Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe2+Fe3+2O4. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism. Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak. Small grains of magnetite are very common in igneous and metamorphic rocks. The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide.
Properties In addition to igneous rocks, magnetite also occurs in sedimentary rocks, including banded iron formations and in lake and marine sediments as both detrital grains and as magnetofossils. Magnetite nanoparticles are also thought to form in soils, where they probably oxidize rapidly to maghemite.
Crystal structure The chemical composition of magnetite is Fe2+(Fe3+)2(O2-)4. This indicates that magnetite contains both ferrous (divalent) and ferric (trivalent) iron, suggesting crystallization in an environment containing intermediate levels of oxygen. The main details of its structure were established in 1915. It was one of the first crystal structures to be obtained using X-ray diffraction. It has an inverse spinel structure, with O2- ions forming a face-centered cubic lattice and iron cations occupying interstitial sites. Half of the Fe3+ cations occupy tetrahedral sites while the other half, along with Fe2+ cations, occupy octahedral sites. The unit cell consists of thirty-two O2- ions and unit cell length is a = 0.839 nm. As a member of the inverse spinel group, magnetite can form solid solutions with similarly structured minerals, including ulvospinel (Fe2TiO4) and magnesioferrite (MgFe2O4). Titanomagnetite, also known as titaniferous magnetite, is a solid solution between magnetite and ulvospinel that crystallizes in many mafic igneous rocks. Titanomagnetite may undergo oxy-exsolution during cooling, resulting in ingrowths of magnetite and ilmenite.
Crystal morphology and size Natural and synthetic magnetite occurs most commonly as octahedral crystals bounded by {111} planes and as rhombic-dodecahedra. Twinning occurs on the {111} plane. Hydrothermal synthesis usually produces single octahedral crystals which can be as large as 10 millimetres (3⁄8 inch) across. In the presence of mineralizers such as 0.1 M HI or 2 M NH4Cl and at 0.207 MPa at 416–800 °C, magnetite grew as crystals whose shapes were a combination of rhombic-dodechahedra forms. The crystals were more rounded than usual. The appearance of higher forms was considered as a result from a decrease in the surface energies caused by the lower surface to volume ratio in the rounded crystals.
Reactions Magnetite has been important in understanding the conditions under which rocks form. Magnetite reacts with oxygen to produce hematite, and the mineral pair forms a buffer that can control how oxidizing its environment is (the oxygen fugacity). This buffer is known as the hematite-magnetite or HM buffer. At lower oxygen levels, magnetite can form a buffer with quartz and fayalite known as the QFM buffer. At still lower oxygen levels, magnetite forms a buffer with wüstite known as the MW buffer. The QFM and MW buffers have been used extensively in laboratory experiments on rock chemistry. The QFM buffer, in particular, produces an oxygen fugacity close to that of most igneous rocks. Commonly, igneous rocks contain solid solutions of both titanomagnetite and hemoilmenite or titanohematite. Compositions of the mineral pairs are used to calculate oxygen fugacity: a range of oxidizing conditions are found in magmas and the oxidation state helps to determine how the magmas might evolve by fractional crystallization. Magnetite also is produced from peridotites and dunites by serpentinization.
Magnetic properties Lodestones were used as an early form of magnetic compass. Magnetite has been a critical tool in paleomagnetism, a science important in understanding plate tectonics and as historic data for magnetohydrodynamics and other scientific fields. The relationships between magnetite and other iron oxide minerals such as ilmenite, hematite, and ulvospinel have been much studied; the reactions between these minerals and oxygen influence how and when magnetite preserves a record of the Earth's magnetic field. At low temperatures, magnetite undergoes a crystal structure phase transition from a monoclinic structure to a cubic structure known as the Verwey transition. Optical studies show that this metal to insulator transition is sharp and occurs around 120 K. The Verwey transition is dependent on grain size, domain state, pressure, and the iron-oxygen stoichiometry. An isotropic point also occurs near the Verwey transition around 130 K, at which point the sign of the magnetocrystalline anisotropy constant changes from positive to negative. The Curie temperature of magnetite is 580 °C (853 K; 1,076 °F). If magnetite is in a large enough quantity it can be found in aeromagnetic surveys using a magnetometer which measures magnetic intensities.
Melting point
Solid magnetite particles melt at about 1,583–1,597 °C (2,881–2,907 °F).
Distribution of deposits
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