Bornite

Last updated
Bornite
Bornite-Quartz-135210.jpg
Lightly iridescent bornite crystal on quartz needles, from Kazakhstan
Specimen size: 3.6 cm × 2.2 cm × 1.2 cm (1.42 in × 0.87 in × 0.47 in)
General
Category Sulfide mineral
Formula
(repeating unit)
Cu5FeS4
IMA symbol Bn [1]
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
ColorCopper 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
Tenacity Brittle
Mohs scale hardness3–3.25
Luster Metallic if fresh, iridescent tarnish
Streak Grayish black
Specific gravity 5.06–5.08
Refractive index Opaque
Pleochroism Weak but noticeable
Other characteristicsMagnetic after heating, iridescent
References [2] [3] [4]

Bornite, also known as peacock ore, is a sulfide mineral with chemical composition Cu 5 Fe S 4 that crystallizes in the orthorhombic system (pseudo-cubic).

Contents

Appearance

Tarnish of bornite Mineraly.sk - bornit.jpg
Tarnish of bornite

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.

Mineralogy

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. [3] It is important as an ore for its copper content of about 63 percent by mass. [2]

Structure

Microscopic picture of Bornite Bornite by petrographic microscope.jpg
Microscopic picture of Bornite

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. [5]

Composition

Substantial variation in the relative amounts of copper and iron is possible and solid solution extends towards chalcopyrite (CuFeS2) and digenite (Cu9S5). Exsolution of blebs and lamellae of chalcopyrite, digenite, and chalcocite is common. [5]

Form and twinning

Rare crystals are approximately cubic, dodecahedral, or octahedral. Usually massive. Penetration twinning on the crystallographic direction, {111}. [5]

Occurrence

Bornite with silver from Zacatecas, Mexico (size: 7.5 x 4.3 x 3.4 cm) Silver-Bornite-171549.jpg
Bornite with silver from Zacatecas, Mexico (size: 7.5 × 4.3 × 3.4 cm)

It occurs globally in copper ores with notable crystal localities in Butte, Montana and at Bristol, Connecticut in the U.S. It is also collected from the Carn Brea mine, Illogan, and elsewhere in Cornwall, England. Large crystals are found from the Frossnitz Alps, eastern Tirol, Austria; the Mangula mine, Lomagundi district, Zimbabwe; from the N'ouva mine, Talate, Morocco, the West Coast of Tasmania and in Dzhezkazgan, Kazakhstan. [3] There are also traces of it found amongst the hematite in the Pilbara region of Western Australia.

History and etymology

It was first described in 1725 for an occurrence in the Ore Mountains, Bohemia, in what is now the Karlovy Vary Region of the Czech Republic. It was named in 1845 for Austrian mineralogist Ignaz von Born. [4]

See also

Related Research Articles

<span class="mw-page-title-main">Pentlandite</span> Iron–nickel sulfide

Pentlandite is an iron–nickel sulfide with the chemical formula (Fe,Ni)9S8. Pentlandite has a narrow variation range in nickel to iron ratios (Ni:Fe), but it is usually described as 1:1. In some cases, this ratio is skewed by the presence of pyrrhotite inclusions. It also contains minor cobalt, usually at low levels as a fraction of weight.

<span class="mw-page-title-main">Chalcopyrite</span> Copper iron sulfide mineral

Chalcopyrite ( KAL-kə-PY-ryte, -⁠koh-) is a copper iron sulfide mineral and the most abundant copper ore mineral. It has the chemical formula CuFeS2 and crystallizes in the tetragonal system. It has a brassy to golden yellow color and a hardness of 3.5 to 4 on the Mohs scale. Its streak is diagnostic as green-tinged black.

<span class="mw-page-title-main">Germanite</span>

Germanite is a rare copper iron germanium sulfide mineral, Cu26Fe4Ge4S32. It was first discovered in 1922, and named for its germanium content. It is only a minor source of this important semiconductor element, which is mainly derived from the processing of the zinc sulfide mineral sphalerite. Germanite contains gallium, zinc, molybdenum, arsenic, and vanadium as impurities.

<span class="mw-page-title-main">Chalcocite</span> Sulfide mineral

Chalcocite, copper(I) sulfide (Cu2S), is an important copper ore mineral. It is opaque and dark gray to black, with a metallic luster. It has a hardness of 2.5–3 on the Mohs scale. It is a sulfide with a monoclinic crystal system.

<span class="mw-page-title-main">Covellite</span> Sulfide mineral

Covellite is a rare copper sulfide mineral with the formula CuS. This indigo blue mineral is commonly a secondary mineral in limited abundance and although it is not an important ore of copper itself, it is well known to mineral collectors.

<span class="mw-page-title-main">Pyrrhotite</span> Magnetic iron sulfide mineral

Pyrrhotite is an iron sulfide mineral with the formula Fe(1-x)S. It is a nonstoichiometric variant of FeS, the mineral known as troilite. Pyrrhotite is also called magnetic pyrite, because the color is similar to pyrite and it is weakly magnetic. The magnetism decreases as the iron content decreases, and troilite is non-magnetic. Pyrrhotite is generally tabular and brassy/bronze in color with a metallic luster. The mineral occurs with mafic igneous rocks like norites, and may form from pyrite during metamorphic processes. Pyrrhotite is associated and mined with other sulfide minerals like pentlandite, pyrite, chalcopyrite, and magnetite, and has been found globally.

<span class="mw-page-title-main">Tetrahedrite</span> Copper antimony sulfosalt mineral

Tetrahedrite is a copper antimony sulfosalt mineral with formula: (Cu,Fe)
12
Sb
4
S
13
. It is the antimony endmember of the continuous solid solution series with arsenic-bearing tennantite. Pure endmembers of the series are seldom if ever seen in nature. Of the two, the antimony rich phase is more common. Other elements also substitute in the structure, most notably iron and zinc, along with less common silver, mercury and lead. Bismuth also substitutes for the antimony site and bismuthian tetrahedrite or annivite is a recognized variety. The related, silver dominant, mineral species freibergite, although rare, is notable in that it can contain up to 18% silver.

<span class="mw-page-title-main">Sperrylite</span>

Sperrylite is a platinum arsenide mineral with the chemical formula PtAs2 and is an opaque metallic tin white mineral which crystallizes in the isometric system with the pyrite group structure. It forms cubic, octahedral or pyritohedral crystals in addition to massive and reniform habits. It has a Mohs hardness of 6 - 7 and a very high specific gravity of 10.6.

<span class="mw-page-title-main">Fukuchilite</span>

Fukuchilite, Cu
3
FeS
8
, is a copper iron sulfide named after the Japanese mineralogist Nobuyo Fukuchi (1877–1934), that occurs in ore bodies of gypsum-anhydrite at the intersection points of small masses of barite, covellite, gypsum and pyrite, and is mostly found in the Hanawa mine in the Akita prefecture of Honshū, Japan where it was first discovered in 1969. It occurs in masses within the third geologic unit of the Kuroko type deposits within the mine.

In ore deposit geology, supergene processes or enrichment are those that occur relatively near the surface as opposed to deep hypogene processes. Supergene processes include the predominance of meteoric water circulation (i.e. water derived from precipitation) with concomitant oxidation and chemical weathering. The descending meteoric waters oxidize the primary (hypogene) sulfide ore minerals and redistribute the metallic ore elements. Supergene enrichment occurs at the base of the oxidized portion of an ore deposit. Metals that have been leached from the oxidized ore are carried downward by percolating groundwater, and react with hypogene sulfides at the supergene-hypogene boundary. The reaction produces secondary sulfides with metal contents higher than those of the primary ore. This is particularly noted in copper ore deposits where the copper sulfide minerals chalcocite (Cu2S), covellite (CuS), digenite (Cu18S10), and djurleite (Cu31S16) are deposited by the descending surface waters.

<span class="mw-page-title-main">Digenite</span> Copper sulfide mineral

Digenite is a copper sulfide mineral with formula: Cu9S5. Digenite is a black to dark blue opaque mineral that crystallizes with a trigonal - hexagonal scalenohedral structure. In habit it is usually massive, but does often show pseudo-cubic forms. It has poor to indistinct cleavage and a brittle fracture. It has a Mohs hardness of 2.5 to 3 and a specific gravity of 5.6. It is found in copper sulfide deposits of both primary and supergene occurrences. It is typically associated with and often intergrown with chalcocite, covellite, djurleite, bornite, chalcopyrite and pyrite. The type locality is Sangerhausen, Thuringia, Germany, in copper slate deposits.

<span class="mw-page-title-main">Djurleite</span> Copper sulfide mineral

Djurleite is a copper sulfide mineral of secondary origin with formula Cu31S16 that crystallizes with monoclinic-prismatic symmetry. It is typically massive in form, but does at times develop thin tabular to prismatic crystals. It occurs with other supergene minerals such as chalcocite, covellite and digenite in the enriched zone of copper orebodies. It is a member of the chalcocite group, and very similar to chalcocite, Cu2S, in its composition and properties, but the two minerals can be distinguished from each other by x-ray powder diffraction. Intergrowths and transformations between djurleite, digenite and chalcocite are common. Many of the reported associations of digenite and djurleite, however, identified by powder diffraction, could be anilite and djurleite, as anilite transforms to digenite during grinding.

<span class="mw-page-title-main">Carrollite</span>

Carrollite, CuCo2S4, is a sulfide of copper and cobalt, often with substantial substitution of nickel for the metal ions, and a member of the linnaeite group. It is named after the type locality in Carroll County, Maryland, US, at the Patapsco mine, Sykesville.

Copper sulfides describe a family of chemical compounds and minerals with the formula CuxSy. Both minerals and synthetic materials comprise these compounds. Some copper sulfides are economically important ores.

<span class="mw-page-title-main">Cubanite</span> Copper iron sulfide mineral

Cubanite is a copper iron sulfide mineral that commonly occurs as a minor alteration mineral in magmatic sulfide deposits. It has the chemical formula CuFe2S3 and when found, it has a bronze to brass-yellow appearance. On the Mohs hardness scale, cubanite falls between 3.5 and 4 and has a orthorhombic crystal system. Cubanite is chemically similar to chalcopyrite, however it is the less common copper iron sulfide mineral due to crystallization requirements.

Fletcherite is a rare thiospinel sulfide mineral with formula Cu(Ni,Co)2S4. It is an opaque metallic steel gray mineral which crystallizes in the cubic crystal system. It is a member of the linnaeite group.

Mooihoekite is a copper iron sulfide mineral with chemical formula of Cu9Fe9S16. The mineral was discovered in 1972 and received its name from its discovery area, the Mooihoek mine in Transvaal, South Africa.

Skaergaardite is an intermetallic platinum group mineral with the general chemical formula PdCu. The mineral is named after its discovery location: the Skaergaard intrusion, Kangerdlugssuaq area, East Greenland. The mineral name was approved by the International Mineralogical Association in 2003. The mineral has also been reported in the Duluth intrusion in Minnesota and the Rum layered intrusion in Scotland.

<span class="mw-page-title-main">Kesterite</span>

Kësterite is a sulfide mineral with a chemical formula of Cu2(Zn,Fe)SnS4. In its lattice structure, zinc and iron atoms share the same lattice sites. Kesterite is the Zn-rich variety whereas the Zn-poor form is called ferrokesterite or stannite. Owing to their similarity, kesterite is sometimes called isostannite. The synthetic form of kesterite is abbreviated as CZTS. The name kesterite is sometimes extended to include this synthetic material and also CZTSe, which contains selenium instead of sulfur.

<span class="mw-page-title-main">Djerfisherite</span>

Djerfisherite is an alkali copper–iron sulfide mineral and a member of the djerfisherite group.

References

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi: 10.1180/mgm.2021.43 . S2CID   235729616.
  2. 1 2 Barthelmy, David (2014). "Bornite Mineral Data". Webmineral.com. Retrieved 12 August 2022.
  3. 1 2 3 Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (2005). "Bornite" (PDF). Handbook of Mineralogy. Mineral Data Publishing. Retrieved 12 August 2022.
  4. 1 2 Bornite, Mindat.org , retrieved 12 August 2022
  5. 1 2 3 Nesse, William D., "Sulfides and Related Minerals" in Introduction to Mineralogy, New York: Oxford University Press, 2000, p 429

Bibliography