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  • 1
    ISSN: 1572-9028
    Keywords: Fischer-Tropsch synthesis ; bimetallic nickel-iron ; cyanide complex ; potassium ; catalysts preparation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Nickel-iron catalysts have been prepared by homogeneous deposition-precipitation of complex nickel-iron cyanides on a titania support. The nickel-iron alloys obtained after calcination and reduction of the cyanide precursors were characterized by Mössbauer spectroscopy, high-temperature X-ray diffraction, and magnetic measurements. Fischer-Tropsch experiments show remarkable results. Catalysts prepared from K3Fe(CN)6 and Na2Fe(CN)5NO cyanide precursors exhibit a high activity and selectivity, whereas catalysts prepared from K4Fe(CN)6 do not show any activity. This lack of activity is caused by the presence of potassium in catalysts prepared from K4Fe(CN)6. Potassium or iron titanate inhibits the adsorption of CO on the nickel-iron surface. Deactivation of active nickel-iron catalysts was caused by the deposition of inactive carbon during Fischer-Tropsch synthesis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-879X
    Keywords: Rutherford backscattering spectrometry (RBS) ; HDS catalyst ; solid state reaction ; cobalt aluminate ; MoO3 ; Co3O4 ; γ-Al2O3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In view of the importance for CoxOy,-MoO3/γ-Al2O3 hydrodesulphurization (HDS) catalysts, the reactivity of cobalt oxide layers towards cobalt aluminate formation was investigated on both MoO3-covered and bare γ-Al2O3 substrates. Co3O4/MoO3/γ-Al2O3 and Co3O4/γ-Al2O3 systems were prepared by vapour-deposition of MoO3 (12 × 1015 Mo atoms/cm2) and Co (400 × 1015 Co atoms/cm2) layers onto a γ-Al2O3 substrate, followed by oxidation of the Co layer to Co3O4. After annealing at 800°C for 40 h, the interfacial reaction to cobalt aluminate was assessed using Rutherford backscattering spectrometry. The presence of molybdenum oxide appeared to enhance cobalt aluminate formation. The Mo atoms, which spread out over the entire cobalt-containing layer, presumably caused a high defect density, which explains the observed higher reaction rate. The amount of MoO3 was much too low to stabilize all cobalt atoms by cobalt molybdate formation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 39 (1996), S. 233-240 
    ISSN: 1572-879X
    Keywords: volatilization ; steam ; transition metal hydroxides ; NiO ; Co3O4 ; CuO ; Al2O3 ; Rutherford backscattering spectrometry (RBS) ; solid state reaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract To study the influence of steam on the solid state reaction between MeO (Me = Ni, Co, Cu or Fe) and Al2O3, MeO/α-Al2O3 and MeO/γ-Al2O3 model catalysts were kept in either N2/20% O2 or N2/O2/30% H2O at 500–1000°C. The samples were subsequently analyzed with RBS and FTIR. Surprisingly, nickel, cobalt and copper volatilized when MeO/α-Al2O3 or MeAl2U4/α-Al2O3 samples were annealed in the presence of 0.3 atm steam at 1000°C. Especially copper was found to volatilize very rapidly in the presence of steam, even at a temperature as low as 800°C. FTIR spectra of steam-treated NiO/α-Al2O3 samples showed the incorporation of hydroxyl groups in the nickel oxide layer. This observation and an excellent agreement with thermochemical calculations support our conclusion that the volatile species are metal hydroxides. The solid state reaction of MeO withγ-Al2O3 was found to proceed at a much higher rate in the presence of 0.3 atm steam at 500–800°C, presumably as a result of an enhanced surface mobility of Me and Al ions along the grain boundaries and the surfaces of the internal pores of theγ-Al2O3 support, when steam is present.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 41 (1996), S. 27-34 
    ISSN: 1572-879X
    Keywords: Fischer-Tropsch synthesis ; nickel-iron ; particle size ; metal-support interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of the titania support and metal particle size on the performance of nickel-iron catalysts in the Fischer-Tropsch synthesis has been studied by varying the nickel-iron loading and, consequently, varying the nickel-iron particle size. Low-loaded titania-supported nickel-iron catalysts (2 wt%) turned out to be more selective towards higher hydrocarbons than high-loaded nickel-iron catalysts (20 wt%), which produce much more methane. From temperature-programmed hydrogenation experiments, magnetic measurements and Mössbauer spectroscopy it followed that different types of carbon are present on the catalysts depending on the metal loading. These types of carbon could be related to the selectivity in Fischer-Tropsch synthesis and to the deactivation of the catalysts with time on stream. These differences in catalytic behaviour are most likely due to the presence of TiO x species on the surface of the active phase, which species decrease the CO and H2 adsorption properties of the catalyst, but increase the dissociation of CO.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 31 (1996), S. 3115-3121 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Literature indicates that application of zirconia in a supported dehydrogenation catalyst is viable. Textural and structural properties of commercial pre-shaped zirconia supports from various suppliers were characterized using electron microscopy, element analysis, nitrogen physisorption, mercury intrusion porosimetry and X-ray diffraction. Most zirconias are sufficiently pure (〉97 %) and thermostable to be applied in supported catalysts. Specific surface areas as large as 10 m2g−1 are stable at temperatures of about 850 °C. Specific surface areas up to about 30 m2g−1 can be established by a thermal treatment in air at temperatures up to the operating temperatures of the dehydrogenation process. Steam treatment affects the texture differently from treatment in dry air: sintering proceeds more rapidly in the presence of steam. The preshaped supports show a porosity (about 50%) which is higher than that reported for zirconia powders with the same pore-size distribution (5%). This is advantageous, both in the catalyst preparation step and in the catalytic reaction. However, the pre-shaped supports exhibit some microporosity.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 132-134 
    ISSN: 0142-2421
    Keywords: palladium ; particles ; AES ; XPS ; oxidation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The palladium M4,5N1N2,3 transition, which is almost absent in palladium metal, becomes quite intense in palladium oxide. The intensity of the transition is linearly proportional to the amount of palladium oxide. This means that AES can be used for quantitative analysis of palladium oxide layers or supported palladium oxide particles.© 1997 by John Wiley & Sons, Ltd.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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