Muscovite

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Muscovite
Muscovite-Albite-122887.jpg
Muscovite with albite from Doce valley, Minas Gerais, Brazil (dimensions: 6 × 5.3 × 3.9 cm)
General
Category Phyllosilicate
Formula
(repeating unit)
KAl2(AlSi3O10)(F,OH)2
IMA symbol Ms [1]
Strunz classification 9.EC.15
Dana classification71.02.02a.01
Crystal system Monoclinic
Crystal class Prismatic (2/m)
(same H-M symbol)
Space group C2/c
Unit cell a = 5.199  Å, b = 9.027 Å,
c = 20.106 Å, β = 95.78°; Z = 4
Identification
ColorWhite, grey, silvery
Crystal habit Massive to platy
Twinning Common on the [310], less common on the {001}
Cleavage Perfect on the {001}
Fracture Micaceous
Tenacity Elastic
Mohs scale hardness2–2.5 parallel to {001}
4 right angle to {001}
Luster Vitreous, silky, pearly
Streak White
Diaphaneity Transparent to translucent
Specific gravity 2.76–3
Optical propertiesBiaxial (−)
Refractive index nα = 1.552–1.576
nβ = 1.582–1.615
nγ = 1.587–1.618
Birefringence δ = 0.035 – 0.042
Pleochroism Weak when colored
Dispersion r > v weak
Ultraviolet fluorescence None
References [2] [3] [4] [5]

Muscovite (also known as common mica, isinglass, or potash mica [6] ) is a hydrated phyllosilicate mineral of aluminium and potassium with formula KAl2(AlSi 3 O 10)(F,OH)2, or (KF)2(Al2O3)3(SiO2)6(H2O). It has a highly perfect basal cleavage yielding remarkably thin laminae (sheets) which are often highly elastic. Sheets of muscovite 5 meters × 3 meters (16.5 feet × 10 feet) have been found in Nellore, India. [7]

Contents

Muscovite has a Mohs hardness of 2–2.25 parallel to the [001] face, 4 perpendicular to the [001] and a specific gravity of 2.76–3. It can be colorless or tinted through grays, violet or red, and can be transparent or translucent. It is anisotropic and has high birefringence. Its crystal system is monoclinic. The green, chromium-rich variety is called fuchsite; mariposite is also a chromium-rich type of muscovite.

Muscovite is the most common mica, found in granites, pegmatites, gneisses, and schists, and as a contact metamorphic rock or as a secondary mineral resulting from the alteration of topaz, feldspar, kyanite, etc. It is characteristic of peraluminous rock, in which the content of aluminum is relatively high. [8] In pegmatites, it is often found in immense sheets that are commercially valuable. Muscovite is in demand for the manufacture of fireproofing and insulating materials and to some extent as a lubricant.

Naming

The name muscovite comes from Muscovy-glass, a name given to the mineral in Elizabethan England due to its use in medieval Russia (Muscovy) as a cheaper alternative to glass in windows. This usage became widely known in England during the sixteenth century with its first mention appearing in letters by George Turberville, the secretary of England's ambassador to the Russian tsar Ivan the Terrible, in 1568.

Muscovite window Muscovite window.jpg
Muscovite window

Distinguishing characteristics

Micas are distinguished from other minerals by their pseudohexagonal crystal shape and their perfect cleavage, which allows the crystals to be pulled apart into very thin elastic sheets. Pyrophyllite, and talc are softer than micas and have a greasy feel, while chlorite is green in color and its cleavage sheets are inelastic. The other common mica mineral, biotite, is almost always much darker in color than muscovite. Paragonite can be difficult to distinguish from muscovite but is much less common, though it is likely mistaken for muscovite often enough that it may be more common that is generally appreciated. [9] Muscovite mica from Brazil is red due to manganese(3+). [10]

Composition and structure

Like all mica minerals, muscovite is a phyllosilicate (sheet silicate) mineral with a TOT-c structure. In other words, a crystal of muscovite consists of layers (TOT) bonded to each other by potassium cations (c). [9]

Each layer is composed of three sheets. The outer sheets ('T' or tetrahedral sheets) consist of silicon-oxygen tetrahedra and aluminium-oxygen tetrahedra, with three of the oxygen anions of each tetrahedron shared with neighboring tetrahedra to form a hexagonal sheet. The fourth oxygen anion in each tetrahedral sheet is called an apical oxygen anion. [9] There are three silicon cations for each aluminium cation but the arrangement of aluminium and silicon cations is largely disordered. [11]

The middle octahedral (O) sheet consists of aluminium cations that are each surrounded by six oxygen or hydroxide anions forming an octahedron, with the octahedrons sharing anions to form a hexagonal sheet similar to the tetrahedral sheets. The apical oxygen anions of the outer T sheets face inwards and are shared by the octahedral sheet, binding the sheets firmly together. The relatively strong binding between oxygen anions and aluminium and silicon cations within a layer, compared with the weaker binding of potassium cations between layers, gives muscovite its perfect basal cleavage. [9]

In muscovite, alternate layers are slightly offset from each other, so that the structure repeats every two layers. This is called the 1M polytype of the general mica structure. [9]

The formula for muscovite is typically given as KAl2(AlSi3O10)(OH)2, but it is common for small amounts of other elements to substitute for the main constituents. Alkali metals such as sodium, rubidium, and caesium substitute for potassium; magnesium, iron, lithium, chromium, titanium, or vanadium can substitute for aluminium in the octahedral sheet; fluorine or chlorine can substitute for hydroxide; and the ratio of aluminium to silicon in the tetrahedral sheets can change to maintain charge balance where necessary (as when magnesium cations, with a charge of +2, substitute for aluminium ions, with a charge of +3). [12]

Up to 10% of the potassium may be replaced by sodium, and up to 20% of the hydroxide by fluorine. Chlorine rarely replaces more than 1% of the hydroxide. Muscovite in which the mole fraction of silicon is greater than aluminium, and magnesium or iron replaces some of the aluminium to maintain charge balance, is called phengite. [12]

Uses

Muscovite can be cleaved into very thin transparent sheets that can substitute for glass, particularly for high-temperature applications such as industrial furnace or oven windows. It is also used in the manufacture of a wide variety of electronics and as a filler in paints, plastic, and wallboard. It lends a silky luster to wallpaper. It is also used in tire manufacture as a mold release agent, in drilling mud, and in various cosmetics for its luster. [13]


Stereo image
Left frame 
Fuschite3d.jpg
Right frame 
Fuschite3d.jpg
Parallel view ( Stereogram guide parallel.png )
Fuschite3d.jpg
Cross-eye view ( Stereogram guide cross-eyed.png )
Fuschite3d.jpg
Fuschite3d.jpg
Small specimen of Muscovite (fuchsite) from Brazil.

Related Research Articles

<span class="mw-page-title-main">Biotite</span> Group of phyllosilicate minerals within the mica group

Biotite is a common group of phyllosilicate minerals within the mica group, with the approximate chemical formula K(Mg,Fe)3AlSi3O10(F,OH)2. It is primarily a solid-solution series between the iron-endmember annite, and the magnesium-endmember phlogopite; more aluminous end-members include siderophyllite and eastonite. Biotite was regarded as a mineral species by the International Mineralogical Association until 1998, when its status was changed to a mineral group. The term biotite is still used to describe unanalysed dark micas in the field. Biotite was named by J.F.L. Hausmann in 1847 in honor of the French physicist Jean-Baptiste Biot, who performed early research into the many optical properties of mica.

<span class="mw-page-title-main">Kyanite</span> Aluminosilicate mineral

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.

<span class="mw-page-title-main">Mineral</span> Crystalline chemical element or compound formed by geologic processes

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.

<span class="mw-page-title-main">Mica</span> Group of phyllosilicate minerals

Micas are a group of silicate minerals whose outstanding physical characteristic is that individual mica crystals can easily be split into extremely thin elastic plates. This characteristic is described as perfect basal cleavage. Mica is common in igneous and metamorphic rock and is occasionally found as small flakes in sedimentary rock. It is particularly prominent in many granites, pegmatites, and schists, and "books" of mica several feet across have been found in some pegmatites.

<span class="mw-page-title-main">Talc</span> Hydrated magnesium phyllosilicate mineral

Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg3Si4O10(OH)2. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form.

<span class="mw-page-title-main">Silicate</span> Any polyatomic anion containing silicon and oxygen

In chemistry, a silicate is any member of a family of polyatomic anions consisting of silicon and oxygen, usually with the general formula [SiO(4-2x)−
4−x
]
n
, where 0 ≤ x < 2. The family includes orthosilicate SiO4−4, metasilicate SiO2−3, and pyrosilicate Si2O6−7. The name is also used for any salt of such anions, such as sodium metasilicate; or any ester containing the corresponding chemical group, such as tetramethyl orthosilicate. The name "silicate" is sometimes extended to any anions containing silicon, even if they do not fit the general formula or contain other atoms besides oxygen; such as hexafluorosilicate [SiF6]2−.Most commonly, silicates are encountered as silicate minerals.

<span class="mw-page-title-main">Hornblende</span> Complex inosilicate series of minerals

Hornblende is a complex inosilicate series of minerals. It is not a recognized mineral in its own right, but the name is used as a general or field term, to refer to a dark amphibole. Hornblende minerals are common in igneous and metamorphic rocks.

<span class="mw-page-title-main">Amphibole</span> Group of inosilicate minerals

Amphibole is a group of inosilicate minerals, forming prism or needlelike crystals, composed of double chain SiO
4
tetrahedra, linked at the vertices and generally containing ions of iron and/or magnesium in their structures. Its IMA symbol is Amp. Amphiboles can be green, black, colorless, white, yellow, blue, or brown. The International Mineralogical Association currently classifies amphiboles as a mineral supergroup, within which are two groups and several subgroups.

<span class="mw-page-title-main">Pyroxene</span> Group of inosilicate minerals with single chains of silica tetrahedra

The pyroxenes are a group of important rock-forming inosilicate minerals found in many igneous and metamorphic rocks. Pyroxenes have the general formula XY(Si,Al)2O6, where X represents calcium (Ca), sodium (Na), iron or magnesium (Mg) and more rarely zinc, manganese or lithium, and Y represents ions of smaller size, such as chromium (Cr), aluminium (Al), magnesium (Mg), cobalt (Co), manganese (Mn), scandium (Sc), titanium (Ti), vanadium (V) or even iron. Although aluminium substitutes extensively for silicon in silicates such as feldspars and amphiboles, the substitution occurs only to a limited extent in most pyroxenes. They share a common structure consisting of single chains of silica tetrahedra. Pyroxenes that crystallize in the monoclinic system are known as clinopyroxenes and those that crystallize in the orthorhombic system are known as orthopyroxenes.

<span class="mw-page-title-main">Lepidolite</span> Light micas with substantial lithium

Lepidolite is a lilac-gray or rose-colored member of the mica group of minerals with chemical formula K(Li,Al)3(Al,Si,Rb)4O10(F,OH)2. It is the most abundant lithium-bearing mineral and is a secondary source of this metal. It is the major source of the alkali metal rubidium.

An oxyanion, or oxoanion, is an ion with the generic formula A
x
Oz
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
z
A
x
O
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.

<span class="mw-page-title-main">Clay mineral</span> Fine-grained aluminium phyllosilicates

Clay minerals are hydrous aluminium phyllosilicates (e.g. kaolin, Al2Si2O5(OH)4), sometimes with variable amounts of iron, magnesium, alkali metals, alkaline earths, and other cations found on or near some planetary surfaces.

<span class="mw-page-title-main">Silicate mineral</span> Rock-forming minerals with predominantly silicate anions

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.

<span class="mw-page-title-main">Chlorite group</span> Type of mineral

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.

<span class="mw-page-title-main">Cleavage (crystal)</span> Tendency of crystalline materials

Cleavage, in mineralogy and materials science, is the tendency of crystalline materials to split along definite crystallographic structural planes. These planes of relative weakness are a result of the regular locations of atoms and ions in the crystal, which create smooth repeating surfaces that are visible both in the microscope and to the naked eye. If bonds in certain directions are weaker than others, the crystal will tend to split along the weakly bonded planes. These flat breaks are termed "cleavage". The classic example of cleavage is mica, which cleaves in a single direction along the basal pinacoid, making the layers seem like pages in a book. In fact, mineralogists often refer to "books of mica".

<span class="mw-page-title-main">Afwillite</span> Nesosilicate alteration mineral also sometimes found in hydrated cement paste

Afwillite is a calcium hydroxide nesosilicate mineral with formula Ca3(SiO3OH)2·2H2O. It occurs as glassy, colorless to white prismatic monoclinic crystals. Its Mohs scale hardness is between 3 and 4. It occurs as an alteration mineral in contact metamorphism of limestone. It occurs in association with apophyllite, natrolite, thaumasite, merwinite, spurrite, gehlenite, ettringite, portlandite, hillebrandite, foshagite, brucite and calcite.

Bityite is considered a rare mineral, and it is an endmember to the margarite mica sub-group found within the phyllosilicate group. The mineral was first described by Antoine François Alfred Lacroix in 1908, and later its chemical composition was concluded by Professor Hugo Strunz. Bityite has a close association with beryl, and it generally crystallizes in pseudomorphs after it, or in cavities associated with reformed beryl crystals. The mineral is considered a late-stage constituent in lithium bearing pegmatites, and has only been encountered in a few localities throughout the world. The mineral was named by Lacroix after Mt. Bity, Madagascar from where it was first discovered.

<span class="mw-page-title-main">Pimelite</span> Nickel-rich smectite deprecated as mineral species in 2006

Pimelite was discredited as a mineral species by the International Mineralogical Association (IMA) in 2006, in an article which suggests that "pimelite" specimens are probably willemseite, or kerolite. This was a mass discreditation, and not based on any re-examination of the type material. Nevertheless, a considerable number of papers have been written, verifying that pimelite is a nickel-dominant smectite. It is always possible to redefine a mineral wrongly discredited.

The spinels are any of a class of minerals of general formulation AB
2
X
4
which crystallise in the cubic (isometric) crystal system, with the X anions arranged in a cubic close-packed lattice and the cations A and B occupying some or all of the octahedral and tetrahedral sites in the lattice. Although the charges of A and B in the prototypical spinel structure are +2 and +3, respectively, other combinations incorporating divalent, trivalent, or tetravalent cations, including magnesium, zinc, iron, manganese, aluminium, chromium, titanium, and silicon, are also possible. The anion is normally oxygen; when other chalcogenides constitute the anion sublattice the structure is referred to as a thiospinel.

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

Ephesite is a rare member of the mica silicate mineral group, phyllosilicate. It is restricted to quartz-free, alumina rich mineral assemblages and has been found in South African deposits in the Postmasburg district as well as Ephesus, Turkey.

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. Mineralienatlas
  3. Muscovite mineral information and data Mindat
  4. Muscovite Mineral Data Webmineral
  5. Handbook of Mineralogy
  6. Encyclopædia Britannica
  7. P. C. Rickwood (1981). "The largest crystals" (PDF). American Mineralogist. 66: 885–907.
  8. Blatt, Harvey and Robert J. Tracy, Petrology, Freeman, 2nd ed., 1995, p. 516 ISBN   0-7167-2438-3
  9. 1 2 3 4 5 Nesse, William D. (2000). Introduction to mineralogy. New York: Oxford University Press. pp. 235–238. ISBN   9780195106916.
  10. "Minerals Colored by Metal Ions". minerals.gps.caltech.edu. Retrieved 2023-03-01.
  11. Guggenheim, Stephen; Chang, Yu-Hwa; Koster van Groos, August F. (1 June 1987). "Muscovite dehydroxylation; high-temperature studies". American Mineralogist. 72 (5–6): 537–550. Retrieved 15 December 2021.
  12. 1 2 Nesse 2000, p. 244.
  13. Nesse 2000, p. 246.