Warikahnite

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Warikahnite
Warikahnite-mf19c.jpg
Warikahnite, Tsumeb mine, Namibia, 0.6 × 0.4 × 0.1 cm
General
Category Arsenate minerals
Formula
(repeating unit)
Zn 3(As O 4)2·2H2O
IMA symbol War [1]
Strunz classification 8.CA.35
Crystal system Triclinic
Crystal class Pinacoidal (1)
(same H-M symbol)
Space group P1
Unit cell a = 6.71  Å, b = 8.98 Å
c = 14.53 Å; α = 105.59°
β = 93.44°, γ = 108.68°; Z = 4
Identification
Formula mass 510.04 g/mol
ColorPale yellow to colorless; honey-yellow; orange
Crystal habit Acicular; radial
Cleavage [001] perfect, [010] good, [100] good
Fracture Brittle
Mohs scale hardness2
Luster Vitreous, waxy
Streak White
Diaphaneity Transparent
Specific gravity 4.28
Optical propertiesBiaxial (+)
Refractive index nα = 1.747 nβ = 1.753 nγ = 1.768
Birefringence δ = 0.021
2V angle 75° measured
References [2] [3] [4] [5]

Warikahnite is a rare zinc arsenate mineral of the triclinic crystal system with Hermann-Mauguin notation 1, belonging to the space group P1. [6] It occurs in the Tsumeb mine in Namibia on corroded tennantite in the second oxidation zone under hydrothermal conditions in a dolomite-hosted polymetallic ore deposit. [5] [7] It is associated with adamite, stranskiite, koritnigite, claudetite, tsumcorite, and ludlockite. The origin of discovery was in a dolomite ore formation within an oxidized hydrothermal zone, in the E9 pillar, 31st level of the Tsumeb Mine in Namibia, Southwest Africa. [2] [5] It has also been found at Lavrion, Greece and Plaka, Greece as microscopic white needles. [6]

Contents

Discovery

Warikahnite, Tsumeb mine, Namibia, 0.9 x 0.4 x 0.1 cm Warikahnite-177594.jpg
Warikahnite, Tsumeb mine, Namibia, 0.9 × 0.4 × 0.1 cm

Warikahnite was discovered by Clive Queit [6] at Tsumeb mine and was first described in 1979 by Keller, Hess, and Dunn. [2] [5] The name "warikahnite" honors Walter Richard Kahn, who was born in 1911. He was from Bad Bayersoien, Germany, and he was a dealer and collector that specialized in Tsumeb minerals. He was honored due to his support of research into rare secondary minerals. [2] The type material is located at the University of Stuttgart, the Smithsonian Institution, and Harvard University. [5] [6]

Physical properties

Warikahnite has perfect cleavage on the c-axis {001}; and good cleavage on both the a- and b-axes ({100} and {010}). [5] It has bladed subhedral crystals up to 3 × .5 × .5 mm, elongated on {100} and flattened on {010}, with a hardness of approximately 2 as presented in table two. Its specific gravity is 4.24 and it exhibits a colorless to pale yellow hue, along with a white streak and vitreous luster. [6] This triclinic 1 specimen classified under the space group P1 features striated crystals up to two centimetres in radial to subparallel aggregates. [7] The Handbook of Mineralogy further states the cell dimensions of biaxial Warikahnite to be calculated as a = 6.710(1) Å, b = 8.989(2) Å, and c = 14.533(2) Å, with unit cell volume as 788.58 Å. [6]

Crystal structure

Structure Structurewarikahnite.jpg
Structure

The crystal structure of Warikahnite, determined from diffractometer data, contained six various coordination polyhedra of zinc with components of As, O, and H2O; with the coordination numbers six, five, and four; and with five different combinations of ligand. [8] The "Die Kristallstruktur von Warikahnit" article also notes that the hydrogen bonds are discussed appertaining to both charge balance and infrared spectra. Recent data shows the Gladstone-Dale relation compatibility of warikahnite is ranked as superior (−0.010). [9]

Chemical composition

Warikahnite has the chemical formula Zn 3(As O 4)2·2H2O. Along with arsenate ions (AsO4)3−, the infrared spectrum revealed H2O. [5] These water molecules present in the warikahnite sample were determined by thermo gravimetric analysis, and lost at 365 °C. Both H2O and (AsO4)3− readily dissolved when hot hydrochloric acid (HCL) or nitric acid (HNO3) were added to the specimen. [10] After a microprobe analysis, the weight percent oxides were calculated as follows in the table directly below. [5]

Chem For.Name %
As2O5(arsenic pentoxide)44.33%
ZnO(zinc oxide)47.85%
MnO(manganese oxide)0.40%
FeO(iron oxide)0.19%
H2O(water)6.32%
Total99.09%

Geologic occurrence

Warikahnite's only known localities to date are the Tsumeb Mine in Namibia, South West Africa; and Plaka and Lavrion, Greece. [6] The first discovery of this type specimen in the mine was found with white koritnigite, blue stranskiite, pale to emerald-green cuprian adamite, crystals of helmutwinklerite, and white corroded crystals of claudetite, ludlockite, tsumcorite, and lavendulan; while the second acquisition was only linked to quartz. [6]

See also

Related Research Articles

<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">Tsumeb</span> City in Oshikoto Region, Namibia

Tsumeb is a city of 15,000 inhabitants and the largest town in the Oshikoto region in northern Namibia. Tsumeb is known as the "gateway to the north" of Namibia. It is the closest town to the Etosha National Park. Tsumeb used to be the regional capital of Oshikoto until 2008 when Omuthiya was proclaimed a town and the new capital. The area around Tsumeb forms its own electoral constituency and has a population of 44,113. The town is the site of a deep mine that in its heyday was known as "TCL", but has since been renamed the Ongopolo Mine.

<i>Agardite</i> Mineral group

Agardite is a mineral group consisting of agardite-(Y), agardite-(Ce), agardite-(Nd), and agardite-(La). They comprise a group of minerals that are hydrous hydrated arsenates of rare-earth elements (REE) and copper, with the general chemical formula (REE,Ca)Cu6(AsO4)3(OH)6·3H2O. Yttrium, cerium, neodymium, lanthanum, as well as trace to minor amounts of other REEs, are present in their structure. Agardite-(Y) is probably the most often found representative. They form needle-like yellow-green (variably hued) crystals in the hexagonal crystal system. Agardite minerals are a member of the mixite structure group, which has the general chemical formula Cu2+6A(TO4)3(OH)6·3H2O, where A is a REE, Al, Ca, Pb, or Bi, and T is P or As. In addition to the four agardite minerals, the other members of the mixite mineral group are calciopetersite, goudeyite, mixite, petersite-(Ce), petersite-(Y), plumboagardite, and zálesíite.

Geigerite is a mineral, a complex hydrous manganese arsenate with formula: Mn5(AsO3OH)2(AsO4)2·10H2O. It forms triclinic pinacoidal, vitreous, colorless to red to brown crystals. It has a Mohs hardness of 3 and a specific gravity of 3.05.

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

Legrandite is a rare zinc arsenate mineral, Zn2(AsO4)(OH)·(H2O).

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

Arthurite is a mineral composed of divalent copper and iron ions in combination with trivalent arsenate, phosphate and sulfate ions with hydrogen and oxygen. Initially discovered by Sir Arthur Russell in 1954 at Hingston Down Consols mine in Calstock, Cornwall, England, arthurite is formed as a resultant mineral in the oxidation region of some copper deposits by the variation of enargite or arsenopyrite. The chemical formula of Arthurite is CuFe23+(AsO4,PO4,SO4)2(O,OH)2·4H2O.

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

Cabalzarite is a rare arsenate mineral with the chemical formula Ca(Mg,Al,Fe3+
)
2
[AsO
4
]
2
•2(H
2
O,OH)
. It is a member of the tsumcorite group. It crystallizes in the monoclinic system and typically occurs as clusters of crystals or granular aggregates.

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">Duftite</span> Arsenate mineral

Duftite is a relatively common arsenate mineral with the formula CuPb(AsO4)(OH), related to conichalcite. It is green and often forms botryoidal aggregates. It is a member of the adelite-descloizite Group, Conichalcite-Duftite Series. Duftite and conichalcite specimens from Tsumeb are commonly zoned in color and composition. Microprobe analyses and X-ray powder-diffraction studies indicate extensive substitution of Zn for Cu, and Ca for Pb in the duftite structure. This indicates a solid solution among conichalcite, CaCu(AsO4 )(OH), austinite, CaZn(AsO4)(OH) and duftite PbCu(AsO4)(OH), all of them belonging to the adelite group of arsenates. It was named after Mining Councilor G Duft, Director of the Otavi Mine and Railroad Company, Tsumeb, Namibia. The type locality is the Tsumeb Mine, Tsumeb, Otjikoto Region, Namibia.

<span class="mw-page-title-main">Plumbogummite</span> Alunite supergroup, phosphate mineral

Plumbogummite is a rare secondary lead phosphate mineral, belonging to the alunite supergroup of minerals, crandallite subgroup. Some other members of this subgroup are:

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

Lavendulan is an uncommon copper arsenate mineral, known for its characteristic intense electric blue colour. It belongs to the lavendulan group, which has four members:

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

Tsumebite is a rare phosphate mineral named in 1912 after the locality where it was first found, the Tsumeb mine in Namibia, well known to mineral collectors for the wide range of minerals found there. Tsumebite is a compound phosphate and sulfate of lead and copper, with hydroxyl, formula Pb2Cu(PO4)(SO4)(OH). There is a similar mineral called arsentsumebite, where the phosphate group PO4 is replaced by the arsenate group AsO4, giving the formula Pb2Cu(AsO4)(SO4)(OH). Both minerals are members of the brackebuschite group.

Sewardite is a rare arsenate mineral with formula of CaFe3+2(AsO4)2(OH)2. Sewardite was discovered in 1982 and named for the mineralogist, Terry M. Seward (born 1940), a professor of geochemistry in Zürich, Switzerland.

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

Keyite is a mineral with the chemical formula Cu2+3Zn4Cd2(AsO4)6 · 2H2O. The name comes from Charles Locke Key, an American mineral dealer who furnished its first specimens. Keyite is monoclinic-prismatic, meaning its crystal form has three unequal axes, two of which have 90° angles between them and one with an angle less than 90°. Keyite belongs to the biaxial optical class, meaning it has more than one axis of anisotropy, in which light travels with zero birefringence, and three indices of refraction, nα = 1.800, nβ, and nγ = 1.870. Being a very rare cadmium copper arsenate, keyite is only found in Tsumeb, Namibia in the Tsumeb mine, a world-famous copper mine known for its abundance of rare and unusual minerals.

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

Tsumcorite is a rare hydrated lead arsenate mineral that was discovered in 1971, and reported by Geier, Kautz and Muller. It was named after the TSUMeb CORporation mine at Tsumeb, in Namibia, in recognition of the Corporation's support for mineralogical investigations of the orebody at its Mineral Research Laboratory.

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

Ianbruceite is a rare hydrated zinc arsenate with the formula [Zn2(OH)(H2O)(AsO4)](H2O)2; material from the Driggith mine has traces of cobalt. It was first discovered at Tsumeb, approved by the International Mineralogical Association as a new mineral species in 2011, reference IMA2011-49, and named for Ian Bruce, who founded "Crystal Classics" in the early 1990s, and was heavily involved in attempts to reopen the famous Tsumeb mine for specimen mining.
In 2013 new occurrences of ianbruceite were reported from the neighbouring Driggith and Potts Gill mines on High Pike in the Caldbeck Fells, Cumbria, England. Here the mineral is probably a post-mining product. Caldbeck Fells and Tsumeb are the only reported localities for ianbruceite to date (May 2013).

<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.

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

Talmessite is a hydrated calcium magnesium arsenate, often with significant amounts of cobalt or nickel. It was named in 1960 for the type locality, the Talmessi mine, Anarak district, Iran. It forms a series with β-Roselite, where cobalt replaces some of the magnesium, and with gaitite, where zinc replaces the magnesium. All these minerals are members of the fairfieldite group. Talmessite is dimorphic with wendwilsonite.

Bartelkeite is an exceptionally rare mineral, one of scarce natural germanium compounds. The formula was originally assumed to be PbFeGe3O8, bartelkeite was later shown to be isostructural with a high-pressure form of the mineral lawsonite. Thus, its correct formula is PbFeGe(Ge2O7)(OH)2•H2O. Bartelkeite and mathewrogersite are minerals with essential (dominant) lead, iron and germanium. Both come from Tsumeb, Namibia - a world's "capital" of germanium minerals.

<span class="mw-page-title-main">Arsendescloizite</span> Lead-zinc mineral

Arsendescloizite is a lead-zinc mineral, approved by the IMA in 1982. It is an arsenate analog of descloizite. Its first description was published in 1982.

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 3 4 http://rruff.geo.arizona.edu/doclib/hom/warikahnite.pdf Mineral Handbook
  3. http://webmineral.com/data/Warikahnite.shtml Webmineral
  4. http://www.mindat.org/min-4244.html Mindat
  5. 1 2 3 4 5 6 7 8 Fleischer, Michael; L. J. Cabri; A. Pabst (1980). "New mineral names" (PDF). American Mineralogist. 65: 406–408. Retrieved 2010-01-03.
  6. 1 2 3 4 5 6 7 8 Pinch, William W. (July 2005). "Warikahnite: some background on the cover specimen". The Mineralogical Record. The Mineralogical, Inc. 36 (4): 315(1).
  7. 1 2 Anthony, J. W., Bideaux, R. A., Bladh, K. W., and Nichols, M. C. (2000) Handbook of Mineralogy. Volume IV: Arsenates, Phosphates and Vanadates. Mineral Data Publishing Company, Tucson, Arizona, p. 644
  8. Riffel, H., P. Keller, and H. Hess (1980) Die Kristallstruktur von Warikahnit, Zn3(AsO4)2·2H2O Tschermaks Mineral. Petrog. Mitt., 27, 187–199 (in German with English abs)
  9. Mandarino, Joseph A. (2006). "The Gladstone-Dale Compatibility of Arsenate Minerals". Periodico di Mineralogia. 75 (2–3): 167–174.
  10. Keller, P., Hess, H., and Dunn, P.J. (1979) Warikahnit, ein neues Mineral aus Tsumeb, Sudwestafrika. Neues Jahrbuch fur mineralogy, Monatshefte, 389–395. Abstracted in American Mineralogist, 65, 408

Literature