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Ca(2+) Ions Decrease Adhesion between Two (104) Calcite Surfaces as Probed by Atomic Force Microscopy
[Image: see text] Solution composition-sensitive disjoining pressure acting between the mineral surfaces in fluid-filled granular rocks and materials controls their cohesion, facilitates the transport of dissolved species, and may sustain volume-expanding reactions leading to fracturing or pore seal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543600/ https://www.ncbi.nlm.nih.gov/pubmed/34712891 http://dx.doi.org/10.1021/acsearthspacechem.1c00220 |
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author | Dziadkowiec, Joanna Ban, Matea Javadi, Shaghayegh Jamtveit, Bjørn Røyne, Anja |
author_facet | Dziadkowiec, Joanna Ban, Matea Javadi, Shaghayegh Jamtveit, Bjørn Røyne, Anja |
author_sort | Dziadkowiec, Joanna |
collection | PubMed |
description | [Image: see text] Solution composition-sensitive disjoining pressure acting between the mineral surfaces in fluid-filled granular rocks and materials controls their cohesion, facilitates the transport of dissolved species, and may sustain volume-expanding reactions leading to fracturing or pore sealing. Although calcite is one of the most abundant minerals in the Earth’s crust, there is still no complete understanding of how the most common inorganic ions affect the disjoining pressure (and thus the attractive or repulsive forces) operating between calcite surfaces. In this atomic force microscopy study, we measured adhesion acting between two cleaved (104) calcite surfaces in solutions containing low and high concentrations of Ca(2+) ions. We detected only low adhesion between calcite surfaces, which was weakly modulated by the varying Ca(2+) concentration. Our results show that the more hydrated calcium ions decrease the adhesion between calcite surfaces with respect to monovalent Na(+) at a given ionic strength, and thus Ca(2+) can sustain relatively thick water films between contacting calcite grains even at high overburden pressures. These findings suggest a possible loss of cohesion and continued progress of reaction-induced fracturing for weakly charged minerals in the presence of strongly hydrated ionic species. |
format | Online Article Text |
id | pubmed-8543600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85436002021-10-26 Ca(2+) Ions Decrease Adhesion between Two (104) Calcite Surfaces as Probed by Atomic Force Microscopy Dziadkowiec, Joanna Ban, Matea Javadi, Shaghayegh Jamtveit, Bjørn Røyne, Anja ACS Earth Space Chem [Image: see text] Solution composition-sensitive disjoining pressure acting between the mineral surfaces in fluid-filled granular rocks and materials controls their cohesion, facilitates the transport of dissolved species, and may sustain volume-expanding reactions leading to fracturing or pore sealing. Although calcite is one of the most abundant minerals in the Earth’s crust, there is still no complete understanding of how the most common inorganic ions affect the disjoining pressure (and thus the attractive or repulsive forces) operating between calcite surfaces. In this atomic force microscopy study, we measured adhesion acting between two cleaved (104) calcite surfaces in solutions containing low and high concentrations of Ca(2+) ions. We detected only low adhesion between calcite surfaces, which was weakly modulated by the varying Ca(2+) concentration. Our results show that the more hydrated calcium ions decrease the adhesion between calcite surfaces with respect to monovalent Na(+) at a given ionic strength, and thus Ca(2+) can sustain relatively thick water films between contacting calcite grains even at high overburden pressures. These findings suggest a possible loss of cohesion and continued progress of reaction-induced fracturing for weakly charged minerals in the presence of strongly hydrated ionic species. American Chemical Society 2021-10-04 2021-10-21 /pmc/articles/PMC8543600/ /pubmed/34712891 http://dx.doi.org/10.1021/acsearthspacechem.1c00220 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Dziadkowiec, Joanna Ban, Matea Javadi, Shaghayegh Jamtveit, Bjørn Røyne, Anja Ca(2+) Ions Decrease Adhesion between Two (104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title | Ca(2+) Ions Decrease Adhesion between Two
(104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title_full | Ca(2+) Ions Decrease Adhesion between Two
(104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title_fullStr | Ca(2+) Ions Decrease Adhesion between Two
(104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title_full_unstemmed | Ca(2+) Ions Decrease Adhesion between Two
(104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title_short | Ca(2+) Ions Decrease Adhesion between Two
(104) Calcite Surfaces as Probed by Atomic Force Microscopy |
title_sort | ca(2+) ions decrease adhesion between two
(104) calcite surfaces as probed by atomic force microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543600/ https://www.ncbi.nlm.nih.gov/pubmed/34712891 http://dx.doi.org/10.1021/acsearthspacechem.1c00220 |
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