Lavendulan | |
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General | |
Category | Arsenate Minerals |
Formula (repeating unit) | NaCaCu5(AsO4)4Cl.5H2O Usually with some K, Co and Ni [1] |
IMA symbol | Lvd [2] |
Strunz classification | 8.DG.05 |
Dana classification | 42.9.4.2 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | P21/n [3] |
Identification | |
Formula mass | 1,062.00 g/mol |
Color | Blue or greenish blue |
Crystal habit | Thin botryoidal crusts of minute radiating fibers or thin rectangular, pseudo-orthorhombic plates [1] [3] |
Twinning | Common [3] |
Cleavage | Good on {010}, distinct on {100} and {001} |
Fracture | Uneven |
Tenacity | Brittle |
Mohs scale hardness | 2+1⁄2 [3] [4] [5] 2+1⁄2 to 3 [1] |
Luster | Vitreous to waxy, satiny in aggregates |
Streak | Light blue |
Diaphaneity | Translucent |
Specific gravity | 3.54 [3] [4] [5] 3.84 [1] |
Optical properties | Biaxial (−), nearly uniaxial (−) |
Refractive index | Nx = 1.645 Ny = 1.715 Nz = 1.725 [1] Nx = 1.660 Ny = 1.715 Nz = 1.734 [3] Contents
|
Pleochroism | O = pale blue to pale greenish blue, E = blue to greenish blue |
Solubility | Easily soluble in hydrochloric acid [6] |
Other characteristics | Not radioactive |
References | [1] [3] [4] [5] |
Lavendulan is an uncommon copper arsenate mineral, known for its characteristic intense electric blue colour. It belongs to the lavendulan group, which has four members:
Lemanskiite and lavendulan are dimorphs; they have the same formula but different structures. Lemanskiite is tetragonal, but lavendulan is monoclinic. [7] Lavendulan has the same structure as sampleite, and the two minerals form a series. [8] It is the calcium analogue of zdenĕkite and the arsenate analogue of sampleite.
Lavendulan was originally named for the lavender color of the "type" specimen, which has since been determined to be a mixture with no relationship to modern lavendulan. The mineral which is now called lavendulan is not a lavender blue color, and has no relationship to the "type" material from Annaberg. [3] It often contains potassium, cobalt and nickel as impurities.
Although lavendulan is monoclinic, the angle β is very close to 90°, making the mineral pseudo-orthorhombic. Most references describe the lavendulan unit cell as an orthorhombic cell containing 8 formula units (Z = 8) but Mindat.org describes a monoclinic unit cell with the length of the c axis halved, and only 4 formula units per unit cell (Z = 4) and space group P21/n. [3] Unit cell parameters are reported as
Lavendulan is a blue or greenish blue translucent mineral, with a vitreous to waxy luster, satiny in aggregates, and a light blue streak. It occurs as thin botryoidal crusts of minute radiating fibers or as thin rectangular, pseudo-orthorhombic plates, with cleavage in three directions, nearly perfect perpendicular to the b crystal axis, [4] and distinct perpendicular to the a and c axes. Twinning is common. [3] The mineral is brittle, with an uneven fracture. It is quite soft, with hardness 2.5, between gypsum and calcite, and relatively dense; its specific gravity is 3.84, close to that of topaz, and much denser than quartz (specific gravity 2.5 to 2.7). It is easily soluble in hydrochloric acid. [6]
The refractive index varies with the direction of propagation of the light, and varies between 1.64 and 1.75. This is quite high, between topaz and ruby. Lavendulan is biaxial (−), and most sources quote values for three refractive indices, for light travelling parallel to the three crystal axes. One source, [5] however, gives lavendulan as nearly uniaxial (−), and quotes only two refractive indices, for the ordinary and extraordinary rays.
Lavendulan is pleochroic, with O = pale blue to pale greenish blue and E = blue to greenish blue. [3] [5]
Lavendulan is a rare secondary mineral in the oxidised zone of some copper-arsenic deposits. [3]
A lavender blue mineral was discovered in 1837 by Johann F. A. Breithaupt in Annaberg in the Ore Mountains, which is a mountainous region spanning the Czech Republic and Germany. [9] The mineral was named "lavendulan" after the color, and Annaberg was the designated type locality. [6] In 1853, Vogel found a specimen of lavendulan from Jáchymov, also in the Ore Mountains, which was similar in appearance and characteristics to the material from Annaberg. [6] In 1877 Goldsmith examined some specimens of a turquoise blue arsenate of copper from the cobalt deposits of San Juan, Chile, and announced that they were also lavendulan. [6]
Nearly fifty years later, In 1924, William Foshag announced that the Chilean material was entirely distinct from that from Jáchymov, and he determined that it was a new mineral, and gave it the name freirinite, from the locality, the Blanca Mine, Freirina, Huasca Province, Atacama Region, Chile. [6]
In 1957, however, Claude Guillemin found that lavendulan and freirinite from the type localities gave identical x-ray powder patterns, and freirinite was discredited as a mineral species. [8] Yet another fifty years passed, and in 2007 Geister et al. re-examined Breithaupt's type specimen and found that it was a mixture unrelated to modern lavendulan. The second locality where lavendulan was found is in the Czech Republic, so the type locality of the species was changed to there, namely Jáchymov, Ore Mountains, Karlovy Vary Region. [3] The type material is held at the Mining Academy, Freiberg, Germany, reference 20944. [5]
At the type locality, lavendulan occurs associated with erythrite and a cobalt molybdate originally called pateraite, but now discredited. [6] At San Juan, Chile, it is associated with erythrite, cuprite, malachite and cobaltian wad. [5] At the Cap Garonne Mine, Pradet, Var, Provence-Alpes-Côte d'Azur, France, associated minerals are chalcophyllite, cyanotrichite, parnauite, mansfieldite, olivenite, tennantite, covellite, chalcanthite, antlerite, brochantite and geminite. [5] It also occurs at Tsumeb, Namibia, associated with cuprian adamite, conichalcite, o'danielite, tsumcorite, fahleite, quartz, calcite and gypsum. [5]
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:
Erythrite or red cobalt is a secondary hydrated cobalt arsenate mineral with the formula Co
3(AsO
4)
2•8H
2O. Erythrite and annabergite, chemical formula Ni
3(AsO
4)
2•8H
2O, or nickel arsenate form a complete series with the general formula (Co,Ni)
3(AsO
4)
2•8H
2O.
Todorokite is a complex hydrous manganese oxide mineral with generic chemical formula (Na,Ca,K,Ba,Sr)
1-x(Mn,Mg,Al)
6O
12·3-4H
2O. It was named in 1934 for the type locality, the Todoroki mine, Hokkaido, Japan. It belongs to the prismatic class 2/m of the monoclinic crystal system, but the angle β between the a and c axes is close to 90°, making it seem orthorhombic. It is a brown to black mineral which occurs in massive or tuberose forms. It is quite soft with a Mohs hardness of 1.5, and a specific gravity of 3.49 – 3.82. It is a component of deep ocean basin manganese nodules.
Tyrolite is a hydrous calcium copper arsenate carbonate mineral with the formula CaCu5(AsO4)2CO3(OH)4⋅6H2O. Tyrolite forms glassy, blue to green orthorhombic radial crystals and botryoidal masses. It has a Mohs hardness of 1.5–2.0 and a specific gravity of 3.1–3.2. It is translucent with refractive indices of nα = 1.694, nβ = 1.726, and nγ = 1.730.
Jarosewichite is a rare manganese arsenate mineral with formula: Mn2+3Mn3+(AsO4)(OH)6. It was first described in Franklin, New Jersey which is its only reported occurrence. Its chemical composition and structure are similar to chlorophoenicite. This mineral is orthorhombic with 2/m2/m2/m point group. Its crystals are prismatic or barrel-shaped. The color of jarosewichite is dark red to black. It has subvitreous luster of fracture surfaces and reddish-orange streak. This mineral occurs with flinkite, franklinite, andradite and cahnite.
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.
Duftite is a relatively common arsenate mineral with the formula CuPb(AsO4)(OH), related to conichalcite. It is green and often forms botryoidal aggregates. It is a member of the adelite-descloizite Group, Conichalcite-Duftite Series. Duftite and conichalcite specimens from Tsumeb are commonly zoned in color and composition. Microprobe analyses and X-ray powder-diffraction studies indicate extensive substitution of Zn for Cu, and Ca for Pb in the duftite structure. This indicates a solid solution among conichalcite, CaCu(AsO4 )(OH), austinite, CaZn(AsO4)(OH) and duftite PbCu(AsO4)(OH), all of them belonging to the adelite group of arsenates. It was named after Mining Councilor G Duft, Director of the Otavi Mine and Railroad Company, Tsumeb, Namibia. The type locality is the Tsumeb Mine, Tsumeb, Otjikoto Region, Namibia.
Cornubite is a rare secondary copper arsenate mineral with formula: Cu5(AsO4)2(OH)4. It was first described for its discovery in 1958 in Wheal Carpenter, Gwinear, Cornwall, England, UK. The name is from Cornubia, the medieval Latin name for Cornwall. It is a dimorph of cornwallite, and the arsenic analogue of pseudomalachite.
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.
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.
Vladimirite is a rare calcium arsenate mineral with a formula of Ca5(HAsO4)2(AsO4)2·5H2O. It is named after the Vladimirovskoye deposit in Russia, where it was discovered in the 1950s.
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.
Warikahnite is a rare zinc arsenate mineral of the triclinic crystal system with Hermann-Mauguin notation 1, belonging to the space group P1. It occurs in the Tsumeb mine in Namibia on corroded tennantite in the second oxidation zone under hydrothermal conditions in a dolomite-hosted polymetallic ore deposit. It is associated with adamite, stranskiite, koritnigite, claudetite, tsumcorite, and ludlockite. The origin of discovery was in a dolomite ore formation within an oxidized hydrothermal zone, in the E9 pillar, 31st level of the Tsumeb Mine in Namibia, Southwest Africa. It has also been found at Lavrion, Greece and Plaka, Greece as microscopic white needles.
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.
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.
Carminite (PbFe3+2(AsO4)2(OH)2) is an anhydrous arsenate mineral containing hydroxyl. It is a rare secondary mineral that is structurally related to palermoite (Li2SrAl4(PO4)4(OH)4). Sewardite (CaFe3+2(AsO4)2(OH)2) is an analogue of carminite, with calcium in sewardite in place of the lead in carminite. Mawbyite is a dimorph (same formula, different structure) of carminite; mawbyite is monoclinic and carminite is orthorhombic. It has a molar mass of 639.87 g. It was discovered in 1850 and named for the characteristic carmine colour.
Talmessite is a hydrated calcium magnesium arsenate, often with significant amounts of cobalt or nickel. It was named in 1960 for the type locality, the Talmessi mine, Anarak district, Iran. It forms a series with β-Roselite, where cobalt replaces some of the magnesium, and with gaitite, where zinc replaces the magnesium. All these minerals are members of the fairfieldite group. Talmessite is dimorphic with wendwilsonite.
Metarauchite is a member of the autunite group, found at the Jáchymov ore district, Czech Republic and in Schneeberg, Germany. The autunite group is a group of structured uranyl phosphates and arsenates; the other members of the group are autunite, bassetite, heinrichite, kahlerite, nováčekite-I, nováčekite-II, rauchite, sabugalite, saléeite, torbernite, uranocircite, uranospinite, and zeunerite. The mineral is named after Czech mineral collector Luděk Rauch, who died in the Jáchymov mines during mineral prospecting.
Lemanskiite is a mineral that was first discovered in a mine at Abundancia mine, El Guanaco mining district, Chile, with the ideal formula of NaCaCu5(AsO4)4Cl·3H2O. Originally, this mineral was discovered as being dimorphus with lavendulan, but in 2018 it was revised to only have 3 water molecules. Lemanskiite typically occurs as rosette-shaped aggregates of thin lamellar or needle-shaped aggregates, such as lammerite. Lemanskiite is dark sky blue with a light blue streak, it is brittle with an excellent cleavage plane. It was found on a dumping site in the abandoned Abundancia mine, El Guanaco mining district, Region II, Antofagasta Province, Chile The new mineral has been named after Chester S. Lemanski, Jr. This mineral and name were then approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association.