Goethite: Difference between revisions
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== Usage == |
== Usage == |
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Its main modern use is as an [[iron ore]], being referred to as ''brown iron ore''.<ref name=Mindat/> |
Its main modern use is as an [[iron ore]], being referred to as ''brown iron ore''.<ref name=Mindat/> Goethite is an important component of [[ochre]] pigments,<ref>{{cite journal |last1=Hradil |first1=David |last2=Grygar |first2=Tomáš |last3=Hradilová |first3=Janka |last4=Bezdička |first4=Petr |title=Clay and iron oxide pigments in the history of painting |journal=Applied Clay Science |date=April 2003 |volume=22 |issue=5 |pages=223–236 |doi=10.1016/S0169-1317(03)00076-0}}</ref> and has been heat-treated for use as a red pigment since [[Paleolithic]] times.<ref>{{cite journal |last1=Cavallo |first1=G. |last2=Fontana |first2=F. |last3=Gialanella |first3=S. |last4=Gonzato |first4=F. |last5=Riccardi |first5=M. P. |last6=Zorzin |first6=R. |last7=Peresani |first7=M. |title=Heat Treatment of Mineral Pigment During the Upper Palaeolithic in North-East Italy: Heat treatment of mineral pigment during the Upper Palaeolithic |journal=Archaeometry |date=October 2018 |volume=60 |issue=5 |pages=1045–1061 |doi=10.1111/arcm.12360}}</ref> Iron-rich [[laterite|lateritic]] soils that have developed over [[serpentinite]] rocks in tropical climates are mined for their iron content, as well as other metals. |
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Fine goethite specimens are rare and therefore are valued collectibles. Banded or iridescent varieties are cut and polished into [[cabochons]] for jewelry making. |
Fine goethite specimens are rare and therefore are valued collectibles. Banded or iridescent varieties are cut and polished into [[cabochons]] for jewelry making. |
Revision as of 23:09, 8 April 2022
Goethite | |
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General | |
Category | oxide minerals hydroxide subgroup |
Formula (repeating unit) | α-FeO(OH) |
IMA symbol | Gth[1] |
Strunz classification | 4.FD.10 |
Crystal system | Orthorhombic |
Crystal class | Dipyramidal (mmm) H-M symbol: (2/m 2/m 2/m) |
Space group | Pbnm |
Identification | |
Color | Yellowish to reddish to dark brown or black |
Crystal habit | radial acicular, mammillary, botryoidal, stalactitic, massive, as encrustation, as pseudomorph; may be banded or iridescent |
Cleavage | Perfect {010} |
Fracture | Uneven to splintery |
Mohs scale hardness | 5 - 5.5 |
Luster | Adamantine to dull |
Streak | Brown, brownish yellow to orange yellow |
Specific gravity | 3.3 - 4.3 |
Refractive index | Opaque to sub-translucent |
Fusibility | Fusible at 5 - 5.5 |
Solubility | HCl soluble |
Other characteristics | weakly magnetic |
References | [2][3][4][5] |
Goethite (/ˈɡɜːrtaɪt/,[6][7] US also /ˈɡoʊθaɪt/[8][9]) is a mineral of the diaspore group, consisting of iron(III) oxide-hydroxide, specifically the "α" polymorph. It is found in soil and other low-temperature environments such as sediment. Goethite has been well known since ancient times for its use as a pigment (brown ochre). Evidence has been found of its use in paint pigment samples taken from the caves of Lascaux in France. It was first described in 1806 based on samples found in the Hollertszug Mine in Herdorf, Germany.[4] The mineral was named after the German polymath and poet Johann Wolfgang von Goethe (1749–1832).
Composition
Goethite is an iron oxyhydroxide containing ferric iron. It is the main component of rust and bog iron ore. Goethite's hardness ranges from 5.0 to 5.5 on the Mohs Scale, and its specific gravity varies from 3.3 to 4.3. The mineral forms prismatic needle-like crystals ("needle ironstone"[3]) but is more typically massive.[2]
Feroxyhyte and lepidocrocite are both polymorphs of the iron oxyhydroxide FeO(OH) which are stable at the pressure and temperature conditions of the Earth's surface. Although they have the same chemical formula as goethite, their different crystalline structures make them distinct minerals.[5]
Additionally, goethite has several high-pressure and high-temperature polymorphs, which may be relevant to the conditions of the Earth's interior. These include ε-FeOOH, which has an orthorhombic crystal structure,[10] a cubic pyrite-type polymorph with[11] or without losing hydrogen[12] and an ultradense hexagonal structure.[13]
Formation
Goethite often forms through the weathering of other iron-rich minerals, and thus is a common component of soils, concentrated in laterite soils. nanoparticulate authigenic goethite is a common diagenetic iron oxyhydroxide in both marine and lake sediments.[14] The formation of goethite is marked by the oxidation state change of Fe2+ (ferrous) to Fe3+ (ferric), which allows for goethite to exist at surface conditions. Because of this oxidation state change, goethite is commonly seen as a pseudomorph. As iron-bearing minerals are brought to the zone of oxidation within the soil, the iron turns from iron(II) to iron(III), while the original shape of the parent mineral is retained. Examples of common goethite pseudomorphs are: goethites after pyrite, goethite, siderite, and marcasite, though any iron(II)-bearing mineral could become a goethite pseudomorph if proper conditions are met. It may also be precipitated by groundwater or in other sedimentary conditions, or form as a primary mineral in hydrothermal deposits. Goethite has also been found to be produced by the excretion processes of certain bacteria types.[15]
Distribution
Goethite is found all over the planet, usually in the form of concretions, stalactitic formations, oolites (a form consisting of tiny round grains cemented together),[4] reniform (kidney shapes) or botryoidal (globular, like bunches of grapes) accumulations. It is also a very common pseudomorph. It is frequently encountered in the swampy areas at the head of spring waters ('bog iron'), on cave floors, and on the bottom of lakes and small creeks. The boxworks or gossan resulting from the oxidation of sulfide ore deposits is formed of goethite along with other iron oxides and quartz.[16][2]
Significant deposits of goethite are found in England; Cuba; and Minnesota, Missouri, Colorado, Alabama, Georgia, Virginia, and Tennessee, in the United States.[16][2]
Deposits significant in location, if not in abundance, have been found in the Martian crater Gusev by NASA's Spirit rover, providing strong evidence for the presence of liquid water on the planet in an earlier stage of its evolution.[17]
Limpets' teeth are composed of about 80% goethite fibres of only tens of nanometers in diameter, small enough to be flaw-insensitive, which accounts for their extreme tensile strength of 3.5–6.0 GPa and elastic modulus of 120±30 GPa.[18] [19]
Usage
Its main modern use is as an iron ore, being referred to as brown iron ore.[4] Goethite is an important component of ochre pigments,[20] and has been heat-treated for use as a red pigment since Paleolithic times.[21] Iron-rich lateritic soils that have developed over serpentinite rocks in tropical climates are mined for their iron content, as well as other metals.
Fine goethite specimens are rare and therefore are valued collectibles. Banded or iridescent varieties are cut and polished into cabochons for jewelry making.
Perhaps the oldest known use of goethite comes from the ancient kingdom of Phrygia. In a royal tomb a body was found believed to be King Gordias, father of the legendary King Midas. The burial shroud had been colored with a dye containing goethite, which in its original unfaded state would have made the shroud look like it was woven from gold. Historians speculate that the legend of King Midas' golden touch might have originated from Phrygian royalty wearing clothes made from such golden-colored textiles.[22]
Gallery
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Iridescent goethite, Filón Sur Mine, Tharsis, Huelva, Spain
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Goethite from Minas Gerais, Brazil
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A sharp, disc-shaped calcite has here been completely replaced by goethite, which preserved the original form perfectly
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Goethite coating/replacing rusted pyrite cubes
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Finely crystallized specimen of goethite from Lake George, Park County, Colorado, USA
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Goethite from Negaunee, Marquette County, Michigan
See also
References
- ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
- ^ a b c d Hurlbut, Cornelius S.; Klein, Cornelis (1985). Manual of Mineralogy (20th ed.). Wiley. ISBN 0-471-80580-7.
- ^ a b Barthelmy, David (2012). "Goethite Mineral Data". Mineralogy Database. Retrieved 8 April 2022.
- ^ a b c d "Goethite". Mindat.org.
- ^ a b Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (2005). "Goethite" (PDF). Handbook of Mineralogy. Mineral Data Publishing. Retrieved 14 March 2022.
- ^ "goethite". Lexico UK English Dictionary. Oxford University Press. n.d.
- ^ "goethite". Merriam-Webster.com Dictionary. Merriam-Webster.
- ^ "goethite". Dictionary.com Unabridged (Online). n.d.
- ^ "goethite". The American Heritage Dictionary of the English Language (5th ed.). HarperCollins.
- ^ Suzuki, Akio (2010). "High-pressure X-ray diffraction study of ε-FeOOH". Physics and Chemistry of Minerals. 37 (3): 153–157. Bibcode:2010PCM....37..153S. doi:10.1007/s00269-009-0319-x. S2CID 92941002.
- ^ Hu, Qingyang; Kim, Duckyoung; Yang, Wenge; Liuxiang, Yang; Yue, Meng; Zhang, Li; Mao, Ho-kwang (2016). "FeO2 and FeOOH under deep lower-mantle conditions and Earth's oxygen–hydrogen cycles". Nature. 534 (7606): 241–244. Bibcode:2016Natur.534..241H. doi:10.1038/nature18018. PMID 27279220.
- ^ Nishi, Masayuki; Kuwayama, Yasuhiro; Tsuchiya, Jun; Tsuchiya, Taku (2017). "The pyrite-type high-pressure form of ε-FeOOH". Nature. 547 (7662): 205–208. Bibcode:2017Natur.547..205N. doi:10.1038/nature22823. PMID 28678774. S2CID 205257075.
- ^ Zhang, Li; Yuan, Hongsheng; Meng, Yue; Mao, Ho-kwang (2017). "Discovery of a hexagonal ultradense hydrous phase in (Fe,Al)OOH". Proceedings of the National Academy of Sciences of the United States of America. 547 (12): 205–208. doi:10.1073/pnas.1720510115. PMC 5866593. PMID 29507221.
- ^ Van Der Zee, Claar; Roberts, Darryl R.; Rancourt, Denis G.; Slomp, Caroline P. (2003). "Nanogoethite is the dominant reactive oxyhydroxide phase in lake and marine sediments". Geology. 31 (11): 993. Bibcode:2003Geo....31..993V. doi:10.1130/G19924.1. hdl:1874/31393.
- ^ Larese-Casanova, Philip; Haderlein, Stefan B.; Kappler, Andreas (2010). "Biomineralization of lepidocrocite and goethite by nitrate-reducing Fe(II)-oxidizing bacteria: Effect of pH, bicarbonate, phosphate, and humic acids". Geochimica et Cosmochimica Acta. 74 (13): 3721–34. Bibcode:2010GeCoA..74.3721L. doi:10.1016/j.gca.2010.03.037.
- ^ a b Sinkankas, John (1964). Mineralogy for amateurs. Princeton, N.J.: Van Nostrand. pp. 342–344. ISBN 0442276249.
- ^ Klingelhöfer, G.; DeGrave, E.; Morris, R. V.; Van Alboom, A.; de Resende, V. G.; De Souza, P. A.; Rodionov, D.; Schröder, C.; Ming, D. W.; Yen, A. (November 2005). "Mössbauer spectroscopy on Mars: goethite in the Columbia Hills at Gusev crater". Hyperfine Interactions. 166 (1–4): 549–554. doi:10.1007/s10751-006-9329-y.
- ^ Webb, Jonathan (18 February 2015). "Limpet teeth set new strength record". BBC News: Science and Environment. BBC News. Retrieved 23 December 2016.
- ^ Barber, Asa H.; Lu, Dun; Pugno, Nicola M. (2015-04-06). "Extreme strength observed in limpet teeth". J. R. Soc. Interface. 12 (105). Royal Society. 20141326. doi:10.1098/rsif.2014.1326. PMC 4387522. PMID 25694539.
- ^ Hradil, David; Grygar, Tomáš; Hradilová, Janka; Bezdička, Petr (April 2003). "Clay and iron oxide pigments in the history of painting". Applied Clay Science. 22 (5): 223–236. doi:10.1016/S0169-1317(03)00076-0.
- ^ Cavallo, G.; Fontana, F.; Gialanella, S.; Gonzato, F.; Riccardi, M. P.; Zorzin, R.; Peresani, M. (October 2018). "Heat Treatment of Mineral Pigment During the Upper Palaeolithic in North-East Italy: Heat treatment of mineral pigment during the Upper Palaeolithic". Archaeometry. 60 (5): 1045–1061. doi:10.1111/arcm.12360.
- ^ Archived at Ghostarchive and the Wayback Machine: Rose, Brian. "Great Myths and Legends: The Golden Age of King Midas". Penn Museum. Retrieved 27 August 2016.
External links
- Spencer, Leonard James (1911). . Encyclopædia Britannica (11th ed.).