Reaction and characterization studies of an industrial Cr-free iron-based catalyst for high-temperature water gas shift reaction

被引:50
作者
Liu, QS [1 ]
Ma, WP [1 ]
He, RX [1 ]
Mu, ZJ [1 ]
机构
[1] Inner Mongolia Univ Technol, Dept Chem Engn, Hohhot 010062, Peoples R China
关键词
water gas shift reaction; gamma-Fe2O3; Fe3O4; Cr-free; redox mechanism;
D O I
10.1016/j.cattod.2005.07.150
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Activity and stability of an industrial Cr-free iron-based catalyst (NBC-1) for high-temperature water gas shift (WGS) reaction were studied in a fixed-bed reactor under 350 degrees C, 1 atm, H2O:gas = 1:1 and 3000 h(-1) (dry-gas basis). Physical properties of the NBC-1 catalyst before and after the WGS reaction, the desorption behavior of H2O, CO, CO2 and H-2, and surface reaction over the catalyst were characterized by BET, X-ray diffraction (XRD), Mossbauer emission spectroscopy (MES), temperature programmed desorption (TPD) and temperature programmed surface reaction (TPSR). The NBC-1 catalyst is active and has excellent thermo-stability even after pretreatment at a high temperature of 530 degrees C. Its activity and thermo-stability are comparable to those of an UCI commercial Fe-Cr catalyst, C12-4. XRD and MES studies show that iron in the fresh NBG-1 catalyst is present as gamma-Fe2O3, most of which is converted to Fe3O4 during reduction and reaction. Results of TPD demonstrate that adsorbed CO2 and CO cannot exist on the NBC-1 surface beyond the temperature of 300 degrees C while higher temperatures (> 400 degrees C) are required to completely desorb H2O. A redox mechanism of WGS on the NBC-1 surface is proposed based on the TPD and TPSR observations. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 56
页数:5
相关论文
共 22 条
[1]   Studies of the water-gas-shift reaction on ceria-supported Pt, Pd, and Rh: implications for oxygen-storage properties [J].
Bunluesin, T ;
Gorte, RJ ;
Graham, GW .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 15 (1-2) :107-114
[2]  
Chinchen G. C., 1982, Euro Patent, Patent No. [A-0 062410, 0062410]
[3]   A COMPARISON OF THE WATER GAS SHIFT REACTION ON CHROMIA-PROMOTED MAGNETITE AND ON SUPPORTED COPPER-CATALYSTS [J].
CHINCHEN, GC ;
SPENCER, MS .
JOURNAL OF CATALYSIS, 1988, 112 (01) :325-327
[4]   PROMOTION OF METHANOL SYNTHESIS AND THE WATER-GAS SHIFT REACTIONS BY ADSORBED OXYGEN ON SUPPORTED COPPER-CATALYSTS [J].
CHINCHEN, GC ;
SPENCER, MS ;
WAUGH, KC ;
WHAN, DA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1987, 83 :2193-2212
[5]   An environmental friendly dopant for the high-temperature shift catalysts [J].
de Araújo, GC ;
Rangel, MD .
CATALYSIS TODAY, 2000, 62 (2-3) :201-207
[6]  
DICKSON DPE, 1986, MOSSBAUER SPECTROSCO, P169
[7]   Reactive behaviors of iron-based shift catalyst promoted by ceria [J].
Hu, YP ;
Jin, HF ;
Liu, JR ;
Hao, DS .
CHEMICAL ENGINEERING JOURNAL, 2000, 78 (2-3) :147-152
[8]  
JIN H, 1999, Patent No. 951218344
[9]   CHARACTERIZATION OF CHROMIA-PROMOTED GAMMA-IRON OXIDE CATALYSTS AND THEIR CO CONVERSION EFFICIENCY [J].
KUNDU, ML ;
SENGUPTA, AC ;
MAITI, GC ;
SEN, B ;
GHOSH, SK ;
KUZNETSOV, VI ;
KUSTOVA, GN ;
YURCHENKO, EN .
JOURNAL OF CATALYSIS, 1988, 112 (02) :375-383
[10]  
Ladebeck J, 1995, STUD SURF SCI CATAL, V91, P1079