Highly active structured catalyst made up of mesoporous Co3O4 nanowires supported on a metal wire mesh for the preferential oxidation of CO

被引:64
作者
Marban, Gregorio [1 ]
Lopez, Irene [1 ]
Valdes-Solis, Teresa [1 ]
Fuertes, Antonio B. [1 ]
机构
[1] CSIC, Inst Nacl Carbon, INCAR, Oviedo 33011, Spain
关键词
PROX; Hydrogen; CO; Oxidation; Co3O4; Cobalt; Spinel; Catalytic activity; Stability;
D O I
10.1016/j.ijhydene.2008.07.067
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 novel structured catalyst made up of mesoporous Co3O4 nanowire arrays (active phase) supported on a stainless steel mesh is presented. An important advantage of this catalytic system is that the formation and growth of cobalt oxide nanowires takes place on the surface of stainless steel wires. These mesoporous Co3O4 nanowires have a diameter of 500 nm, a BET surface area of 71 m(2)/g and a pore size of similar to 3.4 nm. The catalytic behavior of this system towards the preferential oxidation of CO was investigated. To this end a microreactor was constructed consisting of a metal wire mesh-Co3O4 nanowire composite rolled and inserted into a standard 1/4 '' stainless steel tube. This structured catalytic system exhibits several important properties: a) a high heat exchange rate and a low pressure drop, b) a remarkable stability over the whole temperature range analyzed (100-175 degrees C) and c) a good catalytic activity which doubles that of the best Co3O4 catalyst previously reported. An added feature of this synthetic procedure is that it allows the simultaneous synthesis of unsupported porous Co3O4 particles (similar to 100 mu m diameter) with slightly different characteristics to those of the supported nanowires. Catalytic tests on these particles highlighted the close relationship between the calcination temperature, the reducibility of the produced spinel and the catalytic activity during the PROX reaction. (C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6687 / 6695
页数:9
相关论文
共 17 条
[1]   Co oxidation by silver cobalt composite oxide [J].
Gulari, E ;
Güldür, C ;
Srivannavit, S ;
Osuwan, S .
APPLIED CATALYSIS A-GENERAL, 1999, 182 (01) :147-163
[2]   On the catalytic activity of Co3O4 in low-temperature CO oxidation [J].
Jansson, J ;
Palmqvist, AEC ;
Fridell, E ;
Skoglundh, M ;
Österlund, L ;
Thormählen, P ;
Langer, V .
JOURNAL OF CATALYSIS, 2002, 211 (02) :387-397
[3]   A mechanistic study of low temperature CO oxidation over cobalt oxide [J].
Jansson, J ;
Skoglundh, M ;
Fridell, E ;
Thormählen, P .
TOPICS IN CATALYSIS, 2001, 16 (1-4) :385-389
[4]   A comparative study of catalysts for the preferential CO oxidation in excess hydrogen [J].
Ko, Eun-Yong ;
Park, Eun Duck ;
Seo, Kyung Won ;
Lee, Hyun Chul ;
Lee, Doohwan ;
Kim, Soonho .
CATALYSIS TODAY, 2006, 116 (03) :377-383
[5]   Application of large pore MCM-41 molecular sieves to improve pore size analysis using nitrogen adsorption measurements [J].
Kruk, M ;
Jaroniec, M ;
Sayari, A .
LANGMUIR, 1997, 13 (23) :6267-6273
[6]   Mesoporous CO3O4 nanowire arrays for lithium ion batteries with high capacity and rate capability [J].
Li, Yanguang ;
Tan, Bing ;
Wu, Yiying .
NANO LETTERS, 2008, 8 (01) :265-270
[7]   Freestanding mesoporous quasi-single-crystalline Co3O4 nanowire arrays [J].
Li, Yanguang ;
Tan, Bing ;
Wu, Yiying .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (44) :14258-14259
[8]   Novel catalytic reactor for oxidative reforming of methanol [J].
Lyubovsky, M ;
Roychoudhury, S .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 54 (04) :203-215
[9]   Towards the hydrogen economy? (vol 32, pg 1625, 2007) [J].
Marban, G. ;
Valdes-Solis, T. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2008, 33 (02) :927-927
[10]   Highly active and selective CuOx/CeO2 catalyst prepared by a single-step citrate method for preferential oxidation of carbon monoxide [J].
Marbán, G ;
Fuertes, AB .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 57 (01) :43-53