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The competition between direct gas-solid reduction and oxygen uncoupling of CuO oxygen carrier in chemical looping with oxygen uncoupling: A single particle simulation study

机译:用氧分耦合中CuO氧载体直接气固降低和CuO氧载体的竞争:单一粒子模拟研究

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摘要

In chemical looping with oxygen uncoupling (CLOU), the oxygen carrier (e.g., CuO-based materials) can be reduced either by direct decomposition or by heterogeneous gas-solid reaction. In most cases, the above two reaction pathways take place in parallel and compete with each other, which therefore make it very difficult to quantify the exact proportion of their contributions to the oxygen carrier conversion. The failure to distinguish the individual significance of each reaction route hinders the acquisition of a convincing reaction kinetic model. In this work, the conversion processes of CuO oxygen carrier in free space and in thermogravimetric crucible were simulated by a single particle model, in which the heterogeneous/homogeneous reactions as well as the heat/mass transfer inside and outside a porous particle were incorporated. The competition between the direct gas-solid reduction (using H-2 as fuel gas) and oxygen uncoupling of the CuO oxygen carrier was analyzed from the aspects of the relative significance of each reaction route and the interactions between them. The results showed that the significances of each reaction route varied with the temperature and H-2 concentration conditions. To quantify the relative significance of each reaction route at different conditions, the controlling regime diagram of CuO conversion in free space was given. The CuO conversion was more likely to be dominated by the oxygen uncoupling process when the particle was in crucible. For the conversion of CuO in free space, the exothermic gas-solid reduction increased the particle temperature and further facilitated the oxygen uncoupling rate, which was considered as the predominant interactions. Differently, for the conversion of CuO in crucible, the key interactions were characterized as: the homogeneous reaction between H-2 and O-2 decreased the O-2 concentration neighboring the CuO particle and thus increased its oxygen uncoupling rate. (C) 2020 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
机译:在具有氧耦合(CLOU)的化学环上,通过直接分解或通过异质气体固体反应可以减少氧载体(例如,基于CUO基材料)。在大多数情况下,上述两种反应途径平行地进行并彼此竞争,因此使其使其对氧载体转化贡献的确切比例非常困难。未能区分每个反应路线的个体意义阻碍了采集令人信服的反应动力学模型。在这项工作中,通过单个粒子模型模拟了基于自由空间和热重坩埚中CuO氧载体的转化方法,其中掺入了多均匀/均匀反应以及内部和外部的热/质量转移。从每个反应途径的相对意义和它们之间的相互作用的方面,分析了直接气固缩减(使用H-2作为燃料气体)和CuO氧载体的氧耦合之间的竞争。结果表明,每个反应路径的重要性随温度和H-2浓度条件而变化。为了量化在不同条件下每种反应途径的相对重要性,给出了自由空间中CuO转化的控制方案图。当颗粒在坩埚中时,CuO转化率更可能是由氧的解耦过程主导。为了在自由空间中转化CuO,放热气体固体降低增加了粒子温度并进一步促进了被认为是主要相互作用的氧脱悬率。不同的是,对于CuO在坩埚中的转化,关键相互作用表征为:H-2和O-2之间的均匀反应降低了与CuO颗粒相邻的O-2浓度,从而提高了其氧的非偶联率。 (c)2020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11期|219-227|共9页
  • 作者

    Su Mingze; Zhao Haibo; Tian Xin;

  • 作者单位

    Huazhong Univ Sci & Technol Sch Energy & Power Engn State Key Lab Coal Combust Wuhan 430074 Peoples R China;

    Huazhong Univ Sci & Technol Sch Energy & Power Engn State Key Lab Coal Combust Wuhan 430074 Peoples R China;

    Huazhong Univ Sci & Technol Sch Energy & Power Engn State Key Lab Coal Combust Wuhan 430074 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

    Chemical looping with oxygen uncoupling; CuO oxygen carrier; Competition reactions; Single particle simulation;

    机译:化学循环与氧气耦合;CuO氧载体;竞争反应;单粒子仿真;

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