Metallic Ni monolith-Ni/MgAl2O4 dual bed catalysts for the autothermal partial oxidation of methane to synthesis gas

被引:22
|
作者
Meng, Fanhui [1 ]
Chen, Guangyin [1 ]
Wang, Yaquan [1 ]
Liu, Yuan [2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Minist Educ, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Chem Engn & Technol, Dept Catalysis Sci & Technol, Tianjin 300072, Peoples R China
关键词
Metallic Ni monolith; Ni/MgAl2O4; Dual bed; Methane; Autothermal partial oxidation; Synthesis gas; SYNGAS; TEMPERATURE; CONVERSION; PATHWAYS; REACTOR; STEAM;
D O I
10.1016/j.ijhydene.2009.12.144
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A dual bed catalyst system consisting of a metallic Ni monolith catalyst in the front followed by a supported nickel catalyst Ni/MgAl2O4 has been studied for the autothermal partial oxidation of methane to synthesis gas. The effects of bed configuration, reforming bed length, feed temperature and gas hourly space velocity on the reaction as well as the stability are investigated. The results show that the metallic Ni monolith in the front functions as the oxidation catalyst, which prevents the exposure of the reforming catalyst in the back to the very high temperature, while the supported Ni/MgAl2O4 in the back functions as the reforming catalyst which further increases the methane conversion by 5%. A typical 5 mmNi monolith-5mmNi/MgAl2O4 dual bed catalyst exhibits methane conversion and hydrogen and carbon monoxide selectivities of 85.3%, 91.5% and 93.0%, respectively, under autothermal conditions at a methane to oxygen molar ratio of 2.0 and gas hourly space velocity of 1.0 x 10(5) h(-1). The dual bed catalyst system is also very stable. (c) 2009 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8182 / 8190
页数:9
相关论文
共 50 条
  • [1] Metallic Ni monolith-Ni/MgAl2O4 dual bed catalysts for the autothermal partial oxidation of methane to synthesis gas
    Key Laboratory of Green Chemical Technology, Tianjin University, Ministry of Education, Tianjin 300072, China
    不详
    Int J Hydrogen Energy, 15 (8182-8190):
  • [2] Combination of dry reforming and partial oxidation of methane over Ni catalysts supported on nanocrystalline MgAl2O4
    Hadian, Narges
    Rezaei, Mehran
    FUEL, 2013, 113 : 571 - 579
  • [3] A dual catalyst bed for the autothermal partial oxidation of methane to synthesis gas
    G. C. M. Tong
    J. Flynn
    C. A. Leclerc
    Catalysis Letters, 2005, 102 : 131 - 137
  • [4] A dual catalyst bed for the autothermal partial oxidation of methane to synthesis gas
    Tong, GCM
    Flynn, J
    Leclerc, CA
    CATALYSIS LETTERS, 2005, 102 (3-4) : 131 - 137
  • [5] Preparation of Ni/Pt catalysts supported on spinel (MgAl2O4) for methane reforming
    Foletto, Edson L.
    Alves, Ricardo W.
    Jahn, Sergio L.
    JOURNAL OF POWER SOURCES, 2006, 161 (01) : 531 - 534
  • [6] Effect of the calcination temperature on Ni/MgAl2O4 catalyst structure and catalytic properties for partial oxidation of methane
    Ozdemir, Hasan
    Oksuzomer, M. A. Faruk
    Gurkaynak, M. Ali
    FUEL, 2014, 116 : 63 - 70
  • [7] Cobalt promoted Ni/MgAl2O4 catalyst in lean methane catalytic oxidation
    Mohammad Varbar
    Seyed Mehdi Alavi
    Mehran Rezaei
    Ehsan Akbari
    Research on Chemical Intermediates, 2022, 48 : 1129 - 1150
  • [8] Cobalt promoted Ni/MgAl2O4 catalyst in lean methane catalytic oxidation
    Varbar, Mohammad
    Alavi, Seyed Mehdi
    Rezaei, Mehran
    Akbari, Ehsan
    RESEARCH ON CHEMICAL INTERMEDIATES, 2022, 48 (03) : 1129 - 1150
  • [9] The deposition of coke from methane on a Ni/MgAl2O4 catalyst
    Guo, Jianjun
    Lou, Hui
    Zheng, Xiaoming
    CARBON, 2007, 45 (06) : 1314 - 1321
  • [10] Coating method for Ni/MgAl2O4 deposition on metallic foams
    Cristiani, Cinzia
    Visconti, Carlo Giorgio
    Latorrata, Saverio
    Bianchi, Enrico
    Tronconi, Enrico
    Groppi, Gianpiero
    Pollesel, Paolo
    SCIENTIFIC BASES FOR THE PREPARATION OF HETEROGENEOUS CATALYSTS: PROCEEDINGS OF THE 10TH INTERNATIONAL SYMPOSIUM, 2010, 175 : 653 - 656