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Dive into the research topics where Roger Kieffer is active.

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Featured researches published by Roger Kieffer.


Applied Catalysis A-general | 1997

Change of catalytic properties of FeZnO/zeolite composite catalyst in the hydrogenation of carbon dioxide

Masahiro Fujiwara; Roger Kieffer; Hisanori Ando; Qiang Xu; Yoshie Souma

Abstract The hydrogenation of carbon dioxide was examined using the composite catalysts which were obtained by the physical mixing of Fe ZnO and HY zeolite. Fe ZnO was a typical F-T (Fischer-Tropsch) catalyst and Fe ZnO/HY is a composite catalyst which is able to induce a combined methanol synthesis and MTG (Methanol-to-Gasoline) reaction. To study these unique catalytic behaviors of Fe ZnO/HY, the adsorption and the dissociation of carbon monoxide on Fe ZnO as well as TPR measurements were carried out. Fe ZnO is able to produce hydrocarbons by F-T reaction and methanol. In the absence of zeolite, Fe ZnO exerts its ability for F-T reaction. However, HY diminishes the activity for F-T reaction and hydrocarbons were obtained via methanol formed over the modified Fe ZnO


Studies in Surface Science and Catalysis | 1996

Oxidative dehydrogenation of propane on rare earth vanadates influence of the presence of CO2 in the feed

Bao Zhaorigetu; Roger Kieffer; Jean-Paul Hindermann

Abstract The oxidative dehydrogenation of propane on rare earth vanadates is always in competition with the total oxidation of the alkane which leads to the formation of CO 2 and CO. Addition of CO 2 into the feed results in an increased C 3 H 6 selectivity together with a decreased CO formation through the total oxidation of the alkane or the formed alkene. For the tested rare earth vanadates as well as for the niobium promoted catalysts an enhancement of the C 3 H 6 selectivity at isoconversion and thus of the C 3 H 6 yields is observed upon CO 2 addition into the feed.


Reaction Kinetics and Catalysis Letters | 2002

Synergetic effect between NiO and Ni3V2O8 in propane oxidative dehydrogenation

Bao Zhaorigetu; Wenzhao Li; Roger Kieffer; Hengyong Xu

The oxidative dehydrogenation (ODH) of propane was investigated on Ni-V-O catalysts in a wide range of vanadium contents (5-40%). The addition of a small amount of vanadium significantly increased the catalytic activity of NiO for oxidative dehydrogenation of propane to propene. The formation of propene has a good correlation with the coexistence of NiO and Ni3V2O8. This result strongly suggests that a synergetic effect exists between them in NiXV1-XOY (X = 0.95 to 0.6). The best results were obtained with a high Ni/V ratio (e.g. X = 0.95 to 0.85). The active sites and selective oxygen species are discussed. The influence of the catalyst preparation technique and the redox properties of the catalyst were also examined.


Studies in Surface Science and Catalysis | 1993

Oxidative Dehydrogenation of Propane in Presence of Rare Earth Vanadates

J. Castiglioni; P. Poix; Roger Kieffer

Publisher Summary V 2 O 5 -containing materials have been used in the oxidative dehydrogenation of light-molecular-weight alkanes. Only few examples have been reported for the use of non-stoichiometric rare-earth vanadates for the reaction of propane. This chapter reports on the activity of rare-earth vanadates of a definite Zirkon structure, LnVO 4 (Ln = Ce, Pr, Nd, Tb, Er, Tb), in the title reaction of propane. Rare-earth vanadates are an original catalytic system for the activation of propene, which can compete with the more classical Mn vanadate catalyst. For each catalyst, a correlation can be established between propane selectivity and total conversion. A high propane conversion leads to a low olefin selectivity in all cases. The oxygen/propane ratio in the feed influences the conversion and the selectivity. An interesting correlation between C 3 H 8 conversion and C 3 H 6 selectivity can be observed. A Mars Van Krevelen mechanism, taking into account the reaction on oxygen vacancies on the catalytic surface, describes these results well.


Studies in Surface Science and Catalysis | 1998

Hydrocarbon synthesis from CO2 over composite catalysts

Yoshie Souma; Masahiro Fujiwara; Roger Kieffer; Hisanori Ando; Qiang Xu

Hydrogenation of CO 2 was carried out using various composite catalysts containing a methanol synthesis catalyst and a zeolite. Hydrocarbons were obtained via methanol by MTG(Methanol to Gasoline) reaction. Cu-Zn-Cr mixed oxide prepared from CuO, ZnO and CrO 3 was an effective component of the composite catalyst for the synthesis of light paraffins. The composite catalyst containing Cu-Zn chromate or Fe-ZnO gave higher hydrocarbons via olefin intermediate formed from methanol. Fe-ZnO had two active sites; iron species formed from Fe 3 O 4 and ZnFe 2 O 4 . When Fe-ZnO was used alone, F-T reaction over iron species was predominant. The addition of HY zeolite to Fe-ZnO deactivated the iron species for F-T reaction, and thus MTG reaction over ZnFe 2 O 4 became predominant.


Catalysis Letters | 2001

Investigations on the promoting effect of metal oxides on La-V-O catalyst in propane oxidative dehydrogenation

Bao Zhaorigetu; Roger Kieffer; Wenzhao Li

The addition of reducible metal oxides as promoters shows a positive effect on the catalytic behavior of lanthanum vanadate (LaVO4). A C3H6 yield increase of 6.5% is observed at 500 °C on molybdenum-promoted LaVO4, which can be attributed to the change of the redox properties, the blocking of the strong oxidation sites of the catalysts and to an increase of the accessibility of the labile oxygen toward the reactant. The influence of the catalyst preparation method and of the Mo loading as well as the additional promoting effect of CO2 in the gas feed was also examined.


Catalysis Letters | 2004

Correlation between the characteristics and catalytic performance of Ni-V-O catalysts in oxidative dehydrogenation of propane

Bao Zhaorigetu; Wenzhao Li; Hengyong Xu; Roger Kieffer


Journal de Chimie Physique | 1982

Réactions CO-H2 et CO2-H2 sur catalyseurs au palladium supportés

Edwin Ramaroson; Roger Kieffer; A. Kiennemann


Archive | 1993

PROCEDE DE PREPARATION D'UN OXYDE D'AU MOINS DEUX METAUX DIFFERENTS.

Patrick Chaumette; Danna Andriamasinoro; Roger Kieffer; A. Kiennemann; Paul Poix; Jean-Luc Rehspringer


Archive | 1991

Procede d'isosynthese en presence d'un catalyseur a base d'un oxyde d'au moins deux metaux differents

Patrick Chaumette; Dama Andriamasinoro; Roger Kieffer; A. Kiennemann; Paul Poix; Jean-Luc Rehspringer

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A. Kiennemann

University of Strasbourg

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Bao Zhaorigetu

Dalian Institute of Chemical Physics

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Wenzhao Li

Dalian Institute of Chemical Physics

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Jean-Luc Rehspringer

Centre national de la recherche scientifique

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Paul Poix

Centre national de la recherche scientifique

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Hengyong Xu

Dalian Institute of Chemical Physics

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Hisanori Ando

National Institute of Advanced Industrial Science and Technology

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Masahiro Fujiwara

National Institute of Advanced Industrial Science and Technology

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Yoshie Souma

National Institute of Advanced Industrial Science and Technology

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