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The Langmuir adsorption model deviates significantly in many cases, primarily because it fails to account for the surface roughness of the adsorbent. Rough inhomogeneous surfaces have multiple site types available for adsorption, with some parameters varying from site to site, such as the heat of adsorption.
The following reactions follow an Langmuir–Rideal mechanism: [4] C 2 H 4 + 1 / 2 O 2 (adsorbed) → (CH 2 CH 2)O The dissociative adsorption of oxygen is also possible, which leads to secondary products carbon dioxide and water. CO 2 + H 2 (ads.) → H 2 O + CO; 2 NH 3 + 1 + 1 / 2 O 2 (ads.) → N 2 + 3H 2 O on a platinum catalyst
The langmuir (symbol: L) is a unit of exposure (or dosage) to a surface (e.g. of a crystal) and is used in ultra-high vacuum (UHV) surface physics to study the adsorption of gases. It is a practical unit, and is not dimensionally homogeneous, and so is used only in this field. It is named after American physicist Irving Langmuir.
While the Langmuir model assumes that the energy of adsorption remains constant with surface occupancy, the Freundlich equation is derived with the assumption that the heat of adsorption continually decrease as the binding sites are occupied. [16] The choice of the model based on best fitting of the data is a common misconception. [15]
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.
The idea of a Langmuir–Blodgett (LB) film was first proven feasible in 1917 when Irving Langmuir (Langmuir, 1917) showed that single water-surface monolayers could be transferred to solid substrates. 18 years later, Katharine Blodgett made an important scientific advance when she discovered that several of these single monolayer films could be stacked on top of one another to make multilayer ...
The sticking probability is the probability that molecules are trapped on surfaces and adsorb chemically. From Langmuir's adsorption isotherm, molecules cannot adsorb on surfaces when the adsorption sites are already occupied by other molecules, so the sticking probability can be expressed as follows:
The Hertz–Knudsen equation describes the non-dissociative adsorption of a gas molecule on a surface by expressing the variation of the number of molecules impacting on the surfaces per unit of time as a function of the pressure of the gas and other parameters which characterise both the gas phase molecule and the surface: [1] [2]