Abstract

Nanocrystalline magnetic particles of Co x Fe (3− x )O 4, with x ranging from 0.79 to 1.15, has been synthesised by combustion reaction method using iron nitrate Fe(NO 3) 3.9H 2O, cobalt nitrate Co(NO 3) 2·6H 2O, and urea CO(NH 2) 2 as fuel without template and subsequent heat treatment. The process is quite simple and inexpensive since it does not involve intermediate decomposition and/or calcining steps. The maximum reaction temperature ranged from 850 to 1010 °C and combustion lasted less then 30 s for all systems. X-ray diffraction patterns of all systems showed broad peaks consistent with cubic inverse spinel structure of CoFe 2O 4. The absence of extra reflections in the diffraction patterns of as-prepared materials ensures phase purity. The average crystallite sizes determined from the prominent (3 1 1) peak of the diffraction using Scherre's equation and TEM micrographs consisted of ca. 27 nm in spherical morphology. FTIR spectra of the as-prepared material showed traces of organic and metallic salts byproducts. However, when the same material was washed with deionised water the byproducts were rinsed off, resulting in pure materials. Magnetic properties such as saturation magnetisation, remanence magnetisation and coercivity field measured at room temperature were 48 emu/g, 15 emu/g and 900 Oe, respectively.

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