Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy

Research output: Contribution to journalJournal articleResearchpeer-review

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Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy. / Iles, Gail N.; Gates, Will P.; Pereira, Jose E. M.; Stampfl, Anton P. J.; Aldridge, Laurence P.; Bordallo, Heloisa N.

In: Journal of Physical Chemistry C, Vol. 126, No. 49, 2022, p. 21061-21070.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Iles, GN, Gates, WP, Pereira, JEM, Stampfl, APJ, Aldridge, LP & Bordallo, HN 2022, 'Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy', Journal of Physical Chemistry C, vol. 126, no. 49, pp. 21061-21070. https://doi.org/10.1021/acs.jpcc.2c06470

APA

Iles, G. N., Gates, W. P., Pereira, J. E. M., Stampfl, A. P. J., Aldridge, L. P., & Bordallo, H. N. (2022). Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy. Journal of Physical Chemistry C, 126(49), 21061-21070. https://doi.org/10.1021/acs.jpcc.2c06470

Vancouver

Iles GN, Gates WP, Pereira JEM, Stampfl APJ, Aldridge LP, Bordallo HN. Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy. Journal of Physical Chemistry C. 2022;126(49):21061-21070. https://doi.org/10.1021/acs.jpcc.2c06470

Author

Iles, Gail N. ; Gates, Will P. ; Pereira, Jose E. M. ; Stampfl, Anton P. J. ; Aldridge, Laurence P. ; Bordallo, Heloisa N. / Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy. In: Journal of Physical Chemistry C. 2022 ; Vol. 126, No. 49. pp. 21061-21070.

Bibtex

@article{aeb1dddc798646ccb8ee45d025fb25a9,
title = "Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy",
abstract = "The capacity of clay minerals to store large amounts of water is utilized in a number of industrial and environmental applications on Earth, for example, as components in geosynthetic clay liners in landfills or ingredients in water-based drilling fluids, and could prove important on Mars to identify future human landing sites where water could be harvested. The subzero behavior of water interacting within the interlayer space of clay minerals is of particular interest in most applications but remains poorly understood. To better understand the hydrothermal mechanism by which water ice bonds and separates from clay interlayers, we have utilized neutron spectroscopy, spectral analysis, and phonon band assignment. The inelastic neutron scattering from sodium montmorillonite, hydrated at 24, 73, and 166% water content, as well as an oven-dried sample, were measured to assess the vibrational density of states. The water contents studied provide a range of pore dimensions within clay gels that have varying degrees of confinement. The type of ice formed from water held in larger intraand interparticle pores differs substantially from that confined within the interlayer (pseudo-two-layer hydrate), and the differences vary with hydration level. Spectral subtraction over an energy transfer range 50 < E < 550 cm-1 (8 < E < 70 meV) produces clearly two different forms of ice: hexagonal and cubic in the two wetter samples. A form of interfacial ice, presumably of a lower density, is observed in the vibrational density of states spectrum of the sample hydrated to a pseudo-two-layer hydrate (ie 24% gravimetric water content (GWC), 10 H2O/Na+). No hexagonal or cubic ice is observed in this sample. The four vibrational modes within the translation band of hexagonal ice are apparent within the sample hydrated to 166% gravimetric water content, in which pores greater than 20 nm are largely water-filled. By considering hydrogen bonding of the water to the clay surface, our data indicate an increase in the strength of the H-bond due to a shorter distance to the hydroxyl. We attribute this decrease to the pores in the clay generating a localized negative pressure or {"}suction{"} effect, thus attracting the water.",
keywords = "HYDRATION PROPERTIES, WATER DESORPTION, SOLID-SURFACES, TRIPLE-AXIS, MONTMORILLONITE, SPECTROMETER, VIBRATIONS, SCATTERING, MINERALOGY, ISOTHERMS",
author = "Iles, {Gail N.} and Gates, {Will P.} and Pereira, {Jose E. M.} and Stampfl, {Anton P. J.} and Aldridge, {Laurence P.} and Bordallo, {Heloisa N.}",
year = "2022",
doi = "10.1021/acs.jpcc.2c06470",
language = "English",
volume = "126",
pages = "21061--21070",
journal = "The Journal of Physical Chemistry Part C",
issn = "1932-7447",
publisher = "American Chemical Society",
number = "49",

}

RIS

TY - JOUR

T1 - Two Forms of Ice Identified in Mars-like Clay Using Neutron Spectroscopy

AU - Iles, Gail N.

AU - Gates, Will P.

AU - Pereira, Jose E. M.

AU - Stampfl, Anton P. J.

AU - Aldridge, Laurence P.

AU - Bordallo, Heloisa N.

PY - 2022

Y1 - 2022

N2 - The capacity of clay minerals to store large amounts of water is utilized in a number of industrial and environmental applications on Earth, for example, as components in geosynthetic clay liners in landfills or ingredients in water-based drilling fluids, and could prove important on Mars to identify future human landing sites where water could be harvested. The subzero behavior of water interacting within the interlayer space of clay minerals is of particular interest in most applications but remains poorly understood. To better understand the hydrothermal mechanism by which water ice bonds and separates from clay interlayers, we have utilized neutron spectroscopy, spectral analysis, and phonon band assignment. The inelastic neutron scattering from sodium montmorillonite, hydrated at 24, 73, and 166% water content, as well as an oven-dried sample, were measured to assess the vibrational density of states. The water contents studied provide a range of pore dimensions within clay gels that have varying degrees of confinement. The type of ice formed from water held in larger intraand interparticle pores differs substantially from that confined within the interlayer (pseudo-two-layer hydrate), and the differences vary with hydration level. Spectral subtraction over an energy transfer range 50 < E < 550 cm-1 (8 < E < 70 meV) produces clearly two different forms of ice: hexagonal and cubic in the two wetter samples. A form of interfacial ice, presumably of a lower density, is observed in the vibrational density of states spectrum of the sample hydrated to a pseudo-two-layer hydrate (ie 24% gravimetric water content (GWC), 10 H2O/Na+). No hexagonal or cubic ice is observed in this sample. The four vibrational modes within the translation band of hexagonal ice are apparent within the sample hydrated to 166% gravimetric water content, in which pores greater than 20 nm are largely water-filled. By considering hydrogen bonding of the water to the clay surface, our data indicate an increase in the strength of the H-bond due to a shorter distance to the hydroxyl. We attribute this decrease to the pores in the clay generating a localized negative pressure or "suction" effect, thus attracting the water.

AB - The capacity of clay minerals to store large amounts of water is utilized in a number of industrial and environmental applications on Earth, for example, as components in geosynthetic clay liners in landfills or ingredients in water-based drilling fluids, and could prove important on Mars to identify future human landing sites where water could be harvested. The subzero behavior of water interacting within the interlayer space of clay minerals is of particular interest in most applications but remains poorly understood. To better understand the hydrothermal mechanism by which water ice bonds and separates from clay interlayers, we have utilized neutron spectroscopy, spectral analysis, and phonon band assignment. The inelastic neutron scattering from sodium montmorillonite, hydrated at 24, 73, and 166% water content, as well as an oven-dried sample, were measured to assess the vibrational density of states. The water contents studied provide a range of pore dimensions within clay gels that have varying degrees of confinement. The type of ice formed from water held in larger intraand interparticle pores differs substantially from that confined within the interlayer (pseudo-two-layer hydrate), and the differences vary with hydration level. Spectral subtraction over an energy transfer range 50 < E < 550 cm-1 (8 < E < 70 meV) produces clearly two different forms of ice: hexagonal and cubic in the two wetter samples. A form of interfacial ice, presumably of a lower density, is observed in the vibrational density of states spectrum of the sample hydrated to a pseudo-two-layer hydrate (ie 24% gravimetric water content (GWC), 10 H2O/Na+). No hexagonal or cubic ice is observed in this sample. The four vibrational modes within the translation band of hexagonal ice are apparent within the sample hydrated to 166% gravimetric water content, in which pores greater than 20 nm are largely water-filled. By considering hydrogen bonding of the water to the clay surface, our data indicate an increase in the strength of the H-bond due to a shorter distance to the hydroxyl. We attribute this decrease to the pores in the clay generating a localized negative pressure or "suction" effect, thus attracting the water.

KW - HYDRATION PROPERTIES

KW - WATER DESORPTION

KW - SOLID-SURFACES

KW - TRIPLE-AXIS

KW - MONTMORILLONITE

KW - SPECTROMETER

KW - VIBRATIONS

KW - SCATTERING

KW - MINERALOGY

KW - ISOTHERMS

U2 - 10.1021/acs.jpcc.2c06470

DO - 10.1021/acs.jpcc.2c06470

M3 - Journal article

VL - 126

SP - 21061

EP - 21070

JO - The Journal of Physical Chemistry Part C

JF - The Journal of Physical Chemistry Part C

SN - 1932-7447

IS - 49

ER -

ID: 330777800