Bismoclite
Bismoclite | |
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General | |
Category | Halide mineral - Oxide mineral |
Formula (repeating unit) | BiOCl |
Strunz classification | 3.DC.25 |
Dana classification | 10.2.1.2 |
Crystal system | Tetragonal |
Unit cell | a = 3.887 Å, c = 7.354 Å; Z=2 |
Identification | |
Color | Cream-white, greyish, yellowish brown |
Crystal habit | Platey to thin rectangular crystals, firous to columnar, massive |
Crystal symmetry |
Tetragonal ditetragonal dipyramidal H-M symbol: (4/m 2/m 2/m) Space group: P 4/nmm |
Cleavage | {001} perfect |
Tenacity | Elastic |
Mohs scale hardness | 2-2.5 |
Luster | Greasy, silky, pearly, dull, earthy |
Streak | White |
Diaphaneity | Transparent to translucent |
Specific gravity | 7.36 (measured), 7.784 (calculated) |
Optical properties | Uniaxial (-) |
Refractive index | nω = 2.150 nε = 1.910 |
Birefringence | δ = 0.240 |
References | [1][2][3] |
Bismoclite is a bismuth oxohalide mineral with formula BiOCl. The name was derived from its chemical constituents. It is a secondary bismuth mineral composed of bismuthyl ions (BiO+) and chloride anions. It is member of the matlockite group.
It was first described in 1935 from alluvium near bismuth-bearing pegmatites in South Africa.[1] It has been found in association with granite pegmatite and in greisen. Associated minerals include: bismutite, mica, jarosite, alunite, cerussite, atacamite, connellite. Occurrences include the type locality at Jackals Water, SW of Prieska, South Africa; Bygoo, Australia; the Tintic district in the East Tintic Mountains of Utah; and from Dalbeattie, Scotland.[2]
References
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