Apatite is a group of phosphate minerals, usually hydroxyapatite, fluorapatite and chlorapatite, with high concentrations of Hydroxide−, Fluoride− and Chloride− ion, respectively, in the crystal. The formula of the admixture of the three most common endmembers is written as Calcium10(Phosphate)6(OH,F,Cl)2, and the crystal unit cell formulae of the individual are written as Ca10(PO4)6(OH)2, Ca10(PO4)6F2 and Ca10(PO4)6Cl2.
The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786,According to Werner himself – (Werner, 1788), p. 85 – the name "apatite" first appeared in print in:
Werner described the mineral in some detail in an article of 1788.
although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word ἀπατάω (apatáō), which means to deceive.
Apatite is the defining mineral for 5 on the Mohs scale. It can be distinguished Field work from beryl and tourmaline by its relative softness. It is often fluorescent under ultraviolet light.
Apatite is one of a few minerals produced and used by biological micro-environmental systems. Hydroxyapatite (IMA name: 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 tooth 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 histories of and of Sedimentary rock in sedimentary basins.
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. Apatite is also occasionally a source of uranium and vanadium, present as trace elements in the mineral.
Fluoro-chloro apatite forms the basis of the now obsolete halophosphor fluorescent lamp 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 alter the shade of white produced. This system has been almost entirely replaced by the tri-phosphor system.Henderson and Marsden, "Lamps and Lighting", Edward Arnold Ltd., 1972,
Apatites are also a proposed host material for storage of nuclear waste, along with other phosphates.
The town of Apatity in the Arctic North of Russia was named for its mining operations for these ores.
Apatite is an ore mineral at the Hoidas Lake rare-earth project. Great Western Minerals Group Ltd. | Projects – Hoidas Lake, Saskatchewan . Gwmg.ca (2010-01-27). Retrieved on 2011-07-24.
Structural and Thermodynamics 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 potentialSee: Born-Huggins-Mayer potential (SklogWiki) 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 stateParsafar, Gholamabbas and Mason, E.A. (1994) "Universal equation of state for compressed solids," Physical Review B Condensed Matter, 49 (5) : 3049–60. 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.
Apatites have been investigated for their potential use as pigments (copper-doped alkaline earth apatites), as and for absorbing and immobilising toxic heavy metals.
In apatite minerals strontium, barium and lead can be substituted for calcium; arsenate and vanadate for phosphate; and the final balancing anion can be fluoride (fluorapatites), chloride (chlorapatites), hydroxide (hydroxyapatites) or oxide (oxyapatites). Synthetic apatites add hypomanganate, hypochromate, bromide (bromoapatites), iodide (iodoapatites), sulfide (sulfoapatites), and selenide (selenoapatites). Evidence for natural sulfide substitution has been found in lunar rock samples.
Furthermore, compensating substitution of monovalent and trivalent cations for calcium, of dibasic and tetrabasic anions for phosphate, and of the balancing anion, can occur to a greater or lesser degree. For example, in biological apatites there is appreciable substitution of sodium for calcium and carbonate for phosphate, in belovite sodium and cerium or lanthanum substitute for a pair of divalent metal ions, in germanate-pyromorphite germanate replaces phosphate and chloride, and in ellestadites silicate and sulphate replace pairs of phosphate anions. Metals forming smaller divalent ions, such as magnesium and iron, cannot substitute extensively for the relatively large calcium ions but may be present in small quantities.
Uses
Gemology
Use as an ore mineral
Thermodynamics
Lunar science
Bio-leaching
Apatite group and supergroup
See also
|
|