Development of dehydrogenation catalyst for hydrogen generation in organic chemical hydride method

被引:302
作者
Okada, Yoshimi [1 ]
Sasaki, Eiji [1 ]
Watanabe, Eiji [1 ]
Hyodo, Shinji [1 ]
Nishijima, Hiroaki [1 ]
机构
[1] Chiyoda Corp, R&D Ctr, Kanagawa Ku, Yokohama, Kanagawa 2210022, Japan
关键词
dehydrogenation catalyst; organic chemical hydrides; OCH method; hydrogen station; low-grade hydrogen; global hydrogen energy chain;
D O I
10.1016/j.ijhydene.2005.11.014
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
The utilization of the organic chemical hydride method (OCH method) for hydrogen storage and transportation using hydrogenation and dehydrogenation chemical reactions with aromatic compounds has been investigated since the 1980s. This method provides for both high gravimetric and volumetric hydrogen densities, and the potential risk is very small due to the storage and transportation in the liquid state under ambient pressure. It also has the advantage that hydrogen storage and transportation is carried out as a conventional petrochemical product. However, this method has not been technically established because the dehydrogenation catalyst does not have a sufficient stability and performance. We have developed a dehydrogenation catalyst using a simple fixed-bed reactor that has a high stability and sufficient performance. This catalyst can generate hydrogen from methyl-cyclobexane (MCH: 99.9%) with a conversion > 95%, toluene selectivity > 99.9%, hydrogen generation rate > 1000 Nm(3)/h/m(3) cat under the reasonable conditions of 593 K, ambient pressure, LHSV: 2.0/h and co-feed hydrogen 5-20 mol% in the feed. The estimated production cost at a hydrogen station for fuel cell vehicle (FCV) is around 64.7 Y/Nm(3) H-2(59c/Nm(3) H-2). Two possible applications of this method are introduced. One is the utilization of low-grade hydrogen including impurities. The other is a future vision of the global hydrogen energy chain. (c) 2005 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1348 / 1356
页数:9
相关论文
共 19 条
[1]  
[Anonymous], 1983, STUD SURF SCI CATAL, DOI DOI 10.1016/S0167-2991(09)60054-9
[2]  
COOPER A, 2005, FY2004 PROGR REPORT
[3]  
CORMA A, 1991, APPL CATAL, V67, P307
[4]   ACTIVITY, YIELD PATTERNS, AND COKING BEHAVIOR OF PT AND PTRE CATALYSTS DURING DEHYDROGENATION OF METHYLCYCLOHEXANE .1. IN THE ABSENCE OF SULFUR [J].
COUGHLIN, RW ;
KAWAKAMI, K ;
HASAN, A .
JOURNAL OF CATALYSIS, 1984, 88 (01) :150-162
[5]   REACTIONS OF METHYLCYCLOHEXANE AND NORMAL-HEPTANE OVER SUPPORTED PT AND PT-RE CATALYSTS [J].
DOOLITTLE, WJ ;
SKOULARIKIS, ND ;
COUGHLIN, RW .
JOURNAL OF CATALYSIS, 1987, 107 (02) :490-502
[6]   STATUS OF THE HYDRO-HYDROGEN PILOT PROJECT (EQHHPP) [J].
GRETZ, J ;
DROLET, B ;
KLUYSKENS, D ;
SANDMANN, F ;
ULLMANN, O .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1994, 19 (02) :169-174
[7]   THE 100 MW EURO-QUEBEC HYDRO-HYDROGEN PILOT PROJECT [J].
GRETZ, J ;
BASELT, JP ;
ULLMANN, O ;
WENDT, H .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1990, 15 (06) :419-424
[8]  
HYNEC S, 1998, INT J HYDROGEN ENERG, V23, P803
[9]  
JOUTHIMURUGESAN K, 1985, IND ENG CHEM FUND, V24, P433
[10]  
JOUTHIMURUGESAN K, 1985, AICHE J, V31, P1997