Georgeite
Sky blue georgeite associated to blue chalconatronite, found in Western Australia
General
CategoryCarbonate mineral
Formula[Cu(OH)2−x(H2O)x][CO3]x/2[1]
IMA symbolGg
Strunz classification5.BA.10
Crystal systemAmorphous
Crystal classAmorphous / gel-like
Identification
ColorSky-blue to bluish
FractureSub-conchoidal
Mohs scale hardness1–2
LusterVitreous to earthy
StreakPale blue
DiaphaneityTransparent to opaque
Specific gravity~2.55
Optical propertiesIsotropic

Georgeite is an extremely rare, X-ray amorphous copper hydroxycarbonate mineral, related to crystalline copper carbonates such as malachite. It occurs as pale blue, powdery or gel-like coatings in the oxidation zones of copper-bearing ores and was first identified in 1979.[2]

Discovery and nomenclature

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Georgeite was named after the late George Herbert Payne, Western Australia Government Chemical Laboratories former mineral division chief. It was first described in 1979, found within the Carr Boyd nickel mine in Western Australia. The mineral was confirmed as a new species after being found to be amorphous to X-rays, distinguishing it from crystalline copper carbonates.[2][3]

The holotype material is held at the Western Australian Museum.[1]

Chemical composition and structure

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Georgeite is a copper hydroxycarbonate, with early analyses giving an approximate empirical composition similar to Cu5(CO3)3(OH)4·6H2O in hydrated form, but the current accepted formula is [Cu(OH)2−x(H2O)x][CO3]x/2, permitting variable structural water. Georgeite is X-ray and electron-beam amorphous, lacking long-range crystallographic order.[2]

Occurrence and associated minerals

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Georgeite forms in supergene environments—oxidation zones of copper (or copper-nickel) sulphide deposits—often where carbonate or alkaline fluids are present. The type locality is Carr Boyd dump in Western Australia. It is also known to exist in Britannia Mine, Snowdonia, Wales.[4] Associated minerals include malachite and chalconatronite, both of which georgeite can recrystallize into.[2]

Because of this tendency to recrystallize, natural occurrences of georgeite are scarce and delicate. However, synthetic georgeite is now of interest in catalysis and materials science, expanding the relevance of georgeite beyond pure mineralogical description.[3][5]

Synthesis

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Despite natural georgeite's rarity, amorphous copper hydroxycarbonate is relatively simple to create in laboratory settings.[6] An early reproducible synthesis was described in 1991, which demonstrated that the amorphous blue precipitate would rapidly recrystallize into more stable crystalline malachite and chalconatronite, especially when agitated.[3] At the time, this instability hindered its detailed study and application.

A significant breakthrough was published to the journal Nature in 2016, where researchers successfully implemented a novel process to create stable georgeite.[5]

Industrial significance

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The primary industrial interest in synthetic georgeite is its role as a superior precursor material for copper-zinc oxide (Cu/ZnO) catalysts.[7] These catalysts are critical for two major industrial processes:

The conventional catalysts for these reactions are made from crystalline precursors like zincian malachite. However, a 2016 study showed that catalysts derived from their stable amorphous georgeite precursor exhibit significantly higher activity and stability.[5] The development of these more efficient catalysts could lead to improved productivity and energy efficiency in these vital chemical industries.[8]

Environmental and geochemical significance

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Georgeite-like precipitates have been observed in controlled laboratory precipitations relevant to copper in water and pipe corrosion systems. Such studies shed light on copper solubility, transport, and potential for forming amorphous phases under environmental conditions.[9]

See also

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References

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  1. ^ a b "Georgeite". www.mindat.org. Retrieved 2025-09-22.
  2. ^ a b c d Bridge, P. J.; Just, J.; Hey, M. H. (1979). "Georgeite, a new amorphous copper carbonate from the Carr Boyd Mine, Western Australia". Mineralogical Magazine. 43 (325): 97–98. doi:10.1180/minmag.1979.043.325.04.
  3. ^ a b c Pollard, A. M.; Thomas, R. G.; Williams, P. A. (1991). "The synthesis and composition of georgeite and its reactions to form other secondary copper(II) carbonates". Mineralogical Magazine. 55 (379): 163–166. doi:10.1180/minmag.1991.055.379.03.
  4. ^ "Mindat.org". www.mindat.org. Retrieved 2025-09-22.
  5. ^ a b c d Kondrat, Simon A.; Smith, Paul J.; Wells, Peter P.; Chater, Philip A.; Carter, James H.; Morgan, David J.; Fiordaliso, Elisabetta M.; Wagner, Jakob B.; Davies, Thomas E.; Lu, Li; Bartley, Jonathan K.; Taylor, Stuart H.; Spencer, Michael S.; Kiely, Christopher J.; Kelly, Gordon J.; Park, Colin W.; Rosseinsky, Matthew J.; Hutchings, Graham J. (2016). "Stable amorphous georgeite as a precursor to a high-activity catalyst". Nature. 531 (7592): 83–87. doi:10.1038/nature16935.
  6. ^ "Ground breaking synthesis of the rare mineral georgeite leads to better catalysts". Cardiff University. Retrieved 2025-09-22.
  7. ^ Pollard, A. M.; Spencer, M. S.; Thomas, R. G.; Williams, P. A.; Holt, J.; Jennings, J. R. (1992-06-04). "Georgeite and azurite as precursors in the preparation of co-precipitated copper/zinc oxide catalysts". Applied Catalysis A: General. 85 (1): 1–11. doi:10.1016/0926-860X(92)80125-V. ISSN 0926-860X.
  8. ^ Behrens, M.; Studt, F.; Kasatkin, I.; Kühl, S.; Hävecker, M.; Abild-Pedersen, F.; Zander, S.; Girgsdies, F.; Kurr, P.; Kniep, B.; Tauer, M.; Flechsig, J.; Trunschke, A.; Haber, J.; Schlögl, R.; Nørskov, J. K. (2012). "The Active Site of Methanol Synthesis over Cu/ZnO/Al2O3 Catalysts". Science. 336 (6083): 893–897. doi:10.1126/science.1219831. hdl:11858/00-001M-0000-000F-D2C9-A.
  9. ^ Lytle, Darren A.; Wahman, David G.; Schock, Michael R.; Nadagouda, Mallikarjuna N.; Harmon, Stephen; Webster, Katherine; Botkins, Jacob (2019). "Georgeite: A rare copper mineral with important drinking water implications". Chemical Engineering Journal. 355: 1–10. doi:10.1016/j.cej.2018.08.106. PMC 6605079.
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