Langite

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Langite
Langite-120989.jpg
Langite from Podlipa and Reinera Mines, Slovakia
General
CategoryCopper minerals
Formula
(repeating unit)
Cu4(SO4)(OH)6·2H2O
IMA symbol Lgt [1]
Strunz classification 7.DD.10
Dana classification31.4.3.1
Crystal system Monoclinic
Crystal class Domatic (m)
(same H-M symbol)
Space group Pc
Unit cell a = 7.118, b = 6.031
c = 11.209 [Å]
β = 90.00–90.02°; Z = 2
Identification
Formula mass 488.32 g/mol
ColorGreenish blue, sky-blue to bluish green
Crystal habit Crystals scaly, or as crusts; earthy
Twinning Common on {110}, typically repeated
Cleavage {001} perfect, {010} distinct
Fracture Uneven
Mohs scale hardness2.5 to 3
Luster Vitreous, crusts silky
Streak Blue green
Diaphaneity Translucent
Specific gravity 3.28 [2] 3.48 to 3.5 [3] 3.5 [4] 2.28 to 3.34 [5]
Optical propertiesBiaxial (−) r>v weak
Refractive index nα = 1.708 nβ = 1.760 nγ = 1.798 [3]
Birefringence δ = 0.090
Pleochroism X = c = light yellowish green
Y = b = blue-green
Z = a = sky blue
Solubility Insoluble in water, easily soluble in dilute acids or NH4OH
Other characteristicsMay be altered to brochantite. Not radioactive
References [3] [2] [4] [5]

Langite is a rare hydrated copper sulfate mineral, with hydroxyl, found almost exclusively in druses of small crystals. It is formed from the oxidation of copper sulfides, and was first described in specimens from Cornwall, United Kingdom. It is dimorphous with wroewolfeite. Langite was discovered in 1864 and named after the physicist and crystallographer Viktor von Lang (1838–1921), who was Professor of Physics at the University of Vienna, Austria. [3]

Contents

Unit cell

Langite belongs to the monoclinic crystal class m, meaning that it has just one mirror plane, and no axes of rotational symmetry. The crystal is built up of identical unit cells stacked together, with no space in between. The unit cell for the monoclinic system has a base which is a rhombus, with sides a and c inclined at angle β. The third side b is perpendicular to both a and c. For langite the angle β is very close to 90°, so the unit cell is almost brick-shaped (as for the orthorhombic system). Different sources give slightly different values for the unit cell parameters, but they all fall within the ranges a = 7.118 Å to 7.137 Å, b = 6.031 Å to 6.034 Å, c = 11.209 Å to 11.217 Å, β = 90.00 to 90.02°, Z (the number of formula units per unit cell) = 2. [3] [2] [4] [5]

Physical properties

Langite usually occurs as druses of small greenish-blue crystals which may be scaly or earthy. It is translucent, with a vitreous to silky luster and a blue-green streak. It has perfect cleavage perpendicular to the c crystal axis, and distinct cleavage perpendicular to b. Twinning is common, and typically repeated to give snowflake or star shaped groupings. [3] [5] The mineral is soft, with hardness 2.5 to 3, a little less than that of calcite. Fracture is uneven, and specific gravity is in the range 3.28 to 3.50, [3] [2] [4] [5] a little less than that of diamond.

Optical properties

Langite is biaxial (−). Since it is monoclinic, it has three different refractive indices, corresponding to the three crystallographic directions. All the refractive indices are in the range 1.64 to 1.80, which is comparatively large, almost as high as garnet. Different sources give these values:

Nx = 1.641, Ny = 1.690, Nz = 1.712 [2]
Nx = 1.708, Ny = 1.760, Nz = 1.798 [3] [4]
Nx = 1.641 to 1.654, Ny = 1.690 to 1.713, Nz = 1.705 to 1.722 [5]
Nx = 1.641, Ny = 1.690, Nz = 1.705 to 1.712 [6]

The mineral is pleochroic, with X light yellowish green, Y blue-green and Z sky blue. [3]

Occurrence

Langite is an uncommon but widespread secondary mineral in the oxidised zone of copper sulfide deposits, which may be of post-mine formation. It is associated with wroewolfeite, posnjakite, serpierite, devilline, chalcophyllite, connellite, brochantite, malachite and gypsum. [5]

There are two type localities for langite, Fowey Consols, Tywardreath, Par Area, St Austell District, and St Just, St Just District, both in Cornwall, England. The type material is conserved at the Natural History Museum, Vienna, Austria, reference A.a.4353.

Other reported occurrences include:

Related Research Articles

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<span class="mw-page-title-main">Ajoite</span>

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<span class="mw-page-title-main">Botallackite</span> Halide mineral

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<span class="mw-page-title-main">Chalcophyllite</span>

Chalcophyllite is a rare secondary copper arsenate mineral occurring in the oxidized zones of some arsenic-bearing copper deposits. It was first described from material collected in Germany. At one time chalcophyllite from Wheal Tamar in Cornwall, England, was called tamarite, but this name is now discredited. At Wheal Gorland a specimen exhibiting partial replacement of liriconite, Cu
2
Al(AsO
4
)(OH)
4
·(4H
2
O)
, by chalcophyllite has been found. The mineral is named from the Greek, chalco "copper" and fyllon, "leaf", in allusion to its composition and platy structure. It is a classic Cornish mineral that can be confused with tabular spangolite.

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<span class="mw-page-title-main">Tsumebite</span>

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<span class="mw-page-title-main">Tsumcorite</span>

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<span class="mw-page-title-main">Tuperssuatsiaite</span>

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<span class="mw-page-title-main">Ianbruceite</span>

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<span class="mw-page-title-main">Brianyoungite</span>

Brianyoungite is a secondary zinc carbonate mineral. The Commission on New Minerals, Nomenclature and Classification (CNMNC) of the International Mineralogical Association (IMA) classifies it as a carbonate with the formula Zn3(CO3)(OH)4, but sulfate groups SO4 also occupy the carbonate CO3 positions, in the ratio of about one sulfate to three carbonates, so other sources give the formula as Zn3(CO3,SO4)(OH)4, and Gaines et al. classify the mineral as a compound carbonate. It is similar in appearance to hydrozincite, another zinc carbonate. It was discovered in 1991 and designated IMA1991-053. In 1993 it was named "brianyoungite" after Brian Young (born 1947), a field geologist with the British Geological Survey, who provided the first specimens.

<span class="mw-page-title-main">Köttigite</span>

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<span class="mw-page-title-main">Serpierite</span>

Serpierite (Ca(Cu,Zn)4(SO4)2(OH)6·3H2O) is a rare, sky-blue coloured hydrated sulfate mineral, often found as a post-mining product. It is a member of the devilline group, which has members aldridgeite (Cd,Ca)(Cu,Zn)4(SO4)2(OH)6·3H2O, campigliaite Cu4Mn2+(SO4)2(OH)6·4H2O, devilline CaCu4(SO4)2(OH)6·3H2O, kobyashevite Cu5(SO4)2(OH)6·4H2O, lautenthalite PbCu4(SO4)2(OH)6·3H2O and an unnamed dimorph of devilline. It is the calcium analogue of aldridgeite and it is dimorphous with orthoserpierite CaCu4(SO4)2(OH)6·3H2O.

<span class="mw-page-title-main">Posnjakite</span>

Posnjakite is a hydrated copper sulfate mineral. It was discovered in the Tungsten deposit of Nura-Taldy in Karaganda Region in Kazakhstan and described in 1967 by Aleksandr Ivanovich Komkov (1926–1987) and Yevgenii Ivanovich Nefedov (1910–1976) and named after geochemist Eugene Valdemar Posnjak (1888–1949).

<span class="mw-page-title-main">Mottramite</span>

Mottramite is an orthorhombic anhydrous vanadate hydroxide mineral, PbCu(VO4)(OH), at the copper end of the descloizite subgroup. It was formerly called cuprodescloizite or psittacinite (this mineral characterized in 1868 by Frederick Augustus Genth). Duhamelite is a calcium- and bismuth-bearing variety of mottramite, typically with acicular habit.

Ophirite is a tungstate mineral first discovered in the Ophir Hill Consolidated mine at Ophir district, Oquirrh Mountains, Tooele County, Utah, United States of America. It was found underground near a calcite cave in one veinlet, six centimeters wide by one meter long, surrounded by different sulfides. Before the closing of the mine in 1972, it was dominated by sulfide minerals, and the Ophir district was known for being a source of zinc, copper, silver, and lead ores. The crystals are formed as tablets. It is the first known mineral to contain a heteropolyanion, a lacunary defect derivative of the Keggin anion. The chemical formula of ophirite is Ca2Mg4[Zn2Mn3+2(H2O)2(Fe3+W9O34)2] · 46•H2O. The mineral has been approved by the Commission on New Minerals and Mineral Names, IMA, to be named ophirite for its type locality, the Ophir Consolidated mine.

References

  1. 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.
  2. 1 2 3 4 5 Gaines et al (1997) Dana’s New Mineralogy Eighth Edition, Wiley
  3. 1 2 3 4 5 6 7 8 9 Mindat.org
  4. 1 2 3 4 5 Webmineral data
  5. 1 2 3 4 5 6 7 Handbook of Mineralogy
  6. American Mineralogist (1964) 49:1143
  7. Australian Journal of Mineralogy (2004) 10-1:3
  8. Australian Journal of Mineralogy (1997) 3-1:43
  9. The Mineralogical Record (2004) 35-4:357
  10. Mines & Minerals (2005)25:6
  11. Rocks & Minerals (2009) 84-4:321