Showing 4 results for Beitollahi
B. Alinejad1,, H. Sarpoolaky1,, A. Beitollahi1, S. Afshar2,
Volume 4, Issue 1 (winter & spring 2007 2007)
Abstract
Abstract: Nanocrystalline MgAl2O4 spinel powder was synthesized using metal nitrates and a
polymer matrix-based composed of sucrose and polyvinyl alcohol (PVA). The precursor and the
calcined powders were characterized by simultaneous thermal analysis (STA), X-ray diffraction
(XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy
(SEM). According to XRD results, the inceptive formation temperature of spinel via this technique
was between 600°C and 700°C. The average crystallite size of calcined powder at 800°C for 2h
was in the range of 8-12nm. In addition, SEM micrograph showed that the synthesized powder had
a spherical morphology.
N. Najmoddin, H.r. Rezaie, A. Beitollahi, M.s. Toprak,
Volume 11, Issue 3 (september 2014)
Abstract
The synthesis of mesoporous CuFe2O4 spinel by several nanocasting strategies (i.e., multi-step nanocasting, one step nanocasting, modified solid-liquid), in which copper and iron nitrates are used as precursors and Pluronic P123 as surfactant, is explored. We have also checked the effect of pH, citric acid and sodium citrate in multi-step nanocasting method. The modified solid-liquid method which contains impregnating mesoporous silica by molten state salts in a non-ionic solvent seems to be the best choice to obtain single phase ordered mesoporous copper ferrite. Other methods suffer from the presence of copper oxide or hematite as impurities or lack of integrity in the mesoporous structure. Increasing pH up to 9.5 does not enhance the phase formation inside the pores of the silica matrix. The citric acid yields a fine structure but does not facilitate the phase formation. Adding sodium citrate neither heals the phase formation nor the structure of the final product. Moreover, vinyl- functionalized mesoporous silica exploited in this study as a hard template entraps both metal nitrates in the pores, assisting impregnation procedure
A. Mohammadpour, S. M. Mirkazemi, A. Beitollahi,
Volume 12, Issue 3 (September 2015)
Abstract
In the present study, the feasibility of α-Fe ferromagnetic phase formation in glass and glass-ceramic by
reduction in hydrogen atmosphere have been investigated. The glass with the composition of 35Na
2
O–24Fe2O3–20B
2O3
–
20SiO
2
–1ZnO (mol %) was melted and quenched by using a twin roller technique. As quenched glass flakes were heat
treated in the range of 400-675 °C for 1-2 h in hydrogen atmosphere, which resulted in reduction of iron cations to α-Fe
and FeO. The reduction of iron cations in glass was not completely occurred. Saturation magnetization of these samples
was 8-37 emu g -1
. For the formation of glass ceramic, As quenched glass flakes heat treated at 590 °C for 1 h. Heat
treatment of glass ceramic containing magnetite at 675°C in hydrogen atmosphere for 1 h led to reduction of almost all of
the iron cations to α-Fe. Saturation magnetization of this sample increased from 19.8 emu g
-1
for glass ceramic to 67 emu
g
-1
S. Mirzaei, H. Saghafian, A. Beitollahi, J. Świerczek, P. Tiberto,
Volume 16, Issue 3 (September 2019)
Abstract
In the present research, rapidly solidified Fe85.3B11P3Cu0.7 ribbons were prepared by melt spinning process. The microstructural variation as well as magnetic properties of the as-spun and annealed ribbons were characterized by X-ray diffraction (XRD), transmission Mossbauer spectroscopy and alternating gradient field magnetometer (AGFM). The results show two separated distinct exothermic peaks during heating resulting from the phase transition from amorphous to α-Fe and then to Fe3B, respectively. The study of magnetic properties in the amorphous and nanocrystalline states revealed that annealing the amorphous ribbons at 440˚C for 10 minutes gives rise to a significant increase in saturation magnetization (220 emu/g) which makes this alloy a good candidate for power applications.
