YCrxAl1-xO3 nanoparticles were synthesized by a reverse micelle processing for inorganic pigment. Y(NO3)2·6H2O, Cr (NO3)2·6H2O and Al (NO3)3·9H2O are used for precursors in order to synthesis YCrxAl1-xO3 nanoparticles. The aqueous solution consists of mixing the molar ratio of Y/Cr/Al at 1:x:1-x and heat treated at 900~1300°C for 2h. The average size and distribution of synthesized YCrxAl1-xO3 powders was in the range of 10-20nm and narrow, respectively. The average size of the synthesized YCrxAl1-xO3 powders increased with increasing water to surfactant molar ratio and heating temperature. The crystallinity of synthesized YCrxAl1-xO3 powder increased with increasing heating temperature. The synthesized YCrxAl1-xO3 powders were characterized by X-ray diffraction analysis (XRD), field emission scanning electron microscopy (FE-SEM) and color spectrophotometer. The properties of the synthesized powders were affected by such variables as molar ratio, heating temperature etc.
CeO2 nanoparticles were synthesized through the solvothermal process. It is observed that the water/ethanol mixed solvents were strongly influenced on the agglomeration. The average size of CeO2 nanoparticles was about in the range of 11-13nm and its distribution was narrow. With the increase of the ethanol composition, the surface area of CeO2 was increased from 65.384m2/g to 84.649m2/g. The synthesized nanoparticles components, particle size, morphology and surface area were characterized by EDS, XRD, FE-SEM, FE-TEM and BET.
Hydrothermal processes have the potential for the direct preparation of crystalline ceramic powders and offer a low-temperature alternative to conventional powder synthesis techniques in the production of oxide powders. These processes can produce fine, high-purity, stoichiometric particles of single and multi-component metal oxides. Furthermore, if process conditions such as solute concentration, reaction temperature, reaction time and the type of solvent are carefully controlled, the desired shape and size of particles can be produced. Uniform distribution of the particles is key for optimal control of grain size and microstructure in order to maintain high reliability. It has been demonstrated that such powders are composed of much softer agglomerates and sinter much better than those prepared by calcination decomposition of the same oxides. These powders could be sintered at low temperature without calcination and milling steps. The objective of this study was to synthesis TiO2-CeO2 nanosized crystalline particles by a hydrothermal process.TiO2-CeO2 nanosized powders were prepared under high temperature and pressure conditions by precipitation from metal nitrates with aqueous potassium hydroxide. The TiO2-CeO2 nanosized powder was obtained at 185°C and 6 h. The average size and size distribution of the synthesized particles were below 10±5 nm and narrow, respectively. The XRD diffraction pattern shows that the synthesized particles were crystalline. This study has shown that the synthesis of TiO2-CeO2 nanosized crystalline particles is possible under hydrothermal conditions in aqueous solution.
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