STUDY OF THE DEACTIVATION MECHANISM OF AL2O3-SUPPORTED COBALT FISCHER-TROPSCH CATALYSTS

被引:142
作者
SCHANKE, D
HILMEN, AM
BERGENE, E
KINNARI, K
RYTTER, E
ADNANES, E
HOLMEN, A
机构
[1] UNIV TRONDHEIM,NORWEGIAN INST TECHNOL,DEPT IND CHEM,N-7034 TRONDHEIM,NORWAY
[2] SINTEF,APPL CHEM,N-7034 TRONDHEIM,NORWAY
[3] STATOIL,RES CTR,N-7005 TRONDHEIM,NORWAY
关键词
FISCHER-TROPSCH SYNTHESIS; COBALT CATALYSTS; DEACTIVATION; OXIDATION; REDUCTION; PROMOTERS; RHENIUM;
D O I
10.1007/BF00806876
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 influence of water on alumina-supported cobalt catalysts has been studied. The deactivation of supported Co catalysts was studied in a fixed-bed reactor using synthesis gas feeds containing different concentrations of water vapour. Supporting model studies were carried out using H2O/H-2 feeds in conjunction with XPS and gravimetry. Rapid deactivation occurs on Re-promoted Co/Al2O3 catalysts when H-2/CO/H2O feeds are used, whereas unpromoted Co/Al2O3 shows more stable activity. The results from the gravimetric studies suggest that only a small fraction of the bulk cobalt metal initially present reoxidizes to cobalt oxide during reaction. However, the XPS results indicate significant reoxidation of surface cobalt atoms or highly dispersed cobalt phases, which is likely to be the cause of the observed deactivation. Rhenium is shown to have a marked effect on the extent of reoxidation of alumina-supported cobalt catalysts.
引用
收藏
页码:269 / 284
页数:16
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