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Synthesis and crystal-chemistry of the synthetic P21/m amphibole Na(NaMg)Mg5Si8O22(OH)2. (Articolo in rivista)
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- Synthesis and crystal-chemistry of the synthetic P21/m amphibole Na(NaMg)Mg5Si8O22(OH)2. (Articolo in rivista) (literal)
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- 2004-01-01T00:00:00+01:00 (literal)
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Iezzi G., Della Ventura G., Oberti R., Cámara F., Holtz F. (2004)
Synthesis and crystal-chemistry of the synthetic P21/m amphibole Na(NaMg)Mg5Si8O22(OH)2.
in The American mineralogist
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- Iezzi G., Della Ventura G., Oberti R., Cámara F., Holtz F. (literal)
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- GIANLUCA IEZZI,1,2,+ GIANCARLO DELLA VENTURA,2,* ROBERTA OBERTI,3 FERNANDO CÁMARA,3
AND FRANÇOIS HOLTZ4
1Bayerisches Geoinstitut, Universität Bayreuth, D-95440 Bayreuth, Germany
2Dipartimento di Scienze Geologiche, Università di Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy
3CNR-Istituto di Geoscienze e Georisorse, sezione di Pavia, via Ferrata 1, I-27100 Pavia, Italy
4Institut für Mineralogie, Universität Hannover, Welfengarten 1, D-30167, Germany (literal)
- Titolo
- Synthesis and crystal-chemistry of the synthetic P21/m amphibole Na(NaMg)Mg5Si8O22(OH)2. (literal)
- Abstract
- In the present work, we characterize the amphibole Na(NaMg)Mg5Si8O22(OH)2 synthesized at
0.4 GPa and 750, 800, and 850 °C, and 0.5 GPa, 900 °C. Experiments at 800 and 900 °C yielded
crystals suitable for single-crystal data collection. Structure refinement shows that synthetic
Na(NaMg)Mg5Si8O22(OH)2 has P21/m symmetry at room T. The two non-equivalent tetrahedral
double-chains differ in their degree of stretching and kinking. The infrared spectrum of synthetic
Na(NaMg)Mg5Si8O22(OH)2 has two well-defined absorption bands at 3742 and 3715 cm-1 which can be
assigned to O-H bands associated with the two independent anion sites (O3A and O3B) in the structure.
The higher frequency band is assigned to the shorter O3B-H2 bond, and the lower frequency band is
assigned to the longer O3A-H1 bond. The broader shape of the 3743 cm-1 band is consistent with a
stronger interaction of the H2 atom with ANa, which is confirmed by structure refinement. Increasing
T of synthesis causes a progressive departure from the ideal stoichiometry via the A1BMg1ANa-1BNa-1
substitution, as confirmed by EMPA, structure refinement, and FTIR spectroscopy. (literal)
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