FISCHER-TROPSCH SYNTHESIS IN A SLURRY REACTOR - PRETREATMENT EFFECT STUDIES

被引:27
作者
BUKUR, DB
NOWICKI, L
LANG, XS
机构
[1] Department of Chemical Engineering, Kinetics, Catalysis and Chemical Reaction Engineering Laboratory, Texas A & M University, College Station
关键词
D O I
10.1021/ef00052a008
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
Effects of pretreatment procedures, using H-2, CO, and syngas (H-2/CO = 0.7) as reductants, on the performance (activity, selectivity, and stability with time) of a precipitated iron catalyst (100 Fe/5 Cu/4.2 K/16 SiO2 on a mass basis) during Fischer-Tropsch (FT) synthesis were studied in a stirred tank slurry reactor. The syngas conversion varied between 70 and 87% during the first 300 h on stream at baseline process conditions (260 degrees C, 1.48 MPa, 1.5 L(STP)/g-cat/h, H-2/CO = 0.67), and the catalyst deactivation rate was less than 1% per day in all three tests, The catalyst selectivity did not vary markedly with time on stream. The reactor space-time-yield increased by 32-47% in all three tests, upon increasing the reaction pressure and gas space velocity to 2.17 MPa and 2.2 L(STP)/g-cat/h, respectively. The catalyst deactivation rate increased and the water-gas-shift (WGS) activity decreased during testing at the higher reaction pressure. This resulted in a slight decrease of secondary olefin hydrogenation and isomerization reactions in all three tests, and in a shift of hydrocarbon distribution toward higher molecular weight products (CO pretreated catalyst). Total olefin content decreased in the following order with the pretreatment conditions: CO > syngas > H-2, whereas the olefin isomerization activity was essentially independent of the pretreatment conditions employed, Methane selectivity varied with the pretreatment conditions in the following order: CO < H-2 < syngas.
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页码:620 / 629
页数:10
相关论文
共 46 条
[11]  
BUKUR DB, 1993, LIQUEFACTION CONTRAC, P943
[12]  
BUKUR DB, 1992, LIQUEFACTION CONTRAC, P493
[13]  
BUKUR DB, IN PRESS APPL CATAL
[14]  
BUKUR DB, 1990, LIQUEFACTION CONTRAC, P221
[15]  
DAVIS BH, 1991, INDIRECT LIQUEFACTIO, P275
[16]   FISCHER-TROPSCH SYNTHESIS OVER REDUCED AND UNREDUCED IRON-OXIDE CATALYSTS [J].
DICTOR, RA ;
BELL, AT .
JOURNAL OF CATALYSIS, 1986, 97 (01) :121-136
[17]   PRODUCT DISTRIBUTIONS OF THE FISCHER-TROPSCH SYNTHESIS ON PRECIPITATED IRON CATALYSTS [J].
DONNELLY, TJ ;
SATTERFIELD, CN .
APPLIED CATALYSIS, 1989, 52 (1-2) :93-114
[18]  
DRY ME, 1981, CATALYSIS SCI TECHNO, V1, P160
[19]   THE POLYFUNCTIONALITY OF IRON CATALYSTS DURING CARBON-MONOXIDE HYDROGENATION .2. THE FORMATION OF SECONDARY PRODUCTS BY ALPHA-OLEFIN ISOMERIZATION [J].
EGIEBOR, NO ;
COOPER, WC .
APPLIED CATALYSIS, 1985, 17 (01) :47-56
[20]  
Hall C., 1952, J I PET, V38, P845