Smithsonite

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Smithsonite
Smithsonite-Willemite-cktsu-23a.jpg
General
Category Carbonate mineral
Formula
(repeating unit)
ZnCO3
IMA symbol Smt [1]
Strunz classification 5.AB.05
Crystal system Trigonal
Crystal class Hexagonal scalenohedral (3m)
H-M symbol: (3 2/m)
Space group R3c
Unit cell a = 4.6526(7)
c = 15.0257(22) [Å]; Z = 6
Identification
ColorWhite, grey, yellow, green to apple-green, blue, pink, purple, bluish grey, and brown
Crystal habit Uncommon as crystals, typically botryoidal, reniform, spherulitic; stalactitic, earthy, compact massive
Twinning None observed
Cleavage Perfect on [1011]
Fracture Uneven, sub-conchoidal
Tenacity Brittle
Mohs scale hardness4.5
Luster Vitreous, may be pearly
Streak White
Diaphaneity Translucent
Specific gravity 4.4–4.5
Optical propertiesUniaxial (−)
Refractive index nω = 1.842 – 1.850 nε = 1.619 – 1.623
Birefringence δ = 0.223 – 0.227
Ultraviolet fluorescence May fluoresce pale green or pale blue under UV
References [2] [3] [4]

Smithsonite, also known as zinc spar, is the mineral form of zinc carbonate (Zn CO3). Historically, smithsonite was identified with hemimorphite before it was realized that they were two different minerals. The two minerals are very similar in appearance and the term calamine has been used for both, leading to some confusion. The distinct mineral smithsonite was named in 1832 by François Sulpice Beudant in honor of English chemist and mineralogist James Smithson (c. 1765–1829), who first identified the mineral in 1802. [3] [5]

Contents

Smithsonite is a variably colored trigonal mineral which only rarely is found in well formed crystals. The typical habit is as earthy botryoidal masses. It has a Mohs hardness of 4.5 and a specific gravity of 4.4 to 4.5.

Smithsonite occurs as a secondary mineral in the weathering or oxidation zone of zinc-bearing ore deposits. It sometimes occurs as replacement bodies in carbonate rocks and as such may constitute zinc ore. It commonly occurs in association with hemimorphite, willemite, hydrozincite, cerussite, malachite, azurite, aurichalcite and anglesite. It forms two limited solid solution series, with substitution of manganese leading to rhodochrosite, and with iron, leading to siderite. [4] A variety rich in cadmium, which gives it a bright yellow color, is sometimes called turkey fat ore. The cause of colour is the presence of greenockite inclusions. [2]

See also

Related Research Articles

<span class="mw-page-title-main">Calamine (mineral)</span> Zinc ore group

Calamine is a historic name for an ore of zinc. The name calamine was derived from lapis calaminaris, a Latin corruption of Greek cadmia (καδμία), the old name for zinc ores in general. The name of the Belgian town of Kelmis, La Calamine in French, which was home to a zinc mine, comes from this. In the 18th and 19th centuries large ore mines could be found near the German village of Breinigerberg.

<span class="mw-page-title-main">Hemimorphite</span> Silicate mineral

Hemimorphite is the chemical compound Zn4(Si2O7)(OH)2·H2O, a component of mineral calamine. It is a silicate mineral which, together with smithsonite (ZnCO3), has been historically mined from the upper parts of zinc and lead ores. Both compounds were originally believed to be the same mineral and classified as calamine. In the second half of the 18th century, it was discovered that these two different compounds were both present in calamine. They closely resemble one another.

<span class="mw-page-title-main">Rhodochrosite</span> Mineral of manganese carbonate

Rhodochrosite is a manganese carbonate mineral with chemical composition MnCO3. In its pure form (rare), it is typically a rose-red colour, but it can also be shades of pink to pale brown. It streaks white, and its Mohs hardness varies between 3.5 and 4.5. Its specific gravity is between 3.45 and 3.6. The crystal system of rhodochrosite is trigonal, with a structure and cleavage in the carbonate rhombohedral system. The carbonate ions (CO2−
3
) are arranged in a triangular planar configuration, and the manganese ions (Mn2+) are surrounded by six oxygen ions in an octahedral arrangement. The MnO6 octahedra and CO3 triangles are linked together to form a three-dimensional structure. Crystal twinning is often present. It can be confused with the manganese silicate rhodonite, but is distinctly softer. Rhodochrosite is formed by the oxidation of manganese ore, and is found in South Africa, China, and the Americas. It is one of the national symbols of Argentina.

<span class="mw-page-title-main">Azurite</span> Copper carbonate mineral

Azurite is a soft, deep-blue copper mineral produced by weathering of copper ore deposits. During the early 19th century, it was also known as chessylite, after the type locality at Chessy-les-Mines near Lyon, France. The mineral, a basic carbonate with the chemical formula Cu3(CO3)2(OH)2, has been known since ancient times, and was mentioned in Pliny the Elder's Natural History under the Greek name kuanos (κυανός: "deep blue," root of English cyan) and the Latin name caeruleum. Copper (Cu2+) gives it its blue color.

<span class="mw-page-title-main">Wulfenite</span> Molybdate mineral

Wulfenite is a lead molybdate mineral with the formula PbMoO4. It often occurs as thin tabular crystals with a bright orange-red to yellow-orange color, sometimes brown, although the color can be highly variable. In its yellow form it is sometimes called "yellow lead ore".

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

Hydrozincite, also known as zinc bloom or marionite, is a white carbonate mineral consisting of Zn5(CO3)2(OH)6. It is usually found in massive rather than crystalline form.

<span class="mw-page-title-main">Aurichalcite</span> Basic carbonate of zinc and copper

Aurichalcite is a carbonate mineral, usually found as a secondary mineral in copper and zinc deposits. Its chemical formula is (Zn,Cu)5(CO3)2(OH)6. The zinc to copper ratio is about 5:4. Copper (Cu2+) gives aurichalcite its green-blue colors.

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

Creedite is a calcium aluminium sulfate fluoro hydroxide mineral with formula: Ca3Al2SO4(F,OH)10·2(H2O). Creedite forms colorless to white to purple monoclinic prismatic crystals. It often occurs as acicular radiating sprays of fine prisms. It is translucent to transparent with indices of refraction of nα = 1.461 nβ = 1.478 nγ = 1.485. It has a Mohs hardness of 3.5 to 4 and a specific gravity of 2.7.

<span class="mw-page-title-main">Siderite</span> Mineral composed of iron(II) carbonate

Siderite is a mineral composed of iron(II) carbonate (FeCO3). Its name comes from the Ancient Greek word σίδηρος (sídēros), meaning "iron". A valuable iron ore, it consists of 48% iron and lacks sulfur and phosphorus. Zinc, magnesium, and manganese commonly substitute for the iron, resulting in the siderite-smithsonite, siderite-magnesite, and siderite-rhodochrosite solid solution series.

<span class="mw-page-title-main">Mimetite</span> Lead arsenate chloride mineral

Mimetite is a lead arsenate chloride mineral (Pb5(AsO4)3Cl) which forms as a secondary mineral in lead deposits, usually by the oxidation of galena and arsenopyrite. The name derives from the Greek Μιμητής mimetes, meaning "imitator" and refers to mimetite's resemblance to the mineral pyromorphite. This resemblance is not coincidental, as mimetite forms a mineral series with pyromorphite (Pb5(PO4)3Cl) and with vanadinite (Pb5(VO4)3Cl). Notable occurrences are Mapimi, Durango, Mexico and Tsumeb, Namibia.

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

Alstonite, also known as bromlite, is a low temperature hydrothermal mineral that is a rare double carbonate of calcium and barium with the formula BaCa(CO
3
)
2
, sometimes with some strontium. Barytocalcite and paralstonite have the same formula but different structures, so these three minerals are said to be trimorphous. Alstonite is triclinic but barytocalcite is monoclinic and paralstonite is trigonal. The species was named Bromlite by Thomas Thomson in 1837 after the Bromley-Hill mine, and alstonite by August Breithaupt of the Freiberg Mining Academy in 1841, after Alston, Cumbria, the base of operations of the mineral dealer from whom the first samples were obtained by Thomson in 1834. Both of these names have been in common use.

<span class="mw-page-title-main">Adamite</span> Zinc arsenate hydroxide mineral

Adamite is a zinc arsenate hydroxide mineral, Zn2AsO4OH. It is a mineral that typically occurs in the oxidized or weathered zone above zinc ore occurrences. Pure adamite is colorless, but usually it possess yellow color due to Fe compounds admixture. Tints of green also occur and are connected with copper substitutions in the mineral structure. Olivenite is a copper arsenate that is isostructural with adamite and there is considerable substitution between zinc and copper resulting in an intermediate called cuproadamite. Zincolivenite is a recently discovered mineral being an intermediate mineral with formula CuZn(AsO4)(OH). Manganese, cobalt, and nickel also substitute in the structure. An analogous zinc phosphate, tarbuttite, is known.

<span class="mw-page-title-main">Willemite</span> Nesosilicate mineral

Willemite is a zinc silicate mineral and a minor ore of zinc. It is highly fluorescent (green) under shortwave ultraviolet light. It occurs in a variety of colors in daylight, in fibrous masses and apple-green gemmy masses. Troostite is a variant in which part of the zinc is partly replaced by manganese, it occurs in solid brown masses.

<span class="mw-page-title-main">Sauconite</span> Trioctahedral (Zn2+) smectite, phyllosilicate mineral

Sauconite is a complex phyllosilicate mineral of the smectite clay group, formula Na0.3Zn3(SiAl)4O10(OH)2·4H2O. It forms soft earthy bluish white to red-brown monoclinic crystals typically massive to micaceous in habit. It has a Mohs hardness of 1 to 2 and a specific gravity of 2.45. Optically it is biaxial positive with refractive index values of nα = 1.550 – 1.580, nβ = 1.590 – 1.620 and nγ = 1.590 – 1.620. It is found in vugs and seams in the oxidized zones of zinc and copper deposits. It occurs in association with hemimorphite, smithsonite, chrysocolla, coronadite and various iron oxides.

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

Fraipontite is a zinc aluminium silicate mineral with a formula of (Zn,Al)3(Si,Al)2O5(OH)4.

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">Carbonate-hosted lead-zinc ore deposits</span>

Carbonate-hosted lead-zinc ore deposits are important and highly valuable concentrations of lead and zinc sulfide ores hosted within carbonate formations and which share a common genetic origin.

Reinerite is a rare arsenite (arsenate(III)) mineral with chemical formula Zn3(AsO3)2. It crystallizes in the orthorhombic crystal system.

<span class="mw-page-title-main">Tarbuttite</span> Phosphate mineral

Tarbuttite is a rare phosphate mineral with formula Zn2(PO4)(OH). It was discovered in 1907 in what is now Zambia and named for Percy Coventry Tarbutt.

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

Köttigite is a rare hydrated zinc arsenate which was discovered in 1849 and named by James Dwight Dana in 1850 in honour of Otto Friedrich Köttig (1824–1892), a German chemist from Schneeberg, Saxony, who made the first chemical analysis of the mineral. It has the formula Zn3(AsO4)2·8H2O and it is a dimorph of metaköttigite, which means that the two minerals have the same formula, but a different structure: köttigite is monoclinic and metaköttigite is triclinic. There are several minerals with similar formulae but with other cations in place of the zinc. Iron forms parasymplesite Fe2+3(AsO4)2·8H2O; cobalt forms the distinctively coloured pinkish purple mineral erythrite Co3(AsO4)2·8H2O and nickel forms annabergite Ni3(AsO4)2·8H2O. Köttigite forms series with all three of these minerals and they are all members of the vivianite 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 Smithsonite: Smithsonite mineral information and data from Mindat
  3. 1 2 Smithsonite mineral data from Webmineral
  4. 1 2 Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (2005). "Smithsonite" (PDF). Handbook of Mineralogy. Mineral Data Publishing. Retrieved 14 March 2022.
  5. "Smithsonite at the National Museum of Natural History". Smithsonian Institution. Retrieved 8 December 2010.

Bibliography