Apatite

From New World Encyclopedia
Apatite
Apatite crystals.jpg
General
CategoryPhosphate mineral group
Chemical formulaCa5(PO4)3(F,Cl,OH)
Identification
ColorTransparent to translucent, usually green, less often colorless, yellow, blue to violet, pink, brown.[1]
Crystal habitTabular, prismatic crystals, massive, compact or granular
Crystal systemHexagonal Dipyramidal (6/m)[2]
Cleavage[0001] Indistinct, [1010] Indistinct [3]
FractureConchoidal to uneven[4]
Mohs Scale hardness5[5]
LusterVitreous[6] to subresinous
Refractive index1.634 - 1.638 (+.012, -.006)[7]
Optical PropertiesDouble refractive, uniaxial negative[8]
Birefringence.002-.008[9]
PleochroismBlue stones - strong, blue and yellow to colorless. Other colors are weak to very weak.[10]
StreakWhite
Specific gravity3.16 - 3.22[11]
DiaphaneityTransparent to translucent[12]

Apatite is the name given to a group of phosphate minerals, usually referring to hydroxylapatite (or hydroxyapatite), fluoroapatite (or fluorapatite), and chloroapatite (or chlorapatite). They are named for the presence of hydroxide (OH-), fluoride (F-), and chloride (Cl-) ions, respectively, in the crystal lattice. These three forms of apatite are not readily distinguishable, as each specimen usually contains all three types of ions. Impure, massive apatite is called phosphorite.

Apatite is distributed widely in igneous, metamorphic, and sedimentary rocks, often in the form of cryptocrystalline fragments. It is usually green, but blue, yellow, purple, and brown varieties have also been found. The crystals range from transparent to translucent, with a vitreous to greasy luster.

This mineral is also a biological material. In particular, hydroxylapatite is the main constituent of tooth enamel, and a special form of apatite is found in bone. When toothpastes and water containing fluoride are used, the fluoride ions substitute for hydroxide ions in tooth enamel, making the enamel more resistant to attack by acids.

Apatite has a diverse range of uses. For example, in medicine, hydroxylapatite is used as a filler to replace amputated bone or as a coating to promote the growth of bone into prosthetic implants. Also, some dental implants are coated with hydroxylapatite, in the belief that it may promote integration into bone tissue. Researchers use hydroxylapatite for a chromatographic technique to purify proteins and other chemicals. Geologists have used a radiometric dating technique (known as fission track dating) with natural deposits of apatite to get a sense of historical changes in temperature in mountain-forming belts and sedimentary basins. In some cases, crystals of apatite have been cut and used as gems.

It should be noted that phosphate, arsenate, and vanadate minerals with similar crystalline structures (hexagonal or pseudohexagonal monoclinic crystals) are known as the Apatite Group. This group includes minerals such as apatite, mimetite, pyromorphite, and vanadinite.

Etymology

The name apatite is derived from a Greek word that means "to deceive," because it appears similar to other minerals, particularly olivine, beryl, and peridot.

Occurrence

Biological: Apatite is one of few minerals that are produced and used by biological systems. Hydroxylapatite is the main component of tooth enamel. A relatively unique form of apatite—in which most OH groups are absent and containing many carbonate and acid phosphate substitutions—is a large component of bone material.

Mineralogical: In mineral form, noteworthy areas of occurrence include Bancroft, Ontario; Durango, Mexico; Germany; and Russia.

Characteristics

The overall chemical formula for apatite is generally given as Ca5(PO4)3(OH, F, Cl). The formulas for the three common species may be written as:

  • Hydroxylapatite: Ca5(PO4)3(OH)
  • Fluoroapatite: Ca5(PO4)3F
  • Chlorapatite: Ca5(PO4)3Cl

Apatite has a hardness of 5 on the Mohs scale, and its specific gravity is between 3.1 and 3.2. Its crystals belong to the hexagonal crystal system, and the crystal habit is typically hexagonal prism, terminating with a hexagonal pyramid or pinacoid shape. In addition, apatite may occur in acicular (needle-like), granular, reniform, and massive forms.

Hydroxylapatite

A sample of hydroxylapatite.

Hydroxylapatite is the hydroxyl endmember of the apatite group. The OH- ion can be replaced by fluoride, chloride or carbonate. As noted above, its formula may be written as Ca5(PO4)3(OH). The formula may also be written as Ca10(PO4)6(OH)2, to indicate that each crystal unit cell combines two molecules.

Purified hydroxylapatite powder is white. Naturally occurring forms can also be brown, yellow, or green.

Hydroxylapatite is the main mineral component of bone. Hydroxylapatite that is deficient in carbonated calcium is the main constituent of dental enamel and dentin.

Fluoroapatite

Fluoroapatite crystal, Mexico.
Fluoroapatite
Unit cell of fluoroapatite
General
Systematic name Fluoroapatite
Other names Fluorapatite
Molecular formula Ca5(PO4)3F
Molar mass 504.3 g/mol
Appearance hard solid, various colors
CAS number 68877-08-7
Properties
Solubility in water almost insoluble
Structure
Crystal structure hexagonal
Related compounds
Related compounds Ca5(PO4)3OH
Ca5(PO4)3Cl
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)

Fluoroapatite is a hard crystalline solid that may be classified as a calcium halophosphate. The pure mineral is colorless, but naturally occurring samples can have various colors, such as green, brown, blue, or violet. It is an important constituent of tooth enamel. It is often combined as a solid solution with hydroxylapatite in biological matrices.

Fluoroapatite can be synthesized in a two-step process. First, calcium phosphate is generated by combining calcium and phosphate salts at neutral pH. This material then reacts further with fluoride sources (such as sodium monofluorophosphate or calcium fluoride (CaF2)) to give the desired material. This reaction is an integral part of the global phosphorous cycle.[13] The reactions may be written as follows:

3Ca2+ + 2PO43- → Ca3(PO4)2
3 Ca3(PO4)2 + CaF2 → 2 Ca5(PO4)3F

Fluoroapatite can also be used as a precursor for the production of phosphorus. The mineral can be reduced by carbon in the presence of quartz, ultimately generating white phosphorus (P4), as follows:

Ca5(PO4)3F + 3SiO2 + 5C → 3CaSiO3 + 5CO + P2
2P2 → P4 (after cooling)

Applications

  • Geologists often use a radiometric dating technique in which they follow fission tracks (of uranium) in apatite to determine the thermal history of orogenic (mountain-forming) belts and sediments in sedimentary basins.
  • Fluoroapatite is more resistant to acid attack than is hydroxylapatite. For this reason, toothpastes typically contain a source of fluoride anions (such as sodium fluoride or sodium monofluorophosphate), allowing for the exchange of fluoride ions for hydroxy groups in the apatite in teeth. Fluoridated water has a similar effect. Too much fluoride, however, results in dental fluorosis or skeletal fluorosis.
  • Hydroxylapatite can be used as a filler to replace amputated bone or as a coating to promote bone ingrowth into prosthetic implants. Although many other phases exist with similar or even identical chemical makeup, the body responds quite differently to them. Coral skeletons can be transformed into hydroxylapatite by high temperatures; their porous structure allows relatively rapid ingrowth at the expense of initial mechanical strength. The high temperature also burns away organic molecules such as proteins, preventing host-versus-graft disease.[14]
  • Some modern dental implants are coated with hydroxylapatite. It has been suggested that this may promote osseointegration, but conclusive clinical proof of this has yet to come.
  • Hydroxylapatite is used to purify proteins and other chemicals by the technique known as hydroxylapatite (HAP) chromatography. The mechanism involved in this technique is complicated and has been described as "mixed-mode" ion exchange.
  • In the United States, apatite is often used to fertilize tobacco. It partially starves the plant of nitrogen, which gives American cigarettes a different taste from those of other countries.
  • Apatite is infrequently used as a gemstone. Transparent stones of clean color have been faceted, and chatoyant specimens have been cabochon cut.[15] Chatoyant stones are known as cat's-eye apatite,.[16]

transparent green stones are known as asparagus stone,[17] and blue stones may be called moroxite.[18] If crystals of rutile have grown in the apatite crystal, the cut stone displays a cat's eye effect when viewed in the right lighting. Major sources[19] for gem-quality apatite are: Brazil, Burma, and Mexico. Additional sources include Canada, Czechoslovakia, Germany, India, Madagascar, Mozambique, Norway, South Africa, Spain, Sri Lanka, and the United States.

See also

Notes

  1. GIA Gem Reference Guide(Carlsbad, CA: Gemological Institute of America, 1995), ISBN 0873110196
  2. B. & C. Gobin, Worldwide Fine Minerals by B & C GobinApatite Mineral Data. Webmineral.com Retrieved May 8, 2007.
  3. Gobin
  4. GIA
  5. Ibid.
  6. Ibid.
  7. Ibid.
  8. Ibid.
  9. Ibid.
  10. Ibid.
  11. Gobin
  12. Ibid.
  13. A. F. Holleman and E. Wiberg, Inorganic Chemistry (San Diego: Academic Press, 2001). ISBN 0123526515
  14. It may be noted that bioactive glasses are the only manmade materials known to bond to both bone and soft tissue and have been clinically used as a bone grafting material for over 20 years in dental, maxillofacial, and orthopedic procedures. Unlike hydroxyapatite, which is said to be “osteoconductive” by conducting new bone growth along the materials surface, bioactive glasses are “osteostimulative” in that the material stimulates the recruitment and differentiation of osteoblasts—cells that produce new bone. As a result, bioactive glass rapidly enhances the production of new bone and is completely resorbed by the body and replaced by new bone. Bioactive glasses have also been used in oral care applications as a tooth remineralizer (calcium sodium phosphosilicate) in both professional dental and consumer oral care products.
  15. GIA
  16. Ibid.
  17. Ibid.
  18. Edwin W. Streeter, Moroxite Precious Stones and Gems, 6th ed. (London: George Bell and Sons, 1898), 306. Retrieved May 8, 2007.
  19. GIA

References
ISBN links support NWE through referral fees

  • Farndon, John. 2006. The Practical Encyclopedia of Rocks & Minerals: How to Find, Identify, Collect and Maintain the World's best Specimens, with over 1000 Photographs and Artworks. London: Lorenz Books. ISBN 0754815412
  • Gobin, B. & C.Worldwide Fine Minerals by B & C GOBINApatite Mineral Data. Webmineral.com. Retrieved May 8, 2007.
  • Holleman, A. F. and E. Wiberg, Inorganic Chemistry (San Diego: Academic Press, 2001). ISBN 0123526515
  • Klein, Cornelis, and Barbara Dutrow. 2007. Manual of Mineral Science, 23rd ed. New York: John Wiley. ISBN 9780471721574
  • Pellant, Chris. 2002. Rocks and Minerals. Smithsonian Handbooks. New York: Dorling Kindersley. ISBN 0789491060
  • Shaffer, Paul R., Herbert S. Zim, and Raymond Perlman. 2001. Rocks, Gems and Minerals, Rev. ed. New York: St. Martin's Press. ISBN 1582381321
  • Streeter, Edwin W. Moroxite Precious Stones and Gems, 6th ed. (London: George Bell and Sons, 1898), 306. Retrieved May 8, 2007.
  • Mineral Gallery. 2006. The Mineral Apatite. Amethyst Galleries.

External links

All links retrieved August 11, 2023.

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