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American Mineralogist; May-June 2007; v. 92; no. 5-6; p. 713-721; DOI: 10.2138/am.2007.2197
© 2007 Mineralogical Society of America
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Single-crystal FTIR and X-ray study of vishnevite, ideally [Na6(SO4)][Na2(H2O)2](Si6Al6O24)

Giancarlo Della Ventura1,*, Fabio Bellatreccia1, Gian Carlo Parodi2, Fernando Cámara3 and Massimo Piccinini1,4

1 Dipartimento di Scienze Geologiche, Università Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy
2 Laboratoire de Minéralogie, Museum National d’Histoire Naturelle, 61, rue Buffon, F-75005 Paris
3 CNR-Istituto di Geoscienze e Georisorse, unità di Pavia, via Ferrata 1, I-27100 Pavia, Italy
4 I.N.F.N., Laboratori Nazionali di Frascati, Via E. Fermi, 40, I-00044 Frascati (Rome), Italy

Correspondence: * E-mail: dellaven{at}uniroma3.it

This paper reports a single-crystal FTIR spectroscopic study of vishnevite, ideally [Na6(SO4)] [Na2(H2O)2](Si6Al6O24), a member of the cancrinite group of feldspathoids. The study was done on several crystals from various geological occurrences. Infrared spectra show that most samples, and in particular the specimens from the holotype locality at Vishnevye Mountains (Urals, Russia), contain molecular CO2 as the main carbon species in the structural pores, while the specimens from Loch Borolan (Scotland) were found to be CO3-rich. Polarized-light measurements show that the linear CO2 molecules are oriented perpendicular to the crystallographic c axis. Structure refinement of sample Pi4 from Latium (Italy) shows usual H2O···Na···H2O sequences within the undecahedral cages; however, difference Fourier maps suggest the presence of additional protons in the channels, possibly forming OH groups. The FTIR spectra show three absorptions in the 3800–3200 cm–1 region. The first one, at 3590 cm–1 is strongly polarized for E{bot}c while the second, at 3535 cm–1, behaves almost isotropic. These two bands are assigned to the stretching vibrations of an asymmetric water molecule in the structural cages. The third broad absorption at 3320 cm–1, is predominantly polarized for E||c and is assigned to additional OH groups in the channels. Detailed microspectroscopic mapping showed several samples from Latium (Italy) to be zoned with respect to the CO2/CO3 content, thus pointing to a possible use of the volatile content of these minerals for petrological modeling.

Key Words: Vishnevite • EMPA • crystal structure refinement • FTIR spectroscopy • channel molecules




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