Langite | |
---|---|
General | |
Category | Copper minerals |
Formula (repeating unit) | Cu4(SO4)(OH)6·2H2O |
IMA symbol | Lgt [1] |
Strunz classification | 7.DD.10 |
Dana classification | 31.4.3.1 |
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 |
Color | Greenish 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 hardness | 2.5 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 properties | Biaxial (−) 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 characteristics | May 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]
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]
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.
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:
The mineral is pleochroic, with X light yellowish green, Y blue-green and Z sky blue. [3]
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:
Stilbite is the name of a series of tectosilicate minerals of the zeolite group. Prior to 1997, stilbite was recognized as a mineral species, but a reclassification in 1997 by the International Mineralogical Association changed it to a series name, with the mineral species being named:
Scolecite is a tectosilicate mineral belonging to the zeolite group; it is a hydrated calcium silicate, CaAl2Si3O10·3H2O. Only minor amounts of sodium and traces of potassium substitute for calcium. There is an absence of barium, strontium, iron and magnesium. Scolecite is isostructural (having the same structure) with the sodium-calcium zeolite mesolite and the sodium zeolite natrolite, but it does not form a continuous chemical series with either of them. It was described in 1813, and named from the Greek word, σκώληξ (sko-lecks) = "worm" because of its reaction to the blowpipe flame.
Ajoite is a hydrated sodium potassium copper aluminium silicate hydroxide mineral. Ajoite has the chemical formula (Na,K)Cu7AlSi9O24(OH)6·3H2O, and minor Mn, Fe and Ca are usually also present in the structure. Ajoite is used as a minor ore of copper.
Djurleite is a copper sulfide mineral of secondary origin with formula Cu31S16 that crystallizes with monoclinic-prismatic symmetry. It is typically massive in form, but does at times develop thin tabular to prismatic crystals. It occurs with other supergene minerals such as chalcocite, covellite and digenite in the enriched zone of copper orebodies. It is a member of the chalcocite group, and very similar to chalcocite, Cu2S, in its composition and properties, but the two minerals can be distinguished from each other by x-ray powder diffraction. Intergrowths and transformations between djurleite, digenite and chalcocite are common. Many of the reported associations of digenite and djurleite, however, identified by powder diffraction, could be anilite and djurleite, as anilite transforms to digenite during grinding.
Kutnohorite is a rare calcium manganese carbonate mineral with magnesium and iron that is a member of the dolomite group. It forms a series with dolomite, and with ankerite. The end member formula is CaMn2+(CO3)2, but Mg2+ and Fe2+ commonly substitute for Mn2+, with the manganese content varying from 38% to 84%, so the formula Ca(Mn2+,Mg,Fe2+)(CO3)2 better represents the species. It was named by Professor Bukowsky in 1901 after the type locality of Kutná Hora, Bohemia, in the Czech Republic. It was originally spelt "kutnahorite" but "kutnohorite" is the current IMA-approved spelling.
Botallackite, chemical formula Cu2(OH)3Cl is a secondary copper mineral, named for its type locality at the Botallack Mine, St Just in Penwith, Cornwall. It is polymorphous with atacamite, paratacamite and clinoatacamite.
Yuksporite is a rare inosilicate mineral with double width, unbranched chains, and the complicated chemical formula K4(Ca,Na)14Sr2Mn(Ti,Nb)4(O,OH)4(Si6O17)2(Si2O7)3(H2O,OH)3. It contains the relatively rare elements strontium, titanium and niobium, as well as the commoner metallic elements potassium, calcium, sodium and manganese. As with all silicates, it contains groups of linked silicon and oxygen atoms, as well as some associated water molecules.
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
2Al(AsO
4)(OH)
4·(4H
2O), 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.
Lavendulan is an uncommon arsenate mineral in the lavendulan group. It is known for its characteristic intense electric blue colour. Lavendulan is very similar to Lemanskiite, the analogue trihydrate mineral, to the point of them being considered dimorphs. Lemanskiite is tetragonal, but lavendulan is monoclinic. Lavendulan has the same structure as sampleite, and the two minerals form a series. It is the calcium analogue of zdenĕkite and the arsenate analogue of sampleite.
Tsumebite is a rare phosphate mineral named in 1912 after the locality where it was first found, the Tsumeb mine in Namibia, well known to mineral collectors for the wide range of minerals found there. Tsumebite is a compound phosphate and sulfate of lead and copper, with hydroxyl, formula Pb2Cu(PO4)(SO4)(OH). There is a similar mineral called arsentsumebite, where the phosphate group PO4 is replaced by the arsenate group AsO4, giving the formula Pb2Cu(AsO4)(SO4)(OH). Both minerals are members of the brackebuschite group.
Mendipite is a rare mineral that was named for the locality where it is found, the Mendip Hills in Somerset, England. It is an oxyhalide of lead with formula Pb3Cl2O2.
Vlasovite is a rare inosilicate (chain silicate) mineral with sodium and zirconium, with the chemical formula Na2ZrSi4O11. It was discovered in 1961 at Vavnbed Mountain in the Lovozero Massif, in the Northern Region of Russia. The researchers who first identified it, R P Tikhonenkova and M E Kazakova, named it for Kuzma Aleksevich Vlasov (1905–1964), a Russian mineralogist and geochemist who studied the Lovozero massif, and who was the founder of the Institute of Mineralogy, Geochemistry, and Crystal Chemistry of Rare Elements, Moscow, Russia.
Tsumcorite is a rare hydrated lead arsenate mineral that was discovered in 1971, and reported by Geier, Kautz and Muller. It was named after the TSUMeb CORporation mine at Tsumeb, in Namibia, in recognition of the Corporation's support for mineralogical investigations of the orebody at its Mineral Research Laboratory.
Tuperssuatsiaite is a rare clay mineral found in Greenland, Namibia and Brazil. It is a hydrated phyllosilicate of sodium and iron.
Ianbruceite is a rare hydrated zinc arsenate with the formula [Zn2(OH)(H2O)(AsO4)](H2O)2; material from the Driggith mine has traces of cobalt. It was first discovered at Tsumeb, approved by the International Mineralogical Association as a new mineral species in 2011, reference IMA2011-49, and named for Ian Bruce, who founded "Crystal Classics" in the early 1990s, and was heavily involved in attempts to reopen the famous Tsumeb mine for specimen mining.
In 2013 new occurrences of ianbruceite were reported from the neighbouring Driggith and Potts Gill mines on High Pike in the Caldbeck Fells, Cumbria, England. Here the mineral is probably a post-mining product. Caldbeck Fells and Tsumeb are the only reported localities for ianbruceite to date (May 2013).
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.
Köttigite is a rare hydrated zinc arsenate which was discovered in 1849 and named by James Dwight Dana in 1850 in honour of Otto Friedrich Köttig (1824–1892), a German chemist from Schneeberg, Saxony, who made the first chemical analysis of the mineral. It has the formula Zn3(AsO4)2·8H2O and it is a dimorph of metaköttigite, which means that the two minerals have the same formula, but a different structure: köttigite is monoclinic and metaköttigite is triclinic. There are several minerals with similar formulae but with other cations in place of the zinc. Iron forms parasymplesite Fe2+3(AsO4)2·8H2O; cobalt forms the distinctively coloured pinkish purple mineral erythrite Co3(AsO4)2·8H2O and nickel forms annabergite Ni3(AsO4)2·8H2O. Köttigite forms series with all three of these minerals and they are all members of the vivianite group.
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.
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).
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.