Magnetic Properties of Ni-Zn Ferrites by Citrate Gel Method


Ni-Zn ferrite with a nominal composition of Ni1-xZnxFe2O4 (x = 0, 0.2, 0.6, 0.8, 0.9) are prepared by citrate gel method and characterized by X-ray diffraction. Magnetic properties of all samples are obtained by using VSM (Vibrating Sample Magnetometer) in the range of 10 Koe. The saturation magnetization values of the samples are carried out from the B-H loop. The effect of composition on saturation magnetization and magnetic moment are studied in this paper. The results showed that Saturation magnetization and magnetic moment values increases gradually as Zn2+ composition increases, it reaches maximum value 70.28 emu/gm for (x = 0.6) and decreases further with increasing Zn2+ composition.

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Krishna, K. , Kumar, K. , Ravindernathgupta, C. and Ravinder, D. (2012) Magnetic Properties of Ni-Zn Ferrites by Citrate Gel Method. Advances in Materials Physics and Chemistry, 2, 149-154. doi: 10.4236/ampc.2012.23022.

1. Introduction

Nickel-Zinc ferrites are considered as one of the most versatile soft ferrites because of its high resistance and low eddy current losses [1]. Mixed Ni-Zn ferrite has been commercially used in radio frequency circuits, high quality filters, rod antennas and transformer cores [2,3]. NiZn ferrite is mixed spinel in which the tetrahedral (A) sites are occupied by Zn2+ and Fe3+ ions, and the octahedral sites (B) are occupied by Ni2+ and Fe3+ ions in the spinel formula AB2o4. The magnetic & dielectric properties depend on this distribution of these ions on tetrahedral and octahedral sites. This distribution is different when the ferrite is synthesized at low temperature [4]. It is also believed that addition of zn2+ ions alter the saturation magnetization, lattice parameter and Curie temperature. Several researchers synthesized Ni-Zn ferrite by conventional methods like double sintering method, solid state reaction method, and chemical co precipitation method, hydro thermal process etc. In this context, the objective of this work is to synthesize zinc doped nickel ferrite produced by Citrate gel method and to study their magnetic properties.

2. Experimental

Five different compositions of Ni1−xZnxFe2O4 with x = 0.0, 0.2, 0.6, 0.8, and 0.9 are prepared by citrate gel method. The citrate process [5,6] is simple, easy and doesn’t require any elaborate and expensive experimental setup. The main advantages of this method is

1) Capacity to yield a homogenous mixture of the constituent ions.

2) As no ball milling is required in this process, there is a little scope of contamination of materials.

3) In case of conventional methods, there is a possibility of introducing iron impurities during milling this leads inhomogenity in sample, which affects the magnetic property.

4) This is a simple method which offers a significant saving in time and energy consumption.

The starting materials used in this preparation are nickel nitrate (Merc, India), zinc nitrate (Merc, India), iron (III) citrate (Merc, India) and citric acid (Merc India) having molar ratio of 1:3 were dissolved in deionized water. Citric acid acts as chelating agent and helps in the homogenous distribution of metal ions. The pH of the solution is adjusted to 7 by using ammonia solution. The solution was uniformly heated at 373 K with constant stirring to transform it into a gel and the dried gel was obtained by de hydration process. The dried gel was combusted with evolution of gases and resulted in formation loose powder. This powder is subjected to micro wave sintering at 1000˚C for 30 minutes to get the final product. The X-ray diffraction patterns of the ferrite powder was taken on powder X-ray diffractometer (X-rd) using Cu-Kα radiation. The Magnetic measurements was carried out by using Vibrating Sample Magneto meter (VSM) in the range of 10 Koe.

3. Results & Discussions

The X-ray diffractogram of Ni-Zn ferrite is shown in figure 1, which reveals a single phase cubic spinel structure. The lattice parameter of


where, a = lattice constantd = inter planar distance and(h, k, l) are the Miller indices.

The variation of lattice parameter with Zn2+ composition is shown in the figure 2. From the figure it can be

Figure 1. X-ray diffraction studies of mixed Ni-Zn ferrites.

Figure 2. Variation of lattice parameter with composition.

seen that lattice parameter increases with Zn2+ composition. There by it indicating that the Ni-Zn ferrite system obeys Vegard’s law [7]. A similar variation also observed by Ravinder in case of Cu-Zn ferrites [8]. This variation can be explained on the basis of ionic radius of Zn2+ (0.82 Å) is greater than Ni2+ (0.78 Å).

3.1. Magnetic Properties

From the VSM data, hystersis loops are plotted as shown in the figure 3. The variation of saturation magnetization with composition is discussed. It can be seen from the table, that the value of saturation magnetization increases gradually from X = 0.0 to 0.6 and reaches to the maximum value of 70.28 emu/gm for X = 0.6 composition and then decreases gradually while Zn2+ composition increases. The behavior of this plot is similar to the [9]. The dependence of saturation magnetization is explained in terms of spin-disorder and spin-canting. In mixed Ni-Zn ferrite, the Zn2+ ions concentrate preferentially in the A site and the Ni2+ ions in B site in cubic spinel lattice. When the concentration of Fe3+ ions in the A site is diluted by low concentration of diamagnetic substances such as Zn2+, the net magnetization increases. However magnetization decreases at higher level doping. The reason for this nature is that low Zn2+ concentration reduce the no of spins occupying the A sub lattice, causing the net magnetization increases. As the Zn2+ content increases the exchange interactions are weakened and the B spins are no longer held rigidly parallel to the few remaining A spins. The decrease in B sub lattice moment, interpreted as spin departure from co linearity causes the effect known as canting. Sattar [10] also described this effect in samples of Cu-Zn ferrite.

3.2. Magnetic Moment

Magnetic Moment is calculated in Bhor Magnetron using the following relation [11] and tabulated in the table 1.

M = Molecular weight of particular compositionMs = Saturation Magnetization.

It can be seen from the table that the ferrite with composition Ni0.4Zn0.6Fe2O4 shows highest value of magnetic moment. It is evident from the table 1, that the magnetic moment increases with Zn2+ composition from X = 0.0 to X = 0.6 reaches to maximum value 70.28 at X = 0.6 and then decreases. It can be concluded that as Zn2+ replaces magnetic ions from “A” sites. The magnitude of A site moment decreases but the difference between the A site and B site moment increases, as a result magnetic moment increases but the decrease in magnetic moment  after X = 0.8 indicates the possibility of canted spin (noncollinear) structure in the present system. The decrease in magnetic moment with increase Zn2+ concentration indicating ferromagnetic behavior which decrease with increasing Zn2+ composition [12].

4. Conclusion

A series of Ni-Zn ferrite with the composition X = 0.0, 0.2, 0.6, 0.8, and 0.9 are prepared by using citrate precursor method. The lattice parameter increases as Zn2+ compositions is increases, the ferrite with X = 0.9 shows highest value of lattice parameter. The values of saturation magnetization, magnetic moment increases gradually from X = 0.0 to X = 0.6 reaches the maximum value at X = 0.6 and then decreases as Zn2+ composition is increases.

Table 1. Values of the Saturation magnetization and Bhor magnetron (mB) as a function of composition.

   X = 0.0              X = 0.2             X = 0.6           X = 0.8           X = 0.9

Figure 3. Magnetic hysteresis loops drawn between magnetic field and magnetic moment.

5. Acknowledgements

The authors are grateful Prof. P. Kistaiah, Head, Department of Physics, Osmania University, Hyderabad for his encouragement in research work. One of the authors K. Rama Krishna is grateful to V. S. K. Reddy, Principal, Malla Reddy College of Engineering & Technology, Hyderabad. And the author K. Vijaya Kumar is great ful to Dr. Koorapati Eshwara Prasad, Principal JNTUH College of Engineering, Nachupally, Karim Nagar (Dist).

Conflicts of Interest

The authors declare no conflicts of interest.


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