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H2O and CO2 in minerals of the haüyne-sodalite group: an FTIR spectroscopy study

Published online by Cambridge University Press:  05 July 2018

F. Bellatreccia*
Affiliation:
Dipartimento di Scienze Geologiche, Universita` Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati (I.N.F.N.-L.N.F.), Via Enrico Fermi 40 I- 00044 Frascati (Roma), Italy
G. Della Ventura
Affiliation:
Dipartimento di Scienze Geologiche, Universita` Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati (I.N.F.N.-L.N.F.), Via Enrico Fermi 40 I- 00044 Frascati (Roma), Italy
M. Piccinini
Affiliation:
Dipartimento di Scienze Geologiche, Universita` Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati (I.N.F.N.-L.N.F.), Via Enrico Fermi 40 I- 00044 Frascati (Roma), Italy
A. Cavallo
Affiliation:
Istituto Nazionale di Geofisica e Vulcanologia (I.N.G.V.), Via di Vigna Murata 605, I-00143 Roma, Italy
M. Brilli
Affiliation:
Istituto di Geologia Ambientale e Geoingegneria (C.N.R.-I.G.A.G.), Via Salaria km 29, 300 - C.P. 10 Monterotondo Stazione, I-00016 Roma, Italy
*

Abstract

This paper reports an infrared spectroscopic study of a set of sodalite-group minerals. The specimens have been identified using a combination of X-ray diffraction and microchemical analysis. As expected, the Si/Al ratio is ~1; the extra framework cation content is characterized by a well-defined Na ⇌ (Ca+K) substitution. The lattice parameters of the studied samples range from sodalite (sample LM11) with a = 8.889(2) Å, to haüyne (sample HR3S) with a = 9.1265(2) Å. The specimens, having the SO2– group as a dominant anion, show a clear correlation between the a cell edge and the K content. Singlecrystal FTIR spectroscopy shows that haüyne and nosean typically contain enclathrated CO2 molecules, inadditionto H2O and minor carbonate, while sodalite is virtually CO2-free. Detailed microspectrometric mappings show a non-homogeneous distribution of volatile constituents across the crystals, which may be related to the presence of fractures in the crystals. Because of such zoning, a relatively wide variation is observed when calibrating extinction coefficients on the basis of a bulk analytical method such as CHN elemental analysis.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2009

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Footnotes

currently at: Porto Conte Ricerche srl SP 55 Porto Conte-Capo Caccia, km 8,300 Loc. Tramariglio, Alghero I-07041 Sassari, Italy

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