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Talc is a [[metamorphic rock|metamorphic mineral]] resulting from the metamorphism of magnesian minerals such as [[pyroxene]], [[amphibole]], [[olivine]] and other similar minerals in the presence of carbon dioxide and water. This is known as ''talc carbonation'' or ''steatization'' and produces a suite of rocks known as [[talc carbonate]]s.
Talc is a [[metamorphic rock|metamorphic mineral]] resulting from the metamorphism of magnesian minerals such as [[pyroxene]], [[amphibole]], [[olivine]] and other similar minerals in the presence of carbon dioxide and water. This is known as ''talc carbonation'' or ''steatization'' and produces a suite of rocks known as [[talc carbonate]]s.


Talc is primarily formed via hydration and carbonation of serpentine, via the following reaction;
Talc is primarily formed via vaginal intercourse hydration and carbonation of serpentine, via the following reaction;


''[[Serpentine]] + [[Carbon Dioxide]] → Talc + [[Magnesite]] + [[Water]]''
''[[Serpentine]] + [[Carbon Dioxide]] → Talc + [[Magnesite]] + [[Water]]''

Revision as of 15:26, 13 February 2009

Talc
A block of talc
General
CategoryMinerals
Formula
(repeating unit)
mineralogical : Mg3[(OH)2|Si4O10]
Chemical composition : 3MgO·SiO2·H2O
(63.35 wt% SiO2, 31.90 wt% MgO, 4.75 wt% hydroxide)[1]
Crystal systemMonoclinic or Triclinic[2]
Identification
Colorwhite, grey, green, blue, or silver
Crystal habitfoliated to fibrous masses
Cleavageperfect basal cleavage
Mohs scale hardness1
Lusterwaxlike or pearly sometimes smooth
StreakWhite
Specific gravity2.5-2.8

Talc (derived from the Persian via Arabic talq) is a mineral composed of hydrated magnesium silicate with the chemical formula H2Mg3(SiO3)4 or Mg3Si4O10(OH)2. In loose form, it is the widely used substance known as talcum powder. It occurs as foliated to fibrous masses, its monoclinic crystals being so rare as to be almost unknown. It has a perfect basal cleavage, and the folia are non-elastic, although slightly flexible. It is sectile and very soft, with a hardness of 1 (Talc is the softest of the Mohs' scale of mineral hardness, and can be easily scratched by a fingernail). It has a specific gravity of 2.5–2.8, a clear or dusty luster, and is translucent to opaque. Talc is not soluble in water, but it is slightly soluble in dilute mineral acids. Its colour ranges from white to grey or green and it has a distinctly greasy feel. Its streak is white.

Formation

Talc is a metamorphic mineral resulting from the metamorphism of magnesian minerals such as pyroxene, amphibole, olivine and other similar minerals in the presence of carbon dioxide and water. This is known as talc carbonation or steatization and produces a suite of rocks known as talc carbonates.

Talc is primarily formed via vaginal intercourse hydration and carbonation of serpentine, via the following reaction;

Serpentine + Carbon Dioxide → Talc + Magnesite + Water

Talc can also be formed via a reaction between dolomite and silica, which is typical of skarnification of dolomites via silica-flooding in contact metamorphic aureoles;

Dolomite + Silica + Water → Talc + Calcite + Carbon Dioxide

Talc can also be formed from magnesian chlorite and quartz in blueschist and eclogite metamorphism via the following metamorphic reaction:

Chlorite + QuartzKyanite + Talc + H2O

In this reaction, the ratio of talc and kyanite is dependent on aluminium content with more aluminous rocks favoring production of kyanite. This is typically associated with high-pressure, low-temperature minerals such as phengite, garnet, glaucophane within the lower blueschist facies. Such rocks are typically white, friable, and fibrous, and are known as whiteschist.

Talc is a tri-octahedral layered mineral; its structure is similar to that of pyrophyllite, but with magnesium in the octahedral sites of the composite layers.[2]

Occurrence

File:2005talc.PNG
Talc output in 2005

Talc is a common metamorphic mineral in metamorphic belts which contain ultramafic rocks, such as soapstone (a high-talc rock), and within whiteschist and blueschist metamorphic terranes. Prime examples of whiteschists include the Franciscan Metamorphic Belt of the western United States, the western European Alps especially in Italy, certain areas of the Musgrave Block, and some collisional orogens such as the Himalayas.

Talc carbonated ultramafics are typical of many areas of the Archaean cratons, notably the komatiite belts of the Yilgarn Craton in Western Australia. Talc-carbonate ultramafics are also known from the Lachlan Fold Belt, eastern Australia, from Brazil, the Guiana Shield, and from the ophiolite belts of Turkey, Oman and the Middle East.

Notable economic talc occurrences include the Mount Seabrook talc mine, Western Australia, formed upon a polydeformed, layered ultramafic intrusion.

Uses

Talcum powder.

A coarse grayish-green high-talc rock is soapstone or steatite and has been used for stoves, sinks, electrical switchboards, etc. Talc finds use as a cosmetic (talcum powder), as a lubricant, and as a filler in paper manufacture. Talc is used in baby powder, an astringent powder used for preventing rashes on the area covered by a diaper (see diaper rash). Most tailor's chalk is talc, as is the chalk often used for welding or metalworking.

Talc is also used as food additive or in pharmaceutical products. In medicine talc is used as a pleurodesis agent to prevent recurrent pneumothorax. In the European Union the additive number is E553b.

Talc is widely used in the ceramics industry in both bodies and glazes. In low-fire artware bodies it imparts whiteness and increases thermal expansion to resist crazing. In stonewares, small percentages of talc are used to flux the body and therefore improve strength and vitrification. It is a source of MgO flux in high temperature glazes (to control melting temperature). It is also employed as a matting agent in earthenware glazes and can be used to produce magnesia mattes at high temperatures.

ISO standard for quality (ISO 3262)

Type Talc content min. wt% Loss on ignition at 1000 °C, wt % Solubility in HCl, max. wt %
A 95 4 – 6.5 5
B 90 4 – 9 10
C 70 4 – 18 30
D 50 4 – 27 30

Patents are pending on the use of magnesium silicate as a cement substitute. Its production requirements are less energy-intensive than ordinary portland cement at around 650C, while it absorbs far more carbon dioxide as it hardens. This results in a negative carbon footprint overall, as the cement removes 0.6 tonnes of CO2 per tonne used. This contrasts with a carbon footprint of 0.4 tonne per tone of conventional cement.[3]

Safety

Several studies have established preliminary links between talc and pulmonary issues,[4] lung cancer,[5][6] skin cancer and ovarian cancer.[7] This is a major concern considering talc's widespread commercial and household use. In 1993, a US National Toxicology Program report found that cosmetic grade talc caused tumours in animals (animal testing), even though it contained no asbestos-like fibres.[5] Scientists have been aware of the toxicity of talc since the late 1960s, and in 1971 researchers found particles of talc embedded in 75 percent of the ovarian tumors studied.[8] However, the U.S. Food and Drug Administration (FDA) considers non-asbestiform talc, that is, talc which does not contain potentially carcinogenic asbestiform amphibole fibers, to be generally recognized as safe (GRAS) for use in cosmetics. [9]

See also

References

  1. ^ Ullmann’s Encyclopedia of Industrial Chemistry, 6th Edition, Talc
  2. ^ a b An Introduction to the Rock-Forming Minerals, second edition, by W.A. Deer, R.A. Howie, and J. Zussman, 1992, Prentice Hall, ISBN 0-582-30094-0.
  3. ^ Revealed: The cement that eats carbon dioxide Alok Jha, The Guardian.co.uk 31 December 2008
  4. ^ Hollinger (1990). "Pulmonary toxicity of inhaled and intravenous talc". {{cite journal}}: Cite journal requires |journal= (help)
  5. ^ a b National Toxicology Program (1993). "NTP Toxicology and Carcinogenesis Studies of Talc (Non-Asbestiform) in Rats and Mice (Inhalation Studies)". {{cite journal}}: Cite journal requires |journal= (help)
  6. ^ NIOSH Worker Notification Program. "Health effects of mining and milling talc". {{cite journal}}: Cite journal requires |journal= (help)(historical)
  7. ^ Harlow, Cramer, Bell; et al. (1992). "Perineal exposure to talc and ovarian cancer risk". {{cite journal}}: Cite journal requires |journal= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  8. ^ Henderson WJ, Joslin CA, Turnbull AC, Griffiths K (1971). "Talc and carcinoma of the ovary and cervix". J Obstet Gynaecol Br Commonw. 78 (3): 266–272.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. ^ CFSAN/Office of Food Additive Safety (2006). "Food Additive Status List". U.S. Food and Drug Administration. Retrieved December 2007. {{cite web}}: Check date values in: |accessdate= (help); Unknown parameter |month= ignored (help)