Nickel nanoparticles inserted in tBuONa matrix deposited on alumina - Part II - Thermal treatment and nickel content effects on their stabilty and catalytitic activity

被引:11
作者
Lefondeur, S
Monteverdi, S
Molina, S
Bettahar, MM
Fort, Y
Zhilinskaya, EA
Aboukais, A
Lelaurain, M
机构
[1] Univ Henri Poincare, Fac Sci, Lab Catalyse Heterogene, CNRS,UMR 7565, F-54506 Vandoeuvre Nancy, France
[2] Univ Henri Poincare, Fac Sci, Lab Synth Organ & React, CNRS,UMR 7565, F-54506 Vandoeuvre Nancy, France
[3] Univ Littoral Cote Opale, Lab Catalyse & Environm, MREID, EA 2598, F-59140 Dunkerque, France
[4] Univ Henri Poincare, Fac Sci, Lab Solide Mineral, CNRS,UMR 7555, F-54506 Vandoeuvre Nancy, France
关键词
D O I
10.1023/A:1017992209078
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanoparticles (1 nm-3 nm) of metallic nickel supported on alumina (4.3% Ni-17.9% Ni w/w) were prepared from a colloidal precursor inserted in an organic matrix. Their structural and stability properties have been studied by X-Ray Diffraction (XRD), Electron Paramagnetic Resonance (EPR) and Thermal Gravimetric Analysis (TGA). Benzene hydrogenation at atmospheric pressure in the temperature range of 75 degreesC-200 degreesC was used as a test reaction of their catalytic capability. The thermal stability of the particles depended on the nature of the reactive atmosphere. Thus, a growth in size (up to around 20 nm) is observed under H-2 flow at 350 degreesC or during benzene hydrogenation but not under air flow at 300 degreesC. The growth may be due to the coalescence of the metal particles during the heating and decomposition of the stabilizing organic matrix. Under oxidative atmosphere, stable nickel oxide particles, firmly attached to the support, are formed. The catalysts pre-treated under H-2/350 degreesC were active and stable in benzene hydrogenation. The observed activities depended on the reaction conditions and nickel composition. (C) 2001 Kluwer Academic Publishers.
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页码:2633 / 2638
页数:6
相关论文
共 40 条
[1]   Self-assembly of a two-dimensional superlattice of molecularly linked metal clusters [J].
Andres, RP ;
Bielefeld, JD ;
Henderson, JI ;
Janes, DB ;
Kolagunta, VR ;
Kubiak, CP ;
Mahoney, WJ ;
Osifchin, RG .
SCIENCE, 1996, 273 (5282) :1690-1693
[2]   EPR STUDY OF NI3+-DOPED ACOO2 (A = H, LI) POWDERS [J].
ANGELOV, S ;
FRIEBEL, C ;
ZHECHEVA, E ;
STOYANOVA, R .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1992, 53 (03) :443-448
[3]   THE PREPARATION OF FINELY DIVIDED METAL AND ALLOY POWDERS [J].
BONNEMANN, H ;
BRIJOUX, W ;
JOUSSEN, T .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1990, 29 (03) :273-275
[4]   ACTIVATION OF REDUCING AGENTS - SODIUM HYDRIDE CONTAINING COMPLEX REDUCING AGENTS .18. STUDY OF THE NATURE OF COMPLEX REDUCING AGENTS PREPARED FROM NICKEL AND ZINC SALTS [J].
BRUNET, JJ ;
BESOZZI, D ;
COURTOIS, A ;
CAUBERE, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (25) :7130-7135
[5]   ACTIVATION OF REDUCING AGENTS - SODIUM HYDRIDE CONTAINING COMPLEX REDUCING AGENTS .12. NEW CONVENIENT, HIGHLY-ACTIVE, AND SELECTIVE NICKEL HYDROGENATION CATALYSTS [J].
BRUNET, JJ ;
GALLOIS, P ;
CAUBERE, P .
JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (10) :1937-1945
[6]  
Cerveny L., 1986, CATALYTIC HYDROGENAT, V27
[7]  
COONEN JWE, 1972, P 5 INT C CAT FLOR 1, P671
[8]   UNSUPPORTED SMALL METAL PARTICLES - PREPARATION, REACTIVITY, AND CHARACTERIZATION [J].
DAVIS, SC ;
KLABUNDE, KJ .
CHEMICAL REVIEWS, 1982, 82 (02) :153-208
[9]   Nickel nanoparticles in silica gel: preparation and magnetic properties [J].
Estournes, C ;
Lutz, T ;
Happich, J ;
Quaranta, T ;
Wissler, P ;
Guille, JL .
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 1997, 173 (1-2) :83-92
[10]   THE COLLOID-CHEMICAL APPROACH TO NANOSTRUCTURED MATERIALS [J].
FENDLER, JH ;
MELDRUM, FC .
ADVANCED MATERIALS, 1995, 7 (07) :607-632