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Geological Institute of the Russian Academy of Science, Pyjzhevsky Street 7, 109017 Moscow, Russia
* Corresponding author, e-mail: dainyak{at}ginras.ru
The literature Mössbauer parameters for a representative collection of muscovites, which were interpreted assuming the possible coexistence of trans- and cis-vacant sheets, were used to prove an alternative interpretation in terms of the local structure. Crystal-chemical models including the assignment of the local cation arrangements (LCA) around Fe3+ and Fe2+ to predicted and tentative quadrupole splitting values, respectively, and the LCA occurrence probabilities provided by the simulation of two-dimensional cation distribution (CD) were used. The obtained CD reconstructions in dioctahedral trans-vacant sheets correspond to the two types of muscovites revealed by Mössbauer spectroscopy. The main contributors into type-I muscovite are the 2R2+Al LCAs around Fe2+ (R2+ stands for Fe2+ and Mg) whereas in type-II muscovite the 3Al and 2AlFe3+ LCAs are more important. This implies a more ordered CD in type-II muscovites than that in type-I muscovites from the point of view of Paulings principle of the homogeneous dispersion of charge.
Key-words: Mössbauer spectroscopy, muscovite, isomorphous cations, order-disorder, crystal-chemical models.
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L. G. Dainyak, V. S. Rusakov, I. A. Sukhorukov, B. B. Zviagina, and V. A. Drits An improved model for the interpretation of Mossbauer spectra of dioctahedral 2:1 trans-vacant Fe-rich micas: refinement of parameters European Journal of Mineralogy, October 1, 2009; 21(5): 995 - 1008. [Abstract] [Full Text] [PDF] |
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