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Geochemistry to produce Widgiemoolthalite

"Widgiemoolthalite is a rare hydrated nickel(II) carbonate mineral with the chemical formula (Ni,Mg)
5(CO
3)
4(OH)
2·5H
2O. Usually bluish-green in color, it is a brittle mineral formed during the weathering of nickel sulfide. Present on gaspéite surfaces".[1]

Widgiemoolthalite (bright green) is intermingled with gaspéite (yellow-green). Field of view is three millimeters (0.12 in). Credit: Leon Hupperichs.{{free media}}

One consequence of the 1966 discovery of nickel deposits in Western Australia and subsequent nickel mining boom was the discovery of novel secondary mineral species in mined regions starting in the mid-1970s.[2][3]

"Widgiemoolthalite was first found at 132 North, a nickel deposit near Widgiemooltha, Western Australia, controlled by the Western Mining Corporation. Blair J. Gartrell collected the holotype widgiemoolthalite specimen from a stockpile of secondary minerals at the site."[1]

The mineral was discovered in 1992 and was first reported in American Mineralogist in 1993 by Ernest H. Nickel, Bruce W. Robinson, and William G. Mumme, when it received its name for its type locality.[4][5] Widgiemoolthalite's existence was confirmed and name was approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association the same year."[1]

The holotype specimen was stored in Perth's Western Australian Museum (specimen M.1.1993).[4]

"Widgiemoolthalite occurs as a secondary mineral."[1]

It is found overlaying nickel sulfide that has undergone weathering, often in hollow spaces on gaspéite surfaces [...], and often exhibiting fibrous and rarely massive crystal habits.[4] Other minerals associated with widgiemoolthalite include annabergite, carrboydite, dolomite, glaukosphaerite, hydrohonessite, kambaldaite, magnesite, nepouite, nullaginite, olivenite, otwayite, paratacamite, pecoraite, reevesite, retgersite, and takovite.[4][6] Two additional unnamed minerals were also reported as associated secondary minerals from the 132 North site, the only locality at which widgiemoolthalite had been found as of 2016.[6][7] The 132 North waste pile from which widgiemoolthalite was first recovered is no longer in existence, making it a rare mineral.[8] In support of the designation of an Anthropocene epoch, the existence and provenance of widgiemoolthalite, along with 207 other mineral species, were cited in 2017 by Robert M. Hazen et al. as evidence of uniquely human action upon global stratigraphy.[9]

Supergene processes

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Idealized mineral vein shows zones of leaching and enrichment. Credit: Strickja.
 
Azurite and Malachite are on Limonite from Bisbee, Arizona, USA. Credit: Robert M. Lavinsky.
 
Chalcocite pseudomorph after Covellite is from Butte, Montana, USA. Credit: Robert M. Lavinsky.

Def. "leached and then deposited by descending waters"[10] is called a supergene process.

"In ore deposit geology sugergene processes or enrichment occurs relatively near the surface. Supergene processes include the predominance of meteoric water circulation with concomittant 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 at which point the metals are redeposited on hypogene sulfides creating a zone of increased ore content."[11]

This is particularly noted in copper ore deposits where the copper sulfide minerals chalcocite Cu2S, covellite CuS, digenite Cu1.8S, and djurleite Cu31S16 are deposited by the descending surface waters.[12]

All such processes take place at essentially atmospheric conditions, 25 °C and atmospheric pressure.[13]

From the surface down there are different zones: a gossan cap, a leached zone, an oxidized zone, the water table, an enriched zone (supergene enriched zone) and the primary zone (hypogene zone).[14]

Gossan cap

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Pyrite FeS2 is generally abundant, and near the surface it oxidises to insoluble compounds such as goethite FeO(OH) and limonite,[13] forming a porous covering to the oxidized zone known as gossan or iron hat.[15]

Leached zone

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The groundwater contains dissolved oxygen and carbon dioxide, and as it travels downwards it leaches out the minerals in the rocks to form sulfuric acid, and other solutions that continue moving downwards.[16]

Oxidized zone

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Above the water table the environment is oxidizing, and below it is reducing.[17] Solutions traveling downward from the leached zone react with other primary minerals in the oxidised zone to form secondary minerals[16] such as sulfates and carbonates, and limonite, which is a characteristic product in all oxidised zones.[14]

Aqueous solutions of nickel sulfate react with sodium carbonate to precipitate nickel carbonate, a precursor to nickel-based catalysts and pigments.[18]

In the formation of secondary carbonates, primary sulfide minerals generally are first converted to sulfates, which in turn react with primary carbonates such as calcite CaCO
3, dolomite CaMg(CO
3)
2 or aragonite (also CaCO
3, polymorphic with calcite) to produce secondary carbonates.[15] Soluble salts continue on down, but insoluble salts are left behind in the oxidised zone where they form. An example is the lead mineral anglesite PbSO
4. Copper may be precipitated as malachite Cu
2(CO
3)(OH)
2 or azurite Cu
3(CO
3)
2(OH)
2.[14] Malachite, azurite, cuprite Cu
2O, pyromorphite Pb
5(PO
4)
3Cl and smithsonite ZnCO
3 are stable in oxidising conditions[17] and they are characteristic of the oxidation zone.[14]

Water table

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At the water table the environment changes from an oxidizing environment to a reducing one.[17]

Enriched zone

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Copper ions that move down into this reducing environment form a zone of supergene sulfide enrichment.[14] Covellite CuS, chalcocite Cu
2S and native copper Cu are stable in these conditions[17] and they are characteristic of the enriched zone.[14]

The net effect of these supergene processes is to move metal ions from the leached zone to the enriched zone, increasing the concentration there to levels higher than in the unmodified primary zone, possibly producing a deposit worth mining.

Primary zone

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The primary zone contains unaltered primary minerals.[16]

Mineral alterations

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Chalcopyrite CuFeS2 (primary) readily alters to the secondary minerals bornite Cu5FeS4, covellite CuS and brochantite Cu4SO4(OH)6.[16]

Galena PbS (primary) alters to secondary anglesite PbSO4 and cerussite PbCO3.[13][16]

Sphalerite ZnS (primary) alters to secondary hemimorphite Zn4Si2O7(OH)2.H2O, smithsonite ZnCO3 and manganese-bearing willemite Zn2SiO4.[13][16]

Pyrite FeS2 (primary) alters to secondary melanterite FeSO4.7H2O.[16]

If the original deposits contain arsenic and phosphorus bearing minerals secondary arsenates and phosphates will be formed.[16]

Gaspéites

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Gaspéite is shown encrusting gossanous magnesite ultramafic, Widgie Townsite gossan. Credit: Robert M. Lavinsky.{{free media}}

"Gaspéite's formula is (Ni,Fe,Mg)CO3 and it is a bright green mineral. It forms massive to reniform pappillary aggregates in fractures, bottryoidal concretions in laterite or fracture infill. It is also present as stains and patinas on iron oxide boxworks of gossanous material."[19]

"Gaspéite is formed in the regolith as a supergene alteration mineral of nickel sulphide minerals, generally in arid or semi-arid environments which produce conditions amenable to concentration of calcareous or carbonate minerals in the weathering profile."[19]

"Gaspéite from Widgiemooltha is associated with talc carbonated komatiite-associated nickel sulphide gossans and is probably formed by substitution of nickel into carbonates such as magnesite which are formed by oxidation of the talc-carbonate lithology, and of primary and supergene nickel sulphide minerals."[19]

"Gaspéite is formed from a similar process to the weathering of other sulphide minerals to form carbonae minerals. The sulphide minerals which are weathered to produce gaspeite are pentlandite, violarite, millerite and rarely niccolite."[19]

Hypogene processes

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Def. formed "underground, often by ascending solutions" is called a hypogene process.

In ore deposit geology, hypogene processes occur deep below the earth's surface, and tend to form deposits of primary minerals, as opposed to supergene processes that occur at or near the surface, and tend to form secondary minerals.[20]

At great depth the pressure is high, and water can remain liquid at temperatures well above 100 °C. Hot aqueous solutions originating in the magma contain metal and other ions derived from the magma itself, and also from leaching of surrounding rocks. Hypogene deposition processes include crystallization from the hot aqueous solutions rising through the earth's crust, driven by heat provided by the magma.[15]

Major dissolved components are chlorine, sodium, calcium, magnesium and potassium, and other important components include iron, manganese, copper, zinc, lead, sulfur (as SO42− or S2− or both) carbon (as HCO3− and CO2) and nitrogen (as NH4). Most ore fluids contain chloride as the dominant anion.[14]

As the solutions rise the temperature and pressure fall. Eventually a point is reached where the minerals start to crystallise out.[15] Minerals formed in this way are called primary, or hypogene, minerals. Sulfur is a common component of the fluids, and most of the common ore metals, lead, zinc, copper, silver, molybdenum and mercury, occur chiefly as sulfide and sulfosalt minerals[14] such as pyrite (FeS2), galena (PbS), sphalerite (ZnS), and chalcopyrite (CuFeS2).

See also

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References

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  1. ↑ 1.0 1.1 1.2 1.3 Collin Knopp-Schwyn, et al. (25 August 2019). "Widgiemoolthalite". WikiJournal of Science 2 (1): 7. doi:10.15347/wjs/2019.007. https://en.wikiversity.org/wiki/WikiJournal_of_Science/Widgiemoolthalite. Retrieved 9 February 2020. 
  2. ↑ Prider, R. T. (May 1970). "Nickel in Western Australia". Nature 226 (5247): 691–693. doi:10.1038/226691a0. 
  3. ↑ Birch, B. (December 1997). "New minerals in Australia". Geology Today 13 (6): 230–234. doi:10.1046/j.1365-2451.1997.t01-1-00017.x. 
  4. ↑ 4.0 4.1 4.2 4.3 Nickel, E. H.; Robinson, B. W.; Mumme, W. G. (August 1993). "Widgiemoolthalite: The new Ni analogue of hydromagnesite from Western Australia". American Mineralogist 78 (7–8): 819–821. http://www.minsocam.org/ammin/AM78/AM78_819.pdf. 
  5. ↑ Gamsjäger, H.; Bugajski, J.; Gajda, T.; Lemire, R. J.; Preis, W. (2005). Chemical thermodynamics of nickel. Amsterdam: Elsevier. p. 216. ISBN 978-0-444-51802-6. 
  6. ↑ 6.0 6.1 Nickel, E. H.; Clout, J. F. M.; Gartrell, B. J. (July 1994). "Secondary nickel minerals from Widgiemooltha". Mineralogical Record 25 (4): 283–291. http://search.proquest.com/docview/211708719. 
  7. ↑ "Widgiemoolthalite". Mindat.org. Hudson Institute of Mineralogy. May 1, 2016. Retrieved May 3, 2016.
  8. ↑ Whitfield, P. S. (December 2014). "Diffraction studies from minerals to organics: Lessons learned from materials analyses". Powder Diffraction 29 (S1): S2–S7. doi:10.1017/S0885715614001146. 
  9. ↑ Hazen, R. M.; Grew, E. S.; Origlieri, M. J.; Downs, R. T. (March 2017). "On the mineralogy of the 'Anthropocene Epoch'". American Mineralogist 102 (3): 595–611. doi:10.2138/am-2017-5875. 
  10. ↑ SemperBlotto (22 May 2011). "supergene". San Francisco, California: Wikimedia Foundation, Inc. Retrieved 10 February 2020. {{cite web}}: |author= has generic name (help)
  11. ↑ Vsmith (14 July 2006). "Supergene (geology)". San Francisco, California: Wikimedia Foundation, Inc. Retrieved 10 February 2020. {{cite web}}: |author= has generic name (help)
  12. ↑ Guilbert, John M. and Charles F. Park, Jr (1986) The Geology of Ore Deposits, W. H. Freeman, ISBN 0-7167-1456-6
  13. ↑ 13.0 13.1 13.2 13.3 Manual of Mineralogy (1993) Klein and Hurlbut. Wiley
  14. ↑ 14.0 14.1 14.2 14.3 14.4 14.5 14.6 14.7 Understanding Mineral Deposits (2000). Kula C Misra. Kluwer Academic Publishers Cite error: Invalid <ref> tag; name "UMD" defined multiple times with different content
  15. ↑ 15.0 15.1 15.2 15.3 The Encyclopedia of Gemstones and Minerals (1991). Martin Holden. Publisher: Facts on File Cite error: Invalid <ref> tag; name "EGM" defined multiple times with different content
  16. ↑ 16.0 16.1 16.2 16.3 16.4 16.5 16.6 16.7 Field Guide to North American Rocks and Minerals (1992) The Audubon Society. Alfred A Knopf
  17. ↑ 17.0 17.1 17.2 17.3 John Rakovan (2003) Rocks & Minerals 78:419
  18. ↑ H. B. W. Patterson, "Catalysts" in Hydrogenation of Fats and Oils G. R. List and J. W. King, Eds., 1994, AOCS Press, Urbana.
  19. ↑ 19.0 19.1 19.2 19.3 Rolinator (13 October 2006). "Gaspéite". San Francisco, California: Wikimedia Foundation, Inc. Retrieved 9 February 2020. {{cite web}}: |author= has generic name (help)
  20. ↑ Rakovan, John (November–December 2003). "A Word to the Wise: Hypogene & Supergene". Rocks & Minerals (Taylor & Francis) 78 (6): 419. doi:10.1080/00357529.2003.9926759. http://www.cas.muohio.edu/~rakovajf/WTTW%20Hypogene%20Supergene.pdf. Retrieved August 18, 2012. 
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