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Noonkanbahite, BaKNaTi2(Si4O12)O2, a new mineral species: description and crystal structure

Published online by Cambridge University Press:  05 July 2018

Y. A. Uvarova*
Affiliation:
Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario K7L 3N6 Canada
E. Sokolova
Affiliation:
Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2 Canada
F. C. Hawthorne
Affiliation:
Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2 Canada
R. P. Liferovich
Affiliation:
Department of Geology, Lakehead University, Thunder Bay, Ontario P7B 5E1 Canada
R. H. Mitchell
Affiliation:
Department of Geology, Lakehead University, Thunder Bay, Ontario P7B 5E1 Canada
I. V. Pekov
Affiliation:
Department of Mineralogy, Faculty of Geology, Moscow State University, Vorob'evy Gory, Moscow, Russia 119992
A. E. Zadov
Affiliation:
NPP Teplokhim, Dmitrovskoye av. 71, Moscow, Russia 127238
*

Abstract

Noonkanbahite, ideally BaKNaTi2(Si4O12)O2, is described as a new mineral species. At Liley [Löhley], Eifel Mountains, Germany (the holotype locality), it occurs as sprays of prismatic crystals (up to 8 mm) or single prismatic crystals (up to 4 mm) on walls of cavities in alkaline igneous rocks. At Murun, Siberia, Russia, noonkanbahite forms coarse lamellar crystals up to 0.05 cm × 0.7 cm × 1.5 cm embedded in kalsilite syenite. Noonkanbahite is brittle, H = 6, Dobs. = 3.39(1), Dcalc. = 3.49 g/cm3, has a vitreous lustre and does not fluoresce in ultraviolet light. It has poor cleavage on {010} and {100} and weak parting on {011}. Noonkanbahite is biaxial positive with 2Vobs. = 75(2)°, 2Vcalc. = 72.7(9)°, α 1.730(5), β 1.740(5) and γ 1.765(5), dispersion is medium, r < v. In transmitted plane-polarized light, noonkanbahite is strongly pleochroic, with X colourless, Y yellowish, Z straw-yellow; X = a, Y = b, Z = c. Noonkanbahite is orthorhombic, space group Imma, a = 8.0884(4), b = 10.4970(5), c = 13.9372(6) Å, V = 1183.3(1) Å3, Z = 4. The strongest ten X-ray diffraction lines in the powder pattern [d in Å (I)(hkl)] are: 2.907(100)(222), 8.353(50)(001), 3.196(50)(220), 2.097(50)(242), 2.241(40)(215), 2.179(40)(035), 3.377(30)(031), 2.694(30)(015), 2.304(30)(233), and 1.564(30)(064). Electron microprobe analysis gives SiO2 37.82, TiO2 15.54, ZrO2 0.42, Nb2O5 3.18, Al2O3 0.17, Fe2O3 (recalculated from FeO) 5.63, MnO 0.32, MgO 0.53, BaO 20.60, CaO 1.36, K2O 5.32, Na2O 6.14, F 0.78, H2O 0.58, sum 98.39 wt.%, (H2O determined by SIMS). The formula unit, calculated on the basis of 14 anions (O+OH+F), is (Ba0.85K0.13)Σ0.98(K0.59Na0.26Ca0.15)Σ1.00Na(Ti1.23Fe0.453+Nb0.15Mg0.08Mn0.03Zr0.02Al0.01)Σ1.97 (Si3.99Al0.01O12)(O1.33OH0.41F0.26)Σ2.00, Z = 4.

The crystal structure was refined to R1 = 2.8% for 970 unique (F0 > 4σF) reflections collected on a Bruker single-crystal P4 diffractometer with a CCD detector and MoKα X-radiation. The crystal structure of noonkanbahite is isostructural with that of batisite, ideally BaNa2Ti2(Si4O12)O2, and scherbakovite, ideally K2NaTi2(Si4O12)O(OH). There are two octahedrally coordinated sites, M(1) and M(2), occupied by (Ti1.23Fe0.453+Nb0.15Mg0.08Mn0.03Zr0.02Al0.01), ideally Ti2 a.p.f.u. There are three interstitial A sites, [9]A(1), [8]A(2) and [6]A(3), occupied by Ba, K and Na, respectively. Si tetrahedra and M octahedra form a framework with interstitial cages occupied by Ba, K and Na atoms at the A sites. Noonkanbahite, BaKNaTi2(Si4O12)O2, is a K analogue of batisite, BaNa2Ti2(Si4O12)O2, and a Ba analogue of shcherbakovite, K2NaTi2(Si4O12)O(OH).

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2010

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References

Brown, I.D. (1981) The bond-valence method: an empirical approach to crystal structure and bonding. Pp. 130 in: Structure and Bonding in Crystals II (O’Keeffe, M. and Navrotsky, A., editors). Academic Press, New York.Google 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
Es’kova, E.M. and Kazakova, M.E. (1954) Shcherbakovite – a new mineral. Doklady Akademii Nauk SSSR, 99, 837840 (in Russian).Google Scholar
Hogarth, D.D. (1997) Mineralogy of leucite-bearing dykes from Napoleon Bay, Baffin Island: multistage Proterozoic lamproites. The Canadian Mineralogist, 35, 5378.Google Scholar
Khomyakov, A.P. (1995) Mineralogy of Hyperagpaitic Alkaline Rocks. Clarendon Press, Oxford, UK, 223 pp.Google Scholar
Konev, A.A., Vorob’ev, E.I. and Lazebnik, K.A. (1996) Mineralogiya Murunskogo Shchelochnogo Massiva (Mineralogy of the Murun Alkaline Massif). SO RAN Publishing, Novosibirsk, Russia, 222 pp. (in Russian).Google Scholar
Kravchenko, S.M., Vlasova, E.V. and Pinevich, N.G. (1960) Batisite – a new mineral. Doklady Akademi Nauk SSSR, 133, 657660. (in Russian).Google Scholar
Lazebnik, K.A. and Makhotko, V.F. (1983) Rare minerals potassic batisite and calciostrontianite in charoite rocks. Mineralogischeskiy Zhurnal, 5(3), 8184 (in Russian).Google Scholar
Merlet, C. (1992) Quantitative electron probe microanalysis: new accurate φ (pz) description. Mikrochimica Acta, 12, 107115.CrossRefGoogle Scholar
Mitchell, R.H. (1990) Shcherbakovite in leucite phlogopite lamproites from the Leucite Hills, Wyoming. Mineralogical Magazine, 54, 645646.CrossRefGoogle Scholar
Nikitin, A.V. and Belov, N.V. (1962) Crystal structure of batisite Na2BaTi2O2[Si4O12]. Doklady Akademii Nauk SSSR, 146, 142143.Google Scholar
Ottolini, L., Cámara, F., Hawthorne, F.C. and Stirling, J. (2002) SIMS matrix effects in the analysis of light elements in silicate minerals: comparison with SREF and EMPA data. American Mineralogist, 87, 14771485.CrossRefGoogle Scholar
Ottolini, L. and Hawthorne, F.C. (2001) SIMS ionization of hydrogen in silicates: a case study of kornerupine. Journal of Analytical Atomic Spectrometry, 16, 12661270.CrossRefGoogle Scholar
Prider, R.T. (1965) Noonkanbahite, a potassic batisite from the lamproites of western Australia. Mineralogical Magazine, 34, 403405.CrossRefGoogle Scholar
Rastsvetaeva, R.K., Pushcharovskii, D.Yu., Konev, A.A. and Evsunin, V.G. (1997) The crystal structure of Kcontaining batisite. Kristallografiya, 42, 837840.Google Scholar
Schmahl, W.W. and Tillmanns, E. (1987) Isomorphic substitutions, straight Si-O-Si geometry, and disorder of tetrahedral tilting in batisite, (Ba,K)(K,Na)Na(Ti,Fe,Na,Zr)Si4O12 . Neues Jahrbuch für Mineralogie Monatshefte, 3, 107118.Google Scholar
Shannon, R.D. (1976) Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides. Acta Crystallographica, A32, 751767.CrossRefGoogle Scholar
Sheldrick, G.M. (1998) SADABS User Guide University of Göttingen, Göttingen, Germany.Google Scholar
Uvarova, Yu.A., Sokolova, E., Hawthorne, F.C., Liferovich, R.P. and Mitchell, R.H. (2003) The crystal chemistry of shcherbakovite from the Khibina Massif, Kola Peninsula, Russia. The Canadian Mineralogist, 41, 11931201.CrossRefGoogle Scholar
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