METHANATION OF CO2 ON H-2-REDUCED NI(II) OR CO(II)-BEARING FERRITES AT 200-DEGREES-C

被引:14
作者
TSUJI, M
KATO, H
KODAMA, T
CHANG, SG
HESEGAWA, N
TAMAURA, Y
机构
[1] Department of Chemistry, Research Center for Carbon Recycling and Utilization, Tokyo Institute of Technology, Tokyo, 152, Ookayama, Meguro-ku
[2] Lawrence Berkeley Laboratory, University of California, Berkeley, 94720, CA
关键词
D O I
10.1007/BF00354564
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The methanation of CO2 gas at 200 degrees C was investigated in Co(II) or Ni(II)-bearing ferrites with substitution of up to 0.262 and 0.143, respectively. The metal substitution in the ferrite facilitated the methanation of the deposited carbon from CO2 gas in the H-2-reduced M(II)-bearing ferrite in comparison with the reactivity of the H-2-reduced magnetite with the same spinel structure. The effect on the reactivity of methanation was found to be much larger in Ni(II)-substitution. The degree of the effect increased with increases in the Ni(II)-substitution, while it remained about the same with increases in the Co(II) -substitution. The maximum methanation (86.9%) of CO2 was attained in the Ni(II)-bearing ferrite activated by H-2 gas for 3.0 h.
引用
收藏
页码:6227 / 6230
页数:4
相关论文
共 19 条
[1]   CARBON-DIOXIDE DECOMPOSITION INTO CARBON WITH THE RHODIUM-BEARING MAGNETITE ACTIVATED BY H-2-REDUCTION [J].
AKANUMA, K ;
NISHIZAWA, K ;
KODAMA, T ;
TABATA, M ;
MIMORI, K ;
YOSHIDA, T ;
TSUJI, M ;
TAMAURA, Y .
JOURNAL OF MATERIALS SCIENCE, 1993, 28 (04) :860-864
[2]   HYDROGENATION OF CO AND CO2 OVER IRON FOILS - CORRELATIONS OF RATE, PRODUCT DISTRIBUTION, AND SURFACE COMPOSITION [J].
DWYER, DJ ;
SOMORJAI, GA .
JOURNAL OF CATALYSIS, 1978, 52 (02) :291-301
[3]  
KATO H, IN PRESS J MATER SCI
[4]   FORMATION OF THE OXIDIZED FE3O4-FE2TIO4 SOLID-SOLUTION BY THE AIR OXIDATION OF THE AQUEOUS SUSPENSION [J].
KATSURA, T ;
TAMAURA, Y ;
CHYO, GS .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1979, 52 (01) :96-100
[5]   DECOMPOSITION OF CO2 TO CARBON BY H-2-REDUCED NI(II)- AND CO(II)-BEARING FERRITES AT 300-DEGREES-C [J].
KODAMA, T ;
KATO, H ;
CHANG, SG ;
HASEGAWA, N ;
TSUJI, M ;
TAMAURA, Y .
JOURNAL OF MATERIALS RESEARCH, 1994, 9 (02) :462-467
[6]   DECOMPOSITION OF CO2 AND CO INTO CARBON WITH ACTIVE WUSTITE PREPARED FROM ZN(II)-BEARING FERRITE [J].
KODAMA, T ;
TABATA, M ;
TOMINAGA, K ;
YOSHIDA, T ;
TAMAURA, Y .
JOURNAL OF MATERIALS SCIENCE, 1993, 28 (02) :547-552
[7]   DECOMPOSITION OF CARBON-DIOXIDE TO CARBON WITH ACTIVE WUSTITE AT 300-DEGREES-C [J].
KODAMA, T ;
TOMINAGA, K ;
TABATA, M ;
YOSHIDA, T ;
TAMAURA, Y .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1992, 75 (05) :1287-1289
[8]   ANION EXCHANGE STUDIES .6. THE DIVALENT TRANSITION ELEMENTS MANGANESE TO ZINC IN HYDROCHLORIC ACID [J].
KRAUS, KA ;
MOORE, GE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) :1460-1462
[9]   CATALYTIC BEHAVIOR AND PHASE-COMPOSITION CHANGE OF IRON CATALYST IN HYDROGENATION OF CARBON-DIOXIDE [J].
LEE, MD ;
LEE, JF ;
CHANG, CS .
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1990, 23 (02) :130-136
[10]   HYDROGENATION OF SURFACE CARBON ON ALUMINA-SUPPORTED NICKEL [J].
MCCARTY, JG ;
WISE, H .
JOURNAL OF CATALYSIS, 1979, 57 (03) :406-416