Defluoridation behavior of nanostructured hydroxyapatite synthesized through an ultrasonic and microwave combined technique.

The absorption performance of a nano-structured hydroxyapatite produced from a combined ultrasonic and microwave technique was examined for the removal of fluoride from contaminated water. The effect of physical and chemical parameters such as initial pH, contact time, initial fluoride concentration and temperature were investigated. The results indicated that the equilibrium adsorption data followed both the Langmuir and Freundlich isotherms, with a maximum monolayer adsorption capacity of 5.5mg/g at 298K. In addition, the kinetic studies have shown that the fluoride adsorption data followed a pseudo-second order model and that the intra-particle diffusion process played a significant role in determining the rate. The thermodynamic analysis also established that the adsorption process was endothermic and spontaneous. The initial and final fluoride loaded nano-hydroxyapatite samples were characterized using FESEM, TEM, XRD, FTIR and XPS methods. The analysis revealed that structural changes to the adsorbent had taken place.

Fine-tuning of catalytic tin nanoparticles by the reverse micelle method for direct deposition of silicon nanowires by a plasma-enhanced chemical vapour technique.

The reverse micelle method was used for the reduction of a tin (Sn) salt solution to produce metallic Sn nanoparticles ranging from 85 nm to 140 nm in diameter. The reverse micellar system used in this process was hexane-butanol-cetyl trimethylammonium bromide (CTAB). The diameters of the Sn nanoparticles were proportional to the concentration of the aqueous Sn salt solution. Thus, the size of the Sn nanoparticles can easily be controlled, enabling a simple, reproducible mechanism for the growth of silicon nanowires (SiNWs) using plasma-enhanced chemical vapour deposition (PECVD). Both the Sn nanoparticles and silicon nanowires were characterised using field-emission scanning electron microscopy (FE-SEM). Further characterisations of the SiNW's were made using transmission electron microscopy (TEM), atomic force microscopy (AFM) and Raman spectroscopy. In addition, dynamic light scattering (DLS) was used to investigate particle size distributions. This procedure demonstrates an economical route for manufacturing reproducible silicon nanowires using fine-tuned Sn nanoparticles for possible solar cell applications.