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José Maria C. Bueno

Researcher at Federal University of São Carlos

Publications -  91
Citations -  3951

José Maria C. Bueno is an academic researcher from Federal University of São Carlos. The author has contributed to research in topics: Catalysis & Steam reforming. The author has an hindex of 33, co-authored 87 publications receiving 3415 citations.

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Colloidal Co nanoparticles supported on SiO2: Synthesis, characterization and catalytic properties for steam reforming of ethanol

TL;DR: In this article, the authors obtained colloidal Co nanoparticles with sizes in the 3-8 nm range and impregnated on SiO2 to prepare SiO 2-supported Co nanocatalysts.
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Designing Pt nanoparticles supported on CeO2-Al2O3: Synthesis, characterization and catalytic properties in the steam reforming and partial oxidation of methane

TL;DR: In this article, a new strategy to synthesize Pt clusters of uniform size supported on mixed oxides was achieved, and the catalysts were characterized by Fourier transform infrared spectroscopy of adsorbed CO, transmission electron microscopy and X-ray absorption fine structure analysis.
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CO2 reforming of methane over zeolite-Y supported ruthenium catalysts

TL;DR: In this article, X-ray diffraction (XRD), transmission electron microscopy (TEM) and nuclear magnetic resonance (NMR) were used to characterize Ru/HY and Ru/NaY catalysts.
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The effects of CeO2 on the activity and stability of Pt supported catalysts for methane reforming, as addressed by in situ temperature resolved XAFS and TEM analysis

TL;DR: In this paper, the effects of Ce as a promoter on the activity and stability of Pt/Al 2 O 3 and Pt/CeO 2 -Al 2 -O 3 catalysts for autothermal reforming and partial oxidation of methane (POM) were investigated.
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Ru-Sn catalysts for selective hydrogenation of crotonaldehyde: Effect of the Sn/(Ru + Sn) ratio

TL;DR: In this article, the effects of the Sn/(Ru+Sn) ratio and Ru loading on the properties of silica-supported RuSn catalysts were investigated, and the results indicated that the Ru/SiO2 catalyst was active only for hydrogenation of the C C bond, while the addition of a small amount of Sn (1.6% of Sn) made the catalyst active for hydrogenating both the C and C O bonds.