Low-temperature reforming of ethanol over CeO2-supported Ni-Rh bimetallic catalysts for hydrogen production

被引:159
作者
Kugai, J [1 ]
Velu, S [1 ]
Song, CS [1 ]
机构
[1] Penn State Univ, Energy Inst, Clean Fuels & Catalysis Program, Dept Energy & Geoenvironm Engn, University Pk, PA 16802 USA
关键词
bio-ethanol; reforming; catalyst; Ni-Rh; ethanol hydrogen;
D O I
10.1007/s10562-005-4901-7
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 new series of Ni-Rh bimetallic catalysts with different Ni and Rh loadings on a high-surface-area CeO2 was developed for the reforming of bio-ethanol at low-temperature (below 450 degrees C) to produce H-2-rich gas for on-site or on-board fuel cell applications. Oxidative steam reforming of ethanol (OSRE) over a Ni-Rh/CeO2 catalyst containing 5 wt% Ni and 1 wt% Rh was found to be more efficient offering about 100% ethanol conversion at 375 degrees C with high H-2 and CO2 selectivity and low CO selectivity compared to the steam reforming of ethanol (SRE) reaction which required a higher temperature of about 450 degrees C to achieve 100% ethanol conversion. The high temperature SRE reaction favors the formation of large amount of CO, which would make the downsteam CO cleanup more complicated for polymer electrolyte membrane fuel cell (PEMFC). The presence of O-2 in the feed gas was found to greatly enhance the conversion of ethanol to produce H-2 and CO2 as major products. Increase in Ni content above 5 wt% in the catalyst formulation decreased the H-2 selectivity while the selectivity of undesirable CH4 and acetaldehyde increased. The 1 wt% Rh/CeO2 catalyst was twice as active as 10 wt% Ni/CO2 catalyst in terms of ethanol conversion and acetaldehyde selectivity and this indicated that Rh was more effective in C-C bond cleavage than Ni. The reaction was found to proceed through the formation of acetaldehyde intermediate, which subsequently underwent decomposition to produce a mixture of CO and CH4 or reforming with H2O and O-2 to produce CO, CO2 and H-2. The role of Rh is mainly to cleave the C-C and C-H bonds of ethanol to produce H-2 and COx while Ni addition helps converting CO into CO2 and H-2 by WGS reaction under the conditions employed.
引用
收藏
页码:255 / 264
页数:10
相关论文
共 28 条
[1]  
AGRELL J, 2002, CATALYSIS SPECIALIST, V16, P67
[2]   Metal-catalysed steam reforming of ethanol in the production of hydrogen for fuel cell applications [J].
Breen, JP ;
Burch, R ;
Coleman, HM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 39 (01) :65-74
[3]  
Brown LF, 2001, INT J HYDROGEN ENERG, V26, P381, DOI 10.1016/S0360-3199(00)00092-6
[4]   Performance of Rh/Al2O3 catalyst in the steam reforming of ethanol:: H2 production for MCFC [J].
Cavallaro, S ;
Chiodo, V ;
Freni, S ;
Mondello, N ;
Frusteri, F .
APPLIED CATALYSIS A-GENERAL, 2003, 249 (01) :119-128
[5]   Hydrogen produced from ethanol for internal reforming molten carbonate fuel cell [J].
Cavallaro, S ;
Mondello, N ;
Freni, S .
JOURNAL OF POWER SOURCES, 2001, 102 (1-2) :198-204
[6]   Hydrogen production by auto-thermal reforming of ethanol on Rh/Al2O3 catalyst [J].
Cavallaro, S ;
Chiodo, V ;
Vita, A ;
Freni, S .
JOURNAL OF POWER SOURCES, 2003, 123 (01) :10-16
[7]   Renewable hydrogen from ethanol by autothermal reforming [J].
Deluga, GA ;
Salge, JR ;
Schmidt, LD ;
Verykios, XE .
SCIENCE, 2004, 303 (5660) :993-997
[8]   Hydrogen production by ethanol reforming over Rh/CeO2-ZrO2 catalysts [J].
Diagne, C ;
Idriss, H ;
Kiennemann, A .
CATALYSIS COMMUNICATIONS, 2002, 3 (12) :565-571
[9]   Production of hydrogen for fuel cells by reformation of biomass-derived ethanol [J].
Fatsikostas, AN ;
Kondarides, DI ;
Verykios, XE .
CATALYSIS TODAY, 2002, 75 (1-4) :145-155
[10]   On-board hydrogen production in a hybrid electric vehicle by bio-ethanol oxidative steam reforming over Ni and noble metal based catalysts [J].
Fierro, V ;
Akdim, O ;
Mirodatos, C .
GREEN CHEMISTRY, 2003, 5 (01) :20-24