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Influence of ozone addition on the low-temperature oxidation of dimethyl ether in a jet-stirred reactor

机译:臭氧添加对喷射反应器中二甲醚低温氧化的影响

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摘要

The influence of ozone addition on the low-temperature oxidation of dimethyl ether (DME) was investigated experimentally in an atmospheric-pressure jet-stirred reactor, over the temperature range of 400-800 K. Detailed speciation information was obtained by employing synchrotron vacuum ultraviolet photoionization mass spectrometry. Experimental results revealed that the ozone addition had a positive influence on the production of the highly reactive intermediates. Moreover, the low-temperature reactivity of DME was significantly enhanced, which resulted in the broadening of the temperature window of fuel consumption and intermediates formation at lower temperatures. Therefore, novel experimental data of the low temperature regime (400-500 K) could be obtained. The data set of this special temperature regime yielded insights into the DME low-temperature kinetics, which were further supported with modeling analysis based on two existing DME models (Metcalfe et al., 2013; Wang et al., 2015) combined with an ozone sub-mechanism (Zhao et al., 2016). The analysis showed that temperature-sensitive reactions such as the second oxygen channel could be nearly "frozen" at this low temperature (T 440 K). Furthermore, the production of some intermediates was found to be strongly governed by reaction pairs, such as CH3OCH2 + O-2 = CH3OCH2O2 and CH3OCH2 + O-2 = 2CH(2)O + OH for the CH2O formation. This finding could be useful for examining branching ratios in both models, and the analysis suggested the further modification of the branching ratios for the oxygen addition to CH3OCH2O2 pathways and the CH3OCH2O2 self-reactions were required. Finally, the influences of the O-3 addition in the sensitive reactions of the fuel initial low-temperature oxidation were investigated in this work. It was interesting to note that O-3 addition could change the dominating reactions in the initial low-temperature oxidation, by the addition of some O-3-related pathways with relatively high sensitivity. (C) 2019 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
机译:实验研究了在大气压喷射搅拌的反应器中实验研究了臭氧加入对二甲醚(DME)的低温氧化的影响,在400-800k的温度范围内。通过使用同步紫外线获得详细的品种信息光离子质谱。实验结果表明,臭氧添加对高反应性中间体的产生具有积极影响。此外,DME的低温反应性显着增强,导致在较低温度下燃料消耗和中间体形成的温度窗口的扩大。因此,可以获得低温调节(400-500k)的新型实验数据。这种特殊温度制度的数据集产生了对DME低温动力学的见解,该洞察DME低温动力学进一步支持基于现有DME模型的建模分析(Metcalfe等,2013; Wang等,2015)与臭氧相结合子机制(Zhao等,2016)。该分析表明,在该低温下(T <440K),诸如第二氧气通道的温度敏感反应可能几乎“冷冻”。此外,发现一些中间体的产生通过反应对强烈地控制,例如CH 3OCH2 + O-2 = CH 3OCH 2 O 2和CH 3OCH2 + O-2 = 2CH(2)O + OH用于CH 2 O的形成。该发现可用于检查两种模型中的分支比,分析表明,需要进一步修饰CH3OCH2O2途径的氧加入的分支比,并且需要CH 3OCH 2 O 2自我反应。最后,在这项工作中研究了燃料初始低温氧化敏感反应的O-3添加的影响。值得注意的是,通过添加一些具有相对高灵敏度的O-3相关途径,O-3添加可以改变初始低温氧化中的主导反应。 (c)2019燃烧研究所。由elsevier Inc.出版的所有权利保留。

著录项

  • 来源
    《Combustion and Flame》 |2020年第4期|277-286|共10页
  • 作者单位

    Tsinghua Univ Ctr Combust Energy Beijing 100084 Peoples R China|Tsinghua Univ Key Lab Thermal Sci & Power Engn MOE Beijing 100084 Peoples R China;

    Tsinghua Univ Ctr Combust Energy Beijing 100084 Peoples R China|Tsinghua Univ Key Lab Thermal Sci & Power Engn MOE Beijing 100084 Peoples R China;

    Sandia Natl Labs Combust Res Facil Livermore CA 94551 USA;

    Univ Sci & Technol China Natl Synchrotron Radiat Lab Hefei 230026 Anhui Peoples R China;

    Tsinghua Univ Ctr Combust Energy Beijing 100084 Peoples R China|Tsinghua Univ Key Lab Thermal Sci & Power Engn MOE Beijing 100084 Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Ozone assisted low-temperature oxidation; DME; Jet-stirred reactor; Synchrotron vacuum ultraviolet; photoionization mass spectrometry; Ozone effect;

    机译:臭氧辅助低温氧化;DME;喷射式反应器;同步紫外线紫外线;光离子质谱;臭氧效果;

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