Abstract
CoMn2O4 nanoparticles were synthesized by reverse micelle processing from the mixed precursor (consisting of Co (NO3)2 ·6H2O and MnCl2·4H2O). The CoMn2O4 was prepared by mixing the aqueous solution at a molar ratio of Co : Mn = 1 : 2. The synthesized powders were calcined at 600°C for 2h. The average size and distribution of synthesized powders were in the range of 10-20nm and narrow, respectively. The average size of the synthesized powders increased with increasing water to surfactant molar ratio. The XRD diffraction patterns show that the phase of CoMn2O4 was spinel (JCPDS no.77-0471). The synthesized and calcined powders were characterized by thermogravimetry-differential scanning calorimeter (TG-DSC), X-ray diffraction analysis (XRD) and transmission electron microscopy (TEM). The magnetic property of the powder was measured by Vibrating Sample Magneto-meter (VSM) at 298K. The effect of synthesis parameter, such as the molar ratio of water to surfactant, is discussed.
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