|Crystal class||Dipyramidal (6/m)
(same H-M symbol)
|Color||Transparent to translucent, usually green, less often colorless, yellow, blue to violet, pink, brown.|
|Crystal habit||Tabular, prismatic crystals, massive, compact or granular|
|Cleavage|| indistinct,  indistinct|
|Fracture||Conchoidal to uneven|
|Mohs scale hardness||5 (defining mineral)|
|Luster||Vitreous to subresinous|
|Diaphaneity||Transparent to translucent|
|Optical properties||Double refractive, uniaxial negative|
|Refractive index||1.634–1.638 (+0.012, −0.006)|
|Pleochroism||Blue stones – strong, blue and yellow to colorless. Other colors are weak to very weak.|
|Ultraviolet fluorescence||Yellow stones – purplish-pink, which is stronger in long wave; blue stones – blue to light-blue in both long and short wave; green stones – greenish-yellow, which is stronger in long wave; violet stones – greenish-yellow in long wave, light-purple in short wave.|
Apatite is a group of phosphate minerals, usually referring to hydroxylapatite, fluorapatite and chlorapatite, with high concentrations of OH, F and Cl ions, respectively, in the crystal. The formula of the admixture of the four most common endmembers is written as Ca10(PO4)6(OH,F,Cl)2, and the crystal unit cell formulae of the individual minerals are written as Ca10(PO4)6(OH)2, Ca10(PO4)6(F)2 and Ca10(PO4)6(Cl)2.
The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786, although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is a mineral that is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word απατείν (apatein), which means to deceive or to be misleading.
Apatite is one of a few minerals produced and used by biological micro-environmental systems. Apatite is the defining mineral for 5 on the Mohs scale. Hydroxyapatite, also known as hydroxylapatite, is the major component of tooth enamel and bone mineral. A relatively rare form of apatite in which most of the OH groups are absent and containing many carbonate and acid phosphate substitutions is a large component of bone material.
Fluorapatite (or fluoroapatite) is more resistant to acid attack than is hydroxyapatite; in the mid-20th century, it was discovered that communities whose water supply naturally contained fluorine had lower rates of dental caries. Fluoridated water allows exchange in the teeth of fluoride ions for hydroxyl groups in apatite. Similarly, toothpaste typically contains a source of fluoride anions (e.g. sodium fluoride, sodium monofluorophosphate). Too much fluoride results in dental fluorosis and/or skeletal fluorosis.
Fission tracks in apatite are commonly used to determine the thermal history of orogenic (mountain) belts and of sediments in sedimentary basins. (U-Th)/He dating of apatite is also well established for use in determining thermal histories and other, less typical applications such as paleo-wildfire dating.
Phosphorite is a phosphate-rich sedimentary rock, that contains between 18% and 40% P2O5. The apatite in phosphorite is present as cryptocrystalline masses referred to as collophane.
The primary use of apatite is in the manufacture of fertilizer – it is a source of phosphorus. It is occasionally used as a gemstone. Green and blue varieties, in finely divided form, are pigments with excellent covering power.
During digestion of apatite with sulfuric acid to make phosphoric acid, hydrogen fluoride is produced as a byproduct from any fluorapatite content. This byproduct is a minor industrial source of hydrofluoric acid.
Fluoro-chloro apatite forms the basis of the now obsolete Halophosphor fluorescent tube phosphor system. Dopant elements of manganese and antimony, at less than one mole-percent, in place of the calcium and phosphorus impart the fluorescence, and adjustment of the fluorine-to-chlorine ratio adjusts the shade of white produced. This system has been almost entirely replaced by the Tri-Phosphor system.
In the United States, apatite-derived fertilizers are used to supplement the nutrition of many agricultural crops by providing a valuable source of phosphate.
Apatites are also a proposed host material for storage of nuclear waste, along with other phosphates.
Apatite is infrequently used as a gemstone. Transparent stones of clean color have been faceted, and chatoyant specimens have been cabochon-cut. Chatoyant stones are known as cat's-eye apatite, transparent green stones are known as asparagus stone, and blue stones have been called moroxite. If crystals of rutile have grown in the crystal of apatite, in the right light the cut stone displays a cat's-eye effect. Major sources for gem apatite are Brazil, Burma, and Mexico. Other sources include Canada, Czech Republic, Germany, India, Madagascar, Mozambique, Norway, South Africa, Spain, Sri Lanka, and the United States.
Apatite is occasionally found to contain significant amounts of rare-earth elements and can be used as an ore for those metals. This is preferable to traditional rare-earth ores, as apatite is non-radioactive and does not pose an environmental hazard in mine tailings. However, some apatite in Florida used to produce phosphate for agriculture does contain uranium, radium, lead-210, polonium-210, and radon.
Apatite is an ore mineral at the Hoidas Lake rare-earth project.
The standard enthalpies of formation in the crystalline state of hydroxyapatite, chlorapatite and a preliminary value for bromapatite, have been determined by reaction-solution calorimetry. Speculations on the existence of a possible fifth member of the calcium apatites family, iodoapatite, have been drawn from energetic considerations.
Structural and thermodynamic properties of crystal hexagonal calcium apatites, Ca10(PO4)6(X)2 (X= OH, F, Cl, Br), have been investigated using an all-atom Born-Huggins-Mayer potential by a molecular dynamics technique. The accuracy of the model at room temperature and atmospheric pressure was checked against crystal structural data, with maximum deviations of c. 4% for the haloapatites and 8% for hydroxyapatite. High-pressure simulation runs, in the range 0.5-75 kbar, were performed in order to estimate the isothermal compressibility coefficient of those compounds. The deformation of the compressed solids is always elastically anisotropic, with BrAp exhibiting a markedly different behavior from those displayed by HOAp and ClAp. High-pressure p-V data were fitted to the Parsafar-Mason equation of state with an accuracy better than 1%.
The monoclinic solid phases Ca10(PO4)6(X)2 (X= OH, Cl) and the molten hydroxyapatite compound have also been studied by molecular dynamics.
Moon rocks collected by astronauts during the Apollo program contain traces of apatite. Re-analysis of these samples in 2010 revealed water trapped in the mineral as hydroxyl, leading to estimates of water on the lunar surface at a rate of at least 64 parts per billion – 100 times greater than previous estimates – and as high as 5 parts per million. If the minimum amount of mineral-locked water was hypothetically converted to liquid, it would cover the Moon's surface in roughly one meter of water.
The ectomycorrhizal fungi Suillus granulatus and Paxillus involutus can release elements from apatite.
|Wikimedia Commons has media related to Apatite.|
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