Showing 14 results for Ferrite
Dehghan Manshadi A., Zarei Hanzaki A., Golmahalleh O.,
Volume 2, Issue 2 (6-2005)
Abstract
The presence of bainite in the microstructure of steels to obtain a proper combination of strength and toughness has always been desired. The previous works however have shown that the presence of preferred bainite morphologies in the microstructure of any steel would not be readily accessible. In addition, the appearance of different bainite morphologies in the microstructure of any steel is dictated by different factors including the steel initial microstructure, austenitization characteristics, thermomechanical processing parameters and so on. Accordingly, in the present work, the effect of prior austenite grain size and the amount of austenite hot deformation on the bainite formation characteristics were investigated in 0.12C-2.5 Ni-1.2Cr steels. The results indicated that the prior austenite grain size and the amount of deformation in the austenite no-recrystallization region resulted in significant changes of the bainite formation kinetics and morphology.
Ghobeiti Hasab M., Seyyed Ebrahimi S.a., Badaee A.,
Volume 2, Issue 2 (6-2005)
Abstract
In this research the sol-gel auto-combustion method was used to prepare strontium hexaferrite nanopowder. A solution of distilled water, ferric and strontium nitrates, citric acid, trimethylamine, and n-decyltrimethylammonium bromide cationic surfactant, was heated to form a viscous gel. The gel was heated and then ignited automatically. As-burnt powder was calcined at temperatures from 700 to 900?C in air to obtain SrO.6Fe2O3 phase. The influence of the calcination temperature on the phase composition of the products has been investigated. X-ray diffraction confirmed the formation of single-phase strontium hexaferrite nanopowder at temperature of 800?C.
Sheikhi Moghaddam K., Ataie A.,
Volume 2, Issue 4 (12-2005)
Abstract
Ultra-fine particles of barium hexaferrite have been synthesized by co-precipitation method using barium nitride and iron chloride precursors with a Fe/Ba molar ratio of 11. Co-precipitation was carried out at 25 and 80°C using NaOH as a precipitant. Effect of coprecipitation and annealing temperatures on the phase composition and morphology of the products have been investigated using XRD and SEM, respectively. XRD results indicated existence of BaFeO3-x as a major phase in co-precipitated samples. Analysis of the XRD results also revealed that barium hexaferrite starts to form at a relatively low temperature of 700°C for sample synthesized at 80°C. SEM micrographs exhibit plate-like hexagonal particles of barium hexaferrite for calcined samples. The SEM results showed that the mean particle size of co-precipitated sample at 25°C is smaller than that of 80°C after calcining.
K. Ghadarghadr Jahromi, , A. Zarei-Hanzaki, O. Golmahalleh,
Volume 5, Issue 1 (3-2008)
Abstract
Abstract: In the present investigation, the effects of thermomechanical processing parameters and
the steel chemical composition on the ultra fine ferrite formation characteristics were studied.
This was programmed relying on the capabilities of strain induced transformation (SIT)
phenomenon and applying to different grades of Si-Mn TRIP (Transformation Induced Plasticity)
steels. Accordingly, wedge shaped specimens were rolled at two different temperatures, above and
below the austenite-to-ferrite transformation temperature (Ar3). An ultra fine ferrite grain size, in
the scale of some hundred nanometers, was obtained by rolling the specimens with lower Si
content at a temperature below the related Ar3 temperature. The amount of reduction, which was
resulted in the latter microstructure, was realized to be about 55%.
M. Esmailian,
Volume 7, Issue 1 (3-2010)
Abstract
Abstract:
transformation temperature and different ferrite morphologies in one Nb-microalloyed (HSLA) steel has been
investigated. Three different austenite grain sizes were selected and cooled at two different cooling rates for obtaining
austenite to ferrite transformation temperature. Moreover, samples with specific austenite grain size have been
quenched, partially, for investigation on the microstructural evolution.
In order to assess the influence of austenite grain size on the ferrite transformation temperature, a temperature
differences method (TDM) is established and found to be a good way for detection of austenite to ferrite, pearlite and
sometimes other ferrite morphologies transformation temperatures.
The results obtained in this way show that increasing of austenite grain size and cooling rate has a significant influence
on decreasing of the ferrite transformation temperature.
Micrographs of different ferrite morphologies show that at high temperatures, where diffusion rates are higher, grain
boundary ferrite nucleates. As the temperature is lowered and the driving force for ferrite formation increases,
intragranular sites inside the austenite grains become operative as nucleation sites and suppress the grain boundary
ferrite growth. The results indicate that increasing the austenite grain size increases the rate and volume fraction of
intragranular ferrite in two different cooling rates. Moreover, by increasing of cooling rate, the austenite to ferrite
transformation temperature decreases and volume fraction of intragranular ferrite increases.
The effect of different austenite grain size and different cooling rates on the austenite to ferrite
Z. Ghiami, S. M. Mirkazemi, S. Alamolhoda,
Volume 12, Issue 2 (6-2015)
Abstract
trontium hexaferrite (SrFe
12
O
19
) nanosized powders were synthesized by sol-gel auto-combustion method
with and without cetyltrimethylammonium boromide (CTAB) addition in the sol with Fe/Sr ratio of 11 (using additional
Sr). The resultant powders were investigated by X-ray Diffraction (XRD), Transmission Electron Microscope (TEM),
Field Emission Scanning Electron Microscope (FESEM) and Vibration Sample Magnetometer (VSM) techniques.
Phase constituents of the synthesized samples which were heat treated at temperatures in the range of 700- 900 ◦C
were studied. XRD results revealed that CTAB addition facilitates the formation of single phase strontium hexaferrite
at 800 ◦C. Microstructural evaluations with FESEM represented that CTAB addition causes formation of larger
particles with a narrower size distribution. VSM results represented that the highest amount of intrinsic coercivity force
(
i
H
C
) was obtained in the sample without CTAB addition and with additional Sr, calcined at 800 ◦C for 1 h which was
equal to 5749.21 Oe, while the value of
i
H
C
was equal to 4950.89 Oe without additional Sr. The amount of maximum
magnetization (M
max
) was raised from 48.41 emu/g to 62.60 emu/g using CTAB and additional Sr. The microstructure
and magnetic properties of the samples have been explained
S. Alamolhoda, S. M. Mirkazemi, T. Shahjooyi, N. Benvidi,
Volume 13, Issue 1 (3-2016)
Abstract
Nano-sized NiFe2O4 powders were synthesized by sol–gel auto-combustion method using pH values from 7 to 9 in the sol. The effect of pH variations on complexing behavior of the species in the sol has been explained. Changes in phase constituents, microstructure and magnetic properties by changes in pH values were evaluated by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and vibration sample magnetometer (VSM) techniques. Changes in pH value from 7 to 9 changes the amounts of NiFe2O4, FeNi3 and α-Fe2O3 phases. Calculated mean crystallite sizes are in the range of 44 to 51nm. FESEM micrographs revealed that increasing the pH value to 9 causes formation of coarse particles with higher crystallinity. Saturation magnetization was increased from 36.96emu/g to 39.35emu/g by increasing pH value from 7 to 8 which is the result of increased FeNi3 content. Using higher pH values in the sol reduces the Ms value.
M. Ebrahimi, S. A. Seyyed Ebrahimi, S. M. Masoudpanah,
Volume 14, Issue 1 (3-2017)
Abstract
In this work, the effects of co-precipitation temperature and post calcination on the magnetic properties and photocatalytic activities of ZnFe2O4 nanoparticles were investigated. The structure, magnetic and optical properties of zinc ferrite nanoparticles were characterized by X-ray diffraction (XRD), vibrating sample magnetometry and UV–Vis spectrophotometry techniques. The XRD results showed that the coprecipitated as well as calcined nanoparticles are single phase with partially inverse spinel structures. The magnetization and band gap decreased with the increasing of co-precipitation temperature through the increasing of the crystallite size. However, the post calcination at 500 °C was more effective on the decreasing of magnetization and band gap. Furthermore, photocatalytic activity of zinc ferrite nanoparticles was studied by the degradation of methyl orange under UV-light irradiation. Compare with the coprecipitated ZnFe2O4 nanoparticles with 5% degradation of methyl orange after 5 h UV-light light radiation, the calcined ZnFe2O4 nanoparticles exhibited a better photocatalytic activity with 20% degradation.
M. Palizdar, Z. Aslam, R. Aghababazadeh, A. Mirhabibi, P. Sangpour, Z. Abadi, Y. Palizdar, R. Brydson,
Volume 16, Issue 4 (12-2019)
Abstract
In this paper the chemical interaction between catalyst and support has been studied to understand the observed different growth rate of CNTs in our previous paper. Both pure MgO and Mg(NO3)2 . 6H2O as sources of the MgO catalyst support and Fe2(SO4)3 · xH2O as the source of the Fe catalyst, were employed. A Fe catalyst supported on MgO has been synthesized using the wet impregnation method followed by calcination. To compare the catalyst grain size and its distribution, the sample were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and BET specific surface area (SSA) measurement and X-ray photoelectron spectroscopy (XPS). XPS technique have utilized complementary to demonstrate the existence of chemical interaction between MgO support and Fe catalyst. Results revealed that the type of precursor used to prepare the support has a significant influence on the morphology of the support and the associated distribution of the Fe catalysts. The highest yield of MgFe2O4 phase was obtained using a pure MgO precursor which after calcination results in a homogenous distribution of nano-sized Fe particles over the support surface
Hedayat Gholami, Hassan Koohestani, Mehdi Ahmadi,
Volume 18, Issue 1 (3-2021)
Abstract
In this research, using impregnation method, spinel cobalt and copper ferrites nanoparticles are synthesized on the surface of hematite. Synthesized powders were characterized and examined by FTIR, XRF, XRD, FESEM, BET and EDS analysis and the dye degradation were investigated by UV-vis and AAS methods. Specific surface area increased especially in the sample containing cobalt, which indicates the precise of synthesis and the creation of high surface nano particles at hematite surface. The size of particles was in the nano scale and a good uniformity observed in the structure. The results indicated a significant increase in the catalytic ability of hematite nano composite after synthesis. Their catalytic capability investigated by the Fenton reaction with complete removal of methylene blue from the solution via UV-vis irradiation. The samples stability discovered to be excellent by the AAS method.
Surekha S. Jadhav, Amit A. Bagade, Tukaram J. Shinde, Kesu Y. Rajpure,
Volume 19, Issue 1 (3-2022)
Abstract
In present work Ni0.7Cd0.3NdxFe2-xO4 ferrite samples (0≤x≤0.03) were prepared by using oxalate co-precipitation technique. The different characterization techniques were achieved using X-ray diffraction (XRD), FT-infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), DC electrical resistivity and dielectric measurements. The crystallographic parameters such as crystal structure, crystallite size, lattice constant, unit cell volume and theoretical density have been systematically analysed. The XRD and FT-IR measurements confirmed the formation of single phase spinel ferrite structure. The cation distribution among the octahedral and tetrahedral sites has been proposed on the basis of analysis of XRD patterns by employing Rietveld refinement analysis. The samples exist as a mixed type spinel with cubic structure. The DC electrical resistivity confirms the semiconducting behaviour and the Curie temperature decreases with increase in Nd3+ content. The dielectric constant and loss tangent decreases with frequency and higher frequencies remain constant, which shows the usual dielectric dispersion due to space charge polarization. The AC conductivity reveals that the small type polarons responsible for conduction process.
Salihah Alkhobrani, Hossein Bayahia, Fares T. Alshorifi,
Volume 20, Issue 3 (9-2023)
Abstract
In this study, CoFe2O4 (CoF) and ZnFe2O4 (ZnF) photocatalysts were successfully prepared by a facile and simple chemical precipitation method for degradation of methylene blue (MB) and methyl orange (MO) dyes under direct sunlight irradiation. The obtained ferrites were then characterized through XRD, TEM, EDS, UV-vis, and SEM. XRD and TEM results exhibited cubic nanostructures with sizes ranging from 9 to 16 nm and 11 to 18 nm for ZnF and CoF, respectively. SEM images showed homogenous, porous flat surfaces. EDS spectra confirmed the successful synthesis of ZnF and CoF nanostructures with high purity. UV-vis spectra results of MB and MO dyes showed maximum sunlight absorbance in the absence of ZnF and CoF, while a regular decrease in the sunlight absorbance was observed in the presence of ZnF and CoF within 15-60 min. The UV-vis results also showed that ZnF had higher photocatalytic activity than CoF. The experimental findings showed that the highest % degradation was 92.89% and 96.89% for MO and MB dyes, respectively, over ZnF compared to CoF photocatalyst (87.55% and 88.41% for MO and MB, respectively). These findings confirm that porous ZnF and CoF nanostructures are critical in promoting the degradation of dyes under sunlight instead of UV-vis light lamps that consume/require electrical energy.
Avinash Ramteke, Pradnya Chougule, Pranali Chavan, Amit Yaul, Gourav Pethe,
Volume 21, Issue 1 (3-2024)
Abstract
Nickel doped CoMn ferrites with high magnetization were synthesized by double sintering solid state route with compositions of Co0.7-xNixMn0.3Fe2O4 with x = 0, 0.05, 0.1 and 0.15. Theoretical Cation distribution for cubic spinel ferrites was suggested on basis of electrical configuration expectations and cation site preferences. Cation distribution suggested was in good agreement with experimental results obtained from VSM and XRD. Values of theoretically calculated magnetic moment, coercivity and magnetization are in good agreement with experimental data obtained from VSM. Maximum saturation magnetization of 37.7emu/gm is obtained for sample Co0.7Mn0.3Fe2O4 at magnetic field of 5K Oe. Magnetostriction was found to increase with increasing magnetic field (from 1KOe to 5KOe.) Maximum magnetostriction of 84ppm was observed for sample Co0.7Mn0.3Fe2O4 at 5KOe. Maximum magnetization of magnetoelectric composites with 30% Co0.7-xNixMn0.3Fe2O4 – 70% PbZr0.48Ti0.52 was found to be 7.4 emu/g for composition with x = 0.
Amit Bandekar, Pravin Tirmali, Paresh Gaikar, Shriniwas Kulkarni, Nana Pradhan,
Volume 21, Issue 1 (3-2024)
Abstract
The Mn-Zn ferrite with a composition of Mn0.25Mg0.08Cu0.25Zn0.42Fe2O4 has been synthesized in this study using the chemical sol-gel technique at a pH of 7. The sample was prepared and subsequently annealed at a temperature of 700°C. The nanocrystalline ferrite samples were subjected to characterization using X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), Thermogravimetry (TG), and Differential thermal analysis (DTA). The findings of these observations are delineated and deliberated. The sample's phase composition was verified using X-ray diffraction examination. The crystalline size was determined using Scherrer's formula and was observed to be within the range of 20-75 nm. Two notable stretching bands were seen in the FTIR spectra within the range of 400-650 cm-1. The spinel structure of the produced nanoparticles was confirmed by these two bands. The magnetic characteristics of the powder were examined using a Vibrating Sample Magnetometer (VSM). The presence of M-H hysteresis loops suggests that the produced nanoparticles have superparamagnetic properties, as evidenced by their low coercive force, remanent magnetization, and saturation magnetization values.
