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FTIR spectroscopy of Ti-rich pargasites from Lherz and the detection of O2 at the anionic O3 site in amphiboles. (Articolo in rivista)
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- FTIR spectroscopy of Ti-rich pargasites from Lherz and the detection of O2 at the anionic O3 site in amphiboles. (Articolo in rivista) (literal)
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- 2007-01-01T00:00:00+01:00 (literal)
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- Della Ventura G.; Oberti R.; Hawthorne F.C.; Bellatreccia F. (literal)
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- GIANCARLO DELLA VENTURA,1,2,* ROBERTA OBERTI,2 FRANK C. HAWTHORNE,3
AND FABIO BELLATRECCIA1
1Dipartimento di Scienze Geologiche, Università Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy
2CNR-Istituto di Geoscienze e Georisorse, Unità di Pavia, via Ferrata 1, I-27100 Pavia, Italy
3Department of Geological Sciences, University of Manitoba, Winnipeg, R3T 2N2 Canada (literal)
- Titolo
- FTIR spectroscopy of Ti-rich pargasites from Lherz and the detection of O2 at the anionic O3 site in amphiboles. (literal)
- Abstract
- suite of well-characterized Ti-rich pargasites from Lherz (French Pyrenees). All amphiboles studied
have fairly constant M-site composition, with [6]Altot ~0.55 atoms per formula unit (apfu), [6]Ti ~0.45
apfu, and [6]Fe3+ ~0.40 apfu. SIMS and SREF data show all samples to have an O3 anion composition
of OH ? O2- ? 1.0 apfu, with negligible F. The FTIR spectra show for all samples a broad absorption
consisting of several overlapping bands; three main components can be recognized: ~3710, 3686, and
3660 cm-1, respectively, with an asymmetric tail extending to lower frequency. Six Gaussian components
can be fi tted to the spectra; comparison with spectra of both synthetic and natural pargasites
allows fi ve of these components to be assigned to local confi gurations involving OH-O2- at the O3 site,
thus showing that coupling with an O2- anion through an A-cation signifi cantly affects band position.
Infrared spectroscopy can detect the presence of O2- in amphiboles in chemically favorable cases, i.e.,
in the absence of F. Moreover, the FTIR spectra show that all octahedral confi gurations involving M1Ti4+
or M1Fe3+ M3Fe3+ are associated with O2- at both adjacent O3 sites, and that M3Al is locally associated
with OH, confi rming SRO models based on structure refi nement results. (literal)
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