Hydration forces between mica surfaces in electrolyte solutions
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The observation of hydration force with two decay lengths in 1 M NaAc indicates that cations gradually lost their hydration shells at small distances under high compression; the large decay length farther away corresponds to a layer of fully hydrated Na+ ions outside the innermost structure.
“The observation of the hydration force with two decay lengths indicated again that the cations gradually lost their hydration shells at small distances under high compression [57,58]; the large decay length farther away from the interface corresponds to a layer of fully hydrated Na + ions outside the innermost structure.”
From Effect of Hofmeister Anions on Interfacial Properties of Mica Surface in Concentrated Aqueous Solution (2020) · cites this paper as [57]
The large energies associated with hydration of charges lead to hydration repulsion effects.
“The large energies associated with hydration of charges lead to hydration repulsion effects [55 -60]”
From Hydration lubrication (2013) · cites this paper as [59]
The same hydration effect can lead to strong short-ranged repulsion when two charged surfaces interact across a high-salt-concentration solution.
“The same hydration effect can also lead to strong short-ranged repulsion when two charged surfaces interact across a high-salt-concentration solution [55, 59].”
From Hydration lubrication (2013) · cites this paper as [59]
When charged surfaces interact across pure or low salt-concentration water, the counterions in the gap are mostly small hydrated protons which may readily condense into and neutralise negatively charged lattice sites, so surfaces come into adhesive van der Waals contact.
“When such surfaces interact across pure or low salt-concentration water, as shown in Fig. 1, the counterions in the gap are mostly small hydrated protons which, as the surfaces approach, may readily condense into, and neutralise, the negatively charged lattice sites, so they come into adhesive van der Waals contact.”
From Hydration lubrication (2013) · cites this paper as [59]
Interactions across high salt solutions above some critical hydration concentration (for Na+, K+ around 0.1-1.0 mM) may be very different.
“In contrast, interactions across high salt solutions, above some critical hydration concentration (which differs with the ion but for Na + , K + is around 0.1 -1.0 mM [57, 59]) may be very different”
From Hydration lubrication (2013) · cites this paper as [59]
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Self-citationOrigins of hydration lubrication
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Dynamic properties of confined hydration layers
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“under high compression [57,58]; the large decay length farther away from the interface corresponds to a layer of fully hydrated Na+ ions outside the innermost structure.”
Background
- Authors
- Pashley, R. M.
- Affiliations
- Australian National University (AU)
- Corresponding author
- Pashley, R.M.
- ORCID
- Pashley, R.M.
- Venue
- Advances in Colloid and Interface Science
- Publisher
- Elsevier BV
- Published
- 1982-07
- Volume
- 16
- Issue
- 1
- Pages
- 57-62
- ISSN
- 0001-8686 (ISSN-L)
- OpenAlex
- W2019135964
- Cited by
- 309
- References
- 0
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 7 · 2023: 6 · 2022: 6 · 2021: 4 · 2020: 14 · 2019: 9 · 2018: 14 · 2017: 12 · 2016: 14 · 2015: 9 · 2014: 6 · 2013: 15 · 2012: 12
- FWCI
- 3.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Advances in Colloid and Interface Science (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Electrostatics and Colloid Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Chemical and Physical Studies
- Physical Sciences › Environmental Science › Water Science and Technology › Minerals Flotation and Separation Techniques
- Keywords
- mica surface, hydration forces, DLVO theory, electrolyte solutions, cation adsorption, ion exchange, site-binding model, surface charging, short-range repulsion, alkali metal chlorides, double exponential decay
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