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1 Dipartimento di Scienze Geologiche, Università Roma Tre, Largo S.
Leonardo Murialdo 1, I-00146 Roma, Italy
2 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
3 Istituto Nazionale di Geofisica e Vulcanologia (I.N.G.V.), Via di Vigna Murata
605, I-00143 Roma, Italy
4 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
* E-mail: bellatre{at}uniroma3.it
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
group as a
dominant anion, show a clear correlation between the a cell edge and
the K content. Single-crystal FTIR spectroscopy shows that haüyne and
nosean typically contain enclathrated CO2 molecules, in addition to
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.
KEYWORDS: sodalite, haüyne, nosean, lazurite, H2O and CO2, cell parameters, EMP analysis, CHN analysis, FTIR powder, single-crystal spectroscopy
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