Thermocatalytic decomposition of methane for hydrogen production using activated carbon catalyst: Regeneration and characterization studies

被引:54
作者
Abbas, Hazzim F. [1 ]
Daud, W. M. A. Wan [1 ]
机构
[1] Univ Malaya, Dept Chem Engn, Kuala Lumpur 50603, Malaysia
关键词
Regeneration; Catalytic methane decomposition; Hydrogen production; Activated carbon; Characterization; FLUIDIZED-BED; COKE CHARACTERIZATION; DIRECT CRACKING; DEACTIVATION; OXIDATION; CO2; PYROLYSIS; KINETICS; BLACKS; CHAR;
D O I
10.1016/j.ijhydene.2009.08.014
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
A series of experiments was conducted to study the deactivation and regeneration of activated carbon catalyst used for methane thermocatalytic decomposition to produce hydrogen. The catalyst becomes deactivated due to carbon deposition and six decomposition cycles of methane at temperatures of 850 and 950 degrees C, and five cycles of regeneration by using CO2 at temperatures of 900, 950 and 1000 degrees C were carried out to evaluate the stability of the catalyst. The experiment was conducted by using a thermobalance by monitoring the mass gain during decomposition or the mass lost during the regeneration with time. The initial activity and the ultimate mass gain of the catalyst decreased after each regeneration cycle at both reaction temperatures of 850 and 950 degrees C, but the amount is smaller under the more severe regenerating conditions. For the reaction at 950 degrees C, comparison between the first and sixth reaction cycles shows that the initial activity decreased by 69, 51 and 42%, while the ultimate mass gain decreased by 62%, 36% and 16% when CO2 gasification carried out at 900, 950 and 1000 degrees C respectively. Temperature-programmed oxidation profiles for the deactivated catalyst at reaction temperature of 950 degrees C and after several cycles showed two peaks which are attributed to different carbon characteristics, while one peak was obtained when the experiment was carried out at 850 degrees C. In conclusion, conducting methane decomposition at 950 degrees C and regeneration at 1000 degrees C showed the lowest decrease in the mass gain with reaction cycles. (C) 2009 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8034 / 8045
页数:12
相关论文
共 48 条
[1]   Hydrogen production via the direct cracking of methane over Ni/SiO2:: catalyst deactivation and regeneration [J].
Aiello, R ;
Fiscus, JE ;
zur Loye, HC ;
Amiridis, MD .
APPLIED CATALYSIS A-GENERAL, 2000, 192 (02) :227-234
[2]  
ALAN MD, 2006, INT J HYDROGEN ENERG, V31, P1989
[3]   COx free hydrogen by methane decomposition over activated carbons [J].
Ashok, J. ;
Kumar, S. Naveen ;
Venugopal, A. ;
Kumari, V. Durga ;
Tripathi, S. ;
Subrahmanyam, M. .
CATALYSIS COMMUNICATIONS, 2008, 9 (01) :164-169
[4]   Catalytic decomposition of CH4 over NiO-Al2O3-SiO2 catalysts: Influence of catalyst preparation conditions on the production of H2 [J].
Ashok, Janyam ;
Raju, Gangadhara ;
Reddy, Padigapati Shiva ;
Subrahmanyam, Machiraju ;
Venugopal, Akula .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2008, 33 (18) :4809-4818
[5]   Comparison on pore development of activated carbon produced from palm shell and coconut shell [J].
Daud, WMAW ;
Ali, WSW .
BIORESOURCE TECHNOLOGY, 2004, 93 (01) :63-69
[6]   KINETIC MEASUREMENT AND MODELING OF CARBON OXIDATION [J].
DU, ZY ;
SAROFIM, AF ;
LONGWELL, JP ;
MIMS, CA .
ENERGY & FUELS, 1991, 5 (01) :214-221
[7]   Catalytic decomposition of methane over a wood char concurrently activated by a pyrolysis gas [J].
Dufour, A. ;
Celzard, A. ;
Fierro, V. ;
Martin, E. ;
Broust, F. ;
Zoulalian, A. .
APPLIED CATALYSIS A-GENERAL, 2008, 346 (1-2) :164-173
[8]   FT-IR study of rockrose and of char and activated carbon [J].
GomezSerrano, V ;
PastorVillegas, J ;
PerezFlorindo, A ;
DuranValle, C .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1996, 36 (01) :71-80
[9]   Processes occurring during deactivation and regeneration of metal and metal oxide catalysts [J].
Jackson, SD .
CHEMICAL ENGINEERING JOURNAL, 2006, 120 (1-2) :119-125
[10]   Hydrogen production by the thermocatalytic decomposition of methane in a fluidized bed reactor [J].
Jang, Hyun Tae ;
Cha, Wang Seog .
KOREAN JOURNAL OF CHEMICAL ENGINEERING, 2007, 24 (02) :374-377