Cobalt-nickel-phosphorus supported on Pd-activated TiO2 (Co-Ni-P/Pd-TiO2) as cost-effective and reusable catalyst for hydrogen generation from hydrolysis of alkaline sodium borohydride solution

被引:95
作者
Rakap, Murat [1 ,2 ]
Kalu, Egwu Eric [1 ]
Ozkar, Saim [2 ]
机构
[1] FAMU FSU Coll Engn, Dept Chem & Biomed Engn, Tallahassee, FL 32312 USA
[2] Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey
基金
美国国家科学基金会;
关键词
Cobalt; Nickel; Sodium borohydride; Hydrolysis; Hydrogen generation; BORON/NICKEL FOAM; AMMONIA-BORANE; B CATALYST; NANOCLUSTERS; KINETICS; STORAGE; ELECTROLESS; DEPOSITION; SYSTEM;
D O I
10.1016/j.jallcom.2011.04.023
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
Catalytically active, low-cost, and reusable transition metal catalysts are desired to develop on-demand hydrogen generation system for practical onboard applications. Electrolessly deposited Pd-activated TiO2-supported Co-Ni-P ternary alloy catalyst (Co-Ni-P/Pd-TiO2) is employed as catalyst in the hydrolysis of alkaline sodium borohydride solution. The catalyst is found to be isolable, redispersible, and reusable in the hydrolysis of alkaline NaBH4. The reported work also includes the full experimental details for the collection of a wealth of kinetic data to determine the activation energy (E-a = 57.0 kJ/mol) and effects of the amount of catalyst, amount of substrate, and temperature on the rate for the catalytic hydrolysis of NaBH4. Maximum H-2 generation rate of similar to 460mLH(2) min(-1) (g catalyst)(-1) and similar to 3780mLH(2) min(-1) (g catalyst)(-1) was measured by the hydrolysis of NaBH4 at 25 degrees C and 55 degrees C respectively. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:7016 / 7021
页数:6
相关论文
共 54 条
[41]   Hydrogen generation and storage from hydrolysis of sodium borohydride in batch reactors [J].
Pinto, A. M. F. R. ;
Falcao, D. S. ;
Silva, R. A. ;
Rangel, C. M. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2006, 31 (10) :1341-1347
[42]   Hydrogen generation from the hydrolysis of ammonia borane using cobalt-nickel-phosphorus (Co-Ni-P) catalyst supported on Pd-activated TiO2 by electroless deposition [J].
Rakap, Murat ;
Kalu, Egwu Eric ;
Ozkar, Saim .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2011, 36 (01) :254-261
[43]   Intrazeolite cobalt(0) nanoclusters as low-cost and reusable catalyst for hydrogen generation from the hydrolysis of sodium borohydride [J].
Rakap, Murat ;
Ozkar, Saim .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 91 (1-2) :21-29
[44]   Effect of alloys modified by sodium borohydride alkaline solutions on the kinetics of hydrogen evolution reaction at Mm(Ni3.6Co0.7Mn0.4Al0.3)1.15 hydride electrodes [J].
Santos, D. M. F. ;
Sequeira, C. A. C. ;
Lobo, R. F. M. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2010, 35 (18) :9901-9909
[45]   Hydrogen-storage materials for mobile applications [J].
Schlapbach, L ;
Züttel, A .
NATURE, 2001, 414 (6861) :353-358
[46]   NEW DEVELOPMENTS IN THE CHEMISTRY OF DIBORANE AND OF THE BOROHYDRIDES .9. SODIUM BOROHYDRIDE, ITS HYDROLYSIS AND ITS USE AS A REDUCING AGENT AND IN THE GENERATION OF HYDROGEN [J].
SCHLESINGER, HI ;
BROWN, HC ;
FINHOLT, AE ;
GILBREATH, JR ;
HOEKSTRA, HR ;
HYDE, EK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (01) :215-219
[47]   Hydrogen generation from catalytic hydrolysis of alkaline sodium borohydride solution using attapulgite clay-supported Co-B catalyst [J].
Tian, Hongjing ;
Guo, Qingjie ;
Xu, Dongyan .
JOURNAL OF POWER SOURCES, 2010, 195 (08) :2136-2142
[48]   Hydrogen generation from catalytic hydrolysis of sodium borohydride for proton exchange membrane fuel cells [J].
Wu, C ;
Zhang, HM ;
Yi, BL .
CATALYSIS TODAY, 2004, 93-5 :477-483
[49]   Carbon-supported cobalt catalyst for hydrogen generation from alkaline sodium borohydride solution [J].
Xu, Dongyan ;
Dai, Ping ;
Liu, Xinmin ;
Cao, Changqing ;
Guo, Qingjie .
JOURNAL OF POWER SOURCES, 2008, 182 (02) :616-620
[50]   Hydrogen generation from hydrolysis of alkaline sodium borohydride solution using Pt/C catalyst [J].
Xu, Dongyan ;
Zhang, Huamin ;
Ye, Wei .
CATALYSIS COMMUNICATIONS, 2007, 8 (11) :1767-1771