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Article

Microstructure and Magnetic Properties of M-Type Sr0.1Ca0.4La0.5Fe12O19 Ferrites: The Impact of Different Precursors

1
School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002, China
2
School of Materials Science and Engineering, Anhui University, Hefei 230601, China
*
Author to whom correspondence should be addressed.
Magnetochemistry 2022, 8(7), 68; https://doi.org/10.3390/magnetochemistry8070068
Submission received: 14 May 2022 / Revised: 21 June 2022 / Accepted: 24 June 2022 / Published: 25 June 2022
(This article belongs to the Special Issue Hexagonal Ferrites: Synthesis, Structure and Properties)

Abstract

:
M-type Sr0.1Ca0.4La0.5Fe12O19 powder specimens doped with different precursors RFe2O4(R = Co, Ni, Cu, Zn, and Mg) were prepared via a traditional solid-state reaction method. The structural and magnetic properties of the specimens were studied. Only nthe single magnetoplumbite phase was found in all the specimens with uniformly distributed particles. The specimen with Zn-type precursor has the highest saturation (Ms), while the specimen with Co-type precursor has the highest remanent magnetism (Mr), coercivity (Hc), and the best comprehensive magnetic properties.

1. Introduction

M-type permanent magnetic ferrite is made from SrCO3, BaCO3 or CaCO3 and Fe2O3 as raw materials via a traditional ceramic process. It is a magnetic material of hexagonal magnetoplumbite structure, with high saturation magnetization (Ms), coercivity (Hc), and magnetic crystal anisotropy constant. It is mainly used in computer, office equipment, automotive, consumer electronics, aerospace, inductor, and electrical equipment industries [1,2]. In order to meet the various applications, many attempts have been made to improve the magnetic properties of M-type strontium ferrites by adding or doping some elements, such as La-Co, La-Ni, La-Zn, La-Cu, La-Mg, and other co-substitution of M-type ferrites [3,4,5,6,7,8]. L. Peng et al. [3] prepared La-Ni substituted M-type strontium ferrite by a microwave sintering method combined with a low-temperature sintering technology and studied the effect of La-Ni substitution amount on the magnetic properties of M-type strontium ferrite. When the La–Ni substitution amount was x = 0.2 (Sr1-xLaxFe12-xNixO19), the material shows high anisotropic field Ha and coercivity Hc. Y. Ogata et al. [4] conducted a comparative study on the magnetic properties of M-type barium ferrite replaced by Cr3+ and La-Co, and the results showed that La–Co substitution could significantly improve the remanent magnetism (Mr) and the coercivity (Hc) at the same time. Y. J. Yang et al. [5] studied the influence of La-Cu substitution on the magnetic properties of M-type Barium/strontium ferrite, and the results showed that the Mr of specimens would increase first and then decrease with the increase in La-Cu substitution. L.S. You et al. [6] prepared M-type strontium ferrite substituted by La-Zn via a self-propagating high-temperature synthesis method, and it was found that La-Zn substitution significantly improved the magnetic properties of M-type strontium ferrite. In our previous study, the performance of ferrite could be significantly improved by the exchange coupling between the soft and hard magnetic phases. However, the influence of precursor addition on the structure and magnetic properties of M-type strontium calcium ferrites is still not reported. This research may help to replace rare earth elements with non-rare earth elements and thus reduce production costs.
In this study, the M-type Sr0.1Ca0.4La0.5Fe12O19 magnetic powders with different precursors RFe2O4 (Co-, Ni-, Cu-, Zn-, and Mg-type) were prepared via a solid-state reaction method. The impact of different precursors on the structure and the magnetic properties of M-type strontium calcium ferrites Sr0.1Ca0.4La0.5Fe12O19 are studied.

2. Experimental Procedure

2.1. RFe2O4 (R = Co, Ni, Cu, Zn and Mg) Precursors Preparation

The raw materials used in this study were analytically pure grade CuO, MgO, ZnO, Ni2O3, Fe2O3, and Co2O3. Here, the preparation of the CoFe2O4 precursor is taken as the typical example. The mixed powders (Fe2O3 and Co2O3) were ball-milled in water for 2 h, and then the as-milled powders were dried at 850 °C in a muffle for 3 h in air. Finally, the calcined samples were pulverized to powders with a size smaller than 100 μm using a vibration mill for use as the Co-type precursor. Similarly, Ni-, Cu-, Zn-, and Mg-type precursors were also obtained according to the above steps, respectively.

2.2. Preparation of M-type Strontium Calcium Ferrite Sr0.1Ca0.4La0.5Fe12O19 Powders with Different Precursors

All samples of M-type s Sr0.1Ca0.4La0.5Fe12O19 powders with different precursors (Co-, Ni-, Cu-, Zn-, and Mg-type) were prepared via a solid-state reaction method. The starting materials were SrCO3 (98% purity), CaCO3 (99% purity), La2O3 (99% purity), and Fe2O3 (98% purity). The mixed powders were placed in a sander containing hard alloy steel balls with a diameter of 6mm. The powders were milled in water for 2 h with an angular velocity of 400 rpm and a ball-to-powder weight ratio of 15:1, together with different RFe2O4 precursors of 3 wt%. Then, the as-milled powders were dried, pressed into pellets and calcined at a temperature of 1300 °C in a muffle for 2 h in air. Finally, the calcined samples were pulverized into powders to a size smaller than 100 μm using a vibration mill.

2.3. Characterization

The phase composition of the samples was identified by an X-ray diffractometer (XRD, PANalytical X’Pert Pro, Almelo, Netherlands) using Cu Kα(λ = 1.5406 Ǻ) radiation. The morphologies of specimens were investigated using a field emission scanning electron microscope (FESEM, HITACHI S-4800, Tokyo, Japan). The room temperature (RT) magnetic hysteresis loops were measured on a vibrating sample magnetometer (VSM, MicroSense EZ7, Lowell, MA, USA) with a maximum external field of 20,000 Oe.

3. Results and Discussion

3.1. Structural Properties

Figure 1 displays the XRD patterns for Sr0.1Ca0.4La0.5Fe12O19 powders with different precursors (Co-, Ni-, Cu-, Zn-, and Mg-type). As is shown, there is only the typical peak information from the magnetoplumbite phase found in this figure, which means that different precursor ions can enter the magnetoplumbite ferrite lattices without forming the second phases. However, the relative intensity of the diffraction peaks varies with the type of precursors. The strongest (008) peak was from the specimen with a Zn-type precursor, and the strongest peaks for the specimen with a Cu-type precursor were the (107) and (114) peaks. This indicates that they have different effects on the growth of each crystal plane with different precursors.
The lattice constants a and c were calculated using Miller indices (h, k, and l) and the inter-planer spacing dhkl of (107) and (114) crystal planes according to the following Formula (1):
d h k l = ( 4 3 h 2 + h k + k 2 a 2 + l 2 c 2 ) 1 / 2
The change of lattice constants (a and c) and the crystal axis ratio of c/a of specimens with different precursors are shown in Figure 2. It can be seen that the lattice constant c of the specimens with Cu-type precursors had a maximum value of 22.9878 Å. However, for the specimen with Co-type precursors, the lattice constant (c) had a minimum value of 22.9624 Å.
From the inset of Figure 2, it can be observed that the crystal axis ratio of c/a is almost the same. According to the opinion of Verstegen and Stevels, the value of the c/a ratio presents the structure type [9]. The c/a is considered to be smaller than 3.98 for the SrM ferrites. The c/a ratios for the specimens with different precursors in this study ranged from 3.8952 to 3.9009, which are in good accord with the expected value of the M-type structure.
Figure 3 displays the density (ρ) of the specimens with different precursors. It can be seen from Figure 3 that the specimen with a Zn-type precursor has a maximum value of ρ (4.8570 g/cm3), while the specimen with an Mg-type precursor has a minimum value of ρ (4.1672 g/cm3).
Figure 4 shows the typical FESEM images of the specimens. The grain size distribution of the specimens is shown in the upper right corner of the micrographs. As is shown in this figure, all the specimens with different precursors have formed the hexagonal structure, and the particles are distributed uniformly in size. In addition, the average particle size of specimens nearly remains unchanged for different precursors.

3.2. Magnetic Properties

Figure 5 shows the RT magnetic hysteresis loops of the specimens with different precursors. The Ms, Hc, and remanent magnetization (Mr) of specimens with different precursors were obtained from Figure 5 and are listed in Table 1. As can be seen, the specimen with Zn-type precursor has the largest Ms (67.18 emu/g) but the smallest Mr (12.52 emu/g) and Hc (267 Oe). The specimens with Co-type precursors have the highest Mr and Hc together with the best comprehensive magnetic properties. However, the Ms, the Mr and the Hc of specimens are lower than those reported by Hessien et al. [10] and Rashad et al. [11].
Within the basic M-type hexaferrite crystal structure, Fe3+ ions occupy five different sites, including spin-up sites (2a, octahedral sites; 2b, trigonal bipyramid site; 12k, octahedral sites) and spin-down sites (4f1, tetrahedral site; 4f2, octahedral sites). The magnetic moment of the Fe3+ ion is 5 μB, and the molar ratio of Fe3+ ion at different lattice positions is Fe(12k):Fe(2a):Fe(2b):Fe(4f1):Fe(4f2) = 6:1:1:2:2. The total magnetic moment according to the molar ratio calculated is 20 μB, which determines the main factor of high saturation magnetization of the materials. At the same time, for different precursors, the difference of Ms mainly resulted from the influence of precursors on grain size, uniformity, and density of materials. It can be seen from Figure 4 that the particle distribution of specimens is uniform, and the average particle size of specimens remains unchanged for different precursors. Therefore, the Ms is mainly affected by density, which results in the same variation tendency as density, shown in Figure 3. Due to the hexagonal structure and the lattice point occupied by Fe3+ ions, the SrM ferrite has high magnetocrystalline anisotropy. For ion substitutions, replacing Fe3+ ions will affect the magnetocrystalline anisotropy field for SrM ferrites and then leads to the change of Hc. The study of Mössbauer spectra of La–Co-substituted SrM ferrites revealed that most of the Co2+ ions were substituted for Fe3+ ions in 4f2 (mainly) and 2a octahedral sites [12,13,14]. The La3+ ions replaced most of the Sr2+ ions. Lechevallier et al. [15] reported that in the M-type ferrite phase, the presence of Co2+ ions could improve the solid solubility of rare-earth ions. E. Roohani et al. [16] reported that Ni2+ replaced the Fe3+in 4f2 and 2b sites, resulting in the changes in the magnetocrystalline anisotropy constant. J.M. Bai et al. [17] reported that for the large substitution amount of La-Zn, the substitution of Fe3+ ions by Zn2+ ions could lead to the weakening of the strength of superexchange, which will lead to the transformation of the colinear arrangement of Fe3+ ions to the non-colinear arrangement, accompanied by the spin-inclined structure. L. Qiao et al. [18] reported that Cu2+ ions might preferentially replace Fe3+ ions at the spin-down 4f2 position. This occupation will increase the number of Fe3+ ions compared to the spin-down position, resulting in an enhanced Fe3+-O-Fe3+ super exchange at 12k and 2b positions. Y.J. Yang et al. [19] reported that Mg2+ have a preference replaced the Fe3+ in 4f1 and 2a sites, which is ineffective in the reduction in the magnetocrystalline anisotropy. Therefore, the different Hc of specimens with different precursors in this study could be ascribed to the different degrees of influence on the magneto-crystalline anisotropic field.

4. Conclusions

The M-type strontium calcium ferrite Sr0.1Ca0.4La0.5Fe12O19 specimens with different precursors were prepared via a solid-state reaction method. The effects of different precursors (Co-, Ni-, Cu-, Zn-, and Mg-type) on the structural and magnetic properties have been studied. The single magnetoplumbite phase was obtained in all the specimens. The SEM study showed that the particles were distributed uniformly in size. For the Zn-type precursor, the specimen has the highest saturation magnetization (Ms) but the lowest remanent magnetization (Mr) and coercivity (Hc). On the whole, the specimen with a Co-type precursor has the best comprehensive magnetic properties.

Author Contributions

Conceptualization, X.Z.; Resources, S.Z., J.L. and Y.Y.; Supervision, A.X.; Writing—original draft, X.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. XRD patterns for Sr0.1Ca0.4La0.5Fe12O19 powders with different precursors.
Figure 1. XRD patterns for Sr0.1Ca0.4La0.5Fe12O19 powders with different precursors.
Magnetochemistry 08 00068 g001
Figure 2. Lattice constants (a) and (c) of the specimens with different precursors; inset shows the crystal axis ratio of c/a of the specimen with different precursors.
Figure 2. Lattice constants (a) and (c) of the specimens with different precursors; inset shows the crystal axis ratio of c/a of the specimen with different precursors.
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Figure 3. Density (ρ) of Sr0.1Ca0.4La0.5Fe12O19 specimens with different precursors.
Figure 3. Density (ρ) of Sr0.1Ca0.4La0.5Fe12O19 specimens with different precursors.
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Figure 4. Typical SEM images of Sr0.1Ca0.4La0.5Fe12O19 specimens with different precursors: (a) Co-, (b) Ni-, (c) Cu-, (d) Zn-, and (e) Mg-type.
Figure 4. Typical SEM images of Sr0.1Ca0.4La0.5Fe12O19 specimens with different precursors: (a) Co-, (b) Ni-, (c) Cu-, (d) Zn-, and (e) Mg-type.
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Figure 5. RT magnetic hysteresis loops of specimens with different precursors: (a) Co-, (b) Ni-, (c) Cu-, (d) Zn- and (e) Mg-type.
Figure 5. RT magnetic hysteresis loops of specimens with different precursors: (a) Co-, (b) Ni-, (c) Cu-, (d) Zn- and (e) Mg-type.
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Table 1. Magnetic properties of specimens with different precursors.
Table 1. Magnetic properties of specimens with different precursors.
Precursors TypeMs (emu/g)Mr (emu/g)Hc (Oe)
Co-type66.2031.831270
Ni-type58.0423.05806
Cu-type65.1923.00503
Zn-type67.1812.52267
Mg-type55.6313.76488
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MDPI and ACS Style

Zhao, X.; Zhang, S.; Li, J.; Xia, A.; Yang, Y. Microstructure and Magnetic Properties of M-Type Sr0.1Ca0.4La0.5Fe12O19 Ferrites: The Impact of Different Precursors. Magnetochemistry 2022, 8, 68. https://doi.org/10.3390/magnetochemistry8070068

AMA Style

Zhao X, Zhang S, Li J, Xia A, Yang Y. Microstructure and Magnetic Properties of M-Type Sr0.1Ca0.4La0.5Fe12O19 Ferrites: The Impact of Different Precursors. Magnetochemistry. 2022; 8(7):68. https://doi.org/10.3390/magnetochemistry8070068

Chicago/Turabian Style

Zhao, Xiubin, Shuang Zhang, Jinsong Li, Ailin Xia, and Yujie Yang. 2022. "Microstructure and Magnetic Properties of M-Type Sr0.1Ca0.4La0.5Fe12O19 Ferrites: The Impact of Different Precursors" Magnetochemistry 8, no. 7: 68. https://doi.org/10.3390/magnetochemistry8070068

APA Style

Zhao, X., Zhang, S., Li, J., Xia, A., & Yang, Y. (2022). Microstructure and Magnetic Properties of M-Type Sr0.1Ca0.4La0.5Fe12O19 Ferrites: The Impact of Different Precursors. Magnetochemistry, 8(7), 68. https://doi.org/10.3390/magnetochemistry8070068

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