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Iron(III) oxide

Chemical compound

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Unit cell of Hematite , chemical compound iron(III) oxide
Benjah-bmm27 · Public domain

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Through Pigment, Oxide and Iron

It is one of the three main oxides of iron, the other two being iron(II) oxide (FeO), which is rare; and iron(II,III) oxide (Fe3O4), which also occurs naturally as the mineral magnetite.

Iron(III) oxide is often called rust, since rust shares several properties and has a similar composition; however, in chemistry, rust is considered an ill-defined material, described as hydrous ferric oxide.

Ferric oxide is readily attacked, even by weak acids. It is a weak oxidising agent, most famously when reduced by aluminium in the thermite reaction.

Structure

Fe2O3 can be obtained in various polymorphs. In the primary polymorph, α, iron adopts octahedral coordination geometry. That is, each Fe center is bound to six oxygen ligands. In the γ polymorph, some of the Fe sit on tetrahedral sites, with four oxygen ligands.

Alpha phase

α-Fe2O3 has the rhombohedral, corundum (α-Al2O3) structure and is the most common form. It occurs naturally as the mineral hematite, which is mined as the main ore of iron. It is antiferromagnetic below ~260 K (Morin transition temperature), and exhibits weak ferromagnetism between 260 K and the Néel temperature, 950 K. It is easy to prepare using both thermal decomposition and precipitation in the liquid phase. Its magnetic properties are dependent on many factors, e.g., pressure, particle size, and magnetic field intensity.

Gamma phase

γ-Fe2O3 has a cubic structure. It is metastable and converted from the alpha phase at high temperatures. It occurs naturally as the mineral maghemite. It is ferromagnetic and finds application in recording tapes, although ultrafine particles smaller than 10 nanometers are superparamagnetic. It can be prepared by thermal dehydratation of gamma iron(III) oxide-hydroxide. Another method involves the careful oxidation of iron(II,III) oxide (Fe3O4). The ultrafine particles can be prepared by thermal decomposition of iron(III) oxalate.

Other solid phases

Several other phases have been identified or claimed. The beta phase (β-phase) is cubic body-centered (space group Ia3), metastable, and at temperatures above 500 °C (930 °F) converts to alpha phase. It can be prepared by reduction of hematite by carbon, pyrolysis of iron(III) chloride solution, or thermal decomposition of iron(III) sulfate.

The epsilon (ε) phase is rhombic, and shows properties intermediate between alpha and gamma, and may have useful magnetic properties applicable for purposes such as high density recording media for big data storage. Preparation of the pure epsilon phase has proven very challenging. Material with a high proportion of epsilon phase can be prepared by thermal transformation of the gamma phase. The epsilon phase is also metastable, transforming to the alpha phase at between 500 and 750 °C (930 and 1,380 °F). It can also be prepared by oxidation of iron in an electric arc or by sol-gel precipitation from iron(III) nitrate. Research has revealed epsilon iron(III) oxide in ancient Chinese Jian ceramic glazes, which may provide insight into ways to produce that form in the lab.

Additionally, at high pressure an amorphous form is claimed.

Liquid phase

Molten Fe2O3 is expected to have a coordination number of close to 5 oxygen atoms about each iron atom, based on measurements of slightly oxygen deficient supercooled liquid iron oxide droplets, where supercooling circumvents the need for the high oxygen pressures required above the melting point to maintain stoichiometry.

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