| People | Locations | Statistics |
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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Especel, Catherine
University of Poitiers
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (8/8 displayed)
- 2015Hydrocarbon fuel synthesis from sorbitol over bifunctional catalysts: Association of tungstated titania with platinum, palladium or iridiumcitations
- 2015Selective ring opening of methylcyclohexane and decalin over Rh-Pd supported catalysts: Effect of the preparation methodcitations
- 2012Selective hydrogenation of citral to unsaturated alcohols over mesoporous Pt/Ti-Al2O3 catalysts. Effect of the reduction temperature and of the Ge additioncitations
- 2012Citral hydrogenation on high surface area mesoporous TiO2-SiO2 supported Pt nanocomposites: Effect of titanium loading and reduction temperature on the catalytic performancescitations
- 2011The relationship between the structural properties of bimetallic Pd-Sn/SiO2 catalysts and their performance for selective citral hydrogenation citations
- 2011Catalytic performances of large pore Ti-SBA15 supported Pt nanocomposites for the citral hydrogenation reaction citations
- 2010Control of titania nanodomain size as a route to modulate SMSI effect in Pt/TiO2 catalystscitations
- 2006Bimetallic Rh-Ge and Pt-Ge catalysts supported on TiO2 for citral hydrogenation I. Preparation and characterization of the catalysts citations
Places of action
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article
Selective ring opening of methylcyclohexane and decalin over Rh-Pd supported catalysts: Effect of the preparation method
Abstract
International audience ; Bimetallic Rh-Pd catalysts prepared by various impregnation methods were evaluated in the selective ring-opening of decalin and methylcyclohexane (MCH) used as model molecules of hydrogenated aromatics of the Light Cycle Oil fraction. Rh and Pt were deposited on Al2O3 and SiO2-Al2O3 (S40) by coimpregnation (Cl) or successive impregnations (SI) with different orders of metal addition. Catalysts were characterized by H-2 chemisorption, temperature-programmed reduction, temperature-programmed desorption of pyridine, and test reactions of cyclopentane hydrogenolysis and isomerization of 3,3-dimethyl-1-butene. Their catalytic behaviors for the ring-opening reaction were deeply influenced by the acidity of the support, and in a lesser extent by the metal deposition method. On both supports, the CI catalysts, displaying the highest dispersion values, exhibited the best ring opening performances. In the case of the SI catalysts, the addition order of both metals modified in a moderate way the properties of the catalyst. The yield to ring opening products obtained in MCH ring opening with CI catalysts supported on Al2O3 was 39-69% higher than those prepared by SI (conversion = 55-60%) while for the catalysts supported on S40, the yield to ring opening products was 8-48% higher for the CI catalysts compared to SI catalysts (conversion = 72-77%). The conversion of decalin for the bimetallic catalysts supported on Al2O3 was lower than 20% being dehydrogenated compounds the main reaction products regardless the preparation method. The catalyst supported on S40 showed decalin conversion values between 46-53% and yield to ring opening near to 30%. Moreover, the CI catalysts have yield to ring opening 10 to 20% higher than the catalysts prepared by SI. The catalyst prepared by coimpregnation supported on S40 was the most appropriate for opening the MCH and decalin due to an optimal balance between the metal and acid functions.