Brucite

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Brucite
Brucite-231242.jpg
General
Category Oxide mineral
Formula
(repeating unit)
Mg(OH)2
IMA symbol Brc [1]
Strunz classification 4.FE.05
Crystal system Trigonal
Crystal class Hexagonal crystal family (3m)
H-M symbol: (3 2/m)
Space group P3m1
Unit cell a = 3.142(1) Å, c = 4.766(2) Å; Z = 1
Identification
ColorWhite, pale green, blue, gray; honey-yellow to brownish red
Crystal habit Tabular crystals; platy or foliated masses and rosettes – fibrous to massive
Cleavage Perfect on {0001}
Fracture Irregular
Tenacity Sectile
Mohs scale hardness2.5 to 3
Luster Vitreous to pearly
Streak White
Diaphaneity Transparent
Specific gravity 2.39 to 2.40
Optical propertiesUniaxial (+)
Refractive index nω = 1.56–1.59
nε = 1.58–1.60
Birefringence 0.02
Other characteristics Pyroelectric
References [2] [3] [4]

Brucite is the mineral form of magnesium hydroxide, with the chemical formula Mg(OH)2. It is a common alteration product of periclase in marble; a low-temperature hydrothermal vein mineral in metamorphosed limestones and chlorite schists; and formed during serpentinization of dunites. Brucite is often found in association with serpentine, calcite, aragonite, dolomite, magnesite, hydromagnesite, artinite, talc and chrysotile.

Contents

It adopts a layered CdI2-like structure with hydrogen-bonds between the layers. [5]

Discovery

Brucite was first described in 1824 by François Sulpice Beudant [6] and named for the discoverer, American mineralogist, Archibald Bruce (1777–1818). A fibrous variety of brucite is called nemalite. It occurs in fibers or laths, usually elongated along [1010], but sometimes [1120] crystalline directions.

Occurrence

A notable location in the US is Wood's Chrome Mine, Cedar Hill Quarry, Lancaster County, Pennsylvania. Yellow, white and blue brucite with a botryoidal habit was discovered in Qila Saifullah District of Province Baluchistan, Pakistan. In a later discovery, brucite also occurred in the Bela Ophiolite of Wadh, Khuzdar District, Province Baluchistan, Pakistan. Brucite has also occurred from South Africa, Italy, Russia, Canada, and other localities as well, but the most notable discoveries are the US, Russian and Pakistani examples.[ citation needed ]

Industrial applications

Synthetic brucite is mainly consumed as a precursor to magnesia (MgO), a useful refractory and thermal insulator. It finds some use as a flame retardant because it thermally decomposes to release water in a similar way to aluminium hydroxide (Al(OH)3) and mixtures of huntite (Mg3Ca(CO3)4) and hydromagnesite (Mg5(CO3)4(OH)2·4H2O). [7] [8] It also constitutes a significant source of magnesium for industry. Although generally deemed safe, brucite can be contaminated with naturally occurring asbestos fibers. [9]

Magnesium attack of cement and concrete

When cement or concrete are exposed to Mg2+, the neoformation of brucite, an expansive material, may induce mechanical stress in the hardened cement paste or may clog the porous network creating a buffering effect[ clarification needed ] and delaying the alteration/transformation of the C-S-H phase (the "glue" phase in the hardened cement paste) into M-S-H phase (a non-cohesive mineral phase). The exact magnitude of impact that brucite has on cement paste is still debatable. Prolonged contact between sea water or brines and concrete may induce durability issues for regularly immersed concrete components or structures.

The use of dolomite as aggregate in concrete can also cause magnesium attack and should be avoided. [10]

See also

Related Research Articles

<span class="mw-page-title-main">Aluminium hydroxide</span> Chemical compound

Aluminium hydroxide, Al(OH)3, is found in nature as the mineral gibbsite and its three much rarer polymorphs: bayerite, doyleite, and nordstrandite. Aluminium hydroxide is amphoteric, i.e., it has both basic and acidic properties. Closely related are aluminium oxide hydroxide, AlO(OH), and aluminium oxide or alumina, the latter of which is also amphoteric. These compounds together are the major components of the aluminium ore bauxite. Aluminium hydroxide also forms a gelatinous precipitate in water.

<span class="mw-page-title-main">Magnesium hydroxide</span> Inorganic compound of formula Mg(OH)2

Magnesium hydroxide is the inorganic compound with the chemical formula Mg(OH)2. It occurs in nature as the mineral brucite. It is a white solid with low solubility in water (Ksp = 5.61×10−12). Magnesium hydroxide is a common component of antacids, such as milk of magnesia.

<span class="mw-page-title-main">Magnesium sulfate</span> Chemical compound with formula MgSO4

Magnesium sulfate or magnesium sulphate (in English-speaking countries other than the US) is a chemical compound, a salt with the formula MgSO4, consisting of magnesium cations Mg2+ (20.19% by mass) and sulfate anions SO2−4. It is a white crystalline solid, soluble in water but not in ethanol.

<span class="mw-page-title-main">Magnesium carbonate</span> Chemical compound

Magnesium carbonate, MgCO3, is an inorganic salt that is a colourless or white solid. Several hydrated and basic forms of magnesium carbonate also exist as minerals.

Cement chemist notation (CCN) was developed to simplify the formulas cement chemists use on a daily basis. It is a shorthand way of writing the chemical formula of oxides of calcium, silicon, and various metals.

<span class="mw-page-title-main">Flame retardant</span> Substance applied to items to slow burning or delay ignition

The term flame retardant subsumes a diverse group of chemicals that are added to manufactured materials, such as plastics and textiles, and surface finishes and coatings. Flame retardants are activated by the presence of an ignition source and are intended to prevent or slow the further development of ignition by a variety of different physical and chemical methods. They may be added as a copolymer during the polymerisation process, or later added to the polymer at a moulding or extrusion process or applied as a topical finish. Mineral flame retardants are typically additive, while organohalogen and organophosphorus compounds can be either reactive or additive.

<span class="mw-page-title-main">Artinite</span> Hydrated basic magnesium carbonate mineral

Artinite is a hydrated basic magnesium carbonate mineral with formula: Mg2(CO3)(OH)2·3H2O. It forms white silky monoclinic prismatic crystals that are often in radial arrays or encrustations. It has a Mohs hardness of 2.5 and a specific gravity of 2.

<span class="mw-page-title-main">Hydromagnesite</span> Hydrated hydroxy-carbonate mineral of magnesium

Hydromagnesite is a hydrated magnesium carbonate mineral with the formula Mg5(CO3)4(OH)2·4H2O.

Sorel cement is a non-hydraulic cement first produced by the French chemist Stanislas Sorel in 1867.

<span class="mw-page-title-main">Fire retardant</span> Substance reducing flammability

A fire retardant is a substance that is used to slow down or stop the spread of fire or reduce its intensity. This is commonly accomplished by chemical reactions that reduce the flammability of fuels or delay their combustion. Fire retardants may also cool the fuel through physical action or endothermic chemical reactions. Fire retardants are available as powder, to be mixed with water, as fire-fighting foams and fire-retardant gels. Fire retardants are also available as coatings or sprays to be applied to an object.

In inorganic chemistry, mineral hydration is a reaction which adds water to the crystal structure of a mineral, usually creating a new mineral, commonly called a hydrate.

An AFm phase is an "alumina, ferric oxide, monosubstituted" phase, or aluminate ferrite monosubstituted, or Al2O3, Fe2O3 mono, in cement chemist notation (CCN). AFm phases are important hydration products in the hydration of Portland cements and hydraulic cements.

<span class="mw-page-title-main">Thaumasite</span> Complex calcium silicate hydrate mineral

Thaumasite is a calcium silicate mineral, containing Si atoms in unusual octahedral configuration, with chemical formula Ca3Si(OH)6(CO3)(SO4)·12H2O, also sometimes more simply written as CaSiO3·CaCO3·CaSO4·15H2O.

<span class="mw-page-title-main">Layered double hydroxides</span> Class of ionic solids characterized by a layered structure

Layered double hydroxides (LDH) are a class of ionic solids characterized by a layered structure with the generic layer sequence [AcB Z AcB]n, where c represents layers of metal cations, A and B are layers of hydroxide anions, and Z are layers of other anions and neutral molecules. Lateral offsets between the layers may result in longer repeating periods.

The alkali–carbonate reaction is an alteration process first suspected in the 1950s in Canada for the degradation of concrete containing dolomite aggregates.

<span class="mw-page-title-main">Concrete degradation</span> Damage to concrete affecting its mechanical strength and its durability

Concrete degradation may have many different causes. Concrete is mostly damaged by the corrosion of reinforcement bars due to the carbonatation of hardened cement paste or chloride attack under wet conditions. Chemical damages are caused by the formation of expansive products produced by various chemical reactions, by aggressive chemical species present in groundwater and seawater, or by microorganisms. Other damaging processes can also involve calcium leaching by water infiltration and different physical phenomena initiating cracks formation and propagation. All these detrimental processes and damaging agents adversely affects the concrete mechanical strength and its durability.

<span class="mw-page-title-main">Huntite</span> Carbonate mineral

Huntite is a carbonate mineral with the chemical formula Mg3Ca(CO3)4. Huntite crystallizes in the trigonal system and typically occurs as platy crystals and powdery masses. For most of recorded history its main use was as a white pigment. Today the most common industrial use of huntite is as a natural mixture with hydromagnesite as a flame retardant or fire retardant additive for polymers.

Magnesium hydroxychloride is the traditional term for several chemical compounds of magnesium, chlorine, oxygen, and hydrogen whose general formula xMgO·yMgCl
2
·zH
2
O
, for various values of x, y, and z; or, equivalently, Mg
x+y
(OH)
2x
Cl
2y
(H
2
O)
zx
. The simple chemical formula that is often used is MgClOH, which appears in high school subject, for example.Other names for this class are magnesium chloride hydroxide, magnesium oxychloride, and basic magnesium chloride. Some of these compounds are major components of Sorel cement.

Cement hydration and strength development mainly depend on two silicate phases: tricalcium silicate (C3S) (alite), and dicalcium silicate (C2S) (belite). Upon hydration, the main reaction products are calcium silicate hydrates (C-S-H) and calcium hydroxide Ca(OH)2, written as CH in the cement chemist notation. C-S-H is the phase playing the role of the glue in the cement hardened paste and responsible of its cohesion. Cement also contains two aluminate phases: C3A and C4AF, respectively the tricalcium aluminate and the tetracalcium aluminoferrite. C3A hydration products are AFm, calcium aluminoferrite monosulfate, and ettringite, a calcium aluminoferrite trisulfate (AFt). C4AF hydrates as hydrogarnet and ferrous ettringite.

<span class="mw-page-title-main">Widgiemoolthalite</span> Carbonate mineral

Widgiemoolthalite is a rare hydrated nickel(II) carbonate mineral with the chemical formula (Ni,Mg)5(CO3)4(OH)2·5H2O. Usually bluish-green in color, it is a brittle mineral formed during the weathering of nickel sulfide. Present on gaspéite surfaces, widgiemoolthalite has a Mohs scale hardness of 3.5 and an unknown though likely disordered crystal structure. Widgiemoolthalite was first discovered in 1992 in Widgiemooltha, Western Australia, which is to date its only known source. It was named the following year by the three researchers who first reported its existence, Ernest H. Nickel, Bruce W. Robinson, and William G. Mumme.

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. Brucite on Mindat.org
  3. Handbook of Mineralogy
  4. Brucite on Webmineral
  5. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN   978-0-08-037941-8.
  6. "Blog | GeoRarities". 2021-01-13. Retrieved 2021-06-02.
  7. Hollingbery, LA; Hull TR (2010). "The Thermal Decomposition of Huntite and Hydromagnesite - A Review". Thermochimica Acta. 509 (1–2): 1–11. doi:10.1016/j.tca.2010.06.012.
  8. Hollingbery, LA; Hull TR (2010). "The Fire Retardant Behaviour of Huntite and Hydromagnesite - A Review". Polymer Degradation and Stability. 95 (12): 2213–2225. doi:10.1016/j.polymdegradstab.2010.08.019.
  9. Malferrari, Daniele; Di Guisseppe, Dario; Scognamiglio, Valentina; Gualtieri, Alessandro F. (2021). "Commercial brucite, a worldwide used raw material deemed safe, can be contaminated by asbestos". Periodico di Mineralogia. 90 (3): 317–324. doi:10.13133/2239-1002/17384.
  10. Lee, Hyomin; Cody, Robert D.; Cody, Anita M.; Spry, Paul G. (1 May 2002). "Observations on brucite formation and the role of brucite in Iowa highway concrete deterioration". Environmental and Engineering Geoscience. 8 (2): 137–145. Bibcode:2002EEGeo...8..137L. doi:10.2113/gseegeosci.8.2.137. ISSN   1078-7275.

Further reading