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Polanyi-Dubinin adsorption equation

Wood, G O., "Affinity Coefficients of the Polanyi/Dubinin Adsorption Isotherm Equations a Review with Compilations and Correlations," Carbon. 2001 39 343 356. [Pg.334]

The Dubinin adsorption isotherm equation is a good tool for the measurement of the micropore volume. This isotherm can be deduced with the help of Dubinin s theory of volume filling, and Polanyi s adsorption potential [11,26], The Dubinin adsorption isotherm equation has the following form [11]... [Pg.292]

In the Dubiiiin-Radushkevitch (DR) equation [115], an adsorption model derived from a concept of Dubinin [20] based on Polanyi potential theory, the fluid volume V adsorbed in micropores at pressure P is represented empirically as... [Pg.237]

An analytical method for applying Polanyi s theory at temperatures near the critical temperature of the adsorbate is described. The procedure involves the Cohen-Kisarov equation for the characteristic curve as well as extrapolated values from the physical properties of the liquid. This method was adequate for adsorption on various molecular sieves. The range of temperature, where this method is valid, is discussed. The Dubinin-Rad/ush-kevich equation was a limiting case of the Cohen-Kisarov s equation. From the value of the integral molar entropy of adsorption, the adsorbed phase appears to have less freedom than the compressed phase of same density. [Pg.382]

The Dubinin-Radushkevieh (DR) equation is usually applied to describe the physical adsorption of organic vapors on microporous adsorbents. It is based on the micropore volume-filling theory and the Polanyi concept of adsorption potential. The DR equation can be expressed as... [Pg.286]

The Dubinin-Radushkevich (DR) equation was originally devised as an empirical expression of the Polanyi adsorption potential theory, and due to its simplicity it has been widely used to correlate adsorption data in many microporous sohds despite its failure in giving the correct Henry constant at extremely low pressures. This equation is based on the premise that adsorption in micropores follows a mechanism of pore filhng rather than the molecular layering and capillary condensation as proposed for mesoporous sofids. It has the form ... [Pg.247]

Now let us overview the theoretical adsorption models for characterization of the pore structures according to the pore size range. For physical adsorption of the gas molecules on such microporous sohds as activated carbons and zeolites, Dubinin and Radushkevich developed an empirical equation, which describes the volume filling process in the micropoies. Their theory incorporates earlier work by Polanyi in regard to the adsorption potential ad defined as... [Pg.151]

In Chapter 2, we discussed the fundamentals of adsorption equilibria for pure component, and in Chapter 3 we presented various empirical equations, practical for the calculation of adsorption kinetics and adsorber design, the BET theory and its varieties for the description of multilayer adsorption used as the yardstick for the surface area determination, and the capillary condensation for the pore size distribution determination. Here, we present another important adsorption mechanism applicable for microporous solids only, called micropore filling. In this class of solids, micropore walls are in proximity to each other, providing an enhanced adsorption potential within the micropores. This strong potential is due to the dispersive forces. Theories based on this force include that of Polanyi and particularly that of Dubinin, who coined the term micropore filling. This Dubinin theory forms the basis for many equations which are currently used for the description of equilibria in microporous solids. [Pg.149]

The potential theory of adsorption was introduced by Polanyi in 1914. Dubinin [48,49] and Stoeckli et al. [50] improved the theory and termed it the theory of volume filling of micropores (TVFM). This theory has been widely used in correlating the effect of temperature on the adsorption isotherms of pure gases. The modern formulationof TVFM is the Dubinin-Astakhov (DA) equation, which is expressed as... [Pg.413]

Based on the Polanyi potential theory, different approaches to describe the adsorption behavior of a purely microporous material (isotherm type I, Figure 21.25) have been undertaken by Dubinin and Stockli in collaboration with different other scientists. The simplest relationship that can be considered the base for all other variants is the Dubinin-Radushkevich equation [58] ... [Pg.475]

The DR isotherm remained known to a relatively small group of researchers until Hobson called attention to its applicability to non porous surfaces. In a letter to the Journal of Chemical Physics, Hobson, not without wonder, observed that the appearance of the Dubinin-Radushkevich equation in the present context (submonolayer adsorption of nitrogen on Pyrex) is surprising for two reasons. First, it is a particular equation within the Polanyi potential theory, which is a theory of condensation and might not be expected to apply to physical adsorption at very low coverage. Second, most of the adsorbents to which the Dubinin-Radushkevich equation have been applied have been porous, whereas our conclusion suggests that Pyrex is non-porous for nitrogen. Thus, unless and until a basic derivation for this equation is provided, it can only be considered as a useful empirical relation . [Pg.60]

This model for mixed adsorption (Grant and Manes 1966) is based upon the idea of equipotential energies among the components of the adsorbed mixture and is thus related to the Polanyi potential theory discussed in Section 3.3.5. As previously recorded, Dubinin and Radushkevich (1947) postulated a direct relation between the affinity coefficient Pi of a component i and the molar volume Vmt of the saturated pure liquid. The equipotential energy concept for two components is thus (eiiPi) = (ey/ft). Hence, by use of equation (3.18) for each component... [Pg.55]


See other pages where Polanyi-Dubinin adsorption equation is mentioned: [Pg.191]    [Pg.3]    [Pg.13]    [Pg.235]    [Pg.219]    [Pg.265]    [Pg.178]    [Pg.210]    [Pg.285]    [Pg.234]    [Pg.582]   
See also in sourсe #XX -- [ Pg.191 ]




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