Reedmergnerite | |
---|---|
General | |
Category | Mineral |
Formula (repeating unit) | NaBSi3O8 |
IMA symbol | Rm [1] |
Strunz classification | 9.FA.35 |
Dana classification | 76.1.4.1 |
Crystal system | Triclinic |
Crystal class | Pinacoidal H-M Symbol: 1 |
Space group | C1 |
Unit cell | 587.34 |
Identification | |
Formula mass | 246.05 |
Color | Colorless to yellow-orange, salmon-orange |
Cleavage | Perfect on {001} |
Mohs scale hardness | 6 – 6.5 |
Luster | Vitreous |
Streak | White |
Diaphaneity | Transparent, translucent |
Density | 2.776 |
Optical properties | Biaxial (−) |
Refractive index | nα = 1.554 nβ = 1.565 nγ = 1.573 |
Birefringence | 0.019 |
2V angle | 80° |
Dispersion | None |
Common impurities | Ti, Al, Fe, Mg, Ca, Ba, K, F, H2O, P |
Reedmergnerite is a borosilicate mineral named in honor of Frank S. Reed and John L. Mergner. It is approved by the International Mineralogical Association but was first described prior to the association's formation, first published in 1955. Although it is approved, it got grandfathered, meaning the name reedmergnerite is still believed to refer to a valid species. Reedmergnerite has a synthetic potassium analogue. [2]
Reedmergnerite is a member of the feldspar group. [2] It grows along bedding laminations as authigenic crystals, as a stubby prismatic to platy crystals. It is wedge-shaped usually, and it may have jagged terminations. Crystals grow in aggregates, and a singular crystal's size can reach up to 10 cm. [3] It is isostructural with low albite. It does not exhibit anisotropy. [4] The mineral has been synthesized using gels. The procedure occurred hydrothermally. The gels that were used in the synthesis contained a 10% weight excess of silicon dioxide. While the pressure and the temperature were constant, the degree of boron and silicon order increased with time, though both lower water content and pressure decrease the rate of ordering. The mineral's ordering behavior occurs to be insensitive to the co-existing fluid's composition.
Although it has three type localities, [3] the most important of those is at Joseph Smith No. 1 well in the United States. The associated minerals at the type locality are eitelite, searlesite, crocidolite, leucosphenite and shortite. It happens to occur in dolomitic shale mostly. [2] However, it can also occur in brown dolomitic rock and black oil shale as well.
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.
Feldspar is a group of rock-forming aluminium tectosilicate minerals, also containing other cations such as sodium, calcium, potassium, or barium. The most common members of the feldspar group are the plagioclase (sodium-calcium) feldspars and the alkali (potassium-sodium) feldspars. Feldspars make up about 60% of the Earth's crust, and 41% of the Earth's continental crust by weight.
A pegmatite is an igneous rock showing a very coarse texture, with large interlocking crystals usually greater in size than 1 cm (0.4 in) and sometimes greater than 1 meter (3 ft). Most pegmatites are composed of quartz, feldspar, and mica, having a similar silicic composition to granite. However, rarer intermediate composition and mafic pegmatites are known.
Orthoclase, or orthoclase feldspar (endmember formula KAlSi3O8), is an important tectosilicate mineral which forms igneous rock. The name is from the Ancient Greek for "straight fracture", because its two cleavage planes are at right angles to each other. It is a type of potassium feldspar, also known as K-feldspar. The gem known as moonstone (see below) is largely composed of orthoclase.
The mineral anorthoclase ((Na,K)AlSi3O8) is a crystalline solid solution in the alkali feldspar series, in which the sodium-aluminium silicate member exists in larger proportion. It typically consists of between 10 and 36 percent of KAlSi3O8 and between 64 and 90 percent of NaAlSi3O8.
Plagioclase is a series of tectosilicate (framework silicate) minerals within the feldspar group. Rather than referring to a particular mineral with a specific chemical composition, plagioclase is a continuous solid solution series, more properly known as the plagioclase feldspar series. This was first shown by the German mineralogist Johann Friedrich Christian Hessel (1796–1872) in 1826. The series ranges from albite to anorthite endmembers (with respective compositions NaAlSi3O8 to CaAl2Si2O8), where sodium and calcium atoms can substitute for each other in the mineral's crystal lattice structure. Plagioclase in hand samples is often identified by its polysynthetic crystal twinning or "record-groove" effect.
Albite is a plagioclase feldspar mineral. It is the sodium endmember of the plagioclase solid solution series. It represents a plagioclase with less than 10% anorthite content. The pure albite endmember has the formula NaAlSi
3O
8. It is a tectosilicate. Its color is usually pure white, hence its name from Latin, albus. It is a common constituent in felsic rocks.
The scapolites are a group of rock-forming silicate minerals composed of aluminium, calcium, and sodium silicate with chlorine, carbonate and sulfate. The two endmembers are meionite and marialite. Silvialite (Ca,Na)4Al6Si6O24(SO4,CO3) is also a recognized member of the group.
Hornfels is the group name for a set of contact metamorphic rocks that have been baked and hardened by the heat of intrusive igneous masses and have been rendered massive, hard, splintery, and in some cases exceedingly tough and durable. These properties are caused by fine grained non-aligned crystals with platy or prismatic habits, characteristic of metamorphism at high temperature but without accompanying deformation. The term is derived from the German word Hornfels, meaning "hornstone", because of its exceptional toughness and texture both reminiscent of animal horns. These rocks were referred to by miners in northern England as whetstones.
The chlorites are the group of phyllosilicate minerals common in low-grade metamorphic rocks and in altered igneous rocks. Greenschist, formed by metamorphism of basalt or other low-silica volcanic rock, typically contains significant amounts of chlorite.
Sanidine is the high temperature form of potassium feldspar with a general formula K(AlSi3O8). Sanidine is found most typically in felsic volcanic rocks such as obsidian, rhyolite and trachyte. Sanidine crystallizes in the monoclinic crystal system. Orthoclase is a monoclinic polymorph stable at lower temperatures. At yet lower temperatures, microcline, a triclinic polymorph of potassium feldspar, is stable.
Illite, also called hydromica or hydromuscovite, is a group of closely related non-expanding clay minerals. Illite is a secondary mineral precipitate, and an example of a phyllosilicate, or layered alumino-silicate. Its structure is a 2:1 sandwich of silica tetrahedron (T) – alumina octahedron (O) – silica tetrahedron (T) layers. The space between this T-O-T sequence of layers is occupied by poorly hydrated potassium cations which are responsible for the absence of swelling. Structurally, illite is quite similar to muscovite with slightly more silicon, magnesium, iron, and water and slightly less tetrahedral aluminium and interlayer potassium. The chemical formula is given as (K,H3O)(Al,Mg,Fe)2(Si,Al)4O10[(OH)2·(H2O)], but there is considerable ion (isomorphic) substitution. It occurs as aggregates of small monoclinic grey to white crystals. Due to the small size, positive identification usually requires x-ray diffraction or SEM-EDS analysis. Illite occurs as an altered product of muscovite and feldspar in weathering and hydrothermal environments; it may be a component of sericite. It is common in sediments, soils, and argillaceous sedimentary rocks as well as in some low grade metamorphic rocks. The iron-rich member of the illite group, glauconite, in sediments can be differentiated by x-ray analysis.
Celsian is an uncommon feldspar mineral, barium aluminosilicate, BaAl2Si2O8. The mineral occurs in contact metamorphic rocks with significant barium content. Its crystal system is monoclinic, and it is white, yellow, or transparent in appearance. In pure form, it is transparent. Synthetic barium aluminosilicate is used as a ceramic in dental fillings and other applications.
Eucryptite is a lithium bearing aluminium silicate mineral with formula LiAlSiO4. It crystallizes in the trigonal - rhombohedral crystal system. It typically occurs as granular to massive in form and may pseudomorphically replace spodumene. It has a brittle to conchoidal fracture and indistinct cleavage. It is transparent to translucent and varies from colorless to white to brown. It has a Mohs hardness of 6.5 and a specific gravity of 2.67. Optically it is uniaxial positive with refractive index values of nω = 1.570 - 1.573 and nε = 1.583 - 1.587.
Leifite is a rare tectosilicate. Tectosilicates are built on a framework of tetrahedra with silicon or aluminium at the centre and oxygen at the vertices; they include feldspars and zeolites, but leifite does not belong in either of these categories. It is a member of the leifite group, which includes telyushenkoite (Cs,Na,K)Na6(Be2Al3Si15O39) and eirikite KNa6Be2(Si15Al3)O39F2). Leifite was discovered in 1915, and named after Leif Ericson who was a Norse explorer who lived around 1000 AD, and was probably the first European to land in North America, nearly 500 years before Christopher Columbus. Eirikite was named in 2007 after Eirik Raude, or Erik the Red, (950–1003), who discovered Greenland and who was the father of Leif Ericson. The third mineral in the group, telyushenkoite, was discovered in 2001. It was not named after any of Leif Ericson's family members, but after a professor of geology in Turkmenistan.
Béhierite is a very rare mineral, a natural tantalum borate of the formula (Ta,Nb)BO4. Béhierite is also one of the most simple tantalum minerals. It contains simple tetrahedral borate anions, instead of more common among minerals, planar BO3 groups. It forms a solid solution with its niobium-analogue, schiavinatoite. Both have zircon-type structure (tetragonal, space group I41/amd) and are found in pegmatites. Béhierite and holtite are minerals with essential tantalum and boron.
Baratovite is a very rare cyclosilicate mineral named after Rauf Baratovich Baratov from Tajikistan. It was discovered in 1974 at Dara-Pioz glacier, Tajikistan, and was approved by the International Mineralogical Association only a year later in 1975. The glacier gives home to 133 valid species, and is the type locality of 33 minerals, one of which is baratovite.
Foitite is a mineral in the tourmaline group, it is a vacancy-dominant member of the group. Foitite is in the 'vacancy' group, due to the absence of atoms in the X site.
Vigezzite is a variant of the mineral aeschynite containing calcium, cerium, niobium, tantalum, and titanium. It was first discovered near Orcesco, Valle Vigezzo, Provo Novara, Northern Italy, in cavities of an albitic rock. The crystals of Vigezzite are flat prismatic crystals up to 2-3 mm length of an orange-yellow color.The name Vigezzite was chosen to draw attention to the locality that has produced the first occurrence of a Ca-Nb-Ta-mineral with Nb dominance over Ta, crystallizing with the aeschynite structure. The ideal chemical formula for vigezzite is (Ca,Ce),(Nb,Ta,Ti)2O6
Bavenite is a calcium beryllium aluminosilicate, and it is a part of the Bavenite-Bohseite series. Its name originates from its type locality, which is Baveno, Italy. This mineral is approved by the IMA, and got grandfathered, meaning it is still believed to refer to a valid mineral species. It was discovered in 1901 in a pink granite mined in Lago Maggiore. When bavenite was discovered, it was considered as a member of the zeolite series. Later it was removed from the series as unlike zeolites, bavenite loses the water stored in its crystal lattice in a way higher temperature, between 210 and 320 °C. It is a cheap mineral considering its rarity.