The formation of silica nano- and microparticles has been studied during growth by the modified Stöber-Fink-Bohn (SFB) method. It has been experimentally found that the density and fractal structure of particles vary with size as they grow from 70 to 2200 nm. We propose a model of particle structure which is a dense primary particle core and is composed of concentric secondary particle shells terminating in dense primary particle layers.

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The efficient development of selective materials for the recovery of uranium from nuclear waste and seawater is necessary for their potential application in nuclear fuel and the mitigation of nuclear pollution. In this work, a graphene oxide/amidoxime hydrogel (AGH) exhibits a promising adsorption performance for uranium from various aqueous solutions, including simulated seawater. We show high adsorption capacities (Qm = 398.4 mg g−1) and high % removals at ppm or ppb levels in aqueous solutions for uranium species. In the presence of high concentrations of competitive ions such as Mg2+, Ca2+, Ba2+ and Sr2+, AGH displays an enhanced selectivity for uranium. For low uranium concentrations in simulated seawater, AGH binds uranium efficiently and selectively. The results presented here reveal that the AGH is a potential adsorbent for remediating nuclear industrial effluent and adsorbing uranium from seawater.

We report experimental and theoretical results on the photoluminescence of CdTeSe nanocrystals, embedded in a silica opaline structure by infiltration of a highly diluted solution. Strong modification of emission diagrams of embedded nanocrystals have been observed in good agreement with theoretical models. At macroscopic scale, we measured the difference of nanocrystals emission lifetime embedded either in an opal for which the emission is in the gap, or in an opal of smaller balls diameter for which the emission is outside the gap. The photonic bandgap effect leads to a lifetime increase of the order of 10%. These lifetime variations are shown to be in good agreement with the calculated local density of states modification due to the pseudogap.

SiC nanowires (NWs) with diameters of 20-200 nm and lengths from tens to hundreds of micrometers have been synthesized by the carbothermal reduction of colloidal silica. The morphology and microstructure of NWs have been studied in detail by electron microscopy techniques. SiC NWs have been found to be hexagonal prisms, ''bamboo-like'' nanorods and nanobelts. The NWs with a [111] growth axis are hexagonal prism nanorods, while the nanobelts have growth directions varying from [110] to [113]. It has been found that NW growth proceeds in two stages. Initially, SiC crystallites grow on the carbon fiber surface. These crystallites serve as seeds, on which the SiC NWs nucleate and grow. The crystallites containing microtwins and stacking faults (SFs) with a preferential [111] growth direction give rise to the growth of nanorods, while the nanobelts start growing on the (111) facets of relatively perfect crystallites. Wires with core (SiC)-shell (SiO 2 ) structure have been obtained under special temperature treatment in air. The core-shell structure has been confirmed by transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDX) mapping techniques.