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Neutron Time-of-Flight Quantification of Water Desorption Isotherms of Montmorillonite

Gates, Will P. ; Bordallo, Heloise LU ; Aldridge, Laurence P. ; Seydel, Tilo ; Jacobsen, Henrik ; Marry, Virginie and Churchman, G. Jock (2012) In Journal of Physical Chemistry C 116(9). p.5558-5570
Abstract
The multiple energy states of water held by surfaces of a clay mineral can be effectively probed with time-of-flight and fixed elastic window neutron scattering. We used these techniques to quantitatively differentiate water types, including rotational and translational diffusions, in Ca- and Na-montmorillonite (SAz-1) and charge-reduced preparations equilibrated at RH = 33% and 55%, whose gravimetric water contents are in proportion with their layer charge. Quasi-elastic neutron scattering results revealed significant differences within interlayer water populations and between interlayer and interparticle waters. Interlayer cationic and H-bonded waters have residence times ranging from a few nanoseconds to tenths of picoseconds, while... (More)
The multiple energy states of water held by surfaces of a clay mineral can be effectively probed with time-of-flight and fixed elastic window neutron scattering. We used these techniques to quantitatively differentiate water types, including rotational and translational diffusions, in Ca- and Na-montmorillonite (SAz-1) and charge-reduced preparations equilibrated at RH = 33% and 55%, whose gravimetric water contents are in proportion with their layer charge. Quasi-elastic neutron scattering results revealed significant differences within interlayer water populations and between interlayer and interparticle waters. Interlayer cationic and H-bonded waters have residence times ranging from a few nanoseconds to tenths of picoseconds, while interparticle water, obtained for the RH = 55% equilibrated samples, showed an average diffusivity faster than interlayer water, yet slower than bulk water. Our results enabled us to differentiate at least two water motions during dehydration of Ca- and Na-SAz-1 (initially equilibrated at RH = 55%) by using a "controlled water loss" time-of-flight procedure. This work confirms that (a) interlayer and cationic water in dioctahedral smectites are characterized by slower motions than interparticle water, (b) interlayer cations influenced the dynamics of water loss, probably through its affect on clay fabric, and (c) interparticle water behaves more like bulk water. At 55% RH the Ca montmorillonite held more interparticle water, but on dehydration under controlled conditions, it retained interlayer and cationic water more strongly than Na montmorillonite. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Journal of Physical Chemistry C
volume
116
issue
9
pages
5558 - 5570
publisher
The American Chemical Society (ACS)
external identifiers
  • wos:000301315700036
  • scopus:84858136490
ISSN
1932-7447
DOI
10.1021/jp2072815
language
English
LU publication?
yes
id
63fc3b97-b699-4853-8580-f879609c6c7a (old id 2515560)
date added to LUP
2016-04-01 11:04:23
date last changed
2022-04-20 08:45:38
@article{63fc3b97-b699-4853-8580-f879609c6c7a,
  abstract     = {{The multiple energy states of water held by surfaces of a clay mineral can be effectively probed with time-of-flight and fixed elastic window neutron scattering. We used these techniques to quantitatively differentiate water types, including rotational and translational diffusions, in Ca- and Na-montmorillonite (SAz-1) and charge-reduced preparations equilibrated at RH = 33% and 55%, whose gravimetric water contents are in proportion with their layer charge. Quasi-elastic neutron scattering results revealed significant differences within interlayer water populations and between interlayer and interparticle waters. Interlayer cationic and H-bonded waters have residence times ranging from a few nanoseconds to tenths of picoseconds, while interparticle water, obtained for the RH = 55% equilibrated samples, showed an average diffusivity faster than interlayer water, yet slower than bulk water. Our results enabled us to differentiate at least two water motions during dehydration of Ca- and Na-SAz-1 (initially equilibrated at RH = 55%) by using a "controlled water loss" time-of-flight procedure. This work confirms that (a) interlayer and cationic water in dioctahedral smectites are characterized by slower motions than interparticle water, (b) interlayer cations influenced the dynamics of water loss, probably through its affect on clay fabric, and (c) interparticle water behaves more like bulk water. At 55% RH the Ca montmorillonite held more interparticle water, but on dehydration under controlled conditions, it retained interlayer and cationic water more strongly than Na montmorillonite.}},
  author       = {{Gates, Will P. and Bordallo, Heloise and Aldridge, Laurence P. and Seydel, Tilo and Jacobsen, Henrik and Marry, Virginie and Churchman, G. Jock}},
  issn         = {{1932-7447}},
  language     = {{eng}},
  number       = {{9}},
  pages        = {{5558--5570}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{Journal of Physical Chemistry C}},
  title        = {{Neutron Time-of-Flight Quantification of Water Desorption Isotherms of Montmorillonite}},
  url          = {{http://dx.doi.org/10.1021/jp2072815}},
  doi          = {{10.1021/jp2072815}},
  volume       = {{116}},
  year         = {{2012}},
}