Search results for "Catalyst support"

showing 3 items of 23 documents

Oxidative dehydrogenation of ethane: A study over the structure and robustness of Ni–W–O catalysts

2014

[EN] The robustness of one selected Ni-W-O catalyst has been studied in the oxidative dehydrogenation of ethane. This catalyst initially deactivates for the first 10 h online decreasing 15% of its catalytic activity compared to its initial stable catalytic activity. However from 10 to 60 h online the catalytic activity keeps almost stable. On the other hand, it has been shown that the Ni-W-O catalyst cannot tolerate an oxygen-free atmosphere (C-2 and He) as nickel oxide is transformed into metallic nickel. Methane and hydrogen as well as abundant coke were formed on the surface of the catalyst in these O-free conditions. However a re-calcination in air leads to the removal of coke, the cata…

inorganic chemicalsEthyleneHydrogenGeneral Chemical EngineeringCatalyst supportInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCatalysisMethaneCatalysisEthylenechemistry.chemical_compoundDehydrogenationNickel tungstenOxidative dehydrogenation of ethaneOxide catalystsEthaneChemistryorganic chemicalsNickel oxideCokeFuel TechnologyNi-W-OHydrogenOxidative dehydrogenationFuel Processing Technology
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Nature of cobalt active species in hydrodesulfurization catalysis: combined support and preparation method effects

2007

Abstract Co/γ-Al2O3, Co/SiO2, Co/MCM-41, Co/ASA and Co/S2 (amorphous aluminosilicate with Al/Si = 0.13 and with Al/Si ≈ 2, respectively) were prepared by the method of wet impregnation and by the method of precipitation in the presence of sodium carbonate. The samples were characterised by XPS, XRD and TPR. The catalytic activity was tested in the hydrodesulfurization of thiophene using a continuous flow reactor. Among the wet impregnated catalysts those supported on the amorphous and ordered mesoporous silica exhibited higher HDS activity as compared to the alumina containing supports. Particularly, the use of the mesoporous, high surface area MCM-41 support, determined the best performing…

inorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryMCM-41Physical and Theoretical ChemistrySodium carbonateMesoporous materialHydrodesulfurizationCobaltNuclear chemistry
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Total oxidation of naphthalene using bulk manganese oxide catalysts

2013

Several Mn2O3 catalysts have been synthesized using different preparation methods and tested for the total oxidation of naphthalene, a model polycyclic aromatic compound. The catalysts have been characterized by several physico-chemical techniques such as XRD, TPR, XPS, EDX and TEM. The surface area of the catalyst seems to be of paramount importance, since the mass normalized activity of catalysts increases as the surface area of the Mn2O3 catalysts increases. Consequently, a high surface area ordered mesoporous Mn2O3 catalyst, obtained through a nanocasting route using mesoporous KIT-6 silica as a hard template, was the most efficient catalyst for the deep oxidation of naphthalene. In add…

inorganic chemicalsorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistryCatalysisCatalysisHopcalitechemistry.chemical_compoundchemistryCatalytic oxidationX-ray photoelectron spectroscopyPhase (matter)heterocyclic compoundsMesoporous materialNaphthaleneApplied Catalysis A: General
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