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A Study of Structural and Magnetic Properties of Mg-Cu Mixed Spinel Ferrites

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This is to confirm that the thesis entitled "A Study of Structural and Magnetic Properties of Mg-Cu Mixed Spinel Ferrites" has been carried out in partial fulfillment of the requirement for the M.Sc. One of the magnetic signals is a sextet that is typical of those associated with a good ferromagnetic at room temperature.

Fig.4.9 The magnetization (MS) versus the applied magnetic field (H) curves of Mg1-xCuxFe2O4 ferrites sintered at 1100°C for 3 hours. Fig.4.11 The magnetization (MS) versus the applied magnetic field (H) curves of Mg1-xCuxFe2O4 ferrites sintered at 1200°C (quenched) for 3 hours.

Fig. 3.3  Ring and disk shapes.  55
Fig. 3.3 Ring and disk shapes. 55

List of Tables

INTRODUCTION

THEROETICAL BACKGROUND

RESULTS AND DISCUSSION

CONCLUSION

The Aims and Objectives of the Present Work

The porosity of the prepared sample has been calculated from the theoretical density and the bulk density of the samples sintered at different temperatures are 1100°C, 1200°C and 1200°C (quenched). we). The magnetization of the samples has been measured as a function of field and temperature using the Vibrating Sample Magnetometer (VSM). we you).

Reason for Choosing this Research Work

Application of Ferrites

Review of the Earlier Research Work

One of the key parameters for increasing permeability in spinel ferrite is lowering the magnetostrictive constant. Therefore, the optimization of the Cu content with respect to the densification and resistivity of the ferrite is very important.

Outline of the Thesis

Mössbauer spectra were observed and interpreted as originating from different temperature dependences of the magnetic hyperfine field at different iron sites. In this chapter, the experimental procedures are briefly explained together with a description of the sample preparation, raw materials.

Origin of Magnetism

  • Diamagnetism
  • Antiferromagnetism

In the absence of an applied magnetic field, the dipole moments are randomly oriented, as shown in Figure [2.2(a)]; therefore, the materials have no net macroscopic magnetization. Therefore, the magnetic field cancels out and the material appears to behave the same as a paramagnetic material.

Figure  2.3:  The  inverse  susceptibility  varies  with  temperature  T  for  (a)  Paramagnetic (b) Ferromagnetic (c) Ferrimagnetic (d) Anti ferromagnetic, T N
Figure 2.3: The inverse susceptibility varies with temperature T for (a) Paramagnetic (b) Ferromagnetic (c) Ferrimagnetic (d) Anti ferromagnetic, T N

Classification of Ferrites and its Relevance

  • Soft Ferrites
  • Hard Ferrites

These ferrites are used in the frequency range from 100 MHz to 500 GHz for waveguides for electromagnetic radiation and in microwave devices such as phase shifters. Hard ferrites such as Ba-ferrites, Sr-ferrites, Pb-ferrites are used in the operation of communication equipment with high frequency currents due to the eddy currents with negligible high resistance and lower power loss due to heating and hysteresis with Joule.

Types of Ferrites

  • Cubic Ferrites with Spinel Structure
    • Normal Spinel Ferrites
    • Intermediate or Mixed Spinel Ferrites
  • Hexagonal ferrites
  • Cubic Ferrites of Garnet

They are also called ferrites spinel is the most widespread family of ferrites and is sometimes called ferrospinels because their crystal structure is closely related to that of the natural mineral spinel. The cubic ferrite has the general formula MO.Fe2O3, where M is one of the divalent cations of the transition elements such as Mn, Ni, Mg, Zn, Cd, Co, etc. Variation of the cation distribution between the cationic sites leads to different electrical and magnetic properties, although the composition of the spine is the same.

In this structure, half of the trivalent (A) sites and half octahedral (B) sites, with the remaining cations randomly distributed among the octahedral (B) sites. A fourth way to vary the composition of barium ferrite is to mix two or more of the classic hexagonal ferrites in different proportions.

Figure  2.4:  Schematic  of  two  sub  cells  of  a  unit  cell  of  the  spinal  structure,  showing octahedral or tetrahedral sites
Figure 2.4: Schematic of two sub cells of a unit cell of the spinal structure, showing octahedral or tetrahedral sites

Magnetic Properties of Ferrites

  • Magnetic Dipole
  • Magnetic Moment
  • Magnetic Moment of Ferrites
  • Super exchange Interactions in Spinel Ferrites
  • Neel’s Collinear Model of Ferrites
  • Non-collinear Model of Ferrimagnetism

However, the N-pole and S-pole are labeled here geographically, which is the opposite of the convention for labeling the poles of a magnetic dipole moment. Electron spin of the two atoms Si and Sj, which is proportional to their products. The magnetic interaction in magnetic oxide cannot be explained on the basis of direct reaction due to the following facts: I).

The magnetic properties of spinel ferrites are determined by the type of magnetic ions located at A and B sites, and the relative strengths of inter-sublattice (JAB) and intra-sublattice (JAA, JBB) exchange are shown in Figure 2.6. In the presence of an applied magnetic field Ha, the total magnetic field on the subgrid can be written as

Table 2.1: Experiment and calculated saturation moments of spinals
Table 2.1: Experiment and calculated saturation moments of spinals

Magnetization Process

  • Magnetization Curve
  • Magnetization and Temperature

The combination of displacement walls with an initial permeability depends entirely on the absence of the studied material. In the second phase, the magnetization curve, the field increases, the intensity of magnetization increases more drastically, it is called the range of irreversible magnetization. If the field is increased further, the magnetization curve becomes less steep and its process becomes reversible once more.

An increase in the temperature of the solid causes an increase in the thermal vibrations of the atoms, allowing the atomic magnetic moments to rotate freely. At temperatures below the Curie point, the magnetic moments are partially aligned within the magnetic domains in ferromagnetic materials.

Figure 2.7: Domain dynamics during various parts of the magnetization curve.
Figure 2.7: Domain dynamics during various parts of the magnetization curve.

Mössbauer Spectroscopy

  • Mössbauer Effect
    • Isomer Shift
    • Electric Quadruple Splitting
    • Magnetic splitting
    • Magnetic Hyperfine Interaction

This would cause differential shifts in the energy of the y-rays from the source nuclei and the absorber nuclei. The line positions are related to the splitting of the energy levels, but the line intensities are related to the angle between the Mössbauer γ-ray and the nuclear spin moment. The internal magnetic field at the nucleus originates from the spin and radial and angular distribution of the electron density in the atom.

Where µB is the Bhor microwave, s and l are operators for the spin and orbital moment of the electron and  0 2 is the electron density in the nucleus. Where 0 is the lifetime of the nucleus in the excited state,  is the electron spin correlation time and L is the Larmour precession time of the nucleus.

Figure  2.10:  simple  spectrum  showing  the  velocities  scale  and  motion  of  source relative to the absorber
Figure 2.10: simple spectrum showing the velocities scale and motion of source relative to the absorber

Methodology of Ferrite Preparation

  • Composition of the Studied Ferrite System

Method of Sample preparation

  • Preparing the Mixture of Mg-Cu Ferrites
  • Pre-firing the Mixture to form ferrite
  • Converting Raw Ferrite into Powder and Pressing Powder
  • Sintering

The scope of work in this step varies greatly depending on the starting materials. When component oxides are used, the corresponding step simply involves mixing the oxides by wet milling for 6 hours. However, in this case, some of the particles can be reduced to a sub-micron level.

Printing a uniformly dense body by this method is difficult due to the frictional gradient of the powder at the wells of the die and between the particles themselves. In this process, atomic mobility of the compact is sufficient to enable the decrease in the free energy associated with the grain boundaries.

Figure 3.2 Hydraulic press used to make different shaped samples.
Figure 3.2 Hydraulic press used to make different shaped samples.

X-ray Diffraction

  • Different Parts of the PHILIPS X’ Pert PRO XRD System
  • Interpretation of the XRD data
  • X-ray Density and Bulk Density
  • Porosity

In equation (3.3), λ is the wavelength of the X-ray beam, θ is the scattering angle, and n is an integer representing the order of the diffraction peak. For the XRD experiment, each sample was mounted on a glass slide and the sample was fixed by applying adhesive to the two ends of the sample. Usually, the lattice parameter of the composition is determined by the Debye-Scherrer method after curve extrapolation.

Where λ is the wavelength of the X-ray, θ is the angle of diffraction, and n is an integer representing the order of diffraction. The bulk density (ρB) is measured by the formula ρB =. 3.8) Where m is the sample mass of the disk and v is its volume.

Figure 3.6 Bragg’s diffraction pattern
Figure 3.6 Bragg’s diffraction pattern

Magnetization Measurement

  • Vibration Sample Magnetometer

It is worth noting that the physical and electromagnetic properties strongly depend on the porosity of the studied samples. Therefore, the amplitude of the voltage produced by the rotating coil is proportional to the magnetic induction and therefore the amplitude can be used to measure the magnetic induction or magnetic field in free space. The output of the differential amplifier is then fed to a tuned amplifier and an internal lock-in amplifier that accepts the signal supplied by the oscillator.

The output of the lock-in amplifier, or the output of the magnetometer itself, is a DC signal proportional to the magnetic moment of the sample being studied. Calibration of the VSM is done by measuring the signal from a pure Ni standard with a known saturation magnetic moment, placed at the saddle point.

Experimental Procedure for Microstructure Study

The VSM detection module detects the in-phase and quadrature phase signals from the encoder and from the amplified voltage of the pickup coil. The sample is attached to the sample holder at the end of a sample rod mounted in an electromechanical transducer. The microstructure measurements of the samples were carried out using the Philips XL30 Scanning Tunneling Microscope at AECD, Dhaka, Bangladesh.

The SEM microstructures of samples sintered at 1200°C (furnace cooled) were studied using Philips XL30 Scanning Tunneling Microscope. To observe the microstructure, the ferrite samples were ground and then polished with fine Al2O3.

Experimental Procedure for Mössbauer Spectrometer

The absorption Mössbauer spectrum is obtained by counting transmitted γ-rays as a function of source to absorber velocity. In our experiment, an Fe-Co nucleus decays to an excited state of the 57Fe nucleus shown in Figure 3.12. If the relative velocity of the source toward the absorber increases, Doppler-shifted y-rays can be made to be highly resonant with the split levels in the absorber.

By varying the velocity of the source, resonance conditions can be achieved for each of. This increases the number of counts (and therefore gives better statistics) and flattens the background profile produced by the difference intensity of the source radiation as the source moves relative to the absorber and detector.

Figure 3.13 Scheme of Mössbauer Spectroscopy
Figure 3.13 Scheme of Mössbauer Spectroscopy

Structural and Physical Characterization of Mg-Cu Ferrites

  • Phase Analysis
  • Lattice Parameters
  • Density and Porosity
  • Microstructure Analysis of Mg-Cu Ferrites
  • Variation of Saturation Magnetization at Room Temperature at Different Sintering Temperature
  • Experimental Results and Analysis of Mössbauer for Mg-Cu Ferrites

The porosity of the sample Mg1-xCuxFe2O4 sintered at 1100°C decreases with the increase in Cu content. The migration of the pores to the grain boundary and thus contributed to the reduction of the sintered density. The porosity is the minimum of the sample Mg1-xCuxFe2O4 shown in table - 4.1 x = 0.4, which can be attributed to experimental error.

The saturation magnetizations (MS) of the Mg1-xCuxFe2O4 ferrites as a function of the Cu content at room temperature for different sintering temperatures are shown in Figure 4.12 and Table 4.2. The sextet pattern is created by the interaction of γ-rays with the magnetic field of the sample.

Figure  4.2(b):  Variation  of  the  lattice  parameter  ‘a’  Å  as  N-R function F(θ)  for x = 0.1 and T s  =1100°C
Figure 4.2(b): Variation of the lattice parameter ‘a’ Å as N-R function F(θ) for x = 0.1 and T s =1100°C

Velocity (mm/sec)

Scope for Future Work

And Nordblad P.; “Behavior of spin-reinforced glass and spin glass of diluted Mg-Zn ferrites”; Cp 1003, Magnetic Materials, International Conference on Magnetic Materials, AIP, 295, 2007. B.; "Magneto-Dielectric properties of ferrites Mg-Cu-Co Ceramics: II Electrical, dielectric and magnetic properties", J. Structural and magnetic properties of nanocrystalline Mg-Cd ferrites prepared by oxalate co-precipitation methods"; J.

Effect of hopping speed and hopping length of hopping electrons on the conductivity and dielectric properties of Co-Cd ferrites”; J. Improvement of magnetic properties of Mn-Ni-Zn ferrite by non-magnetic replacement of Al3+ ions”; J.

Gambar

Figure  2.3:  The  inverse  susceptibility  varies  with  temperature  T  for  (a)  Paramagnetic (b) Ferromagnetic (c) Ferrimagnetic (d) Anti ferromagnetic, T N
Figure  2.4:  Schematic  of  two  sub  cells  of  a  unit  cell  of  the  spinal  structure,  showing octahedral or tetrahedral sites
Figure 2.7: Domain dynamics during various parts of the magnetization curve.
Figure  2.10:  simple  spectrum  showing  the  velocities  scale  and  motion  of  source relative to the absorber
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