Methane steam reforming for hydrogen production using low water-ratios without carbon formation over ceria coated Ni catalysts

被引:114
作者
Xu, Jiahui [1 ]
Yeung, Connie M. Y. [3 ]
Ni, Jun [2 ]
Meunier, Frederic [2 ]
Acerbi, Nadia [1 ]
Fowles, Martin [3 ]
Tsang, Shik Chi [1 ]
机构
[1] Univ Oxford, Inorgan Chem Lab, Wolfson Catalysis Ctr, Oxford OX1 3QR, England
[2] Queens Univ Belfast, Sch Chem & Chem Engn, CenTACat, Belfast BT41 1LB, Antrim, North Ireland
[3] Johnson Matthey Catalysts, Billingham TS23 1LB, Cleveland, England
关键词
sol-gel method; ceria; Ni catalyst; methane steam reforming (MSR); carbon deposition;
D O I
10.1016/j.apcata.2008.02.044
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
There are many advantages for hydrogen production from the catalytic methane steam reforming reaction (MSR) using low water to methane ratios. However, conventional Ni based catalysts suffer from severe carbon deposition under these conditions. A typical supported Ni catalyst at water to methane ratios < 1 at 800 degrees C shows rapid deactivation (within few hours). Incorporation of CeO2 is known to offer a kinetic resistance to carbon deposition for many hydrocarbon oxidation reactions because of its facilitated redox activity. As a result, a study of blending ceria into a supported Ni catalyst by a number of deposition methods has been carried out. Catalyst characterization including DRIFTS, XRD, TPR, TGA, TEM and EDX suggests the prime importance of an intimate contact between Ni and CeO2 in reducing the extent of carbon deposition during the reforming reaction, which critically depends on the preparation method in catalyst synthesis. As a result, a stable and high level of hydrogen production with no significant carbon deposition for over 110 h is demonstrated over the same Ni commercial catalyst pre-coated with ceria using a sol-gel method, which offers the best interface for the reaction. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:119 / 127
页数:9
相关论文
共 33 条
[1]   Acetylene cyclotrimerization over Ni/SiO2 catalysts in hydrogen atmosphere [J].
Boudjahem, AG ;
Monteverdi, S ;
Mercy, M ;
Bettahar, MM .
APPLIED CATALYSIS A-GENERAL, 2003, 250 (01) :49-64
[2]   NEW DEVELOPMENTS IN ELECTROCHEMICAL INFRARED-SPECTROSCOPY - ADLAYER STRUCTURES OF CARBON-MONOXIDE ON MONOCRYSTALLINE METAL-ELECTRODES [J].
CHANG, SC ;
ROTH, JD ;
HO, YH ;
WEAVER, MJ .
JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1990, 54 :1185-1203
[3]   Active-site coating for molecular discrimination in heterogeneous catalysis [J].
Collier, P ;
Golunski, S ;
Malde, C ;
Breen, J ;
Burch, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (41) :12414-12415
[4]   DRIVE -: The future of automotive power:: Fuel cells perspective [J].
Duesterwald, H. G. ;
Guennewig, J. ;
Radtke, P. .
FUEL CELLS, 2007, 7 (03) :183-189
[5]   New nickel catalysts for the formation of filamentous carbon in the reaction of methane decomposition [J].
Ermakova, MA ;
Ermakov, DY ;
Kuvshinov, GG ;
Plyasova, LM .
JOURNAL OF CATALYSIS, 1999, 187 (01) :77-84
[6]   Electrochemical separation of hydrogen from reformate using PEM fuel cell technology [J].
Gardner, C. L. ;
Ternan, M. .
JOURNAL OF POWER SOURCES, 2007, 171 (02) :835-841
[7]   Spectrokinetic investigation of reverse water-gas-shift reaction intermediates over a Pt/CeO2 catalyst [J].
Goguet, A ;
Meunier, FC ;
Tibiletti, D ;
Breen, JP ;
Burch, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (52) :20240-20246
[8]   Carbon deposition on Ni/YSZ composites exposed to humidified methane [J].
He, Hongpeng ;
Hill, Josephine M. .
APPLIED CATALYSIS A-GENERAL, 2007, 317 (02) :284-292
[9]   Critical assessment of power trains with fuel-cell systems and different fuels [J].
Höhlein, B ;
von Andrian, S ;
Grube, T ;
Menzer, R .
JOURNAL OF POWER SOURCES, 2000, 86 (1-2) :243-249
[10]   A comparison of oxygen-vacancy effect on activity behaviors of carbon dioxide and steam reforming of methane over supported nickel catalysts [J].
Huang, TJ ;
Lin, HJ ;
Yu, TC .
CATALYSIS LETTERS, 2005, 105 (3-4) :239-247