Investigation of sintered cobalt-zinc ferrite synthesized by coprecipitation at different temperatures: a relation between microstructure and hysteresis curves

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Investigation of sintered cobalt-zinc ferrite synthesized by coprecipitation at different temperatures: a relation between microstructure and hysteresis curves

Ana Maria Rangel de Figueiredo TeixeiraI, ^*; Tsuneharu Ogasawara^II; Maria Cecília de Souza Nóbrega^II

^IDepartment of the Analytical Chemistry, Fluminense Federal University, Niteroi, RJ, Brazil

^IIDepartment of Metallurgical and Materials Engineering of COPPE, Federal University of Rio de Janeiro, RJ, Brazil

ABSTRACT

The magnetic properties of sintered samples of cobalt-zinc ferrites produced from the corresponding coprecipitate were calculated based on hysteresis curves (Hc). The Hc values confirmed that soft ferrites were obtained by the procedure. A possible relation between the magnetic hysteresis curves and the microstructure of the sintered samples was investigated. X ray diffraction, thermal analysis and scanning electron microscopy were used to characterize the microstructure and the phases present in the sintered ceramic pieces, as well as those of their coprecipitated tri-metallic hydroxide precursor powders. It was found that sintering of Co_0.5Zn_0.5Fe₂O₄ at 1400 °C led to "honeycombing" of the ferrite grains and that there was no single phase in the microstructure of a sample sintered at 1400 °C. Thus, a more complete study was made of the behavior of the microstructure at lower sintering temperatures, i.e., in the 1100-1350 °C range.

Keywords: cobalt-zinc ferrite, hysteresis curve, coprecipitation

1. Introduction

Studies of spinel ferrites are highly relevant to modern technologies, so the synthesis and sintering of ferrites have become an important part of modern ceramic research^1-3. Cobalt-zinc ferrite is one of the soft ferrites used in electronic devices such as transformer cores, electric motors and generators. In its applications, it is subjected to alternating magnetic fields, and should therefore present low energy losses. Co_(1-x)Zn_xFe₂O₄ ferrites with x ranging from 0.1 to 0.5 prepared by the coprecipitation method have not yet been as extensively studied as Mn-Zn and Ni-Zn substituted ferrites^2,4,5 have.

The distribution of the cations in cobalt-zinc ferrite can be represented by Zn²⁺_xFe³⁺_1-x [Co²⁺_1-xFe³⁺_1+x ]O₄^6-8. The substitution of Zn²⁺ for Fe³⁺ reduces the Curie temperature of the ferrite^6,7,9. On the other hand, increasing the zinc content of cobalt-zinc ferrites increases their lattice parameter^10-12 while decreasing the saturation magnetization due to augmented B-B interaction followed by reduced A-B interaction. Also, the presence of Co²⁺ ion in the cobalt-zinc ferrite hastens the Co²⁺ + Fe³⁺Û Co³⁺ + Fe²⁺ exchange reaction in octahedral sites, while tetrahedral sites are preferentially occupied by zinc cations. This exchange reaction supports the electronic conduction mechanism in cobalt-zinc ferrites^12,13; the octahedral sites become enlarged when they are occupied by Fe²⁺ ions instead of Co²⁺ ions^6,8,14.

In this study, the cobalt-zinc ferrite precursor was prepared by coprecipitation from an aqueous solution of the pure salts of the cations, a method that offers the advantage of easy and homogeneous mixing of the main components. The purpose of this study was to investigate the possible relation between the magnetic hysteresis curves and the microstructure of sintered Co_0.5Zn_0.5Fe₂O₄.

2. Experimental Procedure

The starting material was an aqueous solution of pure cobalt, zinc and ferric nitrates in a molar ratio of 1: 1: 4. Titration by NH₄OH or NaOH yielded a triple hydroxide precipitate at pH 10. Filtration, careful drying in a furnace and calcination at 400 °C for 5 hours resulted in anhydrous triple-oxide with minimum particle aggregation.

The heat-treated samples were characterized by X ray diffraction to ascertain the effective formation of the desired cobalt-zinc ferrite. All the samples were analyzed with a Phillips X ray diffractometer using CoKa (l = 1.79 A°) radiation.

The thermal behavior of the ferrite powder was monitored by TG and DTA, with the sample heated to a maximum of 1400 °C under synthetic air (Neztsch, Luxx 409 STA). The Co_0.5Zn_0.5Fe₂O₄ powder containing 2 wt. (%) of polyvynil alcohol (PVA) was pressed into ring-shaped compacts (rectangular cross section, 1.7 cm outer diameter and 0.6 cm inner diameter) under 1.5 ton/cm² for 1 minute in a steel die. The compacts weighed about 2.50 g before sintering and were sintered at preset temperatures (950, 1100, 1200, 1300, 1350 and 1400 °C) for 5 hours. The heating rate applied was 4 °C/min up to 600 °C, where the compacts were held for 1 hour to eliminate PVA, after which this rate was increased to 8 °C/min up to the sintering temperature. The sintered compacts were analyzed by atomic absorption spectrometry, X ray diffraction (XRD), and scanning electron microscopy (SEM). One sintered compact from each sintering temperature was equipped with varnished copper wire winding for use as a solenoid, which was then subjected to magnetic hysteresisgraphy using a Walker Scientific model AMH-20 hysteresisgraph at a frequency of 60 Hz.

3. Results and Discussion

3.1. Characterization of the powder

Figure 1 presents a TGA-DTA graph in the range of 25 to 1000 °C for a Co_0.5Zn_0.5Fe₂O₄ powder coprecipitate. The DTA graph shows an endothermic reaction at about 260 °C, which corresponds, on the TGA graph, to a 35.85% weight loss (elimination of ammonium hydroxide used as precipitant; dehydration of hydroxides).

An exothermic reaction between 575 and 925 °C, corresponding on the TGA graph to a 16.75% weight loss, suggests that the ferrite still contains hydroxyl groups, which is congruent with the exothermic band depicted in the DTA graph. According to the literature⁵, hydroxyl groups are retained in Co_0.5Zn_0.5Fe₂O₄ even after sintering at 700 °C and are completely removed after sintering at 925 °C. A similar behavior was observed⁵ for Co_0.2Zn_0.8Fe₂O₄ prepared by coprecipitation, but the exothermic band ended at 550 °C. The presence of hydroxyl groups has also been reported³ in nanocrystalline ferrite powders prepared by hydrothermal synthesis. The weight loss occurring between 300 and 600 °C is not significant but, in this range, the DTA graph shows an exothermic band, which may be due to the formation of spinel ferrite.

Figure 2 shows the X ray diffraction patterns of the powder samples precipitated by NaOH and NH₄OH in the same time period but at different temperatures. The peaks observed here were found to correspond to those of standard diffraction patterns of a spinel ferrite¹⁵ with no extra peaks, confirming that the cubic ferrite phase was formed in all the samples.

An X ray diffraction pattern similar to that shown in Figures 2a and 2b indicated that both precipitants can be used. However, when ammonium hydroxide is used as the precipitating agent, the pH must be strictly controlled because complexes with zinc¹⁷ can be formed and zinc ions may remain in the solution, influencing the ferrite's molar ratio. Therefore, sodium hydroxide was chosen as the precipitant in this study. The XRD pattern also showed that the ferrite phase was dependent on the reaction temperature. The sample heated to 200 °C presented mostly an amorphous phase (Figure 2c), but peaks (311) and (440) attributed to the spinel phase began to appear. The powders treated at 400 °C presented a high level of crystallization. The literature^1,5,17 cites similar results for several spinel ferrites with high levels of crystallization.

The lattice parameter for the ferrite powder prepared at 400 °C was calculated as 8.38 Å based on the XRD pattern. This result was confirmed by the literature^1,6 (which cites values of 8.37 and 8.36 Å).

3.2. Characterization of the sintered material

The sintered compacts were characterized by XRD to confirm the phase purity and crystallinity. The diffraction angles (2q) of the cobalt-zinc ferrite were calculated at different sintering temperatures (Table 1), based on the X ray diffraction pattern. The values remained essentially constant in the range of 950-1350 °C, but clearly differed at 1400 °C, indicating the onset of a phase transformation just above 1350 °C, which means that Co_0.5Zn_0.5Fe₂O₄ cannot be produced above that temperature. The strongest reflection came from the (3,1,1) plane for all ferrites sintered from 950 to 1350 °C, while the strongest reflection for the ferrite sintered at 1400 °C came from the (4,4,4) plane.

Table 2 presents the true density (Dx) of sintered Co_0.5Zn_0.5Fe₂O₄ obtained in this work, which was calculated based on the XRD as a function of the sintering temperature. These values range from 5.29 to 5.35 g/cm³ and are congruent with the reported⁹ value of 5.30 g/cm³ for Co-Zn ferrite also prepared by coprecipitation. The true density of the material sintered at 1400 °C was not calculated because the diffraction peaks could not be assigned to the Co_0.5Zn_0.5Fe₂O₄. This is evidence of the presence of extra phases.

The morphologies of the coprecipitated Co_0.5Zn_0.5Fe₂O₄ compacts sintered at different temperatures (950 °C to 1400 °C) were examined. The compact sintered at 950 °C was characterized by the presence of different grain sizes (ranging from 1 µm to 10 µm), as depicted in Figure 3a. Sintering at 1100 and 1200 °C (Figures 3b, 3c) produced the familiar spinel crystals (15 µm and 20 µm, respectively). The cobalt-zinc ferrite compact sintered at 1300 °C (Figure 3d) showed rounder grains larger than 30 µm, indicating signs of the onset of intragranular "honeycombing". This honeycombing phenomenon intensified in the ferrite compact sintered at 1350 °C (Figure 3e), whose grains welded into a continuous mass dispersed in the honeycomb holes. Honeycombing in the material sintered at 1400 °C (Figure 3f) was so intense that numerous large channels emerged to the sample's surface. This phenomenon is likely related with the decomposition of cobalt-zinc ferrite and loss of zinc by evaporation^18-20.

 

The magnetic behavior of Co_0.5Zn_0.5Fe₂O₄ was examined. Figure 4 presents the hysteresis curves of the sintered Co_0.5Zn_0.5Fe₂O₄ compacts.

Table 2 summarizes the main findings of the material's magnetic behavior.

It can be considered that B_r (remanescent magnetic induction), B_max (maximum magnetic induction), HL (magnetic hysteresis loss) and µ_max (maximum magnetic permeability) increase as the temperature rises from 950 °C to 1400 °C, while the H_c (magnetic coercive force) shows the opposite trend, decreasing as the temperature increases in the same range.

The difference in the Hc values is understandable because of the substantial increase in grain size in response to the increase in sintering temperature from 950 to 1350 °C. In other words, above 1100 °C the mean grain size far exceeded 5 µm, facilitating the movement of the magnetic domain. However, a comparison of Figures 3a and 3d leaves room for doubt concerning this substantial grain growth. The low coercive force, which confirms that the cobalt-zinc ferrite produced here is a soft ferrite, is congruent with the values reported in the literature^1,21 for some substituted cobalt-zinc-ferrite powders prepared by coprecipitation.

On the other hand, the values of the other magnetic properties were more difficult to interpret because of the influence of many variables, including the zinc substitution. Tetrahedral sites in the spinel structure are suitable for cationic radii in the range of 0.58 Å to 0.67 Å, while octahedral sites can accept cations with radii in the range of 0.70 Å to 0.75 Ų². Therefore, in the unit cell structure, Co²⁺ (0.72 Å) and Fe²⁺(0.75 Å) may replace Zn²⁺(0.74 Å), while Co³⁺(0.63 Å) can exchange sites with Fe³⁺(0.64 Å)^12,13. This cation exchange depends on the sintering conditions, since the oxygen partial pressure affects cobalt and iron oxidation states and, hence, influences the magnetic properties of ferrite.

4. Conclusions

a)

The powder coprecipitation method produced well crystallized cobalt-zinc ferrite powder upon heating the coprecipitated triple hydroxide to 400 °C for 5 hours, as confirmed by X ray diffraction;

b)

The coprecipitation method provided the densest compact when the green compact was sintered for 5 hours at 1350 °C. Furthermore, the method required relatively low temperatures and short calcination times to produce well crystallized cobalt-zinc ferrite powders;

c)

Coprecipitated Co_0.5Zn_0.5Fe₂O₄ ceramics should be sintered at temperatures up to 1350 °C, as indicated by "honeycombing" degradation of the ceramic sample above this temperature, and by the sharp change in the X ray diffraction pattern in response to the increase in the sintering temperature from 1350 °C to 1400 °C; and

d)

In spite of the change in the microstructure caused by the sintering process, all the Hc values were sufficiently low to confirm that the ferrite was a soft ferrite.

Acknowledgments

The authors thank the Brazilian institutions CAPES, CNPq, FINEP, PADCT, FAPERJ, UFRJ and UFF for their support of this work.

Received: August 1, 2005; Revised: August 16, 2006

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Publication Dates

• Publication in this collection
  19 Oct 2006
• Date of issue
  Sept 2006

History

• Received
  01 Aug 2005
• Reviewed
  16 Aug 2006