1. High-pressure synthesis of skiagite-majorite garnet and investigation of its crystal structure.
- Author
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ISMAILOVA, LEYLA, BOBROV, ANDREY, BYKOV, MAXIM, BYKOVA, ELENA, CERANTOLA, VALERIO, KANTOR, INNOKENTY, KUPENKO, ILYA, MCCAMMON, CATHERINE, DYADKIN, VADIM, CHERNYSHOV, DMITRY, PASCARELLI, SAKURA, CHUMAKOV, ALEXSANDR, DUBROVINSKAIA, NATALIA, and DUBROVINSKY, LEONID
- Subjects
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CHEMICAL synthesis , *GARNET , *CRYSTAL structure , *SINGLE crystals , *X-ray diffraction - Abstract
Skiagite-rich garnet was synthesized as single crystals at 9.5 GPa and 1100 °C using a multi-anvil apparatus. The crystal structure [cubic, space group Ia...d, a = 11.7511(2) Å, V = 1622.69(5) ų, Dcalc = 4.4931 g/cm³] was investigated using single-crystal synchrotron X-ray diffraction. Synchrotron Mössbauer source spectroscopy revealed that Fe2+ and Fe3+ predominantly occupy dodecahedral (X) and octahedral (Y) sites, respectively, as expected for the garnet structure, and confirmed independently using nuclear forward scattering. Single-crystal X-ray diffraction suggests the structural formula of the skiagite-rich garnet to be Fe32+(Fe 0.234(2)2+Fe1.532(1)3+Si0.234(2)4+)(SiO4)3, in agreement with electron microprobe chemical analysis. The formula is consistent with X-ray absorption near-edge structure spectra. The occurrence of Si and Fe2+ in the octahedral Y-site indicates the synthesized garnet to be a solid solution of end-member skiagite with ~23 mol% of the Fe-majorite end-member Fe32+(Fe2+Si4+)(SiO4)3. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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