Hostname: page-component-76fb5796d-qxdb6 Total loading time: 0 Render date: 2024-04-26T19:08:17.088Z Has data issue: false hasContentIssue false

Joteite, Ca2CuAl[AsO4][AsO3(OH)]2(OH)2·5H2O, a new arsenate with a sheet structure and unconnected acid arsenate groups

Published online by Cambridge University Press:  05 July 2018

A. R. Kampf*
Affiliation:
Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA
S. J. Mills
Affiliation:
Geosciences, Museum Victoria, GPO Box 666, Melbourne 3001, Australia
R. M. Housley
Affiliation:
Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA
G. R. Rossman
Affiliation:
Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA
B. P. Nash
Affiliation:
Department of Geology and Geophysics, University of Utah, Salt Lake City, UT 84112, USA
M. Dini
Affiliation:
Pasaje San Agustin 4045, La Serena, Chile
R. A. Jenkins
Affiliation:
4521 N Via Madre, Tucson, AZ 85749, USA
*
* E-mail: akampf@nhm.org

Abstract

Joteite (IMA2012-091), Ca2CuAl[AsO4][AsO3(OH)]2(OH)2·5H2O, is a new mineral from the Jote mine, Tierra Amarilla, Copiapó Province, Atacama, Chile. The mineral is a late-stage, low-temperature, secondary mineral occurring with conichalcite, mansfieldite, pharmacoalumite, pharmacosiderite and scorodite in narrow seams and vughs in the oxidized upper portion of a hydrothermal sulfide vein hosted by volcanoclastic rocks. Crystals occur as sky-blue to greenish-blue thin blades, flattened and twinned on {001}, up to ~300 μm in length, and exhibiting the forms {001}, {010}, {10}, {20} and {111}. The blades are commonly intergrown in wheat-sheaf-like bundles, less commonly in sprays, and sometimes aggregated as dense crusts and cavity linings. The mineral is transparent and has a very pale blue streak and vitreous lustre. The Mohs hardness is estimated at 2 to 3, the tenacity is brittle, and the fracture is curved. It has one perfect cleavage on {001}. The calculated density based on the empirical formula is 3.056 g/cm3. It is optically biaxial (–) with α = 1.634(1), β = 1.644(1), γ = 1.651(1) (white light), 2Vmeas = 78(2)° and 2Vcalc = 79.4°. The mineral exhibits weak dispersion, r < v. The optical orientation is Xc*; Yb*. The pleochroism is Z (greenish blue) > Y (pale greenish blue) > X (colourless). The normalized electron-microprobe analyses (average of 5) provided: CaO 15.70, CuO 11.22, Al2O38.32, As2O546.62, H2O 18.14 (structure), total 100 wt.%. The empirical formula (based on 19 O a.p.f.u.) is: Ca1.98Cu1.00Al1.15As2.87H14.24O19. The mineral is slowly soluble in cold, concentrated HCl. Joteite is triclinic, P, with the cell parameters: a = 6.0530(2), b = 10.2329(3), c = 12.9112(4) Å, α = 87.572(2), β = 78.480(2), γ = 78.697(2)°, V = 768.40(4) Å3 and Z = 2. The eight strongest lines in the X-ray powder diffraction pattern are [dobs Å (I)(hkl)]: 12.76(100)(001), 5.009(23)(020), 4.206(26)(120,003,121), 3.92(24)(022,02,02), 3.40(25)(13), 3.233(19)(031,023,123,03), 2.97(132,201) and 2.91(15)(22,13). In the structure of joteite (R1 = 7.72% for 6003 Fo > 4σF), AsO4 and AsO3 (OH) tetrahedra, AlO6 octahedra and Cu2+O5 square pyramids share corners to form sheets parallel to {001}. In addition, 7- and 8-coordinate Ca polyhedra link to the periphery of the sheets yielding thick slabs. Between the slabs are unconnected AsO3(OH) tetrahedra, which link the slabs only via hydrogen bonding. The Raman spectrum shows features consistent with OH and/or H2O in multiple structural environments. The region between the slabs may host excess Al in place of some As.

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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Brown, I.D. and Altermatt, D. (1985) Bond-valence parameters from a systematic analysis of the inorganic crystal structure database. Acta Crystallographica, B41, 244247 CrossRefGoogle Scholar
Ferraris, G. and Franchini-Angela, M. (1973) Hydrogen bonding in the crystalline state. Crystal structure of MgHAsO4·7H2 Oroesslerite. A c t a Crystallographica, B29, 286292 Google Scholar
Ferraris, G., Fuess, H. and Joswig, W. (1986) Neutron diffraction study of MgNH4PO4(H2O)6O (struvite) and survey of water molecules donating short hydrogen bonds. Acta Crystallographica, B42, 253258 CrossRefGoogle Scholar
Hawthorne, F.C., Krivovichev, S.V. and Burns, P.C. (2000) The crystal chemistry of sulfate minerals. Pp. 1112 in: Sulfate Minerals – Crystallography, Geochemistry, and Environmental Signifcance. Reviews in Mineralogy, 40. Mineralogical Society of America, Washington, D.C.Google Scholar
Kampf, A.R. (2009) Miguelromeroite, the Mn analogue of sainfeldite, and redefinition of villyaellenite as an ordered intermediate in the sainfeldite-miguelromeroite series. American Mineralogist, 94, 15351540 CrossRefGoogle Scholar
Mandarino, J.A. (2007) The Gladstone–Dale compatibility of minerals and its use in selecting mineral species for further study. The Canadian Mineralogist, 45, 13071324 CrossRefGoogle Scholar
Parker, R.L., Salas, R.O. and Perez, G.R. (1963) Geologia de los distritos mineros Checo de Cobre Pampa Larga y Cabeza de Vaca. Instituto de Investigaciones Geologicas, 14, 4042 Google Scholar
Popova, V.I., Popov, V.A., Clark, A. Polyakov, V.O. and Borisovskii, S.E. (1986) Alacranite – a new mineral. Zapiski Vsesoyuznogo Mineralogicheskogo Obshchestva, 115, 360368 (in Russian).Google Scholar
Pouchou, J.-L. and Pichoir, F. (1991) Quantitative analysis of homogeneous or stratified microvolumes applying the model "PAP." Pp. 3175 in: Electron Probe Quantitation (K.F.J. Heinrich and D.E. Newbury, editors). Plenum Press, New York.CrossRefGoogle Scholar
Sheldrick, G.M. (2008) A short history of SHELX. Acta Crystallographica, A64, 112122 CrossRefGoogle Scholar
Sipos, P. (2009) The structure of Al(III) in strongly alkaline aluminate solutions – a review. Journal of Molecular Liquids, 146, 114 CrossRefGoogle Scholar
Street, R.L.T. and Whitaker, A. (1973) The isostructurality of rosslerite and phosphorosslerite. Zeitschrift für Kristallographie, 137, 246255 Google Scholar
Watling, H.R., Sipos, P.M., Byrne, L., Hefter, G.T. and May, P.M. (1999) Raman,, IR, and Al-27 MAS NMR spectroscopic studies of sodium (hydroxy)aluminates. Applied Spectroscopy, 53, 415422 CrossRefGoogle Scholar
Yang, H., Jenkins, R.A., Downs, R.T., Evans, S.H. and Tait, K.T. (2011) Rruffite, Ca2Cu(AsO4)2·2H2O, a new member of the roselite group, from Tierra Amarilla, Chile. The Canadian Mineralogist, 49, 877884 CrossRefGoogle Scholar
Supplementary material: File

Kampf et al. supplementary material

Structure factors

Download Kampf et al. supplementary material(File)
File 278.5 KB
Supplementary material: File

Kampf et al. supplementary material

CIF

Download Kampf et al. supplementary material(File)
File 64 KB