Activation study of precipitated iron Fischer-Tropsch catalysts

被引:110
作者
OBrien, RJ [1 ]
Xu, LG [1 ]
Spicer, RL [1 ]
Davis, BH [1 ]
机构
[1] UNIV KENTUCKY,CTR APPL ENERGY RES,LEXINGTON,KY 40511
关键词
D O I
10.1021/ef9502315
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Slurry phase Fischer-Tropsch synthesis (FTS) was conducted with two precipitated iron catalysts (100 Fe/3.6 Si/0.71 K and 100 Fe/4.4 Si/1.0 K, atomic percent relative to Fe) at 543 K, 1.31 MPa, and a synthesis gas (H-2/CO = 0.7) space velocity of 3.1 normal L h(-1) (g of Fe)(-1). The impact of activation gas (GO, H-2/CO = 0.7, or H-2/CO = 0.1), temperature (543 or 573 K), and pressure (1.31 or 0.10 MPa) on the long-term (>500 h) activity and selectivity of the catalysts was explored. Pretreatment with CO under the conditions employed gave highly active and stable catalysts. Catalyst performance when synthesis gas activation was used was found to be dependent upon the partial pressure of hydrogen in the activating gas, with low hydrogen partial pressures resulting in the highest catalyst activity. X-ray diffraction results indicate that carbon monoxide activations and synthesis gas activations with low hydrogen partial pressure result in the formation of the carbides chi-Fe5C2 and epsilon'-Fe2.2C, while activation with synthesis gas with high hydrogen partial pressure results in the formation of only Fe3O4. It was found that treating the 100 Fe/3.6 Si/0.71 K catalyst activated with synthesis gas at 1.31 MPa and 543 K with carbon monoxide caused the activity to increase dramatically and the Fe3O4 to be partially converted to iron carbides. It is concluded that Fe3O4 is relatively inactive for FTS, while the presence of some bulk iron carbide is necessary for high FTS activity to be achieved.
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页码:921 / 926
页数:6
相关论文
共 18 条
[11]  
KUO JC, 1983, DOEPC3002210
[12]  
KUO JCW, 1985, DOEPC600199
[13]   ELECTRON AND X-RAY DIFFRACTION STUDIES OF IRON FISCHER-TROPSCH CATALYSTS [J].
MCCARTNEY, JT ;
HOFER, LJE ;
SELIGMAN, B ;
LECKY, JA ;
PEEBLES, WC ;
ANDERSON, RB .
JOURNAL OF PHYSICAL CHEMISTRY, 1953, 57 (07) :730-736
[14]   BEHAVIOR OF METALLIC IRON CATALYSTS DURING FISCHER-TROPSCH SYNTHESIS STUDIED WITH MOSSBAUER-SPECTROSCOPY, X-RAY-DIFFRACTION, CARBON CONTENT DETERMINATION, AND REACTION KINETIC MEASUREMENTS [J].
NIEMANTSVERDRIET, JW ;
VANDERKRAAN, AM ;
VANDIJK, WL ;
VANDERBAAN, HS .
JOURNAL OF PHYSICAL CHEMISTRY, 1980, 84 (25) :3363-3370
[15]   FISCHER-TROPSCH SYNTHESIS - IMPACT OF POTASSIUM AND ZIRCONIUM PROMOTERS ON THE ACTIVITY AND STRUCTURE OF AN ULTRAFINE IRON-OXIDE CATALYST [J].
OBRIEN, RJ ;
XU, LG ;
MILBURN, DR ;
LI, YX ;
KLABUNDE, KJ ;
DAVIS, BH .
TOPICS IN CATALYSIS, 1995, 2 (1-4) :1-15
[16]   ACTIVATION AND PROMOTION STUDIES IN A MIXED SLURRY REACTOR WITH AN IRON-MANGANESE FISCHER-TROPSCH CATALYST [J].
PENNLINE, HW ;
ZAROCHAK, MF ;
STENCEL, JM ;
DIEHL, JR .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1987, 26 (03) :595-601
[17]   CHANGES IN THE SURFACE-STRUCTURE AND COMPOSITION OF AN IRON CATALYST OF REDUCED OR UNREDUCED FE2O3 DURING THE REACTION OF CARBON-MONOXIDE AND HYDROGEN [J].
REYMOND, JP ;
MERIAUDEAU, P ;
TEICHNER, SJ .
JOURNAL OF CATALYSIS, 1982, 75 (01) :39-48
[18]  
1946, REPORT PETROLEUM SYN, P96