Spertiniite

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Spertiniite
Spertiniite-93262.jpg
Spertiniite from Dzhezkazgan, Kazakhstan (size: 5 mm)
General
Category Oxide mineral
Formula
(repeating unit)
Cu(OH)2
IMA symbol Sni [1]
Strunz classification 4.FD.05
Dana classification6.2.4.1
Crystal system Orthorhombic
Crystal class Pyramidal (mm2)
H-M symbol: (mm2)
Space group Cmc21
Unit cell a = 2.95  Å, b = 10.59 Å
c = 5.27 Å; Z = 4
Identification
Formula mass 97.56 g/mol
ColorBlue, blue-green
Crystal habit Flat tabular crystals occurring in radial to botryoidal aggregates
Cleavage None
Tenacity Brittle
Mohs scale hardnessSoft
Luster Vitreous
Diaphaneity Transparent
Specific gravity 3.93
Optical propertiesBiaxial
Refractive index nα = 1.720, nβ= n.d., nγ = > 1.800
Pleochroism Strong; X = colorless; Z = dark blue
Other characteristicsDecomposes in hot water (synthetic)
References [2] [3] [4]

Spertiniite is a rare copper hydroxide mineral. Chemically it is copper(II) hydroxide with formula Cu(OH)2. It occurs as blue to blue green tabular orthorhombic crystal aggregates in a secondary alkaline environment altering chalcocite. Associated minerals include chalcocite, atacamite, native copper, diopside, grossular and vesuvianite. [3]

Discovery and occurrence

It was first described in 1981 for an occurrence in the Jeffrey quarry of the Johns-Manville mine, Asbestos, Estrie, Québec. It was named for mine geologist Francesco Spertini (born 1937). [2] [3] In addition to the type locality, it has also been reported from Mont Saint-Hilaire, Quebec; Ely, White Pine County, Nevada; and Bisbee, Cochise County, Arizona. It has been reported from Dzhezkazgan, Kazakhstan; from slag at Juliushutte, Astfeld, Harz Mountains, Germany; and from Tsumeb, Namibia. [3]

A 2006 study has produced evidence the blue mineral chrysocolla may be a microscopic mixture of spertiniite, amorphous silica and water. [5] [6]

Crystal structure of spertiniite Kristallstruktur Kupfer(II)-hydroxid.png
Crystal structure of spertiniite

Related Research Articles

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Bornite, also known as peacock ore, is a sulfide mineral with chemical composition Cu5FeS4 that crystallizes in the orthorhombic system (pseudo-cubic).

<span class="mw-page-title-main">Chalcocite</span> Sulfide mineral

Chalcocite, copper(I) sulfide (Cu2S), is an important copper ore mineral. It is opaque and dark gray to black, with a metallic luster. It has a hardness of 2.5–3 on the Mohs scale. It is a sulfide with a monoclinic crystal system.

<span class="mw-page-title-main">Chrysocolla</span> Phyllosilicate mineral

Chrysocolla is a hydrated copper phyllosilicate mineral and mineraloid with formula Cu
2–x
Al
x
{H
2–x
Si
2
O
5
)(OH)
4
•nH
2
O
(x<1) or (Cu,Al)
2
H
2
Si
2
O
5
(OH)
4
•nH
2
O)
.

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

Atacamite is a copper halide mineral: a copper(II) chloride hydroxide with formula Cu2Cl(OH)3. It was first described for deposits in the Atacama Desert of Chile in 1802 by Dmitri de Gallitzin. The Atacama Desert is also the namesake of the mineral.

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

Tenorite is a copper oxide mineral with the chemical formula CuO.

<span class="mw-page-title-main">Brochantite</span> Copper sulfate mineral

Brochantite is a sulfate mineral, one of a number of cupric sulfates. Its chemical formula is Cu4SO4(OH)6. Formed in arid climates or in rapidly oxidizing copper sulfide deposits, it was named by Armand Lévy for his fellow Frenchman, geologist and mineralogist A. J. M. Brochant de Villiers.

<span class="mw-page-title-main">Linarite</span> Copper lead sulfate hydroxide mineral

Linarite is a somewhat rare, crystalline mineral that is known among mineral collectors for its unusually intense, pure blue color. It is formed by the oxidation of galena and chalcopyrite and other copper sulfides. It is a combined copper lead sulfate hydroxide with formula PbCuSO4(OH)2. Linarite occurs as monoclinic prismatic to tabular crystals and irregular masses. It is easily confused with azurite, but does not react with dilute hydrochloric acid as azurite does. It has a Mohs hardness of 2.5 and a specific gravity of 5.3 - 5.5.

<span class="mw-page-title-main">Enargite</span> Sulfosalt mineral

Enargite is a copper arsenic sulfosalt mineral with formula Cu3AsS4. It takes its name from the Greek word enarge, "distinct". Enargite is a steel gray, blackish gray, to violet black mineral with metallic luster. It forms slender orthorhombic prisms as well as massive aggregates. It has a hardness of 3 and a specific gravity of 4.45.

<span class="mw-page-title-main">Niedermayrite</span> Sulfate mineral

Niedermayrite is a rare hydrated copper cadmium sulfate hydroxide mineral with formula: Cu4Cd(SO4)2(OH)6·4H2O. It crystallizes in the monoclinic system and occurs as encrustations and well formed vitreous blue-green prismatic crystals. It has a specific gravity of 3.36.

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

Volborthite is a mineral containing copper and vanadium, with the formula Cu3V2O7(OH)2·2H2O. Found originally in 1838 in the Urals, it was first named knaufite but was later changed to volborthite for Alexander von Volborth (1800–1876), a Russian paleontologist.

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

Libethenite is a rare copper phosphate hydroxide mineral. It forms striking, dark green orthorhombic crystals. It was discovered in 1823 in Ľubietová, Slovakia and is named after the German name of that locality (Libethen). Libethenite has also been found in the Miguel Vacas Mine, Conceição, Vila Viçosa, Évora District, Portugal, and in Tier des Carrières, Cahai, Vielsaim, Stavelot Massif, Luxembourg Province, Belgium.

<span class="mw-page-title-main">Rosasite</span> Mineral of copper zinc carbonate

Rosasite is a carbonate mineral with minor potential for use as a zinc and copper ore. Chemically, it is a copper zinc carbonate hydroxide with a copper to zinc ratio of 3:2, occurring in the secondary oxidation zone of copper-zinc deposits. It was originally discovered in 1908 in the Rosas mine in Sardinia, Italy, and is named after the location. Fibrous blue-green rosasite crystals are usually found in globular aggregates, often associated with red limonite and other colorful minerals. It is very similar to aurichalcite, but can be distinguished by its superior hardness.

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

Fornacite is a rare lead, copper chromate arsenate hydroxide mineral with the formula: Pb2Cu(CrO4)(AsO4)(OH). It forms a series with the phosphate mineral vauquelinite. It forms variably green to yellow, translucent to transparent crystals in the monoclinic - prismatic crystal system. It has a Mohs hardness of 2.3 and a specific gravity of 6.27.

<span class="mw-page-title-main">Djurleite</span> Copper sulfide mineral

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.

<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.

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

Ashburtonite is a rare lead copper silicate-bicarbonate mineral with formula: HPb4Cu2+4Si4O12(HCO3)4(OH)4Cl.

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

Pseudomalachite is a phosphate of copper with hydroxyl, named from the Greek for “false” and “malachite”, because of its similarity in appearance to the carbonate mineral malachite, Cu2(CO3)(OH)2. Both are green coloured secondary minerals found in oxidised zones of copper deposits, often associated with each other. Pseudomalachite is polymorphous with reichenbachite and ludjibaite. It was discovered in 1813. Prior to 1950 it was thought that dihydrite, lunnite, ehlite, tagilite and prasin were separate mineral species, but Berry analysed specimens labelled with these names from several museums, and found that they were in fact pseudomalachite. The old names are no longer recognised by the IMA.

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

Plancheite is a hydrated copper silicate mineral with the formula Cu8Si8O22(OH)4•(H2O). It is closely related to shattuckite in structure and appearance, and the two minerals are often confused.

Geerite is a copper sulfide mineral with the chemical formula Cu8S5. The mineral is named after the original collector, Adam Geer, of Utica, New York, US.

Mawsonite is a brownish orange sulfosalt mineral, containing copper, iron, tin, and sulfur: Cu6Fe2SnS8.

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 Spertiniite on Mindat
  3. 1 2 3 4 Spertiniite in the Handbook of Mineralogy
  4. Spertiniite on Webmineral
  5. François Farges, Karim Benzerara, Gordon E. Brown, Jr.; Chrysocolla Redefined as Spertiniite; SLAC-PUB-12232; 13th International Conference On X-Ray Absorption Fine Structure (XAFS13); July 9-14, 2006; Stanford, California
  6. Chrysocolla on Mindat