RESUMO
A general approach to transfer water-soluble nanoparticles with different shapes, sizes, and surface charges into organic solvents, retaining their surface charge properties was developed, and its application in fabrication of hybrid Janus particles with opposite charges in solution was also demonstrated.
RESUMO
A deposition-precipitation (DP) process was used to prepare silica-titania core-shell pebbles decorated with nanocrystalline gold suitable for low-temperature catalytic oxidation of carbon monoxide (CO). The microstructure, phase content, crystallography, and catalytic activity were correlated with the pH (3-8), aging time (15, 30, 60 min), and heat treatment employed for gold crystallization (200-400 degrees C). A homogeneous metal distribution, high gold loading (3.7-4.4 wt %), and superior interfacial adhesion between gold and titania were obtained when the support pebbles were prepared at 600 degrees C, a temperature lower than that required for the anatase-to-rutile transformation. Nucleation and growth of {111} faceted gold was favored at mid-pH (6.4-8), while smaller crystals (<7.5 nm) were obtained at short aging times (
RESUMO
A monodispersed silica-titania core-shell photocatalyst was synthesized via a sol-gel route without the need of pH adjustment, cationic polyelectrolytes, or surfactants in a process where silica spheres were impregnated with hydrolyzed titanium tetrabutoxide, incubated at room temperature, and then condensed using an ethanol/water (1:1) solvent. Four coating cycles in a 10% v/v titania sol produced homogeneous titania shells. The quality of catalysts was assessed quantitatively using Rietveld analysis of powder X-ray diffraction patterns combined with X-ray fluorescence spectrometry. During calcination, the anatase-to-rutile transformation was delayed to 1000 degrees C, which is approximately 300 degrees C higher than usually observed. The thermal stability and surface area of titania were enhanced through the slow crystal growth of anatase. The photocatalytic activity of the core-shell photocatalysts calcined at 400-600 degrees C was found to be proportional to the thickness of titania but did not directly correlate with the surface area.
RESUMO
A new heterogeneous Fenton-like system, consisting of supported Au catalysts and hydrogen peroxide, was proved to be effective in removing low level organic compounds (ca. 100 ppm) such as phenol, ethanol, formaldehyde, and acetone in aqueous solution. Among all gold catalysts the Au/ hydroxyapatite (Au/HAp) exhibits the highest activity, and even better than the conventional iron ions exchanged zeolite (Fe/ ZSM-5) catalyst. In particular, unlike the limited operational pH range (pH: 2 approximately 5) for the other heterogeneous Fenton catalysts such as Fe/ZSM-5, Au/HAp shows higher stability even in strong acid solution (pH approximately 2), due to almost no leaching of active metal from supports into solution. It can be potentially applied in treating the industrial wastewaters with strong acidity and purifying drinking water. In addition, in the case of complete oxidation of phenol, a plausible route was suggested for deep understanding of this process.
Assuntos
Ouro/química , Compostos Orgânicos/isolamento & purificação , Abastecimento de Água , Catálise , Durapatita , Recuperação e Remediação Ambiental , Microscopia Eletrônica de Transmissão , Oxirredução , Fenóis/análise , SoluçõesRESUMO
A direct process for preparing contiguous gold shells (15-25 nm thick) over amorphous silica spheres (200 nm) is described. In this method, gold seeds are synthesized from HAuCl(4) in a dilute NaOH solution using deposition-precipitation with subsequent metallization by sodium borohydride (NaBH(4)). The ease of dispersing gold nanocrystals on spheres of bare silica and spheres after grafting with ammonia was studied as a function of pH (4-8), reaction temperature (65-96 degrees C), and time (5-30 min). Additional parameters requiring optimization included the quantity of NaBH4 and the HAuCl(4) in K(2)CO(3) solution to silica volume ratio. The evolution of gold nanocrystal growth was monitored by transmission electron microscopy, and the bathochromic shift of ultraviolet-visible absorption was correlated with shell perfection and thickness.
Assuntos
Ouro/química , Dióxido de Silício/síntese química , Nanopartículas Metálicas/química , Nanopartículas Metálicas/ultraestrutura , Microscopia Eletrônica de Transmissão , Dióxido de Silício/químicaRESUMO
Highly dispersed gold nanocrystals decorating silica spheres were prepared from HAuCl4 and NaOH via a deposition-precipitation (DP) process, in which the isoelectric point (IEP) of the substrate was adjusted during sphere synthesis by interaction of the surface with ammonia molecules. Through the systematic variation of pH (4-8), reaction temperature (65-96 degrees C), and time (10-30 min), a superior product with small (2-5 nm), homogeneously distributed gold crystals was obtained at pH 7 and a reaction temperature of 96 degrees C. These materials will offer enhanced performance as catalysts and contrast enhancers in biomedical imaging.