H2 production from aqueous-phase reforming of glycerol over Cu-Ni bimetallic catalysts supported on carbon nanotubes

被引:54
作者
Rahman, M. M. [1 ]
机构
[1] Chittagong Univ Engn & Technol, Dept Mech Engn, Chittagong 4349, Bangladesh
关键词
Bimetallic catalyst; Aqueous phase reforming; Glycerol; Hydrogen; WATER-GAS SHIFT; BIOMASS-DERIVED HYDROCARBONS; OXYGEN-CONTAINING GROUPS; HYDROGEN-PRODUCTION; ETHYLENE-GLYCOL; RENEWABLE HYDROGEN; PLATINUM CATALYSTS; METAL-CATALYSTS; METHANOL ELECTROOXIDATION; ALUMINA CATALYSTS;
D O I
10.1016/j.ijhydene.2015.09.015
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
Aqueous-phase reforming of glycerol was investigated over a series of Ni and Cu-Ni bimetallic catalysts supported on multiwalled carbon nanotubes (MWNT). The reaction was carried out in a continuous flow fixed bed reactor (240 degrees C, 40 atm) with a solution of 1 wt% glycerol in DI water at a flow rate of 0.05 mL/min. Amongst the catalysts tested, bimetallic 1Cu-12Ni/MWNT catalyst gave the higher H-2 selectivity (86%) and glycerol conversion (84%) than the benchmark 12Ni/MWNT catalyst. Irrespective of Cu and Ni ratio, bimetallic Cu-Ni catalysts showed higher selectivity and glycerol conversion towards H-2 production than the Ni catalyst. The presence of Cu in bimetallic catalysts resulted in suppression of undesirable methanation reaction. Catalysts characterized by XRD and XPS showed a significant peak shift of Ni in bimetallic Cu-Ni catalysts than the Ni catalyst, suggesting a strong interaction between Cu and Ni. Also H-2-TPR analysis showed that introducing Cu increased Ni reducibility. The bimetallic interaction is thought to be responsible for the lowered methane yield and ultimately, higher hydrogen yield observed. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14833 / 14844
页数:12
相关论文
共 86 条
[1]   Hydrogen production from glycerol: An update [J].
Adhikari, Sushil ;
Fernando, Sandun D. ;
Haryanto, Agus .
ENERGY CONVERSION AND MANAGEMENT, 2009, 50 (10) :2600-2604
[2]   Catalytic conversion of biomass to biofuels [J].
Alonso, David Martin ;
Bond, Jesse Q. ;
Dumesic, James A. .
GREEN CHEMISTRY, 2010, 12 (09) :1493-1513
[3]  
Anderson J.R., 1975, Structure of metallic catalysts
[4]   Biomass as renewable feedstock in standard refinery units. Feasibility, opportunities and challenges [J].
Antonio Melero, Juan ;
Iglesias, Jose ;
Garcia, Alicia .
ENERGY & ENVIRONMENTAL SCIENCE, 2012, 5 (06) :7393-7420
[5]   Hydrotalcite structure derived Ni-Cu-Al catalysts for the production of H2 by CH4 decomposition [J].
Ashok, Jangam ;
Subrahmanyam, Machiraju ;
Venugopal, Akula .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2008, 33 (11) :2704-2713
[6]   Coprecipitated Ni-alumina and Ni-Cu-alumina catalysts of methane decomposition and carbon deposition .2. Evolution of the catalysts in reaction [J].
Avdeeva, LB ;
Goncharova, OV ;
Kochubey, DI ;
Zaikovskii, VI ;
Plyasova, LM ;
Novgorodov, BN ;
Shaikhutdinov, SK .
APPLIED CATALYSIS A-GENERAL, 1996, 141 (1-2) :117-129
[7]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[8]   Improved utilisation of renewable resources: New important derivatives of glycerol [J].
Behr, Arno ;
Eilting, Jens ;
Irawadi, Ken ;
Leschinski, Julia ;
Lindner, Falk .
GREEN CHEMISTRY, 2008, 10 (01) :13-30
[9]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[10]  
Callister WD, 2007, MAT SCI ENG INTRO, P184