Microlite

Last updated
Microlite
Microlite-bem-42a.jpg
General
Category Oxide minerals
Formula
(repeating unit)
(Na,Ca)2Ta2O6(O,OH,F)
IMA symbol Mic [1]
Strunz classification 04.DH.15
Crystal system Cubic
Space group Fd3m (no. 227)
Identification
References [2]

Microlite was once[ when? ] known as a pale-yellow, reddish-brown, or black isometric mineral composed of sodium calcium tantalum oxide with a small amount of fluorine. Its chemical formula is (Na,Ca)2Ta2O6(O,OH,F). Today[ when? ] it is a name of a group of oxide minerals of a similar stoichiometry having tantalum prevailing over titanium and niobium. The microlite group belongs to a large pyrochlore supergroup that occurs in pegmatites and constitutes an ore of tantalum. It has a Mohs hardness of 5.5 and a variable specific gravity of 4.2 to 6.4. It occurs as disseminated microscopic subtranslucent to opaque octahedral crystals with a refractive index of 2.0 to 2.2. Microlite is also called djalmaite, but both names are now obsolete.

"Microlite" occurs as a primary mineral in lithium-bearing granite pegmatites, and in miarolitic cavities in granites. Association minerals include: albite, lepidolite, topaz, beryl, tourmaline, spessartine, tantalite and fluorite.

"Microlite" was first described in 1835 for an occurrence on the Island of Uto, State of Stockholm, Sweden. Another occurrence of microlite is the Clark Ledges pegmatite, Chesterfield, Hampshire County, Massachusetts. The name is from Greek mikros for "small" and lithos for "stone".

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.

<span class="mw-page-title-main">Pyrochlore</span> Niobium mineral of A2B2O7 general formula

Pyrochlore2Nb2O6(OH,F) is a mineral group of the niobium end member of the pyrochlore supergroup. Pyrochlore is also a term for the crystal structure Fd3m. The name is from the Greek πῦρ, fire, and χλωρός, green because it typically turns green on ignition in classic blowpipe analysis.

<span class="mw-page-title-main">Brazilianite</span> Yellow-green phosphate mineral

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

Tantite is a rare tantalum oxide mineral with formula: Ta2O5. Tantite forms transparent microscopic colorless triclinic - pedial crystals with an adamantine luster. It has a Mohs hardness of 7 and a high specific gravity of 8.45. Chemical analyses show minor inclusion (1.3%) of niobium oxide.

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

Hydrokenoelsmoreite is a hydrous tungsten oxide mineral with formula □2W2O6(H2O). Hydrokenoelsmoreite is a colorless to white, translucent isometric mineral. It has a Mohs hardness of 3, exhibits no cleavage and has a splintery fracture. It has a vitreous to adamantine luster. It is optically isotropic with an index of refraction of n = 2.24.

<span class="mw-page-title-main">Loparite-(Ce)</span> Oxide mineral

Loparite-(Ce) is a granular, brittle oxide mineral of the perovskite class. It is black to dark grey and may appear grey to white in reflected light on polished thin section with reddish brown internal reflections. It has the chemical formula of (Ce,Na,Ca)(Ti,Nb)O3. Nioboloparite is a variation of loparite-(Ce) containing niobium.

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

Roméite is a calcium antimonate mineral with the chemical formula (Ca,Fe,Mn,Na)2(Sb,Ti)2O6(O,OH,F). It is a honey-yellow mineral crystallizing in the hexoctahedral crystal system. It has a Mohs hardness of 5.5-6.0. It occurs in Algeria, Australia, Brazil, China, Europe, Japan, New Zealand, and the United States in metamorphic iron-manganese deposits and in hydrothermal antimony-bearing veins.

<span class="mw-page-title-main">Betafite</span> Mineral group

Betafite is a mineral group in the pyrochlore supergroup, with the chemical formula (Ca,U)2(Ti,Nb,Ta)2O6(OH). Betafite typically occurs as a primary mineral in granite pegmatites, rarely in carbonatites. Originally defined by the B-site atom Ti, the development of new nomenclature for mineral names led to modernization of the system for nomenclature of pyrochlore and betafite in order to further rationalize the naming process of this grouping of minerals. Only two of the mineral species that were formerly recognized as betafite are presently retained. They are oxyuranobetafite and oxycalciobetafite. The term betafite is now a synonym or varietal group name under the pyrochlore super group.

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

Wodginite is a manganese, tin, tantalum oxide mineral with the chemical formula Mn2+(Sn,Ta)Ta2O8. It may also include significant amounts of niobium.

<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

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

Hagendorfite is an iron phosphate mineral with the chemical formula of (Na,Ca)MnFe2(PO4)3 and is named after where the mineral was discovered, Hagendorf-Süd, Bavaria, Germany.

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

Simpsonite has a general formula of Al4(Ta,Nb)3O13(OH). It occurs as euhedral to subhedral tabular to short and prismatic crystals, commonly in subparallel groups. Under the petrographic microscope it has a very high relief.

<span class="mw-page-title-main">Donnayite-(Y)</span> Rare-earth carbonate mineral containing the rare-earth metal yttrium

Donnayite-(Y) is a rare-earth carbonate mineral containing the rare-earth metal yttrium. It was first discovered in 1978 at Mont Saint-Hilaire, Quebec. Donnayite was subsequently identified and named after Joseph D. H. Donnay and his wife, Gabrielle Donnay. Both were prominent mineralogists and crystallographers, and J. D. H. Donnay was awarded the Roebling Award by the Mineralogical Society of America in 1971 for his emphasis on the importance of optical mineralogy and crystal morphology. Donnayite tends to occur in small quantities in the pegmatite dykes and miarolitic cavities of mountainous regions. It crystallizes in this environment with increasing alkalinity values until the alkalinity suddenly drops during the last stage of crystallization. This results in increasing amounts of Na carbonates and REE minerals. First discovered at Mont St-Hilaire, donnayite has since been found in the Southern Ural Mountains of Russia and the Narssarssuk pegmatite of South Greenland. Donnayite crystals tend to be small and the color is commonly pale yellow to yellow with a white streak and a vitreous luster. Donnayite crystals usually display trigonal or hexagonal symmetry and have a hardness of 3. Twinning is extremely common in this mineral. Minerals closely related to donnayite include synchysite, calcite, sphalerite, microcline, and analcime. Donnayite is isomorphous with weloganite and mckelveyite.

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

Ixiolite is an accessory oxide mineral found in granitic pegmatites. It is an oxide with the general chemical formula (Ta,Nb,Sn,Mn,Fe)4O8 or (Ta,Mn,Nb)O2.

<span class="mw-page-title-main">Oxyyttropyrochlore-(Y)</span>

Oxyyttropyrochlore-(Y), also referred to as "obruchevite" or "yttropyrochlore-(Y)", is a potential (not yet accepted) zero-valent-dominant mineral of the pyrochlore group. Its formula can be written as (Y,◻)2Nb2O2O.

<span class="mw-page-title-main">Ferronigerite-2N1S</span>

Ferronigerite-2N1S is an iron, tin, alumino-hydroxide mineral that naturally occurs around sillimanite-quartz veins. Ferronigerite-2N1S belongs to the nigerite group, högbomite supergroup. The other constituents of the nigerite group are ferronigerite-6N6S, magnesionigerite-2N1S, magnesionigerite-6N6S, zinconigerite-2N1S and zinconigerite-6N6S. The 2N1S ending stands for the nolanite and spinel structural layers.

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

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.

Szklaryite is an extremely rare mineral with the formula []Al6BAs33+O15. It is essentially vacant ("[]"), arsenic-dominant member of dumortierite supergroup, giving a name of szklaryite group. It is one of three quite recently found minerals of this group, the other two being nioboholtite and titanoholtite, all coming from the Szklary village near Ząbkowice Śląskie in Poland. They occur in a unique pegmatite of probable anatectic origin.

Uranopolycrase is an oxide mineral first discovered in the Fonte del Prete vein of a pegmatite vein in San Piero in Campo, Elba Island, Tuscany, Italy. Uranopolycrase is a member of the Euxenite Group and is the uranium bearing analog of polycrase-(Y). The type specimen is almost entirely metamict. The ideal formula for uranopolycrase is (U,Y)(Ti,Nb)2O6. The mineral has been approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association to be named uranopolycrase for its similarity to polycrase-(Y) and was approved 5 December, 1991.

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. Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (eds.). Handbook of Mineralogy (PDF). Chantilly, VA 20151-1110, USA: Mineralogical Society of America. Retrieved 12 February 2022.{{cite book}}: CS1 maint: location (link)

Additional reading