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Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy
We have collected neutron powder diffraction data from MgSO(4)·11D(2)O (the deuterated analogue of meridianiite), a highly hydrated sulfate salt that is thought to be a candidate rock-forming mineral in some icy satellites of the outer solar system. Our measurements, made using the PEARL/HiPr and OS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289305/ http://dx.doi.org/10.1107/S2052520616018254 |
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author | Fortes, A. Dominic Fernandez-Alonso, Felix Tucker, Matthew Wood, Ian G. |
author_facet | Fortes, A. Dominic Fernandez-Alonso, Felix Tucker, Matthew Wood, Ian G. |
author_sort | Fortes, A. Dominic |
collection | PubMed |
description | We have collected neutron powder diffraction data from MgSO(4)·11D(2)O (the deuterated analogue of meridianiite), a highly hydrated sulfate salt that is thought to be a candidate rock-forming mineral in some icy satellites of the outer solar system. Our measurements, made using the PEARL/HiPr and OSIRIS instruments at the ISIS neutron spallation source, covered the range 0.1 < P < 800 MPa and 150 < T < 280 K. The refined unit-cell volumes as a function of P and T are parameterized in the form of a Murnaghan integrated linear equation of state having a zero-pressure volume V (0) = 706.23 (8) Å(3), zero-pressure bulk modulus K (0) = 19.9 (4) GPa and its first pressure derivative, K′ = 9 (1). The structure’s compressibility is highly anisotropic, as expected, with the three principal directions of the unit-strain tensor having compressibilities of 9.6 × 10(−3), 3.4 × 10(−2) and 3.4 × 10(−3) GPa(−1), the most compressible direction being perpendicular to the long axis of a discrete hexadecameric water cluster, (D(2)O)(16). At high pressure we observed two different phase transitions. First, warming of MgSO(4)·11D(2)O at 545 MPa resulted in a change in the diffraction pattern at 275 K consistent with partial (peritectic) melting; quasielastic neutron spectra collected simultaneously evince the onset of the reorientational motion of D(2)O molecules with characteristic time-scales of 20–30 ps, longer than those found in bulk liquid water at the same temperature and commensurate with the lifetime of solvent-separated ion pairs in aqueous MgSO(4). Second, at ∼ 0.9 GPa, 240 K, MgSO(4)·11D(2)O decomposed into high-pressure water ice phase VI and MgSO(4)·9D(2)O, a recently discovered phase that has hitherto only been formed at ambient pressure by quenching small droplets of MgSO(4)(aq) in liquid nitrogen. The fate of the high-pressure enneahydrate on further compression and warming is not clear from the neutron diffraction data, but its occurrence indicates that it may also be a rock-forming mineral in the deep mantles of large icy satellites. |
format | Online Article Text |
id | pubmed-5289305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-52893052017-02-10 Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy Fortes, A. Dominic Fernandez-Alonso, Felix Tucker, Matthew Wood, Ian G. Acta Crystallogr B Struct Sci Cryst Eng Mater Research Papers We have collected neutron powder diffraction data from MgSO(4)·11D(2)O (the deuterated analogue of meridianiite), a highly hydrated sulfate salt that is thought to be a candidate rock-forming mineral in some icy satellites of the outer solar system. Our measurements, made using the PEARL/HiPr and OSIRIS instruments at the ISIS neutron spallation source, covered the range 0.1 < P < 800 MPa and 150 < T < 280 K. The refined unit-cell volumes as a function of P and T are parameterized in the form of a Murnaghan integrated linear equation of state having a zero-pressure volume V (0) = 706.23 (8) Å(3), zero-pressure bulk modulus K (0) = 19.9 (4) GPa and its first pressure derivative, K′ = 9 (1). The structure’s compressibility is highly anisotropic, as expected, with the three principal directions of the unit-strain tensor having compressibilities of 9.6 × 10(−3), 3.4 × 10(−2) and 3.4 × 10(−3) GPa(−1), the most compressible direction being perpendicular to the long axis of a discrete hexadecameric water cluster, (D(2)O)(16). At high pressure we observed two different phase transitions. First, warming of MgSO(4)·11D(2)O at 545 MPa resulted in a change in the diffraction pattern at 275 K consistent with partial (peritectic) melting; quasielastic neutron spectra collected simultaneously evince the onset of the reorientational motion of D(2)O molecules with characteristic time-scales of 20–30 ps, longer than those found in bulk liquid water at the same temperature and commensurate with the lifetime of solvent-separated ion pairs in aqueous MgSO(4). Second, at ∼ 0.9 GPa, 240 K, MgSO(4)·11D(2)O decomposed into high-pressure water ice phase VI and MgSO(4)·9D(2)O, a recently discovered phase that has hitherto only been formed at ambient pressure by quenching small droplets of MgSO(4)(aq) in liquid nitrogen. The fate of the high-pressure enneahydrate on further compression and warming is not clear from the neutron diffraction data, but its occurrence indicates that it may also be a rock-forming mineral in the deep mantles of large icy satellites. International Union of Crystallography 2017-01-31 /pmc/articles/PMC5289305/ http://dx.doi.org/10.1107/S2052520616018254 Text en © A. D. Fortes et al. 2017 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/ |
spellingShingle | Research Papers Fortes, A. Dominic Fernandez-Alonso, Felix Tucker, Matthew Wood, Ian G. Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title | Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title_full | Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title_fullStr | Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title_full_unstemmed | Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title_short | Isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (MgSO(4)·11D(2)O) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
title_sort | isothermal equation of state and high-pressure phase transitions of synthetic meridianiite (mgso(4)·11d(2)o) determined by neutron powder diffraction and quasielastic neutron spectroscopy |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289305/ http://dx.doi.org/10.1107/S2052520616018254 |
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