Brucite | |
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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 | |
Color | White, 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 hardness | 2.5 to 3 |
Luster | Vitreous to pearly |
Streak | White |
Diaphaneity | Transparent |
Specific gravity | 2.39 to 2.40 |
Optical properties | Uniaxial (+) |
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.
It adopts a layered CdI2-like structure with hydrogen-bonds between the layers. [5]
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.
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 ]
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]
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]
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
2O, for various values of x, y, and z; or, equivalently, Mg
x+y(OH)
2xCl
2y(H
2O)
z−x. 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.
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.