Kinetics modelling of Fischer-Tropsch synthesis over an industrial Fe-Cu-K catalyst

被引:151
作者
Wang, YN
Ma, WP
Lu, YJ
Yang, J
Xu, YY
Xiang, HW
Li, YW
Zhao, YL
Zhang, BJ
机构
[1] Chinese Acad Sci, State Key Lab Coal Convers, Inst Coal Chem, Taiyuan 030001, Peoples R China
[2] Jinan Univ, Dept Chem, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
Fischer-Tropsch synthesis; Fe-Cu-K catalyst; detailed kinetics model; olefin re-adsorption mechanism;
D O I
10.1016/S0016-2361(02)00154-0
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
The kinetic experiments of Fischer-Tropsch synthesis (FFS) over an industrial Fe-Cu-K catalyst are carried out in a micro-fixed-bed reactor under the conditions as follows: temperature of 493-542 K, pressure of 10.9-30.9 bar, H-2/CO feed ratio of 0.98-2.99, and space velocity of 4000-10 000 h(-1). The effects of secondary reactions of oletins are investigated by co-feeding C2H4 and C3H6. A detailed kinetics model taking into account the increasingly proven evidence of the olefin re-adsorption mechanism is then proposed. In this model, different sites are assumed for FTS reactions and water gas shift (WGS) reaction, respectively. Rate expressions for FTS reactions are based on the carbide polymerisation mechanism, in which olefin re-adsorption is considered to be a reverse step of olefin desorption reaction. Rate expression for WGS reaction is based on the formate mechanism. An integral reactor model considering both FTS and WGS kinetics is used to describe the reaction system, and the simultaneous estimation of kinetic-parameters is conducted with non-linear regression procedure. The optimal model shows that the rate determining steps in FrS reactions proceed via the desorption of hydrocarbon products and the adsorption of CO and the slowest step in WGS reaction is the desorption of gaseous carbon dioxide. via formate intermediate species. The activation energies of FTS reactions and WGS reaction are in good agreement with literature values. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:195 / 213
页数:19
相关论文
共 67 条
[1]   A THEORETICAL CORRELATION BETWEEN CHAIN GROWTH-FACTOR AND FEED COMPOSITION FOR THE FISCHER TROPSCH MECHANISMS [J].
ADESINA, AA .
JOURNAL OF MOLECULAR CATALYSIS, 1990, 62 (02) :L23-L27
[2]  
Anderson R., 1956, CATALYSTS FISCHER TR, V4
[3]   A RATE EQUATION FOR THE FISCHER-TROPSCH SYNTHESIS ON IRON CATALYSTS [J].
ANDERSON, RB ;
KARN, FS .
JOURNAL OF PHYSICAL CHEMISTRY, 1960, 64 (06) :805-808
[4]  
Anderson RB., 1984, FISCHER TROPSCH SYNT
[5]  
[Anonymous], C1 MOL CHEM
[6]  
[Anonymous], 1952, J I PET
[7]   KINETICS OF FISCHER-TROPSCH REACTION OVER IRON [J].
ATWOOD, HE ;
BENNETT, CO .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1979, 18 (01) :163-170
[8]   CATALYTIC SYNTHESIS OF HYDROCARBONS OVER GROUP-VIII METALS - A DISCUSSION OF THE REACTION-MECHANISM [J].
BELL, AT .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1981, 23 (1-2) :203-232
[9]   MECHANISM OF HYDROCARBON SYNTHESIS OVER FISCHER-TROPSCH CATALYSTS [J].
BILOEN, P ;
SACHTLER, WMH .
ADVANCES IN CATALYSIS, 1981, 30 :165-216
[10]   ON THE MECHANISM OF THE FISCHER-TROPSCH SYNTHESIS INVOLVING UNREDUCED IRON CATALYST [J].
BLANCHARD, F ;
REYMOND, JP ;
POMMIER, B ;
TEICHNER, SJ .
JOURNAL OF MOLECULAR CATALYSIS, 1982, 17 (2-3) :171-181