RAMAN SPECTROSCOPIC STUDY OF HYDROUS γ-MG2SIO4 TO 56.5 GPA

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dc.contributor.author Kleppe A.K.
dc.contributor.author Jephcoat A.P.
dc.contributor.author Smyth J.R.
dc.date.accessioned 2021-06-03T06:25:19Z
dc.date.available 2021-06-03T06:25:19Z
dc.date.issued 2002
dc.identifier https://elibrary.ru/item.asp?id=1367548
dc.identifier.citation Physics and Chemistry of Minerals, 2002, 29, 7, 473-476
dc.identifier.issn 0342-1791
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/28801
dc.description.abstract Raman spectra of a single-crystal fragment of hydrous γ-Mg2SiO4, synthesized in a multianvil press, have been measured in a diamond-anvil cell with helium as pressure-transmitting medium to 56.5 GPa at room temperature. All five characteristic spinel Raman modes shift continuously up to the highest pressure, showing no evidence for a major change in the crystal structure despite compression well beyond the stability field of ringwoodite in terms of pressure. At pressures above ~30 GPa a new mode on the low-frequency site of the two silicate-stretching modes is clearly identifiable, indicating a modification in the spinel structure which is reversible on pressure release. The frequency of the new mode (802 cm-1 extrapolated to 1 bar) suggests the presence of Si-O-Si linkages and/or a partial increase in the coordination of Si. Direct determination of the subtle structural change causing the new Raman mode would require high-pressure, single-crystal synchrotron X-ray diffraction experiments. The Raman modes of hydrous and anhydrous Mg-end-member ringwoodite are nearly identical up to 20 GPa, suggesting that protonation has only minor effect on the lattice dynamics over the entire pressure stability range for ringwoodite in the mantle.
dc.subject RINGWOODITE
dc.subject HYDROUS MINERALS
dc.subject RAMAN SPECTROSCOPY
dc.subject DIAMOND-ANVIL CELL
dc.subject HIGH-PRESSURE
dc.title RAMAN SPECTROSCOPIC STUDY OF HYDROUS γ-MG2SIO4 TO 56.5 GPA
dc.type Статья


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