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Keggin-type H_4PVMo_(11)O_(40)-based catalysts for the isobutane selective oxidation

Science China Chemistry 2010年第9期53卷 2039-2046页

作者： PAUL Sébastien SULTAN Manzoor bordes-richard elisabeth Université Lille Nord de France ECLilleUnité de Catalyse et de Chimie du Solide(UMR CNRS 8181)Cité Scientifique Université Lille Nord de France ENSCLUnité de Catalyse et de Chimie du Solide(UMR CNRS 8181)Cité Scientifique

Cesium heteropolysalts Cs3PMo12O40 and HCs3PVMo11O40 were synthesized by modifying the preparation conditions in order to get materials with a much higher surface area than the original Keggin-type heteropolyacids(H3PMo12O40 and H4PVMo11O40).These solids were used as carriers for the dispersion of H4PVMo11O40 heteropolyacid by the incipient wetness impregnation *** textural and structural properties of supports and catalysts were examined by scanning electron microscopy,N2 adsorption-desorption isotherms and Raman *** supported catalysts were studied before and after red/ox pretreatments by X-ray photoelectron spectroscopy,which showed that both the surface composition and oxidized to reduced species ratio depend on the used *** catalytic performances of these novel supported catalysts in the selective oxidation of isobutane to methacrylic acid and methacrolein were *** best catalytic properties were obtained when H4PVMo11O40 was supported on *** isobutane conversion and yield of the desired oxygenates increased along the unsupported H4PVMo11O40

关键词： cesium heteropolysalts supports supported H4PVMo11O40 red/ox XPS isobutane selective oxidation Keggin-type heteropolycompounds

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Nickel ferrite spinel as catalyst precursor in the dry reforming of methane:Synthesis,characterization and catalytic properties

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Journal of Natural Gas Chemistry 2012年第5期21卷 595-604页

作者： Rafik Benrabaa Hamza Boukhlouf Axel Lfberg Annick Rubbens Rose-Nelle Vannier elisabeth bordes-richard Akila Barama Laboratoire de Matériaux Catalytiques & Catalyse en Chimie Organique Faculté de ChimieUSTHBBP32 El Alia16111 Bab EzzouarAlgerAlgérie Unité de Catalyse et de Chimie du Solide UMR CNRS 8181Ecole Nationale Supérieure de Chimie de LilleUniversitédes Sciences et Technologies de LilleCité Scientif ique59655 Villeneuve d'AscqFrance

Dry reforming of methane by CO2 using nickel ferrite as precursor of catalysts was *** ferrite crystalline particles were prepared by coprecipitation of nitrates with NaOH or ammonia followed by calcination,or by hydrothermal synthesis without calcination *** textural and structural properties were determined by a number of analysis methods,including X-ray diffraction （XRD）,Raman spectroscopy and X-ray photoelectron spectroscopy （XPS）,among which X-ray diffraction （XRD） was at room and variable *** synthesized oxides showed the presence of micro or nanoparticles of NiFe2O4 inverse spinel,but Fe2O3 （hematite） was also present when ammonia was used for *** reducibility by hydrogen was studied by temperature-programmed reduction （TPR） and in situ XRD,which showed the influence of the preparation *** surface area （BET）,particle size （Rietveld refinement）,as well as surface Ni/Fe atomic ratio （XPS） and the behavior upon reduction varied according to the synthesis *** catalytic reactivity was investigated using isopropanol decomposition to determine the acid/base *** catalytic performance of methane reforming with CO2 was measured with and without the pre-treatment of catalysts under H2 in 650-800 C *** catalytic conversions of methane and CO2 were quite low but they increased when the catalysts were pre-reduced.A significant contribution of reverse water gas shift reaction accounted for the low values of H2 /CO *** coking was observed as shown by the reoxidation step performed after the catalytic *** possible formation of nickel-iron alloy observed during the study of reducibility by hydrogen was invoked to account for the catalytic behavior.

关键词： dry reforming of methane NiFe2O4 spinel hydrothermal synthesis coprecipitation isopropanol decomposition

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