NiW/γ-Al2O3 catalysts prepared by modified equilibrium deposition filtration (MEDF) and non-dry impregnation (NDI) -: Characterization and catalytic activity evaluation for the production of low sulfur gasoline in a HDS pilot plant

被引:39
作者
Kordulis, C
Lappas, AA
Fountzoula, C
Drakaki, K
Lycourghiotis, A
Vasalos, IA
机构
[1] Univ Patras, Dept Chem, GR-26500 Patras, Greece
[2] Inst Chem Engn & High Temp Chem Proc, GR-26500 Patras, Greece
[3] Univ Thessaloniki, Chem Proc Engn Res Inst, Salonika 57001, Greece
[4] Univ Thessaloniki, Dept Chem Engn, Salonika 57001, Greece
关键词
hydrodesulfurization; nickel-tungsten/alumina catalysts; catalyst preparation; equilibrium deposition filtration; hydrogenation; isomerization; XPS;
D O I
10.1016/S0926-860X(00)00748-1
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 aim of this study was to investigate the desulfurization of fluid catalytic cracking (FCC) gasoline using NiW supported on gamma -Al2O3 catalysts prepared by conventional non-dry impregnation (NDI) method and a new one, the equilibrium deposition filtration, (EDF). The latter has been modified (MEDF) to produce the required catalyst quantity for its evaluation in a hydrodesulfurization (HDS) pilot plant. The modification of the typical EDF method showed that it is possible to apply the principles of this technique for practical catalyst preparations. In the first part of this work, the catalyst preparation methodology and the catalyst characterization results are presented. In the second part, the catalyst evaluation is described, in relation to a commercial catalyst, concerning their HDS, hydrogenation (HYG) and isomerization (ISO) activities. The main conclusion of this study was that the MEDF method is more promising than the conventional NDI method for preparing NiW hydrotreatment catalysts. The catalyst prepared by MEDF exhibited higher HDS activity than that of the NDI one, comparable to that of a commercial CoMo catalyst and the highest HYG and ISO activities. The enhanced catalytic activity of the NiW-MEDF catalyst was attributed to the high dispersity of the supported phases achieved by the corresponding preparation method. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:85 / 95
页数:11
相关论文
共 44 条
[1]  
AbsiHalabi M, 1997, HYDROCARB PROCESS, V76, P45
[2]  
[Anonymous], HYDROTREATING CATALY
[3]   Mechanism of deposition of vanadium-oxo, species on the ''anatase/electrolytic solution'' interface [J].
Bourikas, K ;
Georgiadou, I ;
Kordulis, C ;
Lycourghiotis, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (42) :8499-8506
[4]   Mechanisms of deposition of species containing catalytically active ions on the oxidic support electrolytic solution interfaces: A unified approach based on the two-pK/one-site and triple-layer models [J].
Bourikas, K ;
Matralis, HK ;
Kordulis, C ;
Lycourghiotis, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (28) :11711-11719
[5]   Efficient catalytic processes for the manufacturing of high-quality transportation fuels [J].
deJong, KP .
CATALYSIS TODAY, 1996, 29 (1-4) :171-178
[6]   EFFECT OF ADDITIVES ON THE STRUCTURE AND REACTIVITY OF THE SURFACE VANADIUM-OXIDE PHASE IN V2O5 TIO2 CATALYSTS [J].
DEO, G ;
WACHS, IE .
JOURNAL OF CATALYSIS, 1994, 146 (02) :335-345
[7]   STUDY OF NI-MO-GAMMA-AL2O3 CATALYSTS BY X-RAY PHOTOELECTRON AND RAMAN-SPECTROSCOPY - COMPARISON WITH CO-MO-GAMMA-AL2O3 CATALYSTS [J].
DUFRESNE, P ;
PAYEN, E ;
GRIMBLOT, J ;
BONNELLE, JP .
JOURNAL OF PHYSICAL CHEMISTRY, 1981, 85 (16) :2344-2351
[8]   DETERMINATION OF THE MO SURFACE ENVIRONMENT OF MO/TIO2 CATALYSTS BY EXAFS, XANES AND PCA [J].
FAY, MJ ;
PROCTOR, A ;
HOFFMANN, DP ;
HOUALLA, M ;
HERCULES, DM .
MIKROCHIMICA ACTA, 1992, 109 (5-6) :281-293
[9]   USE OF ESCA VALENCE BANDS TO INFER STRUCTURAL INFORMATION ABOUT THE MOLYBDENUM PHASE IN SUPPORTED MOLYBDENUM CATALYSTS [J].
FIEDOR, JN ;
PROCTOR, A ;
HOUALLA, M ;
SHERWOOD, PMA ;
MULCAHY, FM ;
HERCULES, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (26) :10967-10970
[10]   Selection of catalysts and reactors for hydroprocessing [J].
Furimsky, E .
APPLIED CATALYSIS A-GENERAL, 1998, 171 (02) :177-206