Journal of Advanced Materials in Engineering (Esteghlal)

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The effects of temperature, time and atmosphere on microstructure and magnetic properties of NiFe2O4 glassceramic were investigated utilizing differential thermal analysis, X-ray diffraction, vibrating sample magnetometer and scanning electron microscope techniques. Various compositions were studied in the Na2O-NiO-Fe2O3-B2O3-SiO2 system to obtain amorphous phase. The sample heat-treated in graphite bed at 510°C for 1 hr showed higher magnetization than the one heattreated in the air under the same condition. XRD analysis showed the presence of nickel ferrite and some non-magnetic phases such as sodium borate and silicate phases in the heat treated samples. The maximum magnetization of samples reduced by increasing the holding time from 1hr to 3 hr at 510°C. Increment of temperature to 700°C increased the amount of NiFe2O4 and maximum magnetization.

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In this investigation, the effect of Polyvinylpyrrolidone (PVP) additive on microstructure, morphology and magnetic properties of cobalt ferrite nanoparticles prepared by hydrothermal method was studied. X-ray diffraction (XRD) studies in different synthesis conditions showed the formation of cobalt ferrite and cobalt oxide. Comparing IR spectrum of PVP additive, sol prepared before hydrothermal process and C-0.1PVP3, 190 obtained by FTIR spectroscopy indicated the formation of bond between PVP and surface of metallic hydroxide and cobalt ferrite particles, which prevented them from growing and coarsening. Scanning electron microscope (SEM) was used to study the morphology of samples. According to vibration sample magnetometer (VSM) results, as PVP amount increases from 0.1 to 0.3 volume percent, coercive field increases from 298 to 684 Oe and saturation magnetization decreases from 58 to 51 emu/g.

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In this investigation, the effect of heat treatment on magnetic properties of glass and nano-structured cobalt-ferrite glass-ceramic was studied. The glass was synthesized in the system of Na2O-Fe2O3-CoO-B2O3-SiO2. Based on DTA results, heat treatment was done at different times and temperatures. X-ray diffraction pattern of glass-ceramic showed the crystallization of CoFe2O4 and some nonmagnetic phases. The highest magnetization of 11.8 emu/g was obtained for the sample heat-treated for 2 hr at 670C in graphite bed. Average crystallite size of CoFe2O4 in this sample was 50 nm. Scanning Electron Microscopy (SEM) confirmed the formation of cobalt ferrite nanoparticles in the glass matrix.

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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.
 

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Electrophoretic Deposition (EPD) weight is highly affected by electrophoretic mobility of powders in suspension. In theoretical aspect, electrophoretic mobility is influenced by suspension viscosity in opposite direction, and increasing in viscosity can decrease electrophoretic mobility and consequently can decrease EPD weight. In non-aqueous suspension, viscosity is determined by ion strengths of suspension. In this study, viscosity, electrical conductivity and deposit weight were determined for electrophoretic deposition (EPD) of alumina suspended in ethanolic solvent of Y-, Mg-, Ce- and La- salts, prepared in dispersant level between 350 to 1350 ppm. The concentration of XCly, (X: Mg, Y, Ce and La), is also found to be a critical factor to control  the viscosity. It is shown that the deposit weight is influenced by precursor concentration, and on the other hand, electrical conductivity, viscosity or the pH of the suspension cannot change the yield. All concentrations interactions, except Mg × Ce concentration are significant in ANOVA model. The viscosity of suspension reached 2.5 mPa.s with Mg-, Y-, La- and Ce- decreased to 100, 100, 100 and 0 ppm in low iodine concentration (400 ppm). The reason is that heavier cations can be adsorbed to alumina surface with iodine adsorption, but lighter Mg- cations can be adsorbed under the influence of OH groups excited on alumina surface.
 

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