Gottlobite | |
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General | |
Category | Hydroxide mineral, Vanadate mineral, Arsenate mineral |
Formula (repeating unit) | CaMg(VO4,AsO4)(OH) |
IMA symbol | Got [1] |
Strunz classification | 08.BH.35 |
Dana classification | 41.05.01.10 |
Crystal system | Orthorhombic |
Space group | P222 |
Unit cell | a = 7.501(4) Å; b = 9.010(7) Å; c = 5.941(4) Å; Z = 4, V = 401.5Å3 |
Identification | |
Formula mass | 205.20 gm |
Color | Orange to orange-brown |
Crystal habit | Isometric to tabular crystals |
Twinning | Not observed |
Cleavage | Not observed |
Fracture | Conchoidal to irregular |
Tenacity | Brittle |
Mohs scale hardness | 4.5 |
Luster | Vitreous to adamantine |
Streak | Light brownish |
Diaphaneity | Transparent |
Specific gravity | 3.46 g/cm3 (calculated) |
Optical properties | Biaxial negative |
Refractive index | nα = 1.797 nβ = 1.805-1.815 nγ = 1.828 |
Pleochroism | Medium strong with X = orange-brown, Y = pale yellowish brown, and Z = orange-brown |
Group | Vandates and arsenates |
References | [2] [3] [4] |
Gottlobite, Ca Mg(V O 4,As O 4)(O H ), is a mineral found as isolated crystals or isometric grains of orange or orange-brown color. The size of the crystals are a half millimeter in diameter and are part of the orthorhombic crystal system. Gottlobite forms a solid solution with adelite, which is an end member composition of CaMg(VO4)(OH), as well as being classified in the adelite group. Gottlobite is also part of the vanadates and arsenates group. With these characteristics, it is similar to the minerals tangeite and austinite by X-ray diffraction methods. [4]
Gottlobite is a relatively rare mineral where only a small quantity of the mineral has been found. It was first observed at the site of a long-abandoned mine on the northern slope of Gottlob hill in Friedrichroda, Thuringia, Germany by Jὒrgen Graf in August of 1996. As such, gottlobite got its name from its locality. Additionally, the German translation of "Lob" means "praise" and the German translation of "Gott" means "God", as deciphered by Google Translate. In the mine at this location, Gottlobite is found in hydrothermal veins of barite that are cutting through conglomerate. The crystals of gottlobite can be found embedded in these barite veins or as stand-alone crystals on surrounding minerals. The associated minerals in the area are hausmannite, barite, vanadian adelite, and muscovite. [4]
Analytical methods used on gottlobite to determine its chemical composition include energy-dispersive X-ray spectrometry (EDX) and wavelength-dispersive X-ray spectrometry (WDX). EDX revealed the presence and quantities of elements present in the mineral, including Ca, V, As, O and small amounts of Sr. This was then measured in terms of oxides, where the weight percents were 24.98 for CaO, 0.92 for SrO, 17.54 for MgO, 1.50 for MnO, 1.44 for CuO, 27.47 for V2O5, 20.32 for As2O5, and 5.4 for H2O. Mg is in gottlobite's chemical formula, but was not found in the EDX testing because of very similar pattern of arsenic lines that were overlapping with magnesium. The full empirical formula of gottlobite is (Ca0.93,Sr0.03)(Mg0.91,Mn0.04,Cu0.04)(V0.63,As0.37)O4O1.08H1.26. As seen in the formula, it was also determined that the arsenic and vanadium atoms are in 4-fold (tetrahedral) coordination with oxygen, and the magnesium atoms are in six-fold (octahedral) coordination. [4]
In geology and mineralogy, a mineral or mineral species is, broadly speaking, a solid substance with a fairly well-defined chemical composition and a specific crystal structure that occurs naturally in pure form.
Vanadinite is a mineral belonging to the apatite group of phosphates, with the chemical formula Pb5(VO4)3Cl. It is one of the main industrial ores of the metal vanadium and a minor source of lead. A dense, brittle mineral, it is usually found in the form of red hexagonal crystals. It is an uncommon mineral, formed by the oxidation of lead ore deposits such as galena. First discovered in 1801 in Mexico, vanadinite deposits have since been unearthed in South America, Europe, Africa, and North America.
An oxyanion, or oxoanion, is an ion with the generic formula A
xOz−
y. Oxyanions are formed by a large majority of the chemical elements. The formulae of simple oxyanions are determined by the octet rule. The corresponding oxyacid of an oxyanion is the compound H
zA
xO
y. The structures of condensed oxyanions can be rationalized in terms of AOn polyhedral units with sharing of corners or edges between polyhedra. The oxyanions adenosine monophosphate (AMP), adenosine diphosphate (ADP) and adenosine triphosphate (ATP) are important in biology.
Forsterite (Mg2SiO4; commonly abbreviated as Fo; also known as white olivine) is the magnesium-rich end-member of the olivine solid solution series. It is isomorphous with the iron-rich end-member, fayalite. Forsterite crystallizes in the orthorhombic system (space group Pbnm) with cell parameters a 4.75 Å (0.475 nm), b 10.20 Å (1.020 nm) and c 5.98 Å (0.598 nm).
Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of minerals and make up approximately 90 percent of Earth's crust.
The rare mineral adelite, is a calcium, magnesium, arsenate with chemical formula CaMgAsO4OH. It forms a solid solution series with the vanadium-bearing mineral gottlobite. Various transition metals substitute for magnesium and lead replaces calcium leading to a variety of similar minerals in the adelite–duftite group.
Geigerite is a mineral, a complex hydrous manganese arsenate with formula: Mn5(AsO3OH)2(AsO4)2·10H2O. It forms triclinic pinacoidal, vitreous, colorless to red to brown crystals. It has a Mohs hardness of 3 and a specific gravity of 3.05.
In inorganic chemistry, mineral hydration is a reaction which adds water to the crystal structure of a mineral, usually creating a new mineral, commonly called a hydrate.
Belite is an industrial mineral important in Portland cement manufacture. Its main constituent is dicalcium silicate, Ca2SiO4, sometimes formulated as 2 CaO · SiO2 (C2S in cement chemist notation).
Wadsleyite is an orthorhombic mineral with the formula β-(Mg,Fe)2SiO4. It was first found in nature in the Peace River meteorite from Alberta, Canada. It is formed by a phase transformation from olivine (α-(Mg,Fe)2SiO4) under increasing pressure and eventually transforms into spinel-structured ringwoodite (γ-(Mg,Fe)2SiO4) as pressure increases further. The structure can take up a limited amount of other bivalent cations instead of magnesium, but contrary to the α and γ structures, a β structure with the sum formula Fe2SiO4 is not thermodynamically stable. Its cell parameters are approximately a = 5.7 Å, b = 11.71 Å and c = 8.24 Å.
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.
Alacránite (As8S9) is an arsenic sulfide mineral first discovered in the Uzon caldera, Kamchatka, Russia. It was named for its occurrence in the Alacrán silver/arsenic/antimony mine. Pampa Larga, Chile. It is generally more rare than realgar and orpiment. Its origin is hydrothermal. It occurs as subhedral to euhedral tabular orange to pale gray crystals that are transparent to translucent. It has a yellow-orange streak with a hardness of 1.5. It crystallizes in the monoclinic crystal system. It occurs with realgar and uzonite as flattened and prismatic grains up to 0.5 mm across.
Picropharmacolite, Ca4Mg(AsO3OH)2(AsO4)2·11H2O, is a rare arsenate mineral. It was named in 1819 from the Greek for bitter, in allusion to its magnesium content, and its chemical similarity to pharmacolite. The mineral irhtemite, Ca4Mg(AsO3OH)2(AsO4)2·4H2O, has the same composition as picropharmacolite, except that it has only four water molecules per formula unit, instead of eleven. It may be formed by the dehydration of picropharmacolite.
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.
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.
This list gives an overview of the classification of non-silicate minerals and includes mostly International Mineralogical Association (IMA) recognized minerals and its groupings. This list complements the List of minerals recognized by the International Mineralogical Association series of articles and List of minerals. Rocks, ores, mineral mixtures, not IMA approved minerals, not named minerals are mostly excluded. Mostly major groups only, or groupings used by New Dana Classification and Mindat.
Arsenoclasite (originally arsenoklasite) is a red or dark orange brown mineral with formula Mn5(AsO4)2(OH)4. The name comes from the Greek words αρσενικόν (for arsenic) and κλάσις (for cleavage), as arsenoclasite contains arsenic and has perfect cleavage. The mineral was discovered in 1931 in Långban, Sweden.
George-ericksenite is a mineral with the chemical formula Na6CaMg(IO3)6(CrO4)2(H2O)12. It is vitreous, pale yellow to bright lemon yellow, brittle, and features a prismatic to acicular crystal habit along [001] and somewhat flattened crystal habit on {110}. It was first encountered in 1984 at the Pinch Mineralogical Museum. One specimen of dietzeite from Oficina Chacabuco, Chile had bright lemon-yellow micronodules on it. These crystals produced an X-ray powder diffraction pattern that did not match any XRD data listed for inorganic compounds. The X-ray diffraction pattern and powder mount were set aside until 1994. By then, the entire mineral collection from the Pinch Mineralogical Museum had been purchased by the Canadian Museum of Nature. The specimen was then retrieved and studied further. This study was successful and the new mineral george-ericksenite was discovered. The mineral was named for George E. Ericksen who was a research economic geologist with the U.S. Geological Survey for fifty years. The mineral and name have been approved by Commission on New Minerals and Mineral Names (IMA). The specimen, polished thin section, and the actual crystal used for the structure determination are kept in the Display Series of the National Mineral Collection of Canada at the Canadian Museum of Nature, Ottawa, Ontario.
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.