Chalcophyllite | |
---|---|
General | |
Category | Arsenate minerals |
Formula (repeating unit) | Cu 18Al 2(AsO 4) 4(SO 4) 3(OH) 24·36(H 2O) [1] [2] [3] or Cu 18Al 2(AsO 4) 3(SO 4) 3(OH) 27·33(H 2O) [4] [5] [6] |
IMA symbol | Chp [7] |
Strunz classification | 8.DF.30 |
Dana classification | 43.5.14.1 |
Crystal system | Trigonal |
Crystal class | Rhomboedral (3) H-M symbol: (3) [2] [3] [4] [6] |
Space group | R3 [8] |
Identification | |
Color | Blue-green to emerald-green |
Crystal habit | Crystals platy and six-sided, also as rosettes, drusy, foliated or massive. |
Twinning | On {1010} as twin plane. |
Cleavage | Perfect on {0001} |
Fracture | Irregular |
Mohs scale hardness | 2 |
Luster | Vitreous to subadamantine, pearly on {0001} |
Streak | Pale green |
Diaphaneity | Transparent to translucent |
Specific gravity | 2.67 to 2.69 [3] [4] [6] or 2.4 to 2.66 [5] |
Optical properties | Uniaxial (−) |
Refractive index | nω = 1.618 to 1.632, nε = 1.552 to 1.575 |
Pleochroism | O blue-green, E almost colorless |
Solubility | Soluble in acids and in ammonia |
Other characteristics | Can be partially dehydrated. Alters to chrysocolla. Nonfluorescent, not radioactive |
References | [8] [3] [4] [5] [6] |
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 [2] (not to be confused with the amphibole mineral taramite, which is quite different). At Wheal Gorland a specimen exhibiting partial replacement of liriconite, Cu
2Al(AsO
4)(OH)
4·(4H
2O), by chalcophyllite has been found. [2] 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.
Two different formulae are quoted in the literature for chalcophyllite, Cu
18Al
2(AsO
4)
4(SO
4)
3(OH)
24·36(H
2O) [1] [2] [3] (molar mass 3098 g) and Cu
18Al
2(AsO
4)
3(SO
4)
3(OH)
27·33(H
2O) [4] [5] [6] (molar mass 2956 g). The difference reflects the fact that the water content varies at room temperature based on relative humidity. [4]
Chalcophyllite crystallizes in the trigonal crystal class, 3 2/m with space group R 3m [5] or 3 with space group R 3. [2] [3] [4] [6] Some authors choose a unit cell with three formula units per cell (Z = 3), and some a smaller unit cell with only 1.5 formula units per cell (Z = 1.5). For the larger unit cell a = 10.77 Å, c = 57.5 Å, Z = 3. [5] [6] [9] For the smaller unit cell c is only half as long, a = 10.756 Å, c = 28.678 Å, Z = 1.5. [3] [4]
Crystals are platy, six-sided and flattened perpendicular to the c crystal axis, and may be striated triangularly on these flattened faces. It may form rosettes, or be drusy, foliated or massive. [4]
Cleavage is perfect perpendicular to the c crystal axis, and twinning occurs with {1010} as the twin plane. Fracture is irregular. The mineral is soft, with hardness only 2, the same as gypsum. Specific gravity is generally given in the range 2.67 to 2.69, but Webmineral has 2.4 to 2.66. Chalcophyllite is soluble in acids and in ammonia. It is not fluorescent, nor radioactive. The water content varies at room temperature based on relative humidity. Chalcophyllite alters to chrysocolla, [4] which is a copper-aluminium silicate with the formula (Cu,Al)
2H
2Si
2O
5(OH)
4·n(H
2O).
Many copper minerals are blue or green in color; chalcophyllite is blue-green to emerald-green, with a pale green streak and vitreous to subadamantine luster, pearly on {0001}. Crystals are transparent to translucent. It is uniaxial (−) with refractive indices nω = 1.618 to 1.632 and nε = 1.552 to 1.575. Indices of refraction vary markedly depending on the relative humidity since the water content varies at ambient temperature. [4] It is pleochroic with O blue-green and E almost colorless.
Chalcophyllite is an uncommon secondary mineral occurring in the oxidized zones of some arsenic-bearing hydrothermal copper deposits. Associated minerals include azurite, malachite, brochantite, chrysocolla, spangolite, connellite, cuprite, cyanotrichite, strashimirite, parnauite, lavendulan, cornubite, langite, clinoclase, pharmacosiderite and mansfieldite. [3] The type material is conserved at the Mining Academy, Freiberg, Germany. [3] Notable occurrences include the Majuba Hill Mine, Antelope District, Nevada, US [2] and Cornwall, including Wheal Gorland, UK.
Chrysocolla ( KRIS-ə-KOL-ə) is a hydrous copper phyllosilicate mineral and mineraloid with the formula Cu
2 – xAl
x(H
2Si
2O
5)(OH)
4⋅nH
2O (x < 1) or (Cu, Al)
2H
2Si
2O
5(OH)
4⋅nH
2O).
Cyanotrichite is a hydrous copper aluminium sulfate mineral with formula Cu4Al2[(OH)12|SO4]·2H2O, also known as lettsomite. Cyanotrichite forms velvety radial acicular crystal aggregates of extremely fine fibers. It crystallizes in the monoclinic system and forms translucent bright blue acicular crystal clusters or drusey coatings. The Mohs hardness is 2 and the specific gravity ranges from 2.74 to 2.95. Refractive indices are nα = 1.588 nβ = 1.617 nγ = 1.655.
Leadhillite is a lead sulfate carbonate hydroxide mineral, often associated with anglesite. It has the formula Pb4SO4(CO3)2(OH)2. Leadhillite crystallises in the monoclinic system, but develops pseudo-hexagonal forms due to crystal twinning. It forms transparent to translucent variably coloured crystals with an adamantine lustre. It is quite soft with a Mohs hardness of 2.5 and a relatively high specific gravity of 6.26 to 6.55.
Liroconite is a complex mineral: Hydrated copper aluminium arsenate hydroxide, with the formula Cu2Al[(OH)4|AsO4]·4(H2O). It is a vitreous monoclinic mineral, colored bright blue to green, often associated with malachite, azurite, olivenite, and clinoclase. It is quite soft, with a Mohs hardness of 2–2.5, and has a specific gravity of 2.9–3.0.
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.
Sauconite is a complex phyllosilicate mineral of the smectite clay group, formula Na0.3Zn3(SiAl)4O10(OH)2·4H2O. It forms soft earthy bluish white to red-brown monoclinic crystals typically massive to micaceous in habit. It has a Mohs hardness of 1 to 2 and a specific gravity of 2.45. Optically it is biaxial positive with refractive index values of nα = 1.550 - 1.580, nβ = 1.590 - 1.620 and nγ = 1.590 - 1.620. It is found in vugs and seams in the oxidized zones of zinc and copper deposits. It occurs in association with hemimorphite, smithsonite, chrysocolla, coronadite and various iron oxides.
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.
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.
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:
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.
Fluor-liddicoatite is a rare member of the tourmaline group of minerals, elbaite subgroup, and the theoretical calcium endmember of the elbaite-fluor-liddicoatite series; the pure end-member has not yet been found in nature. Fluor-liddicoatite is indistinguishable from elbaite by X-ray diffraction techniques. It forms a series with elbaite and probably also with olenite. Liddiocoatite is currently a non-approved mineral name, but Aurisicchio et al. (1999) and Breaks et al. (2008) found OH-dominant species. Formulae are
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.
Fluorellestadite is a rare nesosilicate of calcium, with sulfate and fluorine, with the chemical formula Ca10(SiO4)3(SO4)3F2. It is a member of the apatite group, and forms a series with hydroxylellestadite.
Pearceite is one of the four so-called "ruby silvers", pearceite Cu(Ag,Cu)6Ag9As2S11, pyrargyrite Ag3SbS3, proustite Ag3AsS3 and miargyrite AgSbS2. It was discovered in 1896 and named after Dr Richard Pearce (1837–1927), a Cornish–American chemist and metallurgist from Denver, Colorado.
Strashimirite is a rare monoclinic mineral containing arsenic, copper, hydrogen, and oxygen. It has the chemical formula Cu8(AsO4)4(OH)4·5(H2O).
Cornwallite is an uncommon copper arsenate mineral with formula Cu5(AsO4)2(OH)4. It forms a series with the phosphate pseudomalachite and is a dimorph of the triclinic cornubite. It is a green monoclinic mineral which forms as radial to fibrous encrustations.
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).
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.
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.