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首页> 外文期刊>Renewable energy >Hydrogen production via steam reforming of glycerol over Rh/γ-Al_2O_3 catalysts modified with CeO_2, MgO or La_2O_3
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Hydrogen production via steam reforming of glycerol over Rh/γ-Al_2O_3 catalysts modified with CeO_2, MgO or La_2O_3

机译:通过CeO_2,MgO或La_2O_3改性rh /γ-Al_2O_3催化剂,通过甘油蒸汽重整氢气生产氢气生产

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摘要

The glycerol steam reforming (GSR) reaction for hydrogen production was investigated over Rh-based catalysts supported on gamma-Al2O3 modified with CeO2, MgO or La2O3. High specific surface area mesoporous supports (Al2O3, CeO2-Al2O3, MgO-Al2O3 and La2O3-Al2O3) were synthesized by the surfactantassisted co-precipitation method using cetyltrimethylammonium bromide (CTAB) as template. Then, highly dispersed Rh-based catalysts were prepared by the wetness impregnation technique. The physicochemical properties of the as-prepared supports and catalysts were investigated by N-2-physisorption, XRD, ICP-AES, CO-chemisorption, TEM, H-2-TPR, CO2-TPD and NH3-TPD measurements. Performance test experiments were carried out in a continuous flow fixed-bed reactor at water-to-glycerol feed ratio (WGFR) of 20:1 (molar), temperatures from 400 degrees C to 750 degrees C, weight hourly space velocity of 50,000 ml g(-1) h(-1) and atmospheric pressure. The stability of all catalysts was also investigated through 12 h time-on-stream (TOS) experiments at 600 degrees C using a WGFR of 9:1. All catalysts were remarkably stable during TOS with total glycerol conversion of =90%, glycerol conversion into gaseous products of =45% and H-2 selectivity of = 78%. The final H-2 yield for all catalysts was 2.4-2.9 mol H-2/mol glycerol. TEM experiments showed that the carbon formed onto the spent catalysts was amorphous and that sintering was mostly avoided during TOS, helping explain the excellent catalytic stability observed. The unpromoted catalyst seems to be following a different reaction pathway than and the promoted ones that depends strongly on the population and kind of acid and basic sites over its surface. (c) 2020 Elsevier Ltd. All rights reserved.
机译:在用CeO2,MgO或La2O3改性的γ-Al2O3上支持的RH基催化剂上研究了用于氢气产生的甘油蒸汽重整(GSR)反应。使用甲酰基三甲基溴化铵(CTAB)作为模板,通过Cetylyrimanticalisted共沉淀法合成了高比表面积介孔载体(Al 2 O 3,CeO 2-Al 2 O 3,MgO-Al2O3和La2O3-Al2O3)。然后,通过湿润浸渍技术制备高度分散的RH基催化剂。通过N-2 - 物理化,XRD,ICP-AES,共级化学吸附,TEM,H-2-TPR,CO2-TPD和NH3-TPD测量来研究由制备的支撑载体和催化剂的物理化学性质。在连续流动固定床反应器中进行性能测试实验在水 - 甘油进料比(WGFR)为20:1(摩尔),400℃至750℃的温度,重量小时空速50,000ml G(-1)H(-1)和大气压。使用WGFR为9:1的WGFR,还在600℃下进行12小时次流(TOS)实验,还研究了所有催化剂的稳定性。在TOS期间,所有催化剂在甘油总转化率= 90%,甘油转化成气态产物的= 45%和H-2选择性> = 78%时,均显着稳定。所有催化剂的最终H-2产率为2.4-2.9molH-2 / mol甘油。 TEM实验表明,形成在废催化剂上的碳是无定形的,并且在TOS期间大部分避免了烧结,有助于解释观察到的优异的催化稳定性。非突出的催化剂似乎遵循不同的反应途径,而促进的反应途径依赖于其表面上的酸和碱性位点的普遍存在的促进途径。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Renewable energy》 |2020年第1期|908-925|共18页
  • 作者单位

    Univ Western Macedonia Dept Chem Engn Lab Alternat Fuels & Environm Catalysis LAFEC GR-50100 Kozani Greece;

    CNR Inst Adv Energy Technol Nicola Giordano ITAE Via S Lucia Contesse 5 I-98126 Messina Italy;

    CNR Inst Adv Energy Technol Nicola Giordano ITAE Via S Lucia Contesse 5 I-98126 Messina Italy;

    Univ Zaragoza CSIC Inst Nanociencia Aragon INA Chem & Environm Engn Dept Zaragoza 50018 Spain|Univ Zaragoza CSIC Inst Ciencia Mat Aragon ICMA Zaragoza 50018 Spain|CIBERBBN Networking Res Ctr Bioengn Biomat & Nanomed Madrid 28029 Spain;

    CNR Inst Adv Energy Technol Nicola Giordano ITAE Via S Lucia Contesse 5 I-98126 Messina Italy;

    Univ Western Macedonia Dept Chem Engn Lab Alternat Fuels & Environm Catalysis LAFEC GR-50100 Kozani Greece;

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

    Hydrogen production; Glycerol; Steam reforming; Rh catalysts; Metal oxide promoters;

    机译:氢气生产;甘油;蒸汽重整;rh催化剂;金属氧化物启动子;

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