Chemical structures of coprecipitated Fe-Ce mixed oxides

被引:160
作者
Pérez-Alonso, FJ
Granados, ML
Ojeda, M
Terreros, P
Rojas, S
Herranz, T
Fierro, JLG
Gracia, M
Gancedo, JR
机构
[1] CSIC, Inst Catalisis & Petr Quim, Madrid 28049, Spain
[2] CSIC, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
关键词
D O I
10.1021/cm0477669
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
Two series of Fe-Ce catalysts were prepared following two different methods: coprecipitation from Fe and Ce nitrate solutions and physical mixing of pure Fe and Ce precursors. Evidence of the presence of a chemical interaction between Fe and Cc was found in the calcined state of the coprecipitated catalysts. Such evidence was obtained with different techniques. The Fe-Ce interaction occurs through the formation of hematite-like and cubic ceria-like solid solutions. In the hematite-like solid solution, Ce cations are dissolved in the hematite structure, whereas in the cubic ceria-like solid solution Fe cations are dissolved in the ceria structure. Such interactions were absent in the samples prepared by the physical mixing. It is suggested that the Fe-Ce interaction present in the calcined state results in a strong Fe-Ce interaction in the final catalyst that defines their better catalytic properties. When tested in the Fischer-Tropsch synthesis of hydrocarbons from CO + H-2 gas mixtures, the coprecipitation method series showed higher CO conversion rates, higher hydrocarbon formation rates, and a higher degree of olefinicity than the pure Fe catalyst sample and the Fe-Ce samples prepared by physical mixing.
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收藏
页码:2329 / 2339
页数:11
相关论文
共 49 条
[1]  
[Anonymous], CATALYSIS CERIA RELA
[2]   Surface and reduction energetics of the CeO2-ZrO2 catalysts [J].
Balducci, G ;
Kaspar, J ;
Fornasiero, P ;
Graziani, M ;
Islam, MS .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (03) :557-561
[3]   AN INSITU FE-57 MOSSBAUER SPECTROSCOPIC INVESTIGATION OF THE REDUCTION OF IRON-CERIUM OXIDE CATALYSTS IN DIFFERENT GASEOUS REDUCING AGENTS [J].
BERRY, FJ ;
JOBSEN, S ;
JONES, SL .
HYPERFINE INTERACTIONS, 1989, 46 (1-4) :613-618
[4]  
Cornell R.M., 1996, The Iron Oxide: Structure, Properties, Reactions, Occurance and Uses
[5]  
Daniels J. M., 1970, Canadian Journal of Physics, V48, P381, DOI 10.1139/p70-054
[6]  
De Grave E., 1989, MOSSBAUER SPECTROSCO, P59
[7]  
deFaria DLA, 1997, J RAMAN SPECTROSC, V28, P873, DOI 10.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO
[8]  
2-B
[9]  
DELEITENBURG C, 1995, CHEM COMMUN, P2181
[10]  
EHASON SH, 1999, APPL CATAL A-GEN, V186, P229