Na2MgSiO4 is a mineralogical phase known in the literature as N2MS and reported in several high-pressure experiments (13.6<P<22GPa) to coexist with wadsleyite, garnet and pyroxene. Although the crystal structure of room-PT Na2MgSiO4 is known, a structural studyof thephase recovered in high-pressure experiments has not been done yet.Herewepresent a chemical and structural study of a crystal of Na2MgSiO4 synthesised in the model system Na2MgSiO4–Mg2SiO4 at 22GPa and 1800 °C. The compound was found to crystallize with the orthorhombic cristobalite-type structure previously described at room conditions, space group Pna21, with lattice parameters a = 10.8193(8), b = 5.2702(3), c = 7.0598(4)A,V = 402.55(4)A3, andZ = 4.The structurewas refined toR1 = 0.0184 using 644 observed reflections [Fo>4s(Fo)] and 73 parameters. The unit-cell of the phase studied here is nearly identical to that of Na2MgSiO4 synthesised at room conditions, thus indicating that it likely relaxed during the pressure release occurring during quenching.

X-ray single-crystal structural characterization of Na2MgSiO4 with cristobalite-type structure synthesised at 22 GPa and 1800 °C / EKATERINA A. SIROTKINA, LUCA BINDI, ANDREY V. BOBROV, ANASTASIA TAMAROVA, DMITRY YU. PUSHCHAROVSKY, TETSUO IRIFUNE. - In: EUROPEAN JOURNAL OF MINERALOGY. - ISSN 0935-1221. - ELETTRONICO. - 30:(2018), pp. 485-489.

X-ray single-crystal structural characterization of Na2MgSiO4 with cristobalite-type structure synthesised at 22 GPa and 1800 °C

LUCA BINDI
;
2018

Abstract

Na2MgSiO4 is a mineralogical phase known in the literature as N2MS and reported in several high-pressure experiments (13.64s(Fo)] and 73 parameters. The unit-cell of the phase studied here is nearly identical to that of Na2MgSiO4 synthesised at room conditions, thus indicating that it likely relaxed during the pressure release occurring during quenching.
2018
30
485
489
EKATERINA A. SIROTKINA, LUCA BINDI, ANDREY V. BOBROV, ANASTASIA TAMAROVA, DMITRY YU. PUSHCHAROVSKY, TETSUO IRIFUNE
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1134176
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