Catalytic decomposition of sulfur trioxide on the binary metal oxide catalysts of Fe/Al and Fe/Ti

被引:69
作者
Kim, Tae-Ho
Gong, Gyeong-Taek
Lee, Byung Gwon
Lee, Kwan-Young
Jeon, Hee-Young
Shin, Chae-Ho
Kim, Honggon
Jung, Kwang-Deog
机构
[1] Korea Adv Inst Sci & Technol, Dept Environm, Seoul 139791, South Korea
[2] Korea Adv Inst Sci & Technol, Proc Technol Div, Seoul 139791, South Korea
[3] Korea Univ, Catalyst & React Engn Lab, Seoul 136701, South Korea
[4] Chungbuk Natl Univ, Dept Chem Engn, Chungbuk 361763, South Korea
关键词
IS cycle; SO3; decomposition; metal sulfate decomposition; hydrogen production;
D O I
10.1016/j.apcata.2006.02.052
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 iodine-sulfur (IS) cycle has been focused for hydrogen production by water splitting using a very high temperature nuclear reactor (VHTR) which is a high temperature heat source. The nuclear energy was absorbed at the temperature ranges of 750-900 degrees C by SO3 decomposition reaction to SO2 and O-2 in IS cycle. In this work, the activity of Fe/Al and Fe/Ti catalysts prepared by a co-precipitation was studied in an attempt to find some suitable catalysts for the decomposition of sulfur trioxide as the oxygen-generating reaction in the thermo-chemical water splitting process. The SO3 decomposition was performed in the temperature range of 750-950 degrees C at a space velocity of 72,000 cm(3)/g cat. h in a fixed bed reactor. The catalytic activity of Fe/Al and Fe/Ti catalysts increased with an increase in Fe loadings, indicating that the Fe component should be active. The mechanism for the SO3 decomposition on metal oxides can be described as follows: the metal sulfate formation (MO + SO3 -> MSO4) and the decomposition of metal sulfate (MSO4 -> MO2 + SO2 and MO2 -> MO + 1/2O(2)). (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
相关论文
共 13 条
[1]  
Barin I., 1989, THERMOCHEMICAL DATA
[2]  
COX KE, 1983, ALTERN ENERGY SOURCE, V3, P385
[3]   STUDY OF THERMOCHEMICAL HYDROGEN PREPARATION .3. OXYGEN-EVOLVING STEP THROUGH THERMAL SPLITTING OF SULFURIC-ACID [J].
DOKIYA, M ;
KAMEYAMA, T ;
FUKUDA, K ;
KOTERA, Y .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1977, 50 (10) :2657-2660
[4]  
FEFEVRE G, 1983, ADV COLLOID INTERF S, V19, P309
[5]   ENERGY REQUIREMENTS IN PRODUCTION OF HYDROGEN FROM WATER [J].
FUNK, JE ;
REINSTRO.RM .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1966, 5 (03) :336-&
[6]   In situ Fourier transform infrared measurements of sulfate adsorption on hematite in aqueous solutions [J].
Hug, SJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 188 (02) :415-422
[7]   CATALYZED THERMAL-DECOMPOSITION OF H2SO4 AND PRODUCTION OF HBR BY THE REACTION OF SO2 WITH BR2 AND H2O [J].
ISHIKAWA, H ;
ISHII, E ;
UEHARA, I ;
NAKANE, M .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1982, 7 (03) :237-246
[8]   Catalytic wet oxidation of H2S to sulfur on Fe/MgO catalyst [J].
Jung, KD ;
Joo, OS ;
Cho, SH ;
Han, SH .
APPLIED CATALYSIS A-GENERAL, 2003, 240 (1-2) :235-241
[9]   Sol-gel synthesis, characterization and catalytic properties of Fe-Ti mixed oxides [J].
Neri, G ;
Rizzo, G ;
Galvagno, S ;
Loiacono, G ;
Donato, A ;
Musolino, MG ;
Pietropaolo, R ;
Rombi, E .
APPLIED CATALYSIS A-GENERAL, 2004, 274 (1-2) :243-251
[10]  
NORMAN JH, 1982, GRI800105 GEN AT COM