RESUMEN
Cerium oxide and mixed Cu/Ce oxide nanoparticles were prepared by the oil-in-water (O/W) microemulsion reaction method in mild conditions. The Cu/Ce molar ratio was varied between 0/100 and 50/50. According to X-ray diffraction (XRD), below 30/70 Cu/Ce molar ratio, the materials presented a single phase consistent with cubic fluorite CeO2. However, above Cu/Ce molar ratio 30/70, an excess monoclinic CuO phase in coexistence with the predominant Cu/Ce mixed oxide was detected by XRD and High-Resolution Transmission Electron Microscopy (HRTEM). Raman spectroscopy showed that oxygen vacancies increased significantly as the Cu content was increased. Band gap (Eg) was investigated as a function of the Cu/Ce molar ratio, resulting in values from 2.91 eV for CeO2 to 2.32 eV for the mixed oxide with 30/70 Cu/Ce molar ratio. These results indicate that below 30/70 Cu/Ce molar ratio, Cu2+ is at least partially incorporated into the ceria lattice and very well dispersed in general. In addition, the photodegradation of Indigo Carmine dye under visible light irradiation was explored for selected samples; it was shown that these materials can remove such contaminants, either by adsorption and/or photodegradation. The results obtained will encourage investigation into the optical and photocatalytic properties of these mixed oxides, for widening their potential applications.
RESUMEN
Indigo carmine and methylene blue dyes in aqueous solution were photodegraded using SiC-TiO(2) catalysts prepared by sol-gel method. After thermal treatment at 450°C, SiC-TiO(2) catalysts prepared in this work showed the presence of SiC and TiO(2) anatase phase. Those compounds showed specific surface area values around 22-25 m(2)g(-1), and energy band gap values close to 3.05 eV. In comparison with TiO(2) (P25), SiC-TiO(2) catalysts showed the highest activity for indigo carmine and methylene blue degradation, but this activity cannot be attributed to the properties above mentioned. Therefore, photocatalytic performance is due to the synergy effect between SiC and TiO(2) particles caused by the sol-gel method used to prepare the SiC-TiO(2) catalysts. TiO(2) nanoparticles are well dispersed onto SiC surface allowing the transfer of electronic charges between SiC and TiO(2) semiconductors, which avoid the fast recombination of the electron-hole pair during the photocatalytic process.
Asunto(s)
Compuestos Inorgánicos de Carbono/química , Carmin de Índigo/química , Azul de Metileno/química , Procesos Fotoquímicos , Compuestos de Silicona/química , Titanio/química , Catálisis , Microscopía Electrónica de Rastreo , Soluciones , Agua , Difracción de Rayos XRESUMEN
In this work, NaTaO(3) compounds doped with 1M% of La and Sm, were prepared by the sol-gel (SG) method and solid state (SS) reaction; and tested as photocatalysts on the degradation of methylene blue (MB) under UV light. The structural characterization by X-ray powder diffraction revealed that the crystallization of the NaTaO(3) phase prepared by the sol-gel method started at 600 degrees C, reaching maximum crystallization at 800 degrees C. It was determined that the presence of Sm and La retard the crystallization of the NaTaO(3) phase. On the other hand, the compounds synthesized in this work showed particle sizes in the nanometric scale, as it was observed by scanning electron microscopy (SEM). The specific surface area of the compounds synthesized by the sol-gel method, showed values 4 times higher than those obtained by the solid state reaction, favoring their functional and photocatalytic performance in the methylene blue degradation. In addition, the best photocatalytic performance was shown by the NaTaO(3) doped with Sm and heated at 600 degrees C, having a half-life time of 65 min.