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Showing 2 results for Sol-Gel Auto-Combustion

S. Alamolhoda, S. M. Mirkazemi, T. Shahjooyi, N. Benvidi,
Volume 36, Issue 2 (9-2017)
Abstract

In this research, nickel ferrite nanoparticles were synthesized by sol-gel auto-combustion route, and the effect of calcination temperature on phase constituents, magnetic properties and microstructure of the synthesized nanoparticles was evaluated using X-ray Diffraction (XRD), Vibrating Sample Magnetometer (VSM) and Scanning Electron Microscopy (SEM). XRD results were submitted to quantitative analysis. Microstructural studies and crystallite size calculations showed formation of nanoparticles. XRD results showed that the combustion product consisted of NiFe2O4, α-Fe2O3, NiO, and FeNi3 phases. FeNi3 was eliminated by calcination, and the amounts of NiO and α-Fe2O3 were modvlated by changing in calcination temperature. Saturation magnetization changed from 37emu/g in combustion product to 30emu/g by calcination at 600°C, due to decomposition of FeNi3 magnetic phase and formation of higher amount of antiferromagnetic hematite phase. Also, the coercivity values increased, that could be due to increasing the amount of nickel ferrite phase and eliminating FeNi3 phase. Saturation magnetization reached to 43emu/g in calcinated sample at 1000°C due to the reaction between hematite and NiO phases that led to formation of higher amount of nickel ferrite to 43emu/g. Coercivity value dropped out to 127Oe by calcination at 1000°C, the reason of which could be incresing of particle size and formation of multi domain magnetic particles.
 


N. Alirezaei Varnosfaderani, S. E. Mousavi Ghahfarokhi, M. Zargar Shoushtari,
Volume 38, Issue 3 (12-2019)
Abstract

In this paper, W-type SrCo2Fe16O27 hexaferrite nanostructures were synthesized by sol-gel auto-combustion method. Effect of annealing temperature on the structural, magnetic and optical properties of these SrCo2Fe16O27 nanostructures was investigated. In order to determine the annealing temperature of samples, the prepared gel was examined by thermo-gravimetric and differential-thermal analyses. Morphology and crystal structure of the prepared samples were characterized by field emission scanning electron microscopy and X-ray diffraction pattern. Based on X-ray diffraction results, at annealing temperature of 1000 °C, the maximum amount of main phase formed. A planar morphology was spectroscopy for the synthesized samples through scanning electron microscope images. Fourier transform infrared analysis was used to confirm the synthesis of the main properties obtained of samples were measured by the vibrating sample magnetometer and the results showed that by increasing temperature, magnetic saturation increases. Moreover, optical properties of samples were investigated by ultraviolet–visible absorption and photoluminescence spectroscopies. The result of measurements of the energy gap approximately is same in the ultraviolet- visible and photoluminescence spectroscopes and also the energy gap is constant with increasing temperature.


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