Bornite | |
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Lightly iridescent bornite crystal on quartz needles from Kazakhstan (size: 3.6 x 2.2 x 1.2 cm)
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General | |
Category | Sulfide mineral |
Formula (repeating unit) |
Cu5FeS4 |
Strunz classification | 2.BA.10 |
Crystal system | Orthorhombic |
Crystal class | Dipyramidal (mmm) H-M symbol: (2/m 2/m 2/m) |
Space group | Pbca |
Unit cell | a = 10.95 Å, b = 21.862 Å, c = 10.95 Å; Z = 16 |
Identification | |
Formula mass | 501.88 g/mol |
Color | Copper red, bronze brown, purple |
Crystal habit | Granular, massive, disseminated - Crystals pseudocubic, dodecahedral, octahedral |
Twinning | Penetration twins on [111] |
Cleavage | Poor on [111]. |
Fracture | Uneven to subconchoidal; brittle |
Tenacity | Brittle |
Mohs scale hardness | 3 - 3.25 |
Luster | Metallic if fresh, iridescent tarnish |
Streak | grayish black |
Specific gravity | 5.06 - 5.08 |
Refractive index | Opaque |
Pleochroism | Weak but noticeable |
Other characteristics | Magnetic after heating, iridescent |
References |
Bornite, also known as peacock ore, is a sulfide mineral with chemical composition Cu5FeS4 that crystallizes in the orthorhombic system (pseudo-cubic).
Bornite has a brown to copper-red color on fresh surfaces that tarnishes to various iridescent shades of blue to purple in places. Its striking iridescence gives it the nickname peacock copper or peacock ore.
Bornite is an important copper ore mineral and occurs widely in porphyry copper deposits along with the more common chalcopyrite. Chalcopyrite and bornite are both typically replaced by chalcocite and covellite in the supergene enrichment zone of copper deposits. Bornite is also found as disseminations in mafic igneous rocks, in contact metamorphic skarn deposits, in pegmatites and in sedimentary cupriferous shales. It is important as an ore for its copper content of about 63 percent by mass.
At temperatures above 228 °C (442 °F), the structure is isometric with a unit cell that is about 5.50 Å on an edge. This structure is based on cubic close-packed sulfur atoms, with copper and iron atoms randomly distributed into six of the eight tetrahedral sites located in the octants of the cube. With cooling, the Fe and Cu become ordered, so that 5.5 Å subcells in which all eight tetrahedral sites are filled alternate with subcells in which only four of the tetrahedral sites are filled; symmetry is reduced to orthorhombic.