1,721,027 research outputs found

    Solid Acid Catalysts from Clays: Preparation of Mesoporous Catalysts by Chemical Activation of Metakaolin under Acid Conditions

    No full text
    Natural kaolin was treated at 850 or 950 °C in air flow to give respectively the metakaolin samples MK8 and MK9. The obtained materials were successively treated at 90 °C with a 1 M solution of H2SO4, for various time lengths. The acid treatment of MK8 was found to give a high surface area microporous material with good catalytic properties related to the high density of acid sites, while MK9 gave an ordered mesoporous material with a low density of acid sites. The materials were characterized by several techniques, X-ray powder diffraction, thermogravimetric analysis, N2 physisorption, scanning electron microscopy, and temperature-programmed desorption of ammonia. The 1-butene isomerization was used as test reaction to evaluate the acidity of the samples

    One-pot mesoporous Al–Ce–Cu oxide systems as catalysts for the preferential carbon monoxide oxidation (CO-PROX)

    No full text
    A series of organized mesoporous Al–Ce–Cu oxide systems, synthesized by a single-step method using aluminum sec-butoxide as Al precursor and Cu and Ce stearates and/or nitrates as metal sources, have been comparatively studied to evaluate the influence of some of the preparation parameters on their catalytic behavior in the preferential oxidation of CO (CO-PROX) to CO2 in H2-rich gas streams. The catalytic activity was tested in the 40–190 °C temperature range

    Photocatalytic performance of Cu-doped titania thin films under UV light irradiation

    No full text
    We investigated the effect of copper doping on the photocatalytic properties of TiO2 thin films. Titania thin films doped with three different copper concentrations were synthesized via radiofrequency-assisted (RF) magnetron sputtering, then annealed at 600 ◦C in controlled atmosphere (Ar, O2, H2 flow). The impact of the annealing in inert, oxidizing or reducing atmosphere on the crystalline and surface structure, and photocatalytic performance in the methylene blue degradation under UV light irradiation was investigated by X-ray diffraction, UV–Vis Spectroscopy, Rutherford Backscattering Spectrometry, Scanning Electron Microscopy. Annealing induced very different crystallization in different atmospheres, with strong copper out-diffusion in samples annealed in reducing atmosphere and formation of large embedded nanoparticles. The Cu-doped titania films exhibited higher photocatalytic activity than pure titania film and the best performing catalyst, treated in H2 atmosphere, suggests that the presence of embedded copper nanoparticles (both metallic and oxidized) is able to strongly enhance the photocatalytic properties of the host titania matrix. Incorporated Cu particles can act as trapped sites for generated electrons, and this leads to the reduction of carrier recombination which, ultimately, plays a significant role in the increase of photoactivity. The recyclability of the best system was ascertained by a suitable 3-cycle stability test

    Low-temperature carbon monoxide oxidation over zirconia-supported CuO–CeO2 catalysts: Effect of zirconia support properties

    No full text
    A study was conducted to investigate the effect of the preparation route of ZrO2 in CuO–CeO2/ZrO2 catalysts for the oxidation of carbon monoxide at low temperature (COX). Four ZrO2 supports were synthetized via either type sol-gel methodology or precipitation. The final Cu-Ce-Zr oxide catalysts were prepared by incipient wetness co-impregnation with copper and cerium solutions (with a loading of 6 wt% of CuO and 20 wt% of CeO2). The catalyst crystalline phases, texture and active species reducibility were determined by XRD, N2 physisorption at −196 °C and H2-TPR, respectively; meanwhile the surface composition and copper-cerium electronic states were studied by XPS. The catalytic activity was evaluated in the oxidation of CO to CO2, in the 40–215 °C temperature range. Catalytic results evidenced that the samples prepared by a sol-gel methodology showed, after the impregnation, a severe decrease of specific surface area and pore volume attributable to a wide degree of pore blockage caused by the presence of metal oxide particles and a collapse of the structure partially burying the active sites. A simple co-impregnation of a zirconia support, obtained through facile and fast precipitation, provided instead a catalyst with very good redox properties and high dispersion of the active phases, which completely oxidizes CO in the range 115–215 °C with T50 of 65 °C. This higher observed activity was ascribed to the formation of a larger fraction of highly dispersed and easily reducible Cu species and ceria nanocrystallites, mainly present as Ce(IV), with an average size of 5 nm
    corecore