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Hylbrownite, Na3MgP3O10·12H2O, a new triphosphate mineral from the Dome Rock Mine, South Australia: description and crystal structure

Published online by Cambridge University Press:  05 July 2018

P. Elliott*
Affiliation:
School of Earth and Environmental Sciences, The University of Adelaide, Adelaide, South Australia 5005, Australia South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia
J. Brugger
Affiliation:
School of Earth and Environmental Sciences, The University of Adelaide, Adelaide, South Australia 5005, Australia South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia
T. Caradoc-Davies
Affiliation:
Australian Synchrotron, 800 Blackburn Road, Clayton, Victoria 3168, Australia
A. Pring
Affiliation:
South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia
*

Abstract

Hylbrownite, ideally Na3MgP3O10·12H2O, the second known triphosphate mineral, is a new mineral species from the Dome Rock mine, Boolcoomatta Reserve, Olary Province, South Australia, Australia. The mineral forms aggregates and sprays of crystals up to 0.5 mm across with individual crystals up to 0.12 mm in length and 0.02 mm in width. Crystals are thin prismatic to acicular in habit and are elongate along [001]. Forms observed are {010}, {100}, {001}, {210} and {201}. Crystals are colourless to white, possess a white streak, are transparent, brittle, have a vitreous lustre and are nonfluorescent. The measured density is 1.81(4) g cm−3; Mohs' hardness was not determined. Cleavage is good parallel to {001} and to {100} and the fracture is uneven. Hylbrownite crystals are nonpleochroic, biaxial (−), with α = 1.390(4), β = 1.421(4), γ = 1.446(4) and 2Vcalc. = 82.2°. Hylbrownite is monoclinic, space group P21/n, with a = 14.722(3), b = 9.240(2), c = 15.052(3) Å, β = 90.01(3)°, V = 2047.5(7) Å3, (single-crystal data) and Z = 4. The strongest lines in the powder X-ray diffraction pattern are [d (Å)(I)(hkl)]: 10.530(60)(10,101), 7.357(80)(200), 6.951(100)(11, 111), 4.754(35)(10, 103), 3.934(40)(022), 3.510(45)(30, 303), 3.336(35)(41, 411). Chemical analysis by electron microprobe gave Na2O 16.08, MgO 7.08, CaO 0.43, P2O5 37.60, H2Ocalc 38.45, total 99.64 wt.%. The empirical formula, calculated on the basis of 22 oxygen atoms is Na2.93Mg0.99Ca0.04P2.99O9.97·12.03H2O. The crystal structure was solved from single-crystal X-ray diffraction data using synchrotron radiation (T = 123 K) and refined to R1 = 4.50% on the basis of 2417 observed reflections with F0 > 4 σ(F0). [Mg(H2O)3P3O10] clusters link in the b direction to Naφ6 octahedra, by face and corner sharing. Edge sharing Naφ6 Octahedra and Naφ7 polyhedra form Na2O9 groups which link via corners to form chains along the b direction. Chains link to [Mg(H2O)3P3O10] clusters via corner-sharing in the c direction and form a thick sheet parallel to (100). Sheets are linked in the a direction via hydrogen bonds.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2013

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References

Bayliss, P., Lawrence, L.J. and Watson, D. (1966) Rare copper arsenates from Dome Rock, South Australia. Australian Journal of Science, 29, 145146.Google Scholar
Brown, H.Y.L. (1893) Catalogue of South Australian minerals: with the mines and other localities where found, and brief remarks on the mode of occurrence of some of the principal metals and ores. Government Printer, Adelaide, 34 pp.Google Scholar
Brown, H.Y.L. (1908) Record of the Mines of South Australia, 4th ed. Government Printer, Adelaide, 382 pp.Google Scholar
Brown, I.D. (1996) VALENCE: a program for calculating bond-valences. Journal of Applied Crystallography, 29, 479480.CrossRefGoogle Scholar
Brown, I.D. and Altermatt, D. (1985) Bond-valence parameters obtained from a systematic analysis of the inorganic crystal structure database. Acta Crystallographica, B41, 244247.CrossRefGoogle Scholar
Cooper, M.A. and Hawthorne, F.C. (1999) The crystal s t ructure of wooldridgeite, Na2CaCu2 2+ (P2O7)2(H2O)10, a novel copper pyrophosphate mineral. The Canadian Mineralogist, 37, 7381.Google Scholar
Dickinson, S.B. (1942) The structural control of ore deposition in some South Australian copperfields. Geological Survey of South Australia Bulletin 20, 139.Google Scholar
Fuchs, L.H., Olsen, E. and Henderson, E.P. (1967) On the occurrence of brianite and panethite, two new phosphate minerals from the Dayton meteorite, Geochimica et Cosmochimica Acta, 31, 17111719.CrossRefGoogle Scholar
Hawthorne, F.C., Cooper, M.A., Green, D.I., Starkey, R.E., Roberts, A.C. and Grice, J.D. (1999) Wooldridgeite, Na2CaCu2 2+(P2O7)2(H2O)10: a new mineral from Judkins Quarry, Warwickshire, England. Mineralogical Magazine, 63, 1316.CrossRefGoogle Scholar
Hunter, B.A. (1998) Rietica – A Visual Rietveld Program. Commission on Powder Diffraction Newsletter, 20, 21.Google Scholar
Jouini, O., Dabbabi, M., Averbuch-Pouchot, M.T., Guitel, J.C. and Durif, A. (1984) Structure du phosphate de cuivre(II) et de trisodium dodecahydrate, CuNa3P3O10(H2O)12 . Acta Crystallographica, C40, 728730.Google Scholar
Kleeman, A.W. and Milnes, A.R. (1973) Phosphorian lavendulan from Dome Rock mine, South Australia. Transactions of the Royal Society of South Australia, 97, 135137.Google Scholar
Le Bail, A., Duroy, H., Fourquet, J.L. (1988) Ab-initio structure determination of LiSbWO6 by X-ray powder diffraction. Materials Research Bulletin 23, 447452.CrossRefGoogle Scholar
Libowitzky, E. (1999) Correlation of O-H stretching frequencies and O-H···O hydrogen bond lengths in minerals. Monatshefte für Chemie, 130, 10471059.CrossRefGoogle Scholar
Liferovich, R.P., Pakhomovsky, Ya.A., Yakubovich, O.V., Massa, W., Laajoki, K., Gehör, S., Bogdanova, A.N. and Sorokhtina, N.V. (2000) Bakhchisaraitsevite, Na2Mg5[PO4]4·7H2O, a new mineral from hydrothermal assemblages related to phoscorite–carbonatite complex of the Kovdor massif, Russia. Neues Jahrbuch für Mineralogie, Monatshefte, 402418.Google Scholar
Lightfoot, P. and Cheetham, A.K. (1987) Structure of manganese(II) trisodium tripolyphosphate dodecahydrate. Acta Crystallographica, C43, 47.Google Scholar
Lutsko, V. and Johansson, G. (1984) The crystal structure of trisodium cadmium triphosphate CdNa3P3O10(H2O)12 . Acta Chemica Scandinavica, A38, 415417.CrossRefGoogle Scholar
Mandarino, J.A. (1981) The Gladstone-Dale relationship: Part IV: The compatibility concept and its application. The Canadian Mineralogist, 19, 441450.Google Scholar
Nickel, E.H. and Birch, W.D. (1988) Cobaltaustinite – a new arsenate mineral from Dome Rock, South Australia. Australian Mineralogist, 3, 5357.Google Scholar
Peacor, D.R., Dunn, P.J., Simmons,W.B. and Wicks, F.J. (1985) Canaphite, a new sodium calcium phosphate from the Paterson area, New Jersey. Mineralogical Record, 16, 467468.Google Scholar
Popova, V.I., Popov, V.A., Sokolova, E.V., Ferraris, G. and Chukanov, N.V. (2002) Kanonerovite, MnNa3P3O10·12H2O, first triphosphate mineral (Kazennitsa pegmatite, Middle Urals, Russia). Neues Jahrbuch für Mineralogie, Monatshefte, 117127.Google Scholar
Pouchou, J.L. and Pichoir, F. (1985) ‘PAP’ f((rZ)) procedure for improved quantitative microanalysis. Pp. 104106. in: Microbeam Analysis (J.T. Armstrong, editor). San Francisco Press, San Francisco, California.Google Scholar
Rakotomahanina, E., Averbuch-Pouchot, M.-T. and Durif, A. (1972) Données cristallographiques sur les triphosphates du type MIINa3P3O10·12H2O pour MII = Ni, Co, Mn, Mg, Zn et Cd. Bulletin Société Franc¸ais de Minéralogie et de Cristallographie, 95, 516520.CrossRefGoogle Scholar
Rouse, R.C., Peacor, D.R. and Freed, R.L. (1988) Pyrophosphate groups in the structure of canaphite, Ca2Na2PO7.4H2O: The first occurrence of a condensed phosphate mineral. American Mineralogist, 73, 168171.Google Scholar
Rulmont, A., Cahay, R., Liegeois-Duyckaerts, M. and Tarte, P. (1991) Vibrational spectroscopy of phosphate: Some general correlations between structure and spectra. European Journal of Solid State and Inorganic Chemistry, 28, 207219.Google Scholar
Ryall, W.R. and Segnit, E.R. (1976) Minerals of the oxidized zone of the Dome Rock copper deposit, South Australia. Australian Mineralogist, 2, 58.Google Scholar
Segnit, E.R. (1978) Further minerals from the Dome Rock Mine, South Australia. Australian Mineralogist, 2, 7374.Google Scholar
Shape Software (1997) ATOMS for Windows and Macintosh V 4.0. Kingsport, Tennessee, USA.Google Scholar
Sheldrick, G.M. (2008) A short history of SHELX. Acta Crystallographica, A64, 112122.CrossRefGoogle Scholar
Yakubovich, O.V., Massa, W., Liferovich, R.P. and Pakhomovsky, Y.A. (2000) The crystal structure of bakhchisaraitsevite, [Na2(H2O)2] {(Mg,Fe)5(H2O)5(PO4)4}, a new mineral species of hydrothermal origin from the Kovdor phoscoritecarbonatite complex, Russia. The Canadian Mineralogist, 38, 831838.CrossRefGoogle Scholar
Yvon, K., Jeitschko, W. and Parthé, E. (1977) LAZY PULVERIX, a computer program, for calculating X-ray and neutron diffraction powder patterns. Journal of Applied Crystallography, 10, 7374.CrossRefGoogle Scholar