Ferrite compounds are extremely low cost, being made of mostly iron oxide, and have excellent corrosion resistance. Yogoro Kato and Takeshi Takei of the Tokyo Institute of Technology synthesized the first ferrite compounds in 1930.
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 (O2−) with A cations occupying one eighth of the tetrahedral holes and B cations occupying half of the octahedral holes, i.e., A2+ B3+ 2O2− 4.
Ferrite crystals do not adopt the ordinary spinel structure, but rather 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−δFe3+δ][M2+δFe3+2−δ]O4 where δ 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.[page needed]
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.
Various ferrite cores used to make small transformers and inductors
Manganese-zinc ferrite (MnZn, with the formula MnaZn(1-a)Fe2O4). MnZn have higher permeability and saturation induction than NiZn.
Nickel-zinc ferrite (NiZn, with the formula NiaZn(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.
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 its 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.
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. Strontium hexaferrite (SrFe12O19) is well known for its high coercivity due to its magnetocrystalline anisotropy. It has been widely used in industrial applications as permanent magnets and, because they can be powdered and formed easily, they are finding their applications into micro and nano-types systems such as biomarkers, bio diagnostics and biosensors.
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 are typically supplied as their carbonates, BaCO3 or SrCO3. During the heating process, these carbonates undergo calcination:
MCO3 → MO + CO2
After this step, the two oxides combine to give the ferrite. The resulting mixture of oxides undergoes sintering.
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.
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 audio magnets, including those used in loudspeakers and electromagnetic instrument pickups, are ferrite magnets. Except for certain "vintage" products, ferrite magnets have largely displaced the more expensive Alnico magnets in these applications. In particular, for hard hexaferrites today the most common uses are still as permanent magnets in refrigerator seal gaskets, microphones and loud speakers, small motors for cordless appliances and in automobile applications.
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 (BaO•6Fe2O3) 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 of permanent magnets.
In the 1960s Philips developed strontium hexaferrite (SrO•6Fe2O3), with better properties than barium hexaferrite. Barium and strontium hexaferrite dominate the market due to their low costs. Other materials have been found with improved properties. BaO•2(FeO)•8(Fe2O3) came in 1980. and Ba2ZnFe18O23 came in 1991.
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