Ferrite (magnet)

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A ferrite is a type of ceramic compound composed of iron(III) oxide (Fe₂O₃) combined chemically with one or more additional metallic elements. They are both electrically nonconductive and ferrimagnetic, meaning they can be magnetized or attracted to a magnet. Ferrites can be divided into two families based on their magnetic coercivity, their resistance to being demagnetized. Hard ferrites have high coercivity, hence they are difficult to demagnetize. They are used to make magnets, for devices such as refrigerator magnets, loudspeakers and small electric motors. Soft ferrites have low coercivity. They are used in the electronics industry to make ferrite cores for inductors and transformers, and in various microwave components. Ferrite compounds have extremely low cost, being made of iron oxide (i.e. rusted iron), and also have excellent corrosion resistance. They are very stable and difficult to demagnetize, and can be made with both high and low coercive forces. Yogoro Kato and Takeshi Takei of the Tokyo Institute of Technology synthesized the first ferrite compounds in 1930.

Video Ferrite (magnet)

Composition, structure, and properties

Ferrites are usually ferrimagnetic ceramic compounds derived from iron oxides. Magnetite (Fe₃O₄) is a famous example. Like most of the other ceramics, ferrites are hard, brittle, and poor conductors of electricity.

Many ferrites adopt the spinel structure with the formula AB₂O₄, where A and B represent various metal cations, usually including iron (Fe). Spinel ferrites usually adopt a crystal motif consisting of cubic close-packed (fcc) oxides (O^2-) with A cations occupying one eighth of the tetrahedral holes and B cations occupying half of the octahedral holes, i.e., A²⁺
B³⁺
₂O^2-
₄. Ferrite adopts not the spinel structure, but the inverse spinel structure: one eighth of the tetrahedral holes are occupied by B cations, one fourth of the octahedral sites are occupied by A cations. and the other one fourth by B cation. It is also possible to have mixed structure spinel ferrites with formula [M²⁺_1-?Fe³⁺_?][M²⁺_?Fe³⁺_2-?]O₄ where ? is the degree of inversion.

The magnetic material known as "ZnFe" has the formula ZnFe₂O₄, with Fe³⁺ occupying the octahedral sites and Zn²⁺ occupy the tetrahedral sites, it is an example of normal structure spinel ferrite.

Some ferrites adopt hexagonal crystal structure, like barium and strontium ferrites BaFe₁₂O₁₉ (BaO:6Fe₂O₃) and SrFe₁₂O₁₉ (SrO:6Fe₂O₃).

In terms of their magnetic properties, the different ferrites are often classified as "soft", "semi-hard" or "hard", which refers to their low or high magnetic coercivity, as follows.

Soft ferrites

Ferrites that are used in transformer or electromagnetic cores contain nickel, zinc, and/or manganese compounds. They have a low coercivity and are called soft ferrites. The low coercivity means the material's magnetization can easily reverse direction without dissipating much energy (hysteresis losses), while the material's high resistivity prevents eddy currents in the core, another source of energy loss. Because of their comparatively low losses at high frequencies, they are extensively used in the cores of RF transformers and inductors in applications such as switched-mode power supplies and loopstick antennas used in AM radios.

The most common soft ferrites are:

• Manganese-zinc ferrite (MnZn, with the formula Mn_aZn_(1-a)Fe₂O₄). MnZn have higher permeability and saturation induction than NiZn.
• Nickel-zinc ferrite (NiZn, with the formula Ni_aZn_(1-a)Fe₂O₄). NiZn ferrites exhibit higher resistivity than MnZn, and are therefore more suitable for frequencies above 1 MHz.

For applications below 5 MHz, MnZn ferrites are used; above that, NiZn is the usual choice. The exception is with common mode inductors, where the threshold of choice is at 70 MHz.

Semi-hard ferrites

• Cobalt ferrite, CoFe₂O₄ (CoO·Fe₂O₃), is in between soft and hard magnetic material and is usually classified as a semi-hard material. It is mainly used for its magnetostrictive applications like sensors and actuators thanks to it high saturation magnetostriction (~200 ppm). CoFe₂O₄ has also the benefits to be rare-earth free, which makes it a good substitute for Terfenol-D. Moreover, its magnetostrictive properties can be tuned by inducing a magnetic uniaxial anisotropy. This can be done by magnetic annealing, magnetic field assisted compaction, or reaction under uniaxial pressure. This last solution has the advantage to be ultra fast (20 min) thanks to the use of spark plasma sintering. The induced magnetic anisotropy in cobalt ferrite is also beneficial to enhance the magnetoelectric effect in composite.

Hard ferrites

In contrast, permanent ferrite magnets are made of hard ferrites, which have a high coercivity and high remanence after magnetization. Iron oxide and barium or strontium carbonate are used in manufacturing of hard ferrite magnets. The high coercivity means the materials are very resistant to becoming demagnetized, an essential characteristic for a permanent magnet. They also have high magnetic permeability. These so-called ceramic magnets are cheap, and are widely used in household products such as refrigerator magnets. The maximum magnetic field B is about 0.35 tesla and the magnetic field strength H is about 30 to 160 kiloampere turns per meter (400 to 2000 oersteds). The density of ferrite magnets is about 5 g/cm³.

The most common hard ferrites are:

• Strontium ferrite, SrFe₁₂O₁₉ (SrO·6Fe₂O₃), used in small electric motors, micro-wave devices, recording media, magneto-optic media, telecommunication and electronic industry.
• Barium ferrite, BaFe₁₂O₁₉ (BaO·6Fe₂O₃), a common material for permanent magnet applications. Barium ferrites are robust ceramics that are generally stable to moisture and corrosion-resistant. They are used in e.g. loudspeaker magnets and as a medium for magnetic recording, e.g. on magnetic stripe cards.

Maps Ferrite (magnet)

Production

Ferrites are produced by heating a mixture of the oxides of the constituent metals at high temperatures, as shown in this idealized equation:

Fe₂O₃ + ZnO -> ZnFe₂O₄

In some cases, the mixture of finely-powdered precursors is pressed into a mold. For barium and strontium ferrites, these metals typically supplied as their carbonates, BaCO₃ or SrCO₃. During the heating process, these carbonates undergo calcination:

MCO₃ -> MO + CO₂

After this decarboxylation step, the two oxides combine to give the ferrite. The resulting mixture of oxides undergoes sintering.

Processing

Having obtained the ferrite, the cooled product is milled to particles smaller than 2 µm, sufficiently small that each particle consists of a single magnetic domain. Next the powder is pressed into a shape, dried, and re-sintered. The shaping may be performed in an external magnetic field, in order to achieve a preferred orientation of the particles (anisotropy).

Small and geometrically easy shapes may be produced with dry pressing. However, in such a process small particles may agglomerate and lead to poorer magnetic properties compared to the wet pressing process. Direct calcination and sintering without re-milling is possible as well but leads to poor magnetic properties.

Electromagnets are pre-sintered as well (pre-reaction), milled and pressed. However, the sintering takes place in a specific atmosphere, for instance one with an oxygen shortage. The chemical composition and especially the structure vary strongly between the precursor and the sintered product.

To allow efficient stacking of product in the furnace during sintering and prevent parts sticking together, many manufacturers separate ware using ceramic powder separator sheets. These sheets are available in various materials such as alumina, zirconia and magnesia. They are also available in fine, medium and coarse particle sizes. By matching the material and particle size to the ware being sintered, surface damage and contamination can be reduced while maximizing furnace loading.

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Uses

Ferrite cores are used in electronic inductors, transformers, and electromagnets where the high electrical resistance of the ferrite leads to very low eddy current losses. They are commonly seen as a lump in a computer cable, called a ferrite bead, which helps to prevent high frequency electrical noise (radio frequency interference) from exiting or entering the equipment.

Early computer memories stored data in the residual magnetic fields of hard ferrite cores, which were assembled into arrays of core memory. Ferrite powders are used in the coatings of magnetic recording tapes. One such type of material is iron (III) oxide.

Ferrite particles are also used as a component of radar-absorbing materials or coatings used in stealth aircraft and in the absorption tiles lining the rooms used for electromagnetic compatibility measurements.

Most common radio magnets, including those used in loudspeakers, are ferrite magnets. Ferrite magnets have largely displaced Alnico magnets in these applications.

It is a common magnetic material for electromagnetic instrument pickups.

Ferrite nanoparticles exhibit superparamagnetic properties.

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History

Yogoro Kato and Takeshi Takei of the Tokyo Institute of Technology synthesized the first ferrite compounds in 1930. This led to the founding of TDK Corporation in 1935, to manufacture the material.

Barium hexaferrite (BaFe₁₂O₁₉) was discovered in 1950 at the Philips Natuurkundig Laboratorium (Philips Physics Laboratory). The discovery was somewhat accidental--due to a mistake by an assistant who was supposed to be preparing a sample of hexagonal lanthanum ferrite for a team investigating its use as a semiconductor material. On discovering that it was actually a magnetic material, and confirming its structure by X-ray crystallography, they passed it on to the magnetic research group. Barium hexaferrite has both high coercivity (170 kA/m) and low raw material costs. It was developed as a product by Philips Industries (Netherlands) and from 1952 was marketed under the trade name Ferroxdure. The low price and good performance led to a rapid increase in the use permanent magnets.

In the 1960s Philips developed strontium hexaferrite (SrFe₁₂O₁₉), with better properties than barium hexaferrite. Barium and strontium hexaferrite dominate the market due to their low costs. However other materials have been found with improved properties. BaFe²⁺₂Fe³⁺₁₆O₂₇ came in 1980. and Ba₂ZnFe₁₈O₂₃ came in 1991.

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See also

• Ferromagnetic material properties
• Ferrite core

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References

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External links

• International Magnetics Association
• What are the bumps at the end of computer cables?

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Sources

• MMPA 0100-00, Standard Specifications for Permanent Magnet Materials
• Meeldijk, Victor Electronic Components: Selection and Application Guidelines, 1997 Wiley ISBN 0-471-18972-3
• Ott, Henry Noise Reduction Techniques in Electronic Systems 1988 Wiley ISBN 0-471-85068-3
• Luecke, Gerald and others General Radiotelephone Operator License Plus Radar Endorsement 2004, Master Pub. ISBN 0-945053-14-2
• Bartlett, Bruce and others Practical Recording Techniques 2005 Focal Press ISBN 0-240-80685-9
• Schaller, George E. Ferrite Processing & Effects on Material Performance

Source of the article : Wikipedia