Highly dispersed NiW/γ-Al2O3 catalyst prepared by hydrothermal deposition method

被引:36
作者
Wang, Hao
Fan, Yu
Shi, Gang
Liu, Zhihong
Liu, Haiyan
Bao, Xiaojun
机构
[1] China Univ Petroleum, China Natl Petr Corp, Key Lab Catalysis, Beijing 102249, Peoples R China
[2] China Univ Petroleum, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[3] PetroChina Co Ltd, Sci & Technol Management Dept, Beijing 100011, Peoples R China
关键词
hydrothermal deposition method; NiW/gamma-Al2O3; catalyst; high dispersion; dibenzothiophene; hydrodesulfurization;
D O I
10.1016/j.cattod.2007.02.025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This article describes a novel hydrothermal deposition method for preparing highly dispersed NiW/gamma-Al2O3 catalysts and demonstrates its advantages over the conventional impregnation method. Via the hydrothermal precipitation reactions between sodium tungstate and hydrochloric acid and between nickel nitrate and urea, respectively, the active species W and Ni were deposited on gamma-Al2O3. In the hydrothermal deposition Of WO3, a surfactant hexadecyltrimethyl ammonium bromide (CTAB) was used to prevent the aggregation of WO3. The characterization results obtained by means of X-ray photoelectron spectroscopy (XPS), N-2 adsorption and high-resolution transmission electron microscopy (HRTEM) measurements showed that compared with the catalyst prepared by the conventional impregnation method, the catalyst with the same metal contents prepared by the hydrothermal deposition had much higher Wand Ni dispersion, higher specific surface area, larger pore volume, the significantly decreased slab length and slightly increased stacking degree of sulfided W species, leading to the significantly enhanced dibenzothiophene (DBT) hydrodesulfurization (HDS) activity. The DBT HDS assessment results also revealed that the catalyst containing 17.7 wt% WO3 and 2.4 wt% NiO prepared by the hydrothermal deposition method had the similar DBT HDS activity as a commercial NiW/gamma-Al2O3 catalyst containing 23 wt% WO3 and 2.6 wt% NiO, resulting in the greatly decreased amount of active metals for achieving the same HDS activity. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 154
页数:6
相关论文
共 36 条
[1]   Catalyst preparation variables that affect the creation of active sites for HDS on Co/Mo/Al2O3 catalytic materials [J].
Adachi, M ;
Contescu, C ;
Schwarz, JA .
JOURNAL OF CATALYSIS, 1996, 162 (01) :66-75
[2]   Influence of support-interaction on the sulfidation behavior and hydrodesulfurization activity of Al2O3-supported W, CoW, and NiW model catalysts [J].
Coulier, L ;
Kishan, G ;
van Veen, JAR ;
Niemantsverdriet, JW .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (23) :5897-5906
[3]   STRUCTURE-FUNCTION RELATIONS IN MOLYBDENUM SULFIDE CATALYSTS - THE RIM-EDGE MODEL [J].
DAAGE, M ;
CHIANELLI, RR .
JOURNAL OF CATALYSIS, 1994, 149 (02) :414-427
[4]   Hydrodesulfurization of dibenzothiophene and 4,6-dimethyldibenzothiophene over sulfided NiMo/γ-Al2O3, CoMo/γ-Al2O3, and Mo/γ-Al2O3 catalysts [J].
Egorova, M ;
Prins, R .
JOURNAL OF CATALYSIS, 2004, 225 (02) :417-427
[5]   A surfactant-assisted hydrothermal deposition method for preparing highly dispersed N/γ-Al2O3 hydrodenitrogenation catalyst [J].
Fan, Yu ;
Bao, Xiaojun ;
Wang, Hao ;
Chen, Chunfang ;
Shi, Gang .
JOURNAL OF CATALYSIS, 2007, 245 (02) :477-481
[6]  
GEUS JW, 1983, PREPARATION CATALYST, V3, P1
[7]   Beneficial effect of carbon on hydrotreating catalysts [J].
Glasson, C ;
Geantet, C ;
Lacroix, M ;
Labruyere, F ;
Dufresne, P .
JOURNAL OF CATALYSIS, 2002, 212 (01) :76-85
[8]   The relation between morphology and hydrotreating activity for supported MoS2 particles [J].
Hensen, EJM ;
Kooyman, PJ ;
van der Meer, Y ;
van der Kraan, AM ;
de Beer, VHJ ;
van Veen, JAR ;
van Santen, RA .
JOURNAL OF CATALYSIS, 2001, 199 (02) :224-235
[9]   Structure of molybdenum supported on α-, γ-, and χ-aluminas in relation to its epoxidation activity [J].
Imamura, S ;
Sasaki, H ;
Shono, M ;
Kanai, H .
JOURNAL OF CATALYSIS, 1998, 177 (01) :72-81
[10]   Hydrothermal synthesis of hexagonal tungsten trioxide from Li2WO4 solution and electrochemical lithium intercalation into the oxide [J].
Komaba, S ;
Kumagai, N ;
Kato, K ;
Yashiro, H .
SOLID STATE IONICS, 2000, 135 (1-4) :193-197