Kosnarite

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Kosnarite
Kosnarite-157545.jpg
General
CategoryAlkali zirconium phosphate
Formula
(repeating unit)
KZr2(PO4)3
IMA symbol Ksn [1]
Strunz classification 7/A. 17-10
Crystal system Trigonal Hexagonal crystal family
Crystal class Hexagonal Scalenohedral (3)m (3)2/m)
(same H-M symbol)
Space group R3c
Unit cell a = 8.687  Å,
c = 23.877 Å; V= 1,560.45 ų
Identification
ColorPale Blue, blue-green, or colorless
Crystal habit Rhombohedral with tiny c pinacolid
Twinning Not observed
Cleavage Perfect at {102}
Fracture Conchoidal fracture
Mohs scale hardness4.5
Luster Vitreous
Streak White
Diaphaneity Transparent to translucent
Specific gravity 3.2
Optical propertiesuniaxial (+)
Refractive index Nw = 1.656(2)
Nc = 1.682(2)
Birefringence δ = 0.026
References [2] [3] [4]

Kosnarite is an alkali zirconium phosphate mineral (KZr2(PO4)3) named after an expert of pegmatites Richard A. Kosnar. [2] Kosnarite contains potassium, oxygen, phosphorus, and zirconium with sodium, rubidium, hafnium, manganese and fluorine (Na, Rb, Hf, Mn, and F) being common impurities found in kosnarite. It was discovered in nature for the first time in 1991 by Vandall T. King. Samples that were found in granitic pegmatites from the Mount Mica Quarry, Paris, Oxford County, Maine, US were sent to Eugene E. Foord for study. This became the first recorded case of naturally occurring kosnarite. [3]

Contents

Occurrence

The first naturally occurring kosnarite was discovered in northern Maine in the United States. Another deposit was later found in Black Mountain, Oxford County, Maine. Both of these deposits were found in zoned granitic pegmatites associated with several minerals such as quartz, lepidolite, and beryl. Another deposit was found in Wycheproof, Northern Victoria, Australia, and this sample of kosnarite was also found in granitic pegmatite. Pegmatite is the term for a form of igneous rock with relatively large interlocking crystals, and there are three popular theories on how pegmatites named metamorphic, magmatic, and metasomatic. The pegmatites that the kosnarite are found in are believed to be formed by a mixture of magmatic and metamorphic as the kosnarite forms in the later stages of paragenesis by the alterations of hydrothermal fluids. [3]

Analysis

Due to the rarity of kosnarite, forms of analysis that involve the powdering of the sample such as X-ray diffraction (XRD) can not be used, so other methods have to be used. To find the data that would have been provided by the XRD, a Gandolfi camera with an 114.6mm diameter was used to find the d-spacing and intensity. Kosnarite's density was found using the sink-float method while using an acetone mixture and methylene iodide. [3] In order to find the chemical composition of kosnarite without damaging any sample, an ARL-SEMQ electron microprobe using an Opus microprobe automation system was used. To help find the chemical composition, CITZAF correction procedures were added to the study. Additionally, emission spectrographic analysis was completed by using a Jarrel-Ash 3.2-m spectrograph using a laser energy source. [3]

Chemical composition

Oxideswt%
P2O543.3%
ZrO244.5%
HfO20.5%
MnO1.0%
FeO0.2%
K2O8.7%
Na2O1.4%
Rb2O0.25%
F-0.20%
Total100.05%

[3]

Properties

The results of the testing found that kosnarite had large amounts of zirconium, phosphorus, and potassium. In the samples, there were also traces of calcium, zinc, and manganese, but these elements make up less than one percent, so they were classified as impurities. Physically, kosnarite from the pegmatites found in Maine occurred as rhombohedral crystals with a hexagonal unit cell [4] and were pseudocubic with a maximum size of around 0.9 mm. This is important as zirconium is in the form of a six coordinated octahedron and potassium is structured in a shape called a trigonal antiprism that is also six coordinated. [4] Kosnarite's structure was then determined by using [100] Patterson projection, and interatomic vector projection was also used to help determine the crystal structure. Special positions in the mineral were then found for potassium, zirconium, and phosphate while the two oxygen atoms had general positions. [4] Multiple refinement cycles using a unit weighing system, and least-squares refinements were used to minimize the deviation of the shifting of the atoms. [4] Later tests showed that zirconium polyhedra groups were joined by groups of phosphate these are both connected to each other by oxygen atoms. However, the oxygens are always bridges between the zirconium and phosphate and one oxygen is never shared between two the same groups and half of the oxygens are also shared with K groups. [4] The pattern of two zirconium polyhedron, one potassium polyhedron, two zirconium polyhedron, and the oxygen and phosphate groups filling in the gaps creates kosnarite's unique crystal structure. [4]

Depending on the impurities present in the sample, the color of kosnarite can range from pale blue to blue-green depending on the amount of iron, manganese, or other impurities, and kosnarite can sometimes appear to be nearly colorless. [3] Other physical properties of kosnarite include its vitreous lust, non-fluorescence, a hardness of 4.5 on the mohs scale of mineral hardness, conchoidal fracturing, and perfect cleavage in the {102} direction. Structurally, kosnarite is part of the hexagonal crystal family meaning that the crystals have three or six-fold symmetry and has a space group of R3c. [2] The unit cell of kosnarite was calculated to be a = 8.687  Å, c = 23.877 Å; V = 1,560.45 Å3, and no twinning growth has been observed. It was discovered that kosnarite is uniaxial (+) with its axes being Nw = 1.656(2), Nc = 1.682(2), and being nonpleochronic. Due to the small number of available samples, some tests have not been carried out, such as infrared spectra. [3]

Kosnarite is part of the alkali zirconium phosphates in which there are only two other known members of this group: gainesite, and a Cs analogue of gainesite. [3]

See also

Related Research Articles

<span class="mw-page-title-main">Pegmatite</span> Igneous rock with very large interlocked crystals

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.

Alforsite is a barium phosphate chloride mineral with formula: Ba5(PO4)3Cl. It was discovered in 1981, and named to honor geologist John T. Alfors (1930–2005) of the California Geological Survey for his work in the area where it was discovered.

<span class="mw-page-title-main">Vivianite</span> Phosphate mineral

Vivianite (Fe2+
3
(PO
4
)
2
·8H
2
O
) is a hydrated iron phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg2+, and calcium Ca2+ may substitute for iron Fe2+ in the structure. Pure vivianite is colorless, but the mineral oxidizes very easily, changing the color, and it is usually found as deep blue to deep bluish green prismatic to flattened crystals.
Vivianite crystals are often found inside fossil shells, such as those of bivalves and gastropods, or attached to fossil bone.

<span class="mw-page-title-main">Brazilianite</span>

Brazilianite, whose name derives from its country of origin, Brazil, is a typically yellow-green phosphate mineral, most commonly found in phosphate-rich pegmatites.

<span class="mw-page-title-main">Lithiophilite</span>

Lithiophilite is a mineral containing the element lithium. It is lithium manganese(II) phosphate with chemical formula LiMnPO4. It occurs in pegmatites often associated with triphylite, the iron end member in a solid solution series. The mineral with intermediate composition is known as sicklerite and has the chemical formula Li(Mn,Fe)PO4). The name lithiophilite is derived from the Greek philos (φιλός) "friend", as lithiophilite is usually found with lithium.

<span class="mw-page-title-main">Triphylite</span>

Triphylite is a lithium iron(II) phosphate mineral with the chemical formula LiFePO4. It is a member of the triphylite group and forms a complete solid solution series with the lithium manganese(II) phosphate, lithiophilite. Triphylite crystallizes in the orthorhombic crystal system. It rarely forms prismatic crystals and is more frequently found in hypidiomorphic rock. It is bluish- to greenish-gray in color, but upon alteration becomes brown to black.

<span class="mw-page-title-main">Whitlockite</span> Phosphate mineral

Whitlockite is a mineral, an unusual form of calcium phosphate. Its formula is Ca9(MgFe)(PO4)6PO3OH. It is a relatively rare mineral but is found in granitic pegmatites, phosphate rock deposits, guano caves and in chondrite meteorites. It was first described in 1941 and named for Herbert Percy Whitlock (1868–1948), American mineralogist and curator at the American Museum of Natural History in New York City.

<span class="mw-page-title-main">Zanazziite</span>

Zanazziite is a complex hydrated phosphate mineral from the roscherite group. It is a magnesium beryllium phosphate mineral. Zanazziite arises as barrel-shaped crystals and can reach up to 4 mm. It grows alongside quartz minerals. It is found in the crevices of Lavra da Ilha pegmatite, near Taquaral, in northeastern Minas Gerais, Brazil. Zanazziite is named after Pier F. Zanazzi. Zanazziite has an ideal chemical formula of Ca2Mg5Be4(PO4)6(OH)4·6H2O.

<span class="mw-page-title-main">Eosphorite</span> Phosphate mineral

Eosphorite is a brown (occasionally pink) manganese hydrous phosphate mineral with chemical formula: MnAl(PO4)(OH)2·H2O. It is used as a gemstone.

<span class="mw-page-title-main">Taranakite</span> Iron-aluminium phosphate mineral

Taranakite is a hydrated alkali iron-aluminium phosphate mineral with chemical formula (K,Na)3(Al,Fe3+)5(PO4)2(HPO4)6·18 H2O. It forms from the reaction of clay minerals or aluminous rocks with solutions enriched in phosphate derived from bat or bird guano or, less commonly, from bones or other organic matter. Taranakite is most commonly found in humid, bat inhabited caves near the boundary of guano layers with the cave surface. It is also found in perennially wet coastal locations that have been occupied by bird colonies. The type location, and its namesake, the Sugar Loaf Islands off Taranaki, New Zealand, is an example of a coastal occurrence.

<span class="mw-page-title-main">Bergenite</span>

Bergenite is a rare uranyl phosphate of the more specific phosphuranylite group. The phosphuranylite-type sheet in bergenite is a new isomer of the group, with the uranyl phosphate tetrahedra varying in an up-up-down, same-same-opposite (uuduudSSOSSO) orientation. All bergenite samples have been found in old mine dump sites. Uranyl minerals are a large constituent of uranium deposits.

<span class="mw-page-title-main">Cyrilovite</span>

Cyrilovite (NaFe33+(PO4)2(OH)4·2(H2O)) is a hydrous sodium iron phosphate mineral. It is isomorphous and isostructural with wardite, the sodium aluminium counterpart.

<span class="mw-page-title-main">Fluor-liddicoatite</span>

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

Zirconium phosphates (zirconium hydrogen phosphate) are acidic, inorganic cation exchange materials that have a layered structure with formula Zr(HPO4)2∙nH2O. These salts have high thermal and chemical stability, solid state ion conductivity, resistance to ionizing radiation, and the capacity to incorporate different types of molecules with different sizes between their layers. There are various phases of zirconium phosphate which vary in their interlaminar spaces and their crystalline structure. Among all the Zirconium phosphate phases the most widely used are the alpha (Zr(HPO4)2∙H2O) and the gamma (Zr(PO4)(H2PO4)∙2H2O) phase. The salts have been widely used in several applications such as: drug delivery, catalysis, nanocomposite, nuclear waste management, clinical dialyzer, among others.

<span class="mw-page-title-main">Maricite</span> Phosphate mineral

Maricite or marićite is a sodium iron phosphate mineral (NaFe2+PO4), that has two metal cations connected to a phosphate tetrahedron. It is structurally similar to the much more common mineral olivine. Maricite is brittle, usually colorless to gray, and has been found in nodules within shale beds often containing other minerals.

<span class="mw-page-title-main">Perhamite</span>

Perhamite is a phosphate mineral with the formula Ca3Al7(SiO4)3(PO4)4(OH)3·16.5(H2O). It occurs in rare isolated masses in amblygonite-rich pegmatite deposits throughout the world. It was discovered in platy sheed form of 1mm hexagonal crystals. It was first described in 1977 by P.J. Dunn and D.E. Appleman from pegmatite collected from Bell Pit, Newry, Maine. Other specimens have been found in Kapunda, South Australia, in Silver Coin mine near Humboldt County, Nevada and various locations throughout Europe.

Bobfergusonite is a mineral with formula Na2Mn5FeAl(PO4)6. The mineral varies in color from green-brown to red-brown. It was discovered in 1986 in Manitoba, Canada, and named for Robert Bury Ferguson (born 1920). As of 2012, the mineral has only been found in Canada and Argentina.

<span class="mw-page-title-main">Grayite</span>

Grayite, ThPO4·(H2O), is a thorium phosphate mineral of the Rabdophane group first discovered in 1957 by S.H.U. Bowie in Rhodesia. It is of moderate hardness occurring occasionally in aggregates of hexagonal crystals occasionally but more commonly in microgranular/cryptocrystalline masses. Due to its thorium content, grayite displays some radioactivity although it is only moderate and the mineral displays powder XRD peaks without any metamict-like effects. The color of grayite is most commonly observed as a light to dark reddish brown but has also been observed as lighter yellows with grayish tints. It has a low to moderate hardness with a Mohs hardness of 3–4 and has a specific gravity of 3.7–4.3. It has been found in both intrusive igneous and sedimentary environments.

<span class="mw-page-title-main">Zigrasite</span>

Zigrasite is a phosphate mineral with the chemical formula of MgZr(PO4)2(H2O)4. Zigrasite was discovered and is only known to occur in the Dunton Quarry at Oxford County, Maine. Zigrasite was specifically found in the giant 1972 gem tourmaline-bearing pocket at the Dunton Quarry. Zigrasite is named after James Zigras who originally discovered and brought the mineral to attention.

<span class="mw-page-title-main">Serrabrancaite</span>

Serrabrancaite is a mineral with the chemical formula MnPO4•H2O and which is named for the locality where it was found, the Alto Serra Branca Pegmatite. The Alto Serra Branca mine has been in operation since the 1940s. It is located in Paraiba, Brazil near a village named Pedra Lavrada. Tantalite is the main mineral mined here. Specimens of serrabrancaite are kept in the Mineralogical Collections of both the Bergakademie Freiberg, Germany and the Martin-Luther Universität Halle, Institut für Geologische Wissenschaften.

References

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi: 10.1180/mgm.2021.43 . S2CID   235729616.
  2. 1 2 3 Kosnar, B. "Kosnarite: Mineral Information, Data, and Localities". Hudson Institute of Mineralogy.
  3. 1 2 3 4 5 6 7 8 9 Brownfield, Michael E.; Foord, Eugene E.; Sutley, Stephen J.; Botinelly, Theodore (1993). "Kosnarite, KZr2(PO4)3, a new mineral from Mount Mica and Black Mountain, Oxford County, Maine". American Mineralogist. 78 (5–6): 653–656.
  4. 1 2 3 4 5 6 7 ŠLJUKIĆ, M.; MATKOVIĆ, B.; PRODIĆ, B.; ANDERSON, D. (1 January 1969). "The crystal structure of KZr2(PO4)3". Zeitschrift für Kristallographie – Crystalline Materials. 130 (1–6): 148–161. doi:10.1524/zkri.1969.130.16.148. S2CID   201841649.