Catalytic reforming of methane with carbon dioxide over nickel catalysts .1. Catalyst characterization and activity

被引:466
作者
Bradford, MCJ [1 ]
Vannice, MA [1 ]
机构
[1] PENN STATE UNIV, UNIVERSITY PK, PA 16802 USA
关键词
methane; carbon dioxide; reforming; nickel; titania; silica; magnesium oxide; carbon;
D O I
10.1016/0926-860X(96)00065-8
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 reforming of methane with carbon dioxide was studied over nickel supported on MgO, TiO2, SiO2, and activated carbon. The influence of the support on catalyst activity and carbon deposition resistivity was markedly different in each case. Although considerable formation of filamentous carbon was observed over Ni/SiO2 (confirmed by TEM and TPO), there was negligible initial loss of catalytic activity. The catalytic activity of Ni/C was very similar to that of Ni/SiO2, but no filamentous carbon appeared to be formed. In contrast to Ni/SiO2, substantially less coking was observed over either the Ni/TiO2 or the Ni/MgO catalysts. Evidence of strong metal-support interaction (SMSI) in the Ni/TiO2 catalyst indicated that large ensembles of nickel atoms, active for carbon deposition, are deactivated or removed by the presence of mobile TiOx species. The identification of two TiOx phases and a Ni5TiO7 phase was made possible by direct measurement of crystalline d spacings with TEM. The Ni/MgO catalyst was both active and very stable for up to 44 h time on stream. Chemisorption, XRD and TEM results indicate the formation of a partially reducible NiO-MgO solid solution, which appears to stabilize the reduced nickel surfaces and provide resistance to carbon deposition.
引用
收藏
页码:73 / 96
页数:24
相关论文
共 91 条
[1]   MAGNESIA-SUPPORTED NICKEL-CATALYSTS .1. FACTORS AFFECTING THE STRUCTURE AND MORPHOLOGICAL PROPERTIES [J].
ARENA, F ;
HORRELL, BA ;
COCKE, DL ;
PARMALIANA, A ;
GIORDANO, N .
JOURNAL OF CATALYSIS, 1991, 132 (01) :58-67
[2]   PARTIAL OXIDATION OF METHANE TO SYNTHESIS GAS-USING CARBON-DIOXIDE [J].
ASHCROFT, AT ;
CHEETHAM, AK ;
GREEN, MLH ;
VERNON, PDF .
NATURE, 1991, 352 (6332) :225-226
[3]  
BAKER RTK, 1995, COMMUNICATION
[4]   VIBRATIONAL SPECTROSCOPY OF CO AT NI(110) - ADSORPTION ENERGY AT ADSORPTION SITES [J].
BAUHOFER, J ;
HOCK, M ;
KUPPERS, J .
SURFACE SCIENCE, 1987, 191 (03) :395-405
[5]   VIBRATIONAL EELS STUDIES OF CO CHEMISORPTION ON CLEAN AND CARBIDED (111), (100) AND (110) NICKEL SURFACES [J].
BERTOLINI, JC ;
TARDY, B .
SURFACE SCIENCE, 1981, 102 (01) :131-150
[6]   THERMODYNAMICS OF 2, TWO-DIMENSIONAL PHASES FORMED BY CO2 CHEMISORPTION ON MGO [J].
BERUTO, D ;
BOTTER, R ;
SEARCY, AW .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (13) :3578-3581
[7]  
BHATTACHARYYA A, 1994, STUD SURF SCI CATAL, V88, P207
[8]   CARBON-DIOXIDE REFORMING OF METHANE OVER LANTHANUM-MODIFIED CATALYSTS IN A FLUIDIZED-BED REACTOR [J].
BLOM, R ;
DAHL, IM ;
SLAGTERN, A ;
SORTLAND, B ;
SPJELKAVIK, A ;
TANGSTAD, E .
CATALYSIS TODAY, 1994, 21 (2-3) :535-543
[9]   A THEORETICAL-STUDY OF THE SITE OF CO DISSOCIATION ON FE(100) [J].
BLYHOLDER, G ;
LAWLESS, M .
SURFACE SCIENCE, 1993, 290 (1-2) :155-162
[10]   CHARACTERIZATION OF CARBONACEAUS DEPOSITS BY TEMPERATURE-PROGRAMMED OXIDATION [J].
BOND, GC ;
DIAS, CR ;
PORTELA, MF .
JOURNAL OF CATALYSIS, 1995, 156 (02) :295-297