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American Mineralogist; April 1999; v. 84; no. 4; p. 536-549
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Iron in kornerupine; a 57 Fe Moessbauer spectroscopic study and comparison with single-crystal structure refinement

Edward S. Grew, Guenther J. Redhammer, Georg Amthauer, Mark A. Cooper, Frank C. Hawthorne, and Karl Schmetzer

University of Maine, Department of Geological Sciences, Orono, ME, United States

Iron is an important constituent of kornerupine, ([]Mg,Fe) (Al,Mg,Fe) 9 (Si,Al,B) 5 O 21 (OH,F). We obtained Mossbauer spectra at 300 K on twelve samples with Sigma Fe = 0.30-1.30 atoms per formula unit (apfu) and Fe (super 3+) /Sigma Fe = 0-0.31; several samples were also run at 77 and 430 K. Models allowing unequivocal refinement of the spectra and determination of site occupancies were developed only when single-crystal refinement (SREF) of six of the samples constrained the number of possibilities. The spectra could then be fitted to three Fe (super 2+) doublets and one Fe (super 3+) doublet. The Fe (super 2+) doublets have nearly identical isomer shifts: delta = 1.14-1.19 mm/s for the octahedral M1 and M2 sites and 1.12-1.20 mm/s for the irregular, eightfold-coordinated X site (relative to alpha -Fe at 300 K). However, they differ to a variable extent in quadrupole splitting, Delta E Q nearly equal 1.06-1.80, 1.83-2.27, and 2.14-3.41 mm/s, respectively, to the M1, M2, and X sites. The Fe (super 3+) doublet corresponds to the M4 site. The Mossbauer and SREF occupancies are in excellent agreement for the six samples. The M1 doublet is split in B-bearing kornerupine and the proportion of Fe corresponding to each doublet, as well as quadrupole splitting, varies with B content. Similarly, the X doublet is split in F-bearing kornerupine, and quadrupole splitting of the X site increases with increasing F content. In contrast to most silicates, resolution of the spectra improves with increasing temperature. Quadrupole splitting of the X, M1, and M2 sites decreases with temperature, the X site at a lesser rate consistent with its being the most distorted site. To a first approximation, the Fe (super 3+) /Sigma Fe ratio in kornerupine determined by SREF and Mossbauer spectroscopy increases with increasing Fe 2 O 3 and Fe (super 3+) /Sigma Fe ratio of the associated sillimanite, sapphirine, and ilmenite-hematite, i.e., the measured Fe (super 3+) /Sigma Fe ratios are related to the oxygen fugacity at which the kornerupine crystallized.

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