Английская Википедия:Huntite

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Шаблон:Short description Шаблон:Infobox mineral

Huntite is a carbonate mineral with the chemical formula Mg3Ca(CO3)4.[1] Huntite crystallizes in the trigonal system and typically occurs as platy crystals and powdery masses. For most of recorded history its main use was as a white pigment.[2][3] Today the most common industrial use of huntite is as a natural mixture with hydromagnesite as a flame retardant or fire retardant additive for polymers.

Discovery

In 1953 a paper by George Faust[4] announced the discovery of a new carbonate mineral found in Currant Creek, Nevada (US). Faust acknowledged that the mineral probably had been discovered previously, but it had been misidentified as impure magnesite by W. E. Ford in 1917. Faust named the new mineral "huntite" in honour of his former teacher, Walter Frederick Hunt (1882–1975),[5] Professor of Petrology at the University of Michigan.[6] Faust carried out analyses of the mineral, and found amongst others that in differential thermal analysis huntite showed two endothermic peaks, which could be attributed to the dissociation of MgCO3 and CaCO3 respectively. Chemical analyses showed huntite to consist of Mg3Ca(CO3)4.

Properties

Huntite often occurs in combination with other Mg/Ca carbonates such as dolomite, magnesite, and hydromagnesite. Large deposits of huntite occur in Turkey and Greece and these are commercially exploited because of its fire retardant properties. Huntite thermally decomposes over a temperature range of about 450–800 °C, releasing carbon dioxide and leaving a residue of magnesium and calcium oxides.[7][8][9]

Occurrences

Huntite has been found in a variety of environments. For example, it occurs in the modern carbonate sediments of the tidal flats bordering the Persian Gulf,[10] in seasonal salt lakes of Turkey,[11][12][13][14] in various playa lakes of British Columbia (Canada),[15] in lacustrine deposits of Greece[16] and in modern sabkha sediments in Tunisia.[17][18]

Caves seem to be well suited for the low-temperature formation of huntite. For example, it has been reported from the caves of the Carlsbad Caverns National Park, New Mexico (US);[19][20][21] in the Castleguard Cave (Alberta, Canada);[22] in the Grotte de Clamouse, France;[23][24] in various caves of the Transvaal Province of South Africa;[25] in Clearwater Cave, Mulu, Sarawak [26] in the Jenolan Caves, Australia;[27] and in the Castañar Cave near Cáceres, Spain.[28][29]

Syntheses

In 1962, huntite was first synthesized by Biedl and Preisinger in experiments conducted at 100 °C and 3.2 bar CO2 pressure.[30]

In 1983 Oomori et al. claimed laboratory synthesis of huntite at 33 °C when adding a sodium carbonate solution to concentrated sea water saturated with calcium bicarbonate.[31] In 2006, Zaitseva et al. noted the precipitation of huntite at room temperature and atmospheric pressure. In laboratory experiments originally intended to synthesize magnesium calcite, they had added cultures of Microcoleus chtonoplastes (cyanobacteria) to sea water brine. After 10 months of continuously shaking the samples they found huntite, magnesite, and aragonite.[32] In 2012, Hopkinson et al. synthesized the mineral at 52 °C by reacting magnesium calcite with nesquehonite (MgCO3·3H2O).[33]

Genesis

Huntite, dolomite and magnesite appear to be so very closely related, that a genetic relationship seems to be implied.[34] In a number of instances all three carbonates are found in close association; for example Faust (1953) described huntite occurring together with dolomite and magnesite (amongst other minerals); Carpenter (1961)[35] found huntite associated with aragonite, magnesium calcite and dolomite; Larrabee (1969)[36] reported on huntite together with (amongst many others) aragonite, calcite, dolomite and magnesite in serpentinite on a weathered dunite rock. A weathered basalt in Australia was found to contain huntite in association with magnesite (Cole & Lancucki, 1975[37]). Huntite together with magnesite was found by Calvo et al. (1995)[38] in lake sediments of Northern Greece. Huntite in combination with magnesite occurs in a weathered serpentinite near Hrubšice, Czech Republic according to Němec (1981)[39] According to the mineral and locations database of "mindat.org" huntite, together with aragonite, calcite, dolomite and magnesite can be found in the "U Pustého Mlýna" quarry near Hrubšice, Czech Republic.[40]

Industrial use

The most common industrial use of huntite is as a natural mixture with hydromagnesite as a flame retardant or fire retardant additive for polymers.[41][42][43] The heat of a fire will cause huntite to decompose releasing carbon dioxide into the flames. This helps to slow the spread of the fire. The release of carbon dioxide is endothermic, meaning that it takes in heat, this action helps to cool the burning material, again slowing the spread of the fire. These types of mixtures are used as alternatives to the more commonly used aluminium hydroxide.

Conite

A mineral with exactly the same composition as that of huntite has been known for more than 200 years; in 1812 for example, John[44] and Stromeyer[45] described it as having a chemical composition of CaCO3 : MgCO3 = 1 : 3. In those days the mineral was known as conite (in German: Konit); a name given to it by Retzius (1798).[46] However, a serious problem concerns the exact location where the mineral conite can be found. Originally Retzius had found the new carbonate in a mineral collection, and had recognized it as a new species because it was harder than any of the known carbonates (even so hard, that it would spark when struck with steel) but no indication was given as to the site where this conite had been found.[46] A number of papers describing conite are known, without the exact location where it can be found. In 1804, Ludwig stated that the sample of conite studied by him, came "from Iceland".[47] In 1805 Leonhard wrote that the conite he had analyzed, came "from Scandinavia".[48] Somewhat more exact was Stromeyer in 1812, who claimed that his sample of conite had been found near the village of Frankenhayn, on the eastern slope of the Hoher Meissner near Kassel, Germany. However, this conite had been found there as a loose boulder, and no outcrop of the new mineral was mentioned. In 1833 Blum summed up how conite could be found in mines near Freiberg (Germany), as boulders on the slopes of Mount Meissner (Germany) and on Iceland.[49] In 1849, Hirzel repeated that conite could be found on the eastern slope of Mount Meissner,[50] and in 1882 Schrauf reported the mineral from the magnesite deposits on the borders of the Schöninger Bach at Křemže near Budweis, Czech Republic.[51] Because of the absence of a type locality for the mineral conite, a historical priority of its description over that of huntite cannot be claimed.

References

Шаблон:Reflist

Партнерские ресурсы
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  1. ↑ Ошибка цитирования Неверный тег <ref>; для сносок Webmin не указан текст
  2. ↑ John Clarke, "Two Aboriginal Rock Art Pigments from Western Australia: Their Properties, Use, and Durability." Studies in Conservation, Volume 21, Issue 3 (1976) pp. 134–142 https://doi.org/10.1179/sic.1976.023
  3. ↑ Richard Parkinson, The Painted Tomb-Chapel of Nebamun: Masterpiece of Ancient Egyptian Art in the British Museum (The British Museum Press: London, 2008) page 50
  4. ↑ Шаблон:Cite journal[1]
  5. ↑ Kraus, E.H., American Mineralogist, v. 38, Jan–Feb, 1953
  6. ↑ Шаблон:Cite journal
  7. ↑ Шаблон:Cite journal
  8. ↑ Шаблон:Cite journal
  9. ↑ Шаблон:Cite journal
  10. ↑ Kinsman, D. J. J. (1967): Huntite from a carbonate – evaporite environment. American Mineralogist, vol. 52, pp. 1332–1340. [2]
  11. ↑ Irion, G. & Müller, G. (1968): Huntite, dolomite, magnesite and polyhalite of Recent age from Tuz Gölü, Turkey. Nature, vol. 220, pp. 1309–1310.
  12. ↑ Irion, G. (1970): Mineralogisch-sedimentpetrographische und geochemische Untersuchungen am Tuz Gölü (Salzsee). Chemie der Erde, vol.29, pp. 163–226.
  13. ↑ Camur, M. Z. & Mutlu, H. (1996): Major-ion geochemistry and mineralogy of the Salt-Lake (Tuz Gölü) basin, Turkey. Chemical Geology, vol.127, pp. 313–329.
  14. ↑ Mutlu, H.; Kadir, S. & Akbulut, A. (1999): Mineralogy and water chemistry of the Lake Acigöl, Denizli, Turkey. Carbonates and Evaporites, vol. 14, pp. 191–199.
  15. ↑ Renaut, R. W. (1990): Recent carbonate sedimentation and brine evolution in the saline lake basins of the Cariboo Plateau, British Columbia, Canada. pp. 67–81, in: Comin, F. A. & Northcote, T. G. (eds.): Saline Lakes. Kluwer, Dordrecht.
  16. ↑ Wetzenstein, W. (1974): Sedimentpetrographische Untersuchungen an limnischen Magnesit – Huntitlagerstätten im Plio-Pleistozän des Serviabeckens / Nordgriechenland. Neues Jahrbuch für Geologie und Paläontologie, Monatshefte, 1974, pp. 625–642.
  17. ↑ Perthuisot, J. P. (1971): Présence de magnésite et de huntite dans le sebkha el Melah de Zarzis. Comptes Rendus des Séances de l'Académie des Sciences de Paris, Série D, vol. 272, pp. 185–188. [3]
  18. ↑ Perthuisot, J. P. (1974): Les dépôts salins de la sebkha El Melah de Zarzis: Conditions et modalités de la sédimentation évaporitique. Revue de la geographie physique et de géologie dynamique, vol. 16, pp. 177–187.
  19. ↑ Thrailkill, J. (1971): Carbonate deposition in Carlsbad caverns. Journal of Geology, vol. 79, pp. 683–695.
  20. ↑ Hill, C. A. (1973): Huntite flowstone in Carlsbad Caverns, New Mexico. Science, vol. 181, pp. 158–159.
  21. ↑ Gonzalez, L. A. & Lohmann, K. C. (1988): Controls on mineralogy and composition of spelean carbonates: Carlsbad Caverns, New Mexico. pp. 81–101, in: James, N. P. & Choquette, P. W. (eds.): Paleokarst. Springer, New York, 416 p.
  22. ↑ Harmon, R. S.; Atkinson, T. C. & Atkinson, J. L. (1983): The Mineralogy of Castleguard Cave, Columbia Icefields, Alberta, Canada]. Arctic and Alpine Research, vol. 15, pp. 503–522.
  23. ↑ Baron, G.; Caillère, S.; Lagrange, R. & Pobeguin, T. (1957): Sur la présence de huntite dans une grotte de l'Hérault (la Clamouse). Comptes Rendus hebdomadaires des séances de l'Académie des Sciences (Paris), vol. 245, pp. 92–94. [4]
  24. ↑ Fischbeck, R. (1976): Mineralogie und Geochemie carbonatischer Ablagerungen in europäischen Höhlen – ein Beitrag zur Bildung und Diagenese von Speleothemen. Neues Jahrbuch für Mineralogie, Abhandlungen, vol. 126, pp. 269–291.
  25. ↑ Martini, J. & Kavalieris, I. (1978): Mineralogy of the Transvaal caves. Transactions of the Geological Society of South Africa, vol. 81, pp. 47–54.
  26. ↑ Laverty, M. (1982): Cave Minerals in the Gunung Mulu National Park, Sarawak. Cave Science 9(2), p. 130
  27. ↑ Pogson, R. E.; Osborne, R. E. & Colchester, D. M. (2001): Minerals of the Jenolan Caves – geosphere meets biosphere. Journal and Proceedings of the Royal Society of New South Wales, vol. 134, p. 111. [5]
  28. ↑ Alonso-Zarza, A. M.; Martín-Pérez, A.; Gil-Peña, I.; Martínez-Flores, E. & Muñoz-Barco, P. (2005): Formacíon de dolomita y huntita en depósitos de moon-milk en la Cueva de Castañar de Ibo (Cáceras). Geogaceta, July 2005, no. 38, pp. 247–250. [6]
  29. ↑ Alonso-Zarza, A. M. & Martín-Pérez, A. (2008): Dolomite in caves: Recent dolomite formation in oxic, non-sulfate environments, Castañar Cave, Spain. Sedimentary Geology, vol. 205, pp. 160–164.
  30. ↑ Biedl, A. & Preisinger, A. (1962): Synthese von Huntit, Mg3Ca(CO3)4. Anzeiger der mathematisch-naturwissenschaftliche Klasse, Österreichische Akademie der Wissenschaften (Wien), 1962, No.10, pp.148–149.
  31. ↑ Oomori, T.; Kaneshima, K.; Taira, T. & Kitano, Y. (1983): Synthetic studies of protodolomite from brine waters. Geochemical Journal, vol.17, pp.147–152.
  32. ↑ Zaitseva, L. V.; Orleanskii, V. K.; Gerasimenko, M. & Ushatinskaya, G. T. (2006): The role of cyanobacteria in crystallization of magnesium calcites. Paleontological Journal, vol.40, pp.125–133.
  33. ↑ Hopkinson, L.; Kristova, P.; Rutt, K. & Cressey, G. (2012): Phase transitions in the system MgO – CO2 – H2O during CO2 degassing of Mg-bearing solutions. Geochimica et Cosmochimica Acta, vol.76, pp.1–13.
  34. ↑ Müller, G.; Irion, G. & Förstner, U. (1972): Formation and diagenesis of inorganic Ca-Mg carbonates in the lacustrine environment. Die Naturwissenschaften, vol.59, pp.158–164.
  35. ↑ Carpenter, A. B. (1961): Mineral assemblage magnesium calcite – aragonite – huntite at Crestmore, California. Geological Society of America, Abstracts for 1961, p.146.
  36. ↑ Larrabee, D. M. (1969) Serpentinite and rodingite in the Hunting Hill Quarry, Montgomery County, Maryland. U.S. Geological Survey Bulletin, no.1283, 34 p. [7]
  37. ↑ Cole, W. F. & Lancucki, C. J. (1975): Huntite, from Deer Park, Victoria, Australia. American Mineralogist, vol.60, pp.1130–1131. [8]
  38. ↑ Calvo, J. P.; Stamatakis, M. G. & Magganas, A. C. (1955): Clastic huntite in Upper Neogene formations of the Kozani Basin, Macedonia, Northern Greece. Journal of Sedimentary Research, vol.A65, pp.627–632.
  39. ↑ Němec, D. (1981): Huntit ze serpentinitové oblasti u Hrubšic na západni Moravě (Huntite from the serpentinite area at Hrubšice, Western Moravia – English summary). Časopis pro mineralogii a geologii, vol.26, pp.75–78.
  40. ↑ Ошибка цитирования Неверный тег <ref>; для сносок Mindat не указан текст
  41. ↑ Шаблон:Cite journal
  42. ↑ Шаблон:Cite journal
  43. ↑ Шаблон:Cite journal
  44. ↑ John, D. (1812): Chemische Analyse des Conits aus der Gegend des Meisseners. Journal für Chemie und Physik, vol.5, pp.13–18. [9]
  45. ↑ Stromeyer, F. (1812): Analyse des sogenannten Konits vom Meissner. Annalen der Physik, vol.41, pp.336–338. [10]
  46. ↑ 46,0 46,1 Retzius, A. J. (1798): Versuch einer Aufstellung des Mineralreiches. S. L. Crusius, Leipzig, 376 p.
  47. ↑ Ludwig, C. F. (1804): Handbuch der Mineralogie nach A. G. Werner. S. L. Crusius, Leipzig, Theil 2 = 226 p. [11]
  48. ↑ Leonhard, C. C. (1805): Handbuch einer allgemeinen topographischen Mineralogie. J. C. Hermann,Frankfurt, vol.1 = 479 p. [12]
  49. ↑ Blum, J. R. (1833): Lehrbuch der Oryktognosie. Schweizerbart, Stuttgart, 509 p. [13]
  50. ↑ Hirzel, H. (1849): Analyse des Konits von Frankenheyn am östlichen Abhange des Meissners. Archiv der Pharmacie, vol.109, pp.154–156.
  51. ↑ Schrauf, A. (1882): Beiträge zur Kenntnis des Associationskreises des Magnesiasilicate. Zeitschrift für Krystallographie und Mineralogie, vol.6, pp.321–388.
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