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Hydrogen production and reduction of Ni-based oxygen carriers during chemical looping steam reforming of ethanol in a fixed-bed reactor

机译:固定床反应器中乙醇的化学循环蒸汽重整过程中氢气的产生和镍基氧载体的还原

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摘要

Hydrogen production and reduction of Ni-based oxygen carriers (OCs) during chemical looping steam reforming (CLSR) of ethanol were studied in a fixed-bed reactor using four OCs with different supports including NiO/SBA-15, NiO/MCM-41, NiO/MMT and NiO/Al2O3. The OCs prepared were characterized by N-2 adsorption-desorption, TPR, TPO, XRD, TEM, FTIR and TGA-DSC. The results demonstrated that NiO component in all the OCs was first reduced by ethanol and the reduced OCs were responsible of catalytic steam reforming and water gas shift for hydrogen production. Mesoporous NiO/SBA-15 presented increasing conversion of NiO reduction and the highest selectivity of hydrogen production. The conversion of ethanol increased with reactions proceeding until the highest value is reached after about similar to 300s, and the negative steam conversion obtained was resulted from H2O formation from ethanol oxidation by OCs. Compared with MMT and Al2O3 supports, the oxidization of NiO with MCM-41 and SBA-15 supports was very fast and less carbon was formed and deposited. Enhancement in hydrogen production from CLSR process was achieved by in-situ CO2 removal. Shrinking Core model (SCM) based on the constant pattern model for fixed-bed reactor indicated the rates of OCs reduction with ethanol were mainly controlled by surface chemical reaction and product layer diffusion. The reduction process was found to undergo three different rate-limiting stages, and the critical times for changes in the rate-limiting steps were determined. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在固定床反应器中研究了乙醇化学循环蒸汽重整(CLSR)过程中氢的产生和镍基氧载体(OCs)的还原,该反应器使用四种带有不同载体的OCs,包括NiO / SBA-15,NiO / MCM-41, NiO / MMT和NiO / Al2O3。通过N-2吸附-脱附,TPR,TPO,XRD,TEM,FTIR和TGA-DSC对所制备的OC进行了表征。结果表明,所有OC中的NiO组分首先被乙醇还原,还原的OC负责催化蒸汽重整和水煤气转化制氢。中孔NiO / SBA-15表现出NiO还原转化率的提高和制氢的最高选择性。乙醇的转化率随反应的进行而增加,直到约300 s后达到最大值,而获得的负蒸汽转化率则是由于乙醇被OCs氧化形成H2O所致。与MMT和Al2O3载体相比,NiO用MCM-41和SBA-15载体的氧化非常快,并且形成和沉积的碳较少。通过原位去除CO2可以提高CLSR工艺制氢的能力。基于恒定床模型的固定床反应堆收缩核模型(SCM)表明乙醇对OCs的还原速率主要受表面化学反应和产物层扩散的控制。发现还原过程经历了三个不同的限速阶段,并确定了限速步骤变化的关键时间。 (C)2017氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2017年第42期|26217-26230|共14页
  • 作者单位

    Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai 200093, Peoples R China;

    Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai 200093, Peoples R China;

    Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai 200093, Peoples R China;

    Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai 200093, Peoples R China;

    Dalian Univ Technol, Sch Energy & Power Engn, Dalian 116023, Peoples R China;

    Dalian Univ Technol, Sch Energy & Power Engn, Dalian 116023, Peoples R China;

    Chinese Acad Sci, Inst Engn Thermophys, Beijing 100190, Peoples R China;

    Chinese Acad Sci, Inst Engn Thermophys, Beijing 100190, 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 steam reforming (CLSR); Ethanol; Ni-based oxygen carriers (OCs); Reaction kinetics;

    机译:化学循环蒸汽重整(CLSR);乙醇;镍基氧载体(OCs);反应动力学;
  • 入库时间 2022-08-18 00:19:31

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