Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fortes, A. Dominic, Fernandez-Alonso, Felix, Tucker, Matthew, Wood, Ian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289305/
http://dx.doi.org/10.1107/S2052520616018254
_version_ 1782504475449098240
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
work_keys_str_mv AT fortesadominic isothermalequationofstateandhighpressurephasetransitionsofsyntheticmeridianiitemgso411d2odeterminedbyneutronpowderdiffractionandquasielasticneutronspectroscopy
AT fernandezalonsofelix isothermalequationofstateandhighpressurephasetransitionsofsyntheticmeridianiitemgso411d2odeterminedbyneutronpowderdiffractionandquasielasticneutronspectroscopy
AT tuckermatthew isothermalequationofstateandhighpressurephasetransitionsofsyntheticmeridianiitemgso411d2odeterminedbyneutronpowderdiffractionandquasielasticneutronspectroscopy
AT woodiang isothermalequationofstateandhighpressurephasetransitionsofsyntheticmeridianiitemgso411d2odeterminedbyneutronpowderdiffractionandquasielasticneutronspectroscopy