Lindgrenite | |
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General | |
Category | Molybdate mineral |
Formula (repeating unit) | Cu3(MoO4)2(OH)2 |
IMA symbol | Lgr [1] |
Strunz classification | 7.GB.05 |
Dana classification | 48.3.1.1 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | P21/n |
Unit cell | a = 5.394, b = 14.023 c = 5.608 [Å]; β = 98.5°; Z = 2 |
Identification | |
Color | Green to yellowish green |
Crystal habit | Tabular to platey crystals, may be acicular, massive or crust forming |
Cleavage | Perfect on {010} and {101}, poor on {100} |
Fracture | Micaceous |
Tenacity | Brittle |
Mohs scale hardness | 4.5 |
Luster | Greasey |
Streak | Pale green |
Diaphaneity | Transparent |
Specific gravity | 4.2 |
Optical properties | Biaxial (-) |
Refractive index | nα = 1.930 nβ = 2.002 nγ = 2.020 |
Birefringence | δ = 0.090 |
2V angle | 71° (measured) |
References | [2] [3] [4] |
Lindgrenite is an uncommon copper molybdate mineral with formula: Cu3(MoO4)2(OH)2. It occurs as tabular to platey monoclinic green to yellow green crystals.
It was first described in 1935 for an occurrence in the Chuquicamata Mine, Antofagasta, Chile, and named for Swedish–American economic geologist Waldemar Lindgren (1860–1939) of the Massachusetts Institute of Technology. [2] [3]
Lindgrenite occurs in the oxidized portions of copper–molybdenum bearing sulfide ore deposits. Associated minerals include antlerite, molybdenite, powellite, brochantite, chrysocolla, iron oxides and quartz. [2]
Molybdenite is a mineral of molybdenum disulfide, MoS2. Similar in appearance and feel to graphite, molybdenite has a lubricating effect that is a consequence of its layered structure. The atomic structure consists of a sheet of molybdenum atoms sandwiched between sheets of sulfur atoms. The Mo-S bonds are strong, but the interaction between the sulfur atoms at the top and bottom of separate sandwich-like tri-layers is weak, resulting in easy slippage as well as cleavage planes. Molybdenite crystallizes in the hexagonal crystal system as the common polytype 2H and also in the trigonal system as the 3R polytype.
Wulfenite is a lead molybdate mineral with the formula PbMoO4. It can be most often found as thin tabular crystals with a bright orange-red to yellow-orange color, sometimes brown, although the color can be highly variable. In its yellow form it is sometimes called "yellow lead ore".
Coffinite is a uranium-bearing silicate mineral with formula: U(SiO4)1−x(OH)4x.
Adamite is a zinc arsenate hydroxide mineral, Zn2AsO4OH. It is a mineral that typically occurs in the oxidized or weathered zone above zinc ore occurrences. Pure adamite is colorless, but usually it possess yellow color due to Fe compounds admixture. Tints of green also occur and are connected with copper substitutions in the mineral structure. Olivenite is a copper arsenate that is isostructural with adamite and there is considerable substitution between zinc and copper resulting in an intermediate called cuproadamite. Zincolivenite is a recently discovered mineral being an intermediate mineral with formula CuZn(AsO4)(OH). Manganese, cobalt, and nickel also substitute in the structure. An analogous zinc phosphate, tarbuttite, is known.
Powellite is a calcium molybdate mineral with formula CaMoO4. Powellite crystallizes with tetragonal – dipyramidal crystal structure as transparent adamantine blue, greenish-brown, yellow-to-grey typically anhedral forms. It exhibits distinct cleavage, and has a brittle-to-conchoidal fracture. It has a Mohs hardness of 3.5 to 4 and a specific gravity of 4.25. It forms a solid solution series with scheelite (calcium tungstate, CaWO4). It has refractive index values of nω=1.974 and nε=1.984.
Datolite is a calcium boron hydroxide nesosilicate, CaBSiO4(OH). It was first observed by Jens Esmark in 1806, and named by him from δατεῖσθαι, "to divide," and λίθος, "stone," in allusion to the granular structure of the massive mineral.
Rickardite is a telluride mineral, a copper telluride (Cu7Te5) or Cu3-x (x = 0 to 0.36)Te2. It was first described for an occurrence in the Good Hope Mine, Vulcan district, Gunnison County, Colorado, US, and named for mining engineer Thomas Arthur Rickard (1864–1953). It is a low temperature hydrothermal mineral that occurs associated with vulcanite, native tellurium, cameronite, petzite, sylvanite, berthierite, pyrite, arsenopyrite and bornite.
Sodium molybdate, Na2MoO4, is useful as a source of molybdenum. This white, crystalline salt is often found as the dihydrate, Na2MoO4·2H2O.
Xocomecatlite is a rare tellurate mineral with formula: Cu3(TeO4)(OH)4. It is an orthorhombic mineral which occurs as aggregates or spherules of green needlelike crystals.
Cubanite is a copper iron sulfide mineral that commonly occurs as a minor alteration mineral in magmatic sulfide deposits. It has the chemical formula CuFe2S3 and when found, it has a bronze to brass-yellow appearance. On the Mohs hardness scale, cubanite falls between 3.5 and 4 and has a orthorhombic crystal system. Cubanite is chemically similar to chalcopyrite, however it is the less common copper iron sulfide mineral due to crystallization requirements.
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.
Iranite (Persian: ایرانیت) is a triclinic lead copper chromate silicate mineral with formula Pb10Cu(CrO4)6(SiO4)2(F,OH)2. It was first described from an occurrence in Iran. It is the copper analogue of hemihedrite (Pb10Zn(CrO4)6(SiO4)2(F,OH)2).
Utahite is an extremely rare secondary copper zinc tellurate mineral found as a product of oxidation. Its chemical formula is Cu5Zn3(Te6+O4)4(OH)8•7H2O.
In chemistry, a molybdate is a compound containing an oxyanion with molybdenum in its highest oxidation state of 6: O−−Mo(=O)2−O−. Molybdenum can form a very large range of such oxyanions, which can be discrete structures or polymeric extended structures, although the latter are only found in the solid state. The larger oxyanions are members of group of compounds termed polyoxometalates, and because they contain only one type of metal atom are often called isopolymetalates. The discrete molybdenum oxyanions range in size from the simplest MoO2−
4, found in potassium molybdate up to extremely large structures found in isopoly-molybdenum blues that contain for example 154 Mo atoms. The behaviour of molybdenum is different from the other elements in group 6. Chromium only forms the chromates, CrO2−
4, Cr
2O2−
7, Cr
3O2−
10 and Cr
4O2−
13 ions which are all based on tetrahedral chromium. Tungsten is similar to molybdenum and forms many tungstates containing 6 coordinate tungsten.
Wairakite is a zeolite mineral with an analcime structure but containing a calcium ion. The chemical composition is Ca8(Al16Si32O96)•16H2O. It is named for the location of its discovery in Wairakei, North Island, New Zealand, by Czechoslovakian mineralogist Alfred Steiner in 1955. The first finds were in hydrothermally altered rhyolitic tuffs, ignimbrites and volcaniclastic rocks. The mineral has since been found in metamorphic rocks and in geothermal areas. It was most likely first successfully synthesized in a laboratory in 1970.
Ferrimolybdite is a hydrous iron molybdate mineral with formula: Fe3+2(MoO4)3·8(H2O) or Fe3+2(MoO4)3·n(H2O). It forms coatings and radial aggregates of soft yellow needles which crystallize in the orthorhombic system.
Gyrolite, NaCa16(Si23Al)O60(OH)8·14H2O, is a rare silicate mineral (basic sodium calcium silicate hydrate: N-C-S-H, in cement chemist notation) belonging to the class of phyllosilicates. Gyrolite is also often associated with zeolites. It is most commonly found as spherical or radial formations in hydrothermally altered basalt and basaltic tuffs. These formations can be glassy, dull or fibrous in appearance.
Nuragheite is a rare natural thorium molybdate, formula Th(MoO4)2·H2O, discovered in Su Seinargiu, Sarroch, Cagliari, Sardegna, Italy. This locality is also a place of discovery of the other thorium molybdate - ichnusaite, which is a trihydrate.
Fumarole minerals are minerals which are deposited by fumarole exhalations. They form when gases and compounds desublimate or precipitate out of condensates, forming mineral deposits. They are mostly associated with volcanoes following deposition from volcanic gas during an eruption or discharge from a volcanic vent or fumarole, but have been encountered on burning coal deposits as well. They can be black or multicoloured and are often unstable upon exposure to the atmosphere.
Szenicsite is a copper hydroxy molybdate mineral, named after husband and wife Terry and Marissa Szenics, American mineral collectors who found the first specimens. When it was first discovered in Atacama, Chile, it was thought to be lindgrenite. The occurrence appeared in an isolated area, which was about one cubic meter in size. The mineral occurred in cavities of copper bearing powellite and matrix rich molybdenite. These cavities were filled with a material resembling clay. Outside of the zone the szenicsite crystals grew, copper levels seemed to decrease, and the mineralization changed to lindgrenite. Moving further from the zone, the minerals growing seemed to be lacking copper, and consisted of powellite blebs in the ore. Szenicsite was approved by the IMA in 1993.
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