Palladium-promoted cobalt catalysts supported on silica prepared by impregnation and reverse micelle for Fischer-Tropsch synthesis

被引:21
作者
Osakoo, Nattawut [1 ,2 ]
Henkel, Robert [2 ]
Loiha, Sirinuch [3 ]
Roessner, Frank [2 ]
Wittayakun, Jatuporn [1 ]
机构
[1] Suranaree Univ Technol, Inst Sci, Sch Chem, Nakhon Ratchasima 30000, Thailand
[2] Carl von Ossietzky Univ Oldenburg, D-26111 Oldenburg, Germany
[3] Khon Kaen Univ, Fac Sci, Dept Chem, Khon Kaen 40002, Thailand
关键词
Fischer-Tropsch synthesis; Cobalt; Palladium; Silica; Impregnation; Reverse micelle; CARBON-MONOXIDE; PARTICLE-SIZE; OXIDE; REDUCTION; OXIDATION; MICROSTRUCTURE; DEACTIVATION; BEHAVIOR; XRD; TPR;
D O I
10.1016/j.apcata.2013.06.008
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 objectives of this work were to compare physicochemical properties of silica-supported cobalt catalysts (with 10 wt% Co) prepared by impregnation (10Co-IP) and precipitation using a reverse micelle technique (10Co-RM) and to investigate influence of palladium as a promoter (0.2 wt% and 1.0 wt%) on properties of 10Co-IP and 10Co-RM. The catalysts were characterized by XRD, H-2-TPR, DR-UV-vis, XANES, EXAFS and the reactivity during Fischer-Tropsch synthesis (FITS) was tested at 230 degrees C, 5 bar with H-2/CO = 2. The particle size of Co3O4 in 10Co-IP was larger than that of 10Co-RM which could contribute to lower selectivity to methane and C-2-C-4 paraffin products. The addition of 0.2 wt% Pd to 10Co-IP and 10Co-RM enhanced the cobalt reducibility, FITS activity and paraffin selectivity. On the other hand, the addition of 1.0 wt% Pd resulted in increased methane formation and lower CO conversion. The most suitable catalyst from this work was 0.2Pd-10Co-IP that gave high CO conversion (34.8%) and high mole fraction of paraffins (0.38) in the gasoline range (C-5-C-9). (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 280
页数:12
相关论文
共 51 条
[1]  
Barreca D, 2001, CHEM MATER, V13, P588, DOI [10.1021/cm001041x, 10.1021/cm00104lx]
[2]   THE ACTIVITY OF PD(110) FOR METHANOL SYNTHESIS [J].
BERLOWITZ, PJ ;
GOODMAN, DW .
JOURNAL OF CATALYSIS, 1987, 108 (02) :364-368
[3]   Cobalt particle size effects in the Fischer-Tropsch reaction studied with carbon nanofiber supported catalysts [J].
Bezemer, GL ;
Bitter, JH ;
Kuipers, HPCE ;
Oosterbeek, H ;
Holewijn, JE ;
Xu, XD ;
Kapteijn, F ;
van Dillen, AJ ;
de Jong, KP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (12) :3956-3964
[4]   Deactivation studies of the SCR of NOx with hydrocarbons on Co-mordenite monolithic catalysts [J].
Boix, Alicia V. ;
Aspromonte, Soledad G. ;
Miro, Eduardo E. .
APPLIED CATALYSIS A-GENERAL, 2008, 341 (1-2) :26-34
[5]   Promotion of Cobalt Fischer-Tropsch Catalysts with Noble metals: a Review [J].
Diehl, F. ;
Khodakov, A. Y. .
OIL & GAS SCIENCE AND TECHNOLOGY-REVUE D IFP ENERGIES NOUVELLES, 2009, 64 (01) :11-24
[6]   Microstructure of Supported Cobalt Fischer-Tropsch Catalysts [J].
Ducreux, O. ;
Rebours, B. ;
Lynch, J. ;
Roy-Auberger, M. ;
Bazin, D. .
OIL & GAS SCIENCE AND TECHNOLOGY-REVUE D IFP ENERGIES NOUVELLES, 2009, 64 (01) :49-62
[7]   In situ XRD study of the influence of thermal treatment on the characteristics and the catalytic properties of cobalt-based Fischer-Tropsch catalysts [J].
Enache, DI ;
Rebours, B ;
Roy-Auberger, M ;
Revel, R .
JOURNAL OF CATALYSIS, 2002, 205 (02) :346-353
[8]   Preparation of supported nano-sized cobalt oxide and fcc cobalt crystallites [J].
Fischer, N. ;
van Steen, E. ;
Claeys, M. .
CATALYSIS TODAY, 2011, 171 (01) :174-179
[9]   Use of different mesostructured materials based on silica as cobalt supports for the Fischer-Tropsch synthesis [J].
Gonzalez, O. ;
Perez, H. ;
Navarro, P. ;
Almeida, L. C. ;
Pacheco, J. G. ;
Montes, M. .
CATALYSIS TODAY, 2009, 148 (1-2) :140-147
[10]   Structure of Pt-Co/Al2O3 and Pt-Co/NaY bimetallic catalysts:: characterization by in situ EXAFS, TPR, XPS and by activity in Co (carbon monoxide) hydrogenation [J].
Guczi, L ;
Bazin, D ;
Kovács, I ;
Borkó, L ;
Schay, Z ;
Lynch, J ;
Parent, P ;
Lafon, C ;
Stefler, G ;
Koppány, Z ;
Sajó, I .
TOPICS IN CATALYSIS, 2002, 20 (1-4) :129-139