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Adsorption Isotherms I01:29

Adsorption Isotherms I

194
Adsorption isotherms are mathematical models that describe how molecules in a gas or liquid phase interact with surfaces. Two of the most common isotherm models are the Langmuir and Freundlich isotherms, which relate to Type I monolayer chemisorption. The Langmuir model is based on four key assumptions:• Adsorption cannot exceed monolayer coverage.• All surface sites are equivalent.• Molecules adsorb only at vacant sites.• There are no interactions between adsorbed...
194
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model01:09

Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model

924
Various dissolution theories provide insight into the factors that influence the dissolution rate. Danckwerts' Model suggests that turbulence, rather than a stagnant layer, characterizes the dissolution medium at the solid-liquid interface. In this model, the agitated solvent contains macroscopic packets that move to the interface via eddy currents, facilitating the absorption and delivery of the drug to the bulk solution. The regular replenishment of solvent packets maintains the...
924
Adsorption Isotherms II01:25

Adsorption Isotherms II

122
Brunauer, Emmett, and Teller (BET) introduced a theory in 1938 that modified Langmuir's assumptions to explain multilayer physical adsorption. This theory is applicable to Type II isotherms and provides a more realistic picture of adsorption processes. The BET theory assumes a uniform solid surface with localized adsorption sites, where adsorption at one site doesn't affect adsorption at neighboring sites. This theory also allows for the possibility of additional molecules being adsorbed on top...
122
Colloids and Suspensions01:17

Colloids and Suspensions

3.9K
Children at play often make suspensions such as mixtures of mud and water, flour and water, or a suspension of solid pigments in water known as tempera paint. These suspensions are heterogeneous mixtures composed of relatively large particles visible to the naked eye or seen with a magnifying glass. They are cloudy, and the suspended particles settle out after mixing. The suspended particles in a suspension settle out after some time of mixing. The separation of particles from a suspension is...
3.9K
Analyte Adsorption and Distribution01:09

Analyte Adsorption and Distribution

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In certain chromatographic separations, solutes transfer between the mobile phase and the stationary phase via sorption, which typically refers to the process of adsorption. For many chromatographic systems, the sorption process often depends on the polarity of the compounds—an expression of the overall dipole moment within the molecule. During the separation process, there is competition between the solute and solvent for adsorption to the stationary phase. Highly polar compounds and...
3.3K
Colloidal precipitates01:09

Colloidal precipitates

6.9K
The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
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Related Experiment Video

Updated: Apr 17, 2026

Study of Short Peptide Adsorption on Solution Dispersed Inorganic Nanoparticles Using Depletion Method
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Study of Short Peptide Adsorption on Solution Dispersed Inorganic Nanoparticles Using Depletion Method

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A colloid model system for interfacial sorption kinetics.

Paul F Salipante1, Steven D Hudson1

  • 1Polymers and Complex Fluids Group, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States.

Langmuir : the ACS Journal of Surfaces and Colloids
|February 26, 2015
PubMed
Summary
This summary is machine-generated.

Researchers studied particle adsorption using micron-sized colloids and total internal reflection microscopy. They found diffusion dynamics significantly impact adsorption and desorption rates when interaction energy is low.

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Area of Science:

  • Colloid and Surface Science
  • Physical Chemistry
  • Soft Matter Physics

Background:

  • Particle adsorption at interfaces is complex, influencing many scientific and industrial processes.
  • Understanding particle characteristics and solution conditions is crucial for controlling adsorption.
  • Weak interfacial interactions are relevant to nanoscale systems like proteins.

Purpose of the Study:

  • To quantitatively measure adsorption and desorption rates of model colloids.
  • To investigate the role of particle diffusion dynamics in adsorption processes.
  • To compare experimental findings with theoretical predictions for weak interaction potentials.

Main Methods:

  • Utilized micron-sized colloids with tunable weak interfacial interactions (<10 kBT).
  • Employed light-emitting diode-based total internal reflection microscopy (TIRM) to track particle motion.
  • Combined depletion, electrostatic, and gravitational forces to control colloid-interface interactions.

Main Results:

  • Observed colloids transitioning between adsorbed and desorbed states via Brownian motion.
  • Demonstrated that diffusion dynamics significantly influence adsorption/desorption rates for low barrier energies.
  • Validated experimental measurements against theoretical models incorporating near-wall diffusivity.

Conclusions:

  • The study provides a model system for investigating interfacial particle dynamics.
  • Highlights the critical role of diffusion in systems with weak colloid-interface interactions.
  • Establishes a foundation for future research on complex interfacial phenomena.