This study reports the preparation of nanostructured cerium-doped titanium dioxide photocatalysts containing different cerium concentrations by a modified sol-gel route involving the use of acetylacetone. The nanocrystalline powders had their structural, morphological, and optical properties characterized by X-ray diffraction, vibrational and Raman spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, Brunauer, Emmett and Teller (BET) surface area analysis, scanning electron microscopy combined with energy dispersive X-ray spectroscopy, total reflection X-ray fluorescence, and diffuse reflectance spectroscopy. Cerium incorporation reduced the bandgap energy of the solids to values that allowed them to absorb visible light. Cerium presence improved the textural properties that are crucial for the catalytic process. The photocatalytic activities were evaluated through photodegradation experiments of methyl orange dye solution. The synthesis with acetylacetone as stabilizer provided nanostructured materials with higher Ce3+/Ce4+ ratio, which enhanced the photocatalytic activity. Smaller quantities of the doped photocatalysts afforded higher degradation rates than the rates reported in the literature.

Abstract CoMo/MgO catalysts with low loading of cobalt and molybdenum were prepared by incipient wetness impregnation and the sol-gel method for high yield production of carbon nanotubes (CNT). A detailed characterization of the catalysts, as-produced CNT and purified CNT, indicated a relationship between carbon nanotube properties, synthesis and purification steps. Excess of molybdenum in the catalyst caused a decrease in carbon yield and produced CNT with a lower degree of graphitization. Catalysts prepared by the sol-gel method and with higher molybdenum loading showed an improved interaction between cobalt and molybdenum, increasing the formation of CoMoO4, which was not completely removed during the purification step. The purification removed all MgO and part of the cobalt and molybdenum present in samples without significant damage to the CNT structure. An increase in sample purity could be achieved by increasing reaction time.

Varias técnicas, como fisissorção, espectroscopia de fotoelétrons excitados por raios X (XPS), difração de raios X (XRD), redução à temperatura programada (TPR) e quimissorção foram usadas para a caracterização de catalisadores de Co/γAl2O3 para a produção de nanotubos de carbono por deposição de metano. Os catalisadores apresentaram três principais espécies de cobalto: CoAl2O4, CoO e Co3O4. As espécies de CoAl2O4 estavam bem dispersas nos catalisadores e apresentaram elevada temperatura de redução, fazendo com que estas espécies sejam inativas para a produção de nanotubos. Para o catalisador 1%Co/Al2O3, a principal espécie encontrada foi o CoAl2O4. Contudo, com o aumento do teor de cobalto nos catalisadores, ocorreu um aumento na formação das espécies Co3O4 em relação às espécies CoO e CoAl2O4. Os catalisadores 2 e 3%Co/Al2O3 apresentaram aglomeração das partículas de cobalto após a etapa de redução e baixa seletividade para produção de nanotubos. Entretanto, o catalisador 4%Co/Al2O3 não apresentou aglomeração, resultando em uma melhor seletividade para formação de nanotubos, 71%, principalmente do tipo nanotubos de carbono de paredes múltiplas (MWNT).

Several analytical techniques, such as N2 physisorption, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), temperature programmed reduction (TPR) and chemisorption were employed to characterize the structure of Co/γAl2O3 catalysts used for the production of carbon nanotubes by methane vapor deposition. The catalysts were studied after the calcination step and presented three main cobalt species, CoAl2O4, CoO and Co3O4. The CoAl2O4 species were well dispersed and were reduced only at high temperatures, rendering them inactive for the carbon nanotube production. In the case of the 1%Co/Al2O3 catalyst, the main cobalt species found was CoAl2O4. However, increasing the cobalt content in the catalysts led to a higher formation of Co3O4 as compared to CoO and CoAl2O4 species. The 2 and 3%Co/Al2O3 catalysts showed particle agglomeration during the pretreatment step that decreased selectivity towards nanotube production. The 4%Co/Al2O3 catalyst did not show particle agglomeration and presented a higher selectivity to carbon nanotube production, 71%, mainly multi-walled carbon nanotubes (MWNT).

A influência do suporte na produção de nanotubos de carbono por deposição química a vapor (CVD) de metano sobre catalisadores de cobalto foi investigada. As técnicas de fisissorção de N2, difratometria de raios X (XRD), redução à temperatura programada (TPR) e quimissorções de H2 e CO foram usadas na caracterização dos catalisadores de cobalto suportados em diferentes óxidos (Al2O3, SiO2, Nb2O5 e TiO2). As técnicas de espectroscopia Raman, oxidação a temperatura programada (TPO) e microscopia eletrônica de varredura (SEM) foram utilizadas na caracterização e quantificação de espécies de carbono produzidas. No crescimento dos nanotubos, o catalisador produziu três espécies principais de carbono: carbono amorfo, nanotubos de carbono de parede única (SWNT) e nanotubos de carbono de parede múltiplas (MWNT). Técnicas de caracterização mostraram que a seletividade catalítica a cada tipo de nanotubo depende da distribuição do tamanho de partículas de cobalto, a qual depende das propriedades texturais do suporte. O catalisador Co/TiO2 apresentou alta seletividade para a produção de nanotubos de parede única. Esta alta seletividade se deve a uma distribuição estreita do tamanho de partículas de cobalto sobre TiO2.

The influence of the support on carbon nanotube production by methane chemical vapor deposition (CVD) on cobalt catalysts was investigated. N2 physisorption, X-ray diffractometry (XRD), temperature programmed reduction (TPR) and H2 and CO chemisorption techniques were used to characterize the structure of cobalt catalysts supported on different metal oxides (Al2O3, SiO2, Nb2O5 and TiO2). Raman spectroscopy, temperature programmed oxidation (TPO) and scanning electron microscopy (SEM) were used for the characterization and quantification of produced carbon species. On carbon nanotube growth, the catalyst produced three main carbon species: amorphous carbon, single walled carbon nanotubes (SWNT) and multi walled carbon nanotubes (MWNT). The characterization techniques showed that the catalyst selectivity to each kind of nanotube depended on the cobalt particle size distribution, which was influenced by the textural properties of the support. Co/TiO2 showed the highest selectivity towards single wall nanotube formation. This high selectivity results from the narrow size distribution of cobalt particles on TiO2.