeling calculations and show relatively good agreement, with the model predicting similar kinetic trends as a function of temperature. These results demonstrate new insight into the kinetics governing plasma-assisted combustion, and provide new experimental data to facilitate the development and validation of PAC-specific kinetic mechanisms. (C) 2015 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
机译:在本研究中,使用等离子体流反应器(PFR)设施设计用于进行稳定(H-2和O-2)和中间(OH自由基)物种检测的非原位和原位实验,以检查等离子体辅助的温度在420 K至1100 K的温度下在I atm压力下的氢氧化特性。通过在氩气中大量稀释反应混合物,在几乎等温的条件下进行了实验,以试图缓解放热化学反应引起的温度变化。这项技术可以从等离子和热(中性)放热效应解耦的角度来解释实验结果,从而基本隔离了等离子化学作用及其对中性化学的影响。结果表明直到860 K时才发生热反应,此时在与反应器相关的流动停留时间内氢被迅速消耗掉。随着等离子放电,氧化开始扩展到较低的温度(T <860 K),同时氧化速率从470 K开始稳定增加,最终消耗了800 K的所有初始氢。 OH摩尔分数表明,在远低于热链支化化学优势的条件下(在T = 668 K时),等离子体对OH的形成产生链增长作用,该作用完全局限在等离子体放电区的边界。反应堆。此外,还进行了时间测量,结果表明,可以基于等离子扰动时标来控制OH形成的程度及其随后对燃料消耗化学物质的总体影响,即对反应流施加高压脉冲的时标产生等离子体放电)。实验结果与模型计算进行了比较,并显示出相对较好的一致性,其中模型预测了相似的动力学趋势随温度的变化。这些结果证明了对控制等离子体辅助燃烧的动力学的新见解,并提供了新的实验数据以促进PAC特定动力学机制的发展和验证。 (C)2015年燃烧研究所。由Elsevier Inc.出版。保留所有权利。

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