Melanophlogite | |
---|---|
General | |
Category | Silicate mineral |
Formula (repeating unit) | SiO2 |
IMA symbol | Mp [1] |
Crystal system | cubic or tetragonal [2] [3] |
Identification | |
Color | Brown, colorless, light yellow, dark reddish brown |
Crystal habit | Forms crust-like aggregates on matrix |
Cleavage | None |
Fracture | Brittle |
Mohs scale hardness | 6.5–7 |
Luster | Vitreous |
Streak | White |
Diaphaneity | Transparent to translucent |
Specific gravity | 1.99–2.11, average = 2.04 |
Optical properties | Isotropic, n=1.425–1.457 |
Other characteristics | Fluorescent, Short UV=weak gray-white, Long UV=gray-white |
References | [4] [5] |
Melanophlogite (MEP) is a rare silicate mineral and a polymorph of silica (SiO2). It has a zeolite-like porous structure which results in relatively low and not well-defined values of its density and refractive index. Melanophlogite often overgrows crystals of sulfur or calcite and typically contains a few percent of organic and sulfur compounds. Darkening of organics in melanophlogite upon heating is a possible origin of its name, which comes from the Greek for "black" and "to be burned". [2] [4]
Melanophlogite was identified and named by Arnold von Lasaulx in 1876 although G. Alessi had described a very similar mineral as early as in 1827. The mineral had a cubic crystal structure; chemical analysis revealed that it is mainly composed of SiO2, but also contains up to 12% of carbon and sulfur. It was suggested that the decomposition of organic matter (carbon) in the mineral was responsible for its blackening upon heating. All studied samples originated from Sicily, and thus the mineral was called Girghenti, an old name for Agrigento town in Sicily. The name was officially changed to melanophlogite in 1927. [2]
Melanophlogite can be grown synthetically at low temperatures and elevated pressures (e.g. 160 °C and 60 bar). It has a zeolite-like porous structure composed of Si5O10 and Si6O12 rings. Its crystalline symmetry depends on the content of its voids: crystals with spherical guest molecules or atoms (e.g. CH4, Xe, Kr) are cubic and the symmetry lowers to tetragonal for non-spherical guests like tetrahydrofuran or tetrahydrothiophene. [6] Since many molecules form unstable guests, the symmetry of melanophlogite can change between cubic and tetragonal upon mild heating (<100 °C). [6]
Even the cubic melanophlogite often shows anisotropic optical properties. They were attributed not to tetragonal fragments but to the organic film in the mineral which could be removed by low-temperature annealing (~400 °C). Otherwise, melanophlogite is thermally stable and its physical properties do not change upon 20-day annealing at 800 °C, but it converts to cristobalite after heating at temperatures above 900 °C. [2]
Melanophlogite is a rare mineral which usually forms round drops (see infobox) or complex intertwinned overgrowth structures over sulfur or calcite crystals. Rarely, it occurs as individual cubic crystallites a few millimeters in size. [2] It is found in Parma, Torino, Caltanissetta and Livorno provinces of Italy; also in several mines of California in the US, in Crimea (Ukraine) and Pardubice Region (Czech Republic). [5]
Analcime (; from Ancient Greek ἀνάλκιμος (análkimos) 'not strong') or analcite is a white, gray, or colorless tectosilicate mineral. Analcime consists of hydrated sodium aluminium silicate in cubic crystalline form. Its chemical formula is NaAlSi2O6·H2O. Minor amounts of potassium and calcium substitute for sodium. A silver-bearing synthetic variety also exists (Ag-analcite). Analcime is usually classified as a zeolite mineral, but structurally and chemically it is more similar to the feldspathoids. Analcime isn't classified as an isometric crystal, as although the crystal structure appears to be isometric, it is usually off only by a fraction of an angle. However, there are truly isometric samples of the mineral, which makes its classification even more difficult. Due to the differences between the samples being too slight, there's no merit from having multiple species names, so as a result analcime is a common example for minerals occurring in multiple crystal systems and space groups. It was first described by French geologist Déodat de Dolomieu, who called it zéolithe dure, meaning hard zeolite. It was found in lava in Cyclops, Italy. The mineral is IMA approved, and had been grandfathered, meaning the name analcime is believed to refer to a valid species til this day.
Kyanite is a typically blue aluminosilicate mineral, found in aluminium-rich metamorphic pegmatites and sedimentary rock. It is the high pressure polymorph of andalusite and sillimanite, and the presence of kyanite in metamorphic rocks generally indicates metamorphism deep in the Earth's crust. Kyanite is also known as disthene or cyanite.
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.
A mineraloid is a naturally occurring mineral-like substance that does not demonstrate crystallinity. Mineraloids possess chemical compositions that vary beyond the generally accepted ranges for specific minerals. For example, obsidian is an amorphous glass and not a crystal. Jet is derived from decaying wood under extreme pressure. Opal is another mineraloid because of its non-crystalline nature. Pearl is considered a mineraloid because the included calcite and/or aragonite crystals are bonded by an organic material, and there is no definite proportion of the components.
Silicon dioxide, also known as silica, is an oxide of silicon with the chemical formula SiO2, most commonly found in nature as quartz. In many parts of the world, silica is the major constituent of sand. Silica is one of the most complex and most abundant families of materials, existing as a compound of several minerals and as a synthetic product. Notable examples include fused quartz, fumed silica, silica gel, opal and aerogels. It is used in structural materials, microelectronics, and as components in the food and pharmaceutical industries.
In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from the intrinsic nature of the constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.
Anatase is a metastable mineral form of titanium dioxide (TiO2) with a tetragonal crystal structure. Although colorless or white when pure, anatase in nature is usually a black solid due to impurities. Three other polymorphs (or mineral forms) of titanium dioxide are known to occur naturally: brookite, akaogiite, and rutile, with rutile being the most common and most stable of the bunch. Anatase is formed at relatively low temperatures and found in minor concentrations in igneous and metamorphic rocks. Thin films of TiO2-coated glass show antifogging and self-cleaning properties under ultraviolet radiation.
Zeolites are microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mn+
1/n(AlO
2)−
(SiO
2)
x・yH
2O where Mn+
1/n is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+
exchanged zeolites are particularly useful as solid acid catalysts.
Zirconium dioxide is a white crystalline oxide of zirconium. Its most naturally occurring form, with a monoclinic crystalline structure, is the mineral baddeleyite. A dopant stabilized cubic structured zirconia, cubic zirconia, is synthesized in various colours for use as a gemstone and a diamond simulant.
Brookite is the orthorhombic variant of titanium dioxide (TiO2), which occurs in four known natural polymorphic forms (minerals with the same composition but different structure). The other three of these forms are akaogiite (monoclinic), anatase (tetragonal) and rutile (tetragonal). Brookite is rare compared to anatase and rutile and, like these forms, it exhibits photocatalytic activity. Brookite also has a larger cell volume than either anatase or rutile, with 8 TiO2 groups per unit cell, compared with 4 for anatase and 2 for rutile. Iron (Fe), tantalum (Ta) and niobium (Nb) are common impurities in brookite.
Cristobalite is a mineral polymorph of silica that is formed at very high temperatures. It has the same chemical formula as quartz, SiO2, but a distinct crystal structure. Both quartz and cristobalite are polymorphs with all the members of the quartz group, which also include coesite, tridymite and stishovite. It is named after Cerro San Cristóbal in Pachuca Municipality, Hidalgo, Mexico.
Tridymite is a high-temperature polymorph of silica and usually occurs as minute tabular white or colorless pseudo-hexagonal crystals, or scales, in cavities in felsic volcanic rocks. Its chemical formula is SiO2. Tridymite was first described in 1868 and the type location is in Hidalgo, Mexico. The name is from the Greek tridymos for triplet as tridymite commonly occurs as twinned crystal trillings (compound crystals comprising three twinned crystal components).
Stishovite is an extremely hard, dense tetragonal form (polymorph) of silicon dioxide. It is very rare on the Earth's surface; however, it may be a predominant form of silicon dioxide in the Earth, especially in the lower mantle.
Lead(IV) oxide, commonly known as lead dioxide, is the inorganic compound with the formula PbO2. It is an oxide where lead is in an oxidation state of +4. It is a dark-brown solid which is insoluble in water. It exists in two crystalline forms. It has several important applications in electrochemistry, in particular as the positive plate of lead acid batteries.
Zeolite facies describes the mineral assemblage resulting from the pressure and temperature conditions of low-grade metamorphism.
Seifertite is a silicate mineral with the formula SiO2 and is one of the densest polymorphs of silica. It has only been found in Martian and lunar meteorites, where it is presumably formed from either tridymite or cristobalite – other polymorphs of quartz – as a result of heating during the atmospheric re-entry and impact to the Earth, at an estimated minimal pressure of 35 GPa. It can also be produced in the laboratory by compressing cristobalite in a diamond anvil cell to pressures above 40 GPa. The mineral is named after Friedrich Seifert (born 1941), the founder of the Bayerisches Geoinstitut at University of Bayreuth, Germany, and is officially recognized by the International Mineralogical Association.
Plattnerite is an oxide mineral and is the beta crystalline form of lead dioxide (β-PbO2), scrutinyite being the other, alpha form. It was first reported in 1845 and named after German mineralogist Karl Friedrich Plattner. Plattnerite forms bundles of dark needle-like crystals on various minerals; the crystals are hard and brittle and have tetragonal symmetry.
Polonium dioxide (also known as polonium(IV) oxide) is a chemical compound with the formula PoO2. It is one of three oxides of polonium, the other two being polonium monoxide (PoO) and polonium trioxide (PoO3). It is a pale yellow crystalline solid at room temperature. Under lowered pressure (such as a vacuum), it decomposes into elemental polonium and oxygen at 500 °C. It is the most stable oxide of polonium and is an interchalcogen.
Keatite is a silicate mineral with the chemical formula SiO2 (silicon dioxide) that was discovered in nature in 2013. It is a tetragonal polymorph of silica first known as a synthetic phase. It was reported as minute inclusions within clinopyroxene (diopside) crystals in an ultra high pressure garnet pyroxenite body. The host rock is part of the Kokchetav Massif in Kazakhstan.
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.