Kernite | |
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General | |
Category | Inoborates |
Formula (repeating unit) |
Na 2B 4O 6(OH) 2·3H 2O |
Strunz classification | 6.DB.05 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | P21/c |
Unit cell | a = 7.0172(2) b = 9.1582(2) c = 15.6774(5) [Å] β = 108.861(2)°; Z = 4 |
Identification | |
Formula mass | 273.22 g/mol |
Color | Colorless, white |
Crystal habit | Crystalline - occurs as well-formed coarse sized crystals |
Cleavage | Perfect on [100] and [001], good on [201] |
Fracture | Splintery |
Tenacity | Brittle |
Mohs scale hardness | 2.5-3 |
Luster | Vitreous - pearly |
Streak | White |
Specific gravity | 1.9 - 1.92 |
Optical properties | Biaxial (-) |
Refractive index | nα=1.454, nβ=1.472, nγ=1.488 |
Birefringence | δ =0.0340 |
2V angle | 80° |
Other characteristics | Non-radioactive, non-fluorescent, non-magnetic |
References |
Kernite, also known as rasorite is a hydrated sodium borate hydroxide mineral with formula Na
2B
4O
6(OH)
2·3H
2O. It is a colorless to white mineral crystallizing in the monoclinic crystal system typically occurring as prismatic to acicular crystals or granular masses. It is relatively soft with Mohs hardness of 2.5 to 3 and light with a specific gravity of 1.91. It exhibits perfect cleavage and a brittle fracture.
Kernite is soluble in cold water and alters to tincalconite when it dehydrates. It undergoes a non-reversible alteration to metakernite (Na
2B
4O
7·5H
2O) when heated to above 100 °C.
The mineral occurs in sedimentary evaporite deposits in arid regions.
Kernite was discovered in 1926 in eastern Kern County, in Southern California, and later renamed after the county. The location was the US Borax Mine at Boron in the western Mojave Desert. This type material is stored at Harvard University, Cambridge, Massachusetts, and the National Museum of Natural History, Washington, D.C.