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critical adsorption point 10.1016/J.ACA.2019.03.017

When the polymers are studied by interaction chromatography (IC) in porous media, the IC separation mechanism competes with the size-exclusion chromatography (SEC) mechanism and under specific conditions close to the critical adsorption point (CAP), the elution times of monodisperse polymer samples nonmonotonically depend on pore sizes.

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critical adsorption point 10.1016/J.POLYMER.2019.05.006

We focused on interaction chromatography (IC) under conditions close to the critical adsorption point (CAP).

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10.1039/c9sm00509a

Our approach accounts for a phenomenon of critical adsorption, therefore, a particle that is adsorptionwise nonneutral is always completely covered by an adsorption layer (droplet).

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10.1016/J.ACA.2019.03.017

When the polymers are studied by interaction chromatography (IC) in porous media, the IC separation mechanism competes with the size-exclusion chromatography (SEC) mechanism and under specific conditions close to the critical adsorption point (CAP), the elution times of monodisperse polymer samples nonmonotonically depend on pore sizes.

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10.1103/PhysRevE.99.062103

022103] it has been shown that, for a fluid film subject to critical adsorption, the resulting critical Casimir force (CCF) may significantly depend on the thermodynamic ensemble.

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10.1088/2053-1591/AB3016

The adsorbability of these three molecules is attributed to the shorter distance of critical adsorption, the larger charge transfer and greater sensitivity to electron band structure.

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10.1016/J.POLYMER.2019.05.006

We focused on interaction chromatography (IC) under conditions close to the critical adsorption point (CAP).

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10.1007/978-3-030-47705-9_15

In this work, two different supercritical carbon dioxide (scCO2) based processes were used to modify KET dissolution rate: the supercritical antisolvent technique to coprecipitate PVP and KET in form of controlled dimensions microparticles for an oral delivery, and the supercritical adsorption to impregnate KET in alginate aerogel for a topical delivery.

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10.1021/acsomega.9b02589

The expansion of ∼4% observed for xenon at a pressure of 48 bar is the largest deformation yet reported for supercritical adsorption on a carbonaceous material.

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10.1016/j.jcis.2019.05.059

Critical adsorption parameters (pH, temperature and PDA thickness) are optimized by the application of experimental design methodology.

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Critical Adsorption

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Oct 16, 2024

What is/are Critical Adsorption?

Critical Adsorption - Our approach accounts for a phenomenon of critical adsorption, therefore, a particle that is adsorptionwise nonneutral is always completely covered by an adsorption layer (droplet). ^[1] When the polymers are studied by interaction chromatography (IC) in porous media, the IC separation mechanism competes with the size-exclusion chromatography (SEC) mechanism and under specific conditions close to the critical adsorption point (CAP), the elution times of monodisperse polymer samples nonmonotonically depend on pore sizes. ^[2] 022103] it has been shown that, for a fluid film subject to critical adsorption, the resulting critical Casimir force (CCF) may significantly depend on the thermodynamic ensemble. ^[3] The adsorbability of these three molecules is attributed to the shorter distance of critical adsorption, the larger charge transfer and greater sensitivity to electron band structure. ^[4] We focused on interaction chromatography (IC) under conditions close to the critical adsorption point (CAP). ^[5] In this work, two different supercritical carbon dioxide (scCO2) based processes were used to modify KET dissolution rate: the supercritical antisolvent technique to coprecipitate PVP and KET in form of controlled dimensions microparticles for an oral delivery, and the supercritical adsorption to impregnate KET in alginate aerogel for a topical delivery. ^[6] The expansion of ∼4% observed for xenon at a pressure of 48 bar is the largest deformation yet reported for supercritical adsorption on a carbonaceous material. ^[7] Critical adsorption parameters (pH, temperature and PDA thickness) are optimized by the application of experimental design methodology. ^[8]

critical adsorption point

When the polymers are studied by interaction chromatography (IC) in porous media, the IC separation mechanism competes with the size-exclusion chromatography (SEC) mechanism and under specific conditions close to the critical adsorption point (CAP), the elution times of monodisperse polymer samples nonmonotonically depend on pore sizes. ^[1] We focused on interaction chromatography (IC) under conditions close to the critical adsorption point (CAP). ^[2]