3T-phlogopite from Kasenyi (SW Uganda) kamafugite: crystal chemistry and structure
Abstract
3T trioctahedral micas are rarer than it is thought. This is likely due to the occurrence of apparent polytypism, so that 1M polytype twins result in a diffraction pattern simulating a 3T periodicity [1, 2]. Most of the 3T trioctahedral micas found in nature to date belong to muscovite-polylithionite-annite system [3, 4, 5, 6]. X-ray diffraction studies on these micas have often reported partial tetrahedral ordering and/or different patterns of octahedral ordering [3, 6]. In the present work, a 3 T trioctahedral mica from Kasenyi (south west Uganda) kamafugite was studied via Electron Probe Microanalysis (EPMA) and Single Crystal X-ray Diffraction (SCXRD). Main EPMA data gave: SiO2 = 38.7(2), Al2O3 = 13.08(9), MgO = 20.4(2), TiO2 = 4.8(1), FeOtot = 5.51(9), Cr2O3 = 0.90(7), K2O = 9.64(5), Na2O = 0.29(1), BaO = 0.15(5) and F = 0.13(5) wt%. The analysed crystal may be classified as a Ti-rich, F-poor mica with a composition intermediate between the annite and phlogopite end members. Anisotropic single crystal X-ray refinement was performed in the <i>P</i>3<sub>1</sub>12 space group and converged to R1 = 4.34 and wR2 = 3.33 %. Unit cell parameters were: a = b = 5.3235(3) and c = 30.188(2) Å. Mean bond length distances of M1, M2 and M3 follow the pattern M1 = M2 < M3, suggesting partial octahedral cation ordering. Conversely, mean bond lengths of T1 and T2 point to a disordered cation distribution over tetrahedral sites. Finally, the overall crystal chemical features indicates the occurrence in the studied sample of the following substitution mechanisms: tetraferriphlogopite; Ti-oxy and Al, Fe3+, Cr-oxy; Al, Fe3+-Tschermak; kinoshitalite and XIIK+ + IVAl3+ « IVSi4+ + XII. Such substitutions are the same as those found in 1M-2M1 coexisting micas from the same rock sample [7].
Autore Pugliese
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SCHINGARO E.;MESTO E.;LACALAMITA M.
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Anno di pubblicazione
2011
ISSN
1972-1552
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