Boracite in the context of "Hilgardite"

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⭐ Core Definition: Boracite

Boracite is a magnesium borate mineral with formula: Mg3B7O13Cl. It occurs as blue green, colorless, gray, yellow to white crystals in the orthorhombic - pyramidal crystal system. Boracite also shows pseudo-isometric cubical and octahedral forms. These are thought to be the result of transition from an unstable high temperature isometric form on cooling. Penetration twins are not unusual. It occurs as well formed crystals and dispersed grains often embedded within gypsum and anhydrite crystals. It has a Mohs hardness of 7 to 7.5 and a specific gravity of 2.9. Refractive index values are nα = 1.658 - 1.662, nβ = 1.662 - 1.667 and nγ = 1.668 - 1.673. It has a conchoidal fracture and does not show cleavage. It is insoluble in water (not to be confused with borax, which is soluble in water).

Boracite is typically found in evaporite sequences associated with gypsum, anhydrite, halite, sylvite, carnallite, kainite and hilgardite. It was first described in 1789 for specimens from its type locality of Kalkberg hill, Lüneburg, Lower Saxony, Germany. It is also found near Sussex, New Brunswick.

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Boracite in the context of Borate mineral

The Borate Minerals are minerals which contain a borate anion group. The borate (BO3) units may be polymerised similar to the SiO4 unit of the silicate mineral class. This results in B2O5, B3O6, B2O4 anions as well as more complex structures which include hydroxide or halogen anions. The [B(O,OH)4] anion exists as well.

Many borate minerals, such as borax, colemanite, and ulexite, are salts: soft, readily soluble, and found in evaporite contexts. However, some, such as boracite, are hard and resistant to weathering, more similar to the silicates.

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Boracite in the context of Leucite

Leucite (from the Greek word leukos meaning white) is a rock-forming mineral of the feldspathoid group, silica-undersaturated and composed of potassium and aluminium tectosilicate KAlSi2O6. Crystals have the form of cubic icositetrahedra but, as first observed by Sir David Brewster in 1821, they are not optically isotropic, and are therefore pseudo-cubic. Goniometric measurements made by Gerhard vom Rath in 1873 led him to refer the crystals to the tetragonal system. Optical investigations have since proved the crystals to be still more complex in character, and to consist of several orthorhombic or monoclinic individuals, which are optically biaxial and repeatedly twinned, giving rise to twin-lamellae and to striations on the faces. When the crystals are raised to a temperature of about 500 °C they become optically isotropic and the twin-lamellae and striations disappear, although they reappear when the crystals are cooled again. This pseudo-cubic character of leucite is very similar to that of the mineral boracite. Leucite is commonly found in igneous rocks, especially at Mt. Vesuvius

The crystals are white or ash-grey in colour, hence the name suggested by A. G. Werner in 1701, from λευκος, '(matt) white'. They are transparent and glassy when fresh, albeit with a noticeably subdued 'subvitreous' lustre due to the low refractive index, but readily alter to become waxy/greasy and then dull and opaque; they are brittle and break with a conchoidal fracture. The Mohs hardness is 5.5, and the specific gravity 2.47. Inclusions of other minerals, arranged in concentric zones, are frequently present in the crystals. On account of the color and form of the crystals the mineral was early known as 'white garnet'. French authors in older literature may employ René Just Haüy's name amphigène, but 'leucite' is the only name for this mineral species that is recognised as official by the International Mineralogical Association.

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