2018
DOI: 10.1016/j.jcis.2018.07.095
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Inferring pore connectivity from sorption hysteresis in multiscale porous media

Abstract: Our formula is able to fit and interpret both primary and scanning sorption/desorption isotherms for a variety of adsorbates (noble gases, water, and organics) and porous materials (cement pastes, dental enamels, porous glasses, carbon black and nanotubes), including cases with broad pore-size distributions and large hysteresis. It allows quantification of the prevalence of percolating macropores in the material, even though these pores are never filled during the sorption experiments. A distinct bump in sorpt… Show more

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Cited by 43 publications
(57 citation statements)
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References 87 publications
(129 reference statements)
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“…Our approach allows us to explain the water hysteresis loop from metastable ink bottleneck states on desorption due to the pore constrictions in cement paste. This contrasts with previous results based on equilibrium thermodynamics for both adsorption and desorption branches and pore connectivity assumption (23, 24).…”
Section: Sorption Hysteresis and Pore Size Distributionscontrasting
confidence: 99%
“…Our approach allows us to explain the water hysteresis loop from metastable ink bottleneck states on desorption due to the pore constrictions in cement paste. This contrasts with previous results based on equilibrium thermodynamics for both adsorption and desorption branches and pore connectivity assumption (23, 24).…”
Section: Sorption Hysteresis and Pore Size Distributionscontrasting
confidence: 99%
“…The difference of ice-water interface curvature is another possible mechanism for freeze-thaw hysteresis. In addition, sorption hysteresis (Pinson et al, 2018) and freezing-induced water redistribution (Mohammed et al, 2014) are also possible alternative mechanisms for hysteresis. Figure 3 shows the SFCC of nonsaline soil with various initial water contents (denoted by w 0 ).…”
Section: Water Resources Researchmentioning
confidence: 99%
“…One argument is that this drop may be caused by measured water in capillary pores changing to in C-S-H pores [32]. Some studies believe that this is caused by cavitation of dissolved gas in pore solution [33,34]. However, the very steep sorption isotherm can also be caused by pore-blocking/percolation in a narrow range of pore necks [35].…”
Section: Fitted Sorption Isothermmentioning
confidence: 99%