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Brunauer–Emmett–Teller (BET) theory aims to explain the physical adsorption of gas molecules on a solid surface and serves as the basis for an important analysis technique for the measurement of the specific surface area of materials. The observations are very often referred to as physical adsorption or physisorption.
Brunauer, Emmett and Teller's model of multilayer adsorption is a random distribution of molecules on the material surface. Adsorption is the adhesion [1] of atoms, ions or molecules from a gas, liquid or dissolved solid to a surface. [2] This process creates a film of the adsorbate on the surface of the adsorbent.
Inherent within this model, the following assumptions [5] are valid specifically for the simplest case: the adsorption of a single adsorbate onto a series of equivalent sites onto the surface of the solid. The surface containing the adsorbing sites is a perfectly flat plane with no corrugations (assume the surface is homogeneous).
Adsorption is the process by which a gas (or solution) phase molecule (the adsorbate) binds to solid (or liquid) surface atoms (the adsorbent). The reverse of adsorption is desorption, the adsorbate splitting from adsorbent. In a reaction facilitated by heterogeneous catalysis, the catalyst is the adsorbent and the reactants are the adsorbate.
The Gibbs adsorption isotherm for multicomponent systems is an equation used to relate the changes in concentration of a component in contact with a surface with changes in the surface tension, which results in a corresponding change in surface energy. For a binary system, the Gibbs adsorption equation in terms of surface excess is
The Langmuir model of adsorption [2] assumes . The maximum coverage is one adsorbate molecule per substrate site. Independent and equivalent adsorption sites. This model is the simplest useful approximation that still retains the dependence of the adsorption rate on the coverage, and in the simplest case, precursor states are not considered.
Created Date: 8/30/2012 4:52:52 PM
The liquid molecules are more attracted to other liquid molecules as compared to the polymer surface. Because the polymer surfaces are solid surfaces, surface tension cannot be measured in a traditional way such as using a Wilhelmy plate. Instead, contact angles can be used to indirectly estimate the surface tension of polymer surfaces. [3]