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American Mineralogist; October 2002; v. 87; no. 10; p. 1297-1306
© 2002 Mineralogical Society of America
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Spectroscopic studies of spessartine from Brazilian pegmatites

Sigrid G. Eeckhout1,2,*, Cristiane Castañeda3, Ana Cláudia M. Ferreira4, Antônio C.S. Sabioni5, Eddy de Grave1 and Daniela C.L. Vasconcelos6

1 Department of Subatomic and Radiation Physics, Ghent University, Belgium
2 Department of Geology and Soil Science, Ghent University, Belgium
3 Instituto de Geociências, Universidade de Brasília, CP 3173 CEP 30140-970, Brasília, Distrito Federal, Brazil
4 Department of Mining and Geology, Federal University of Paraíba, Paraíba, Brazil
5 Department of Physics/ICEB, Federal University of Ouro Preto, Minas Gerais, Brazil
6 Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, Minas Gerais, Brazil

Correspondence: * E-mail: sigrid.eeckhout{at}rug.ac.be

Mössbauer spectra (MS) at room temperature (RT) and Fourier-transform infrared (FTIR) spectra in the OH stretching region were acquired for natural spessartine-almandine garnet samples from different Brazilian pegmatites, including the complex, zoned Alto Mirador pegmatite, the simple, zoned Escondido pegmatite, and the simple Poaiá pegmatite. From MS, it is obvious that in the samples from the Alto Mirador pegmatite, ferrous iron is present at the dodecahedral site and ferric iron at the octahedral site of the garnet structure. The Fe2+/Fe3+ ratio is comparable for all samples from this pegmatite, i.e., ~10%, implying the same geological history, namely similar oxygen fugacities at the moment of garnet formation. In the simple pegmatites, however, almost no ferric iron was detected. On the basis of the multi-band FTIR spectra the nature of the point defects involved in the process of hydrogen uptake in spessartine-almandine garnet has been elucidated, if not completely clarified. The behavior of the absorption bands provides no evidence for multiple incorporation mechanisms, hence the hydrogarnet substitution is proposed to be the only mechanism for the incorporation of hydrogen in the samples studied. As geological setting is difficult to separate from chemical composition, FTIR spectra have the potential to provide useful information on some aspects of the geological history of the samples.




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S. G. Eeckhout, C. Corteel, E. Van Coster, E. De Grave, and P. De Paepe
Crystal-chemical characterization of tourmalines from the English Lake District: Electron-microprobe analyses and Mossbauer spectroscopy
American Mineralogist, November 1, 2004; 89(11-12): 1743 - 1751.
[Abstract] [Full Text] [PDF]




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