chalcopyrite

(kăl'kə-pī'rīt')

[New Latin chalcopyrites : Greek khalkos, copper + PYRITES.]

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A mineral having composition CuFeS₂. Crystals are usually small and resemble tetrahedra. Chalcopyrite is usually massive with a metallic luster, brass-yellow color, and sometimes an iridescent tarnish. The Mohs hardness is 3.5–4.0, and the density 4.1–4.3. Chalcopyrite is a so-called fool's gold, but is brittle while gold is sectile. Pyrite, the most widespread fool's gold, is harder than chalcopyrite. See also Pyrite.

Chalcopyrite is the most widespread primary copper ore mineral. It is commonly found in veins (Braden mine, Chile; Cornwall, England; Butte, Montana; Freiberg, Saxony; Tasmania; Rio Tinto, Spain). Chalcopyrite is also found in contact metamorphic deposits in limestone (Bisbee, Arizona) and as sedimentary deposits (Mansfeld, Germany). See also Copper.

Environment

Common in multitemperature sulfide veins, and often disseminated through porphyritic igneous rocks.

Though tetragonal, the characteristically sphenoidal crystals of chalcopyrite resemble tetrahedra. Crystals of 2-3 cm are common; often they are even larger, with faces usually somewhat uneven and tarnished from black to brilliant iridescent hues. Usually massive, often making up golden sulfide mixtures of several minerals. Structurally close to sphalerite, it often makes oriented intergrowths, with small crystals studded over sphalerite surfaces.

Golden. Luster metallic, often with iridescent tarnish; hardness 3Ɖ-4; gravity 4.1-4.3; fracture uneven; cleavage 1 poor (and rarely noted). Brittle.

Sulfide of copper and iron (34.5% Cu, 30.5% Fe, 35% S).

On charcoal, fuses to magnetic black globule; touched with HCl, tints flame with blue flash. Solution with strong nitric acid is green; ammonia precipitates red iron hydroxide and leaves a blue solution.

Confused with gold, but is brittle, crushes to a green-black powder, gives black streak, and dissolves in acid. Distinguished from pyrite by ease of scratching and by copper tests. The color is a richer yellow than pyrite. Also, obviously hard and shiny pyrite will frequently show smooth flat surfaces, striated cubes or pyritohedrons, whereas chalcopyrite, when not massive, is in characteristic sphenoidal crystals.

The basic copper ore. Widely distributed and may be found in all types of primary occurrences. Often associated with other copper minerals: pyrite, sphalerite, galena, and pyrrhotite. The economically important "porphyry coppers" of Bingham, Utah; Ely, Nevada; and Ajo, Arizona; are representative of open-pit-mined, worldwide low-grade (1-3 percent) copper disseminations through igneous rocks. Some of the best crystals are from Cornwall, England; Akita and Tochigi prefectures, Japan; French Creek, Pennsylvania; and several Colorado localities. Often crystallized in the parallel growths on and through crystals of sphalerite in the Joplin District of Missouri, Kansas, and Oklahoma. Giant 6-in. (15 cm) crystals were found in Freirina, n. Chile. Abundant in n. Mexico, another good source of large crystals.

Chalcopyrite is the generic copper ore that, by alteration and successive removals of iron, produces a series starting with chalcopyrite and going through bornite (Cu ₅ FeS ₄ ), covellite (CuS), and chalcocite (Cu ₂ S), and ending (rarely) as native copper (Cu). (See discussion of secondary enrichment under chalcocite.)

• Mineral compounds

Chalcopyrite
Twinned chalcopyrite crystal from the Camp Bird Mine, Ouray County, Colorado (size:5.2 x 3.6 x 2.7 cm)
General
Category	Sulfide mineral
Chemical formula	CuFeS2
Strunz classification	02.CB.10a
Crystal symmetry	Tetragonal 42m – scalenohedral
Unit cell	a = 5.289 Å, c = 10.423 Å; Z = 4
Identification
Molar mass	183.54
Color	Brass yellow, may have iridescent purplish tarnish.
Crystal habit	Predominantly the disphenoid and resembles a tetrahedron, commonly massive, and sometimes botryoidal.
Crystal system	Tetragonal Scalenohedral 42m
Twinning	Penetration twins
Cleavage	Indistinct on {011}
Fracture	Irregular to uneven
Tenacity	Brittle
Mohs scale hardness	3.5
Luster	Metallic
Streak	Greenish black
Diaphaneity	Opaque
Specific gravity	4.1 – 4.3
Solubility	Soluble in HNO3
Other characteristics	magnetic on heating
References	[1][2][3][4][5]

Chalcopyrite ( /ˌkælkɵˈpaɪraɪt/ kal-ko-py-ryt) is a copper iron sulfide mineral that crystallizes in the tetragonal system. It has the chemical composition CuFeS₂. 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.

On exposure to air, chalcopyrite oxidises to a variety of oxides, hydroxides and sulfates. Associated copper minerals include the sulfides bornite (Cu₅FeS₄), chalcocite (Cu₂S), covellite (CuS), digenite (Cu₉S₅); carbonates such as malachite and azurite, and rarely oxides such as cuprite (Cu₂O). Chalcopyrite is rarely found in association with native copper.

Contents 1 Identification 2 Chemistry 3 Paragenesis 4 Occurrence 5 Structure 6 See also 7 References

Identification

Chalcopyrite and dolomite from the Tri-state district (size: Size: 16.8 x 11.1 x 5.2 cm)

Chalcopyrite is often confused with pyrite, although the latter has a cubic and not a tetragonal crystal system. Further, chalcopyrite is often massive, rarely crystalline, and less brittle. Chalcopyrite is also a darker yellow in color, with a greenish tinge and diagnostic greasy luster.

Due to its color and high copper content, chalcopyrite has often been referred to as "yellow copper" or "fool's gold".

Chemistry

The unit cell of chalcopyrite. Copper is shown in pink, iron in blue and sulfur in yellow.

Natural chalcopyrite has no solid solution series with any other sulfide minerals. There is limited substitution of Zn with Cu despite chalcopyrite having the same crystal structure as sphalerite.

However, it is often contaminated by a variety of other trace elements such as Co, Ni, Mn, Zn and Sn substituting for Cu and Fe. Se, Fe and As substitute for sulfur, and trace amounts of Ag, Au, Pt, Pd, Pb, V, Cr, In, Al and Sb are reported.

It is likely many of these elements are present in finely intergrown minerals within the chalcopyrite crystal, for instance lamellae of arsenopyrite representing As, molybdenite representing Mo, etc.

Paragenesis

Chalcopyrite is present with many ore bearing environments via a variety of ore forming processes.

Chalcopyrite is present in volcanogenic massive sulfide ore deposits and sedimentary exhalative deposits, formed by deposition of copper during hydrothermal circulation. Chalcopyrite is concentrated in this environment via fluid transport.

Porphyry copper ore deposits are formed by concentration of copper within a granite stock during the ascent and crystallisation of a magma. Chalcopyrite in this environment is produced by concentration within a magma system.

Chalcopyrite is an accessory mineral in Kambalda type komatiitic nickel ore deposits, formed from an immiscible sulfide liquid in sulfur-saturated ultramafic lavas. In this environment chalcopyrite is formed by a sulfide liquid stripping copper from an immiscible silicate liquid.

Occurrence

Fine brassy chalcopyrite crystals below large striated pyrite cubes (size:8.8 x 6.3 x 4.5 cm)

Chalcopyrite is the most important copper ore. Chalcopyrite ore occurs in a variety of ore types, from huge masses as at Timmins, Ontario, to irregular veins and disseminations associated with granitic to dioritic intrusives as in the porphyry copper deposits of Broken Hill, the American cordillera and the Andes. The largest deposit of nearly pure chalcopyrite ever discovered in Canada was at the southern end of the Temagami greenstone belt where Copperfields Mine extracted the high-grade copper.^[6]

Chalcopyrite is present in the supergiant Olympic Dam Cu-Au-U deposit in South Australia.

Chalcopyrite may also be found in coal seams associated with pyrite nodules, and as disseminations in carbonate sedimentary rocks.

Structure

Crystallographically the structure of chalcopyrite is closely related to that of zinc blende ZnS (sphalerite). The unit cell is twice as large, reflecting an alternation of Cu⁺ and Fe³⁺ ions replacing Zn²⁺ ions in adjacent cells. In contrast to the pyrite structure chalcopyrite has single S^2- sulfide anions rather than disulfide pairs. Another difference is that the iron cation is not diamagnetic low spin Fe(II) as in pyrite.

See also

Earth sciences portal

• Classification of minerals
• List of minerals
• Kesterite

References

Wikimedia Commons has media related to: Chalcopyrite

1. ^ Klein, Cornelis and Cornelius S. Hurlbut, Jr., Manual of Mineralogy, Wiley, 20th ed., 1985, pp. 277 – 278 ISBN 0-471-80580-7
2. ^ Palache, C., H. Berman, and C. Frondel (1944) Dana’s system of mineralogy, (7th edition), v. I, 219–224
3. ^ http://www.mindat.org/min-955.html mindat.org
4. ^ http://webmineral.com/data/Chalcopyrite.shtml Webmineral.com
5. ^ Handbook of Mineralogy
6. ^ Barnes, Michael (2008). More Than Free Gold. Renfrew, Ontario: General Store Publishing House. p. 31. ISBN 978-1-897113-90-5. 

v · d · e Ore minerals, mix of minerals and ore deposits Ores Oxides Cassiterite (tin) Chromite (chromium) Hematite (iron) Ilmenite (titanium) Magnetite (iron) Sulfides Acanthite (silver) Chalcopyrite (copper) Chalcocite (copper) Cinnabar (mercury) Galena (lead) Pentlandite (nickel) Sphalerite (zinc) Other Bauxite (aluminium) Scheelite (tungsten) Ore deposit types Banded iron formation Carbonate hosted lead zinc ore deposits Heavy mineral sands Iron oxide copper gold Kambalda type komatiitic nickel ore deposits Lateritic nickel Magmatic nickel-copper-iron-PGE deposits Porphyry copper Sedimentary exhalative deposits Volcanogenic massive sulfide

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