Abstract
Nanocrystalline MgAl2O4 powders were prepared by a thermal decomposition method, i.e. by use of molten salts. This method involves co-melting stoichiometric amounts of magnesium nitrate hydrate Mg(NO3)2.6H 2O and aluminium nitrate hydrate Al(N O3) 3.9H2O at 500°C. The spinel content of the co-melted and calcined powders at different firing temperatures up to 1000°C was determined by chemical analysis and the powders were characterised with respect to spinel formation, crystallite and particle sizes by X RD, T EM, and IR spectroscopy. The results obtained revealed that the co-melted materials were amorphous. After heat treatment of the amorphous materials at up to 1000°C, pure spinel powder was obtained, reaching over 98% spinel content. During calcination at different firing temperatures up to 1000°C the amorphous material progressively crystallised, forming nanocrystalline spinel with a maximum crystallite size of about 10 nm and particle size of around 300 nm. Bands in IR spectra were observed corresponding to the ex istence of AlO6 groups prior to magnesium spinel formation, which was the only crystalline phase at 1000°C.
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