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A model for the structure of the hydrated aluminum phosphate, kingite determined by ab initio powder diffraction methods

  • Kia S. Wallwork , Allan Pring EMAIL logo , Max R. Taylor and Brett A. Hunter
Published/Copyright: March 31, 2015
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Abstract

[The crystal structure of kingite, Al3(PO4)2(F5OH)B(H2O, OH), a secondary mineral from a Cambrian-Precambrian phosphate deposit at Tom’s Quarry, near Kapunda, South Australia, has been determined from a powder sample using synchrotron X-ray diffraction data. The structure was determined ab initio by direct methods and refined to Rbragg = 0.022 and Rwp = 0.039 using the Rietveld method. The triclinic structure was solved and refined in the space group P1̅, a = 9.377(1), b = 10.113(1), c = 7.138(1) A, σ = 97.60(1), β= 100.88(1), γ = 96.01(1)°, V= 653.0(1) A3, Z= 2. The structure of kingite contains finite strings of three corner sharing AlΦ6 octahedra (where Φ represents O, OH-, F-, or H2O). These strings are cross-linked via PO4 tetrahedra to produce layers that are perpendicular to [100]. The layers are linked via hydrogen bonding through H2O located in the interlayer space. Kingite is shown to have a different stoichiometry to that reported earlier. The relationship of kingite to the structures of wavellite, Al3(P04)2(OH)5H2O, and mitryaevaite, A15(PO4)2[(P,S)O3(OH,O)]2F2(OH)2(H2O)8-6.48H2O, are briefly discussed.

Received: 2002-4-1
Accepted: 2002-6-10
Published Online: 2015-3-31
Published in Print: 2003-1-1

© 2015 by Walter de Gruyter Berlin/Boston

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