Hematite
Hematite, also spelled as haematite, is a common iron oxide compound with the formula Fe2O3 and is widely found in rocks and soils. Hematite crystals belong to the rhombohedral lattice system which is designated the alpha polymorph of. It has the same crystal structure as corundum and ilmenite. With this crystal structure geometry it forms a complete solid solution at temperatures above.
Hematite occurs naturally in black to steel or silver-gray, brown to reddish-brown, or red colors. It is mined as an important ore mineral of iron. It is electrically conductive. Hematite varieties include kidney ore, martite, iron rose and specularite. While these forms vary, they all have a rust-red streak. Hematite is not only harder than pure iron, but also much more brittle. The term kidney ore may be broadly used to describe botryoidal, mammillary, or reniform hematite. Maghemite is a polymorph of hematite with the same chemical formula, but with a spinel structure like magnetite.
Large deposits of hematite are found in banded iron formations. Gray hematite is typically found in places that have still, standing water, or mineral hot springs, such as those in Yellowstone National Park in North America. The mineral may precipitate in the water and collect in layers at the bottom of the lake, spring, or other standing water. Hematite can also occur in the absence of water, usually as the result of volcanic activity.
Clay-sized hematite crystals also may occur as a secondary mineral formed by weathering processes in soil, and along with other iron oxides or oxyhydroxides such as goethite, which is responsible for the red color of many tropical, ancient, or otherwise highly weathered soils.
Etymology and history
The name hematite is derived from the Greek word for blood, wikt:αἷμα , due to the red coloration found in some varieties of hematite. The color of hematite is often used as a pigment. The English name of the stone is derived from Middle French hématite pierre, which was taken from Latin lapis haematites the 15th century, which originated from Ancient Greek αἱματίτης λίθος.Ochre is a clay that is colored by varying amounts of hematite, varying between 20% and 70%. Red ochre contains unhydrated hematite, whereas yellow ochre contains hydrated hematite. The principal use of ochre is for tinting with a permanent color.
Use of the red chalk of this iron-oxide mineral in writing, drawing, and decoration is among the earliest in human history. To date, the earliest known human use of the powdery mineral is 164,000 years ago by the inhabitants of the Pinnacle Point caves in what now is South Africa, possibly for social purposes. Hematite residues are also found in graves from 80,000 years ago. Near Rydno in Poland and Lovas in Hungary red chalk mines have been found that are from 5000 BC, belonging to the Linear Pottery culture at the Upper Rhine.
Rich deposits of hematite have been found on the island of Elba that have been mined since the time of the Etruscans.
Underground hematite mining is classified as a carcinogenic hazard to humans.
Magnetism
Hematite shows only a very feeble response to a magnetic field. Unlike magnetite, it is not noticeably attracted to an ordinary magnet. Hematite is an antiferromagnetic material below the Morin transition at, and a canted antiferromagnet or weakly ferromagnetic above the Morin transition and below its Néel temperature at, above which it is paramagnetic.The magnetic structure of α-hematite was the subject of considerable discussion and debate during the 1950s, as it appeared to be ferromagnetic with a Curie temperature of approximately, but with an extremely small magnetic moment. Adding to the surprise was a transition with a decrease in temperature at around to a phase with no net magnetic moment. It was shown that the system is essentially antiferromagnetic, but that the low symmetry of the cation sites allows spin–orbit coupling to cause canting of the moments when they are in the plane perpendicular to the c axis. The disappearance of the moment with a decrease in temperature at is caused by a change in the anisotropy which causes the moments to align along the c axis. In this configuration, spin canting does not reduce the energy. The magnetic properties of bulk hematite differ from their nanoscale counterparts. For example, the Morin transition temperature of hematite decreases with a decrease in the particle size. The suppression of this transition has been observed in hematite nanoparticles and is attributed to the presence of impurities, water molecules and defects in the crystals lattice. Hematite is part of a complex solid solution oxyhydroxide system having various contents of H2O, hydroxyl groups and vacancy substitutions that affect the mineral's magnetic and crystal chemical properties. Two other end-members are referred to as protohematite and hydrohematite.
Enhanced magnetic coercivities for hematite have been achieved by dry-heating a two-line ferrihydrite precursor prepared from solution. Hematite exhibited temperature-dependent magnetic coercivity values ranging from. The origin of these high coercivity values has been interpreted as a consequence of the subparticle structure induced by the different particle and crystallite size growth rates at increasing annealing temperature. These differences in the growth rates are translated into a progressive development of a subparticle structure at the nanoscale. At lower temperatures, single particles crystallize. However, at higher temperatures, the growth of crystalline aggregates, and a subparticle structure is favored.