Page 55 - Adsorption by Powders and Porous Solids
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40                             ADSORPTION BY POWDERS AND POROUS SOLIDS

   The drfferential standard entropy of adsorption, A ,,  J;,,,   is:
                             A~~~S';,~=~';,,-                    (2.55)
                                          SF'
   The differential entropy of adsorption can be readily calculated from the differential
   enthalpy of adsorption since from Equations (2.46), (2.5 1) and (2.54) we obtain:

                             A  ads  T. f  =-
                                        T
   It is important not to confuse the differential (or isosteric) enthalpy of adsorption with
   the transformed differential enthalpy of adsorption A ,hT,,  which is derived from
   Equation (2.45):




   so that:






   2.5.2.  Definitions of the integral molar quantities of adsorption
   The difference between a molar surface excess thermodynamic quantity x;, , and the
   corresponding molar quantity x;,,  for the gaseous adsorptive at the same equilibrium
   T and p is usually called the integral molar quantity of adsorption, and is denoted
   A4SxT.r:
                             AadsxT,r= ';,f  - 'tSp
   We can thus define the integral molar energy of adrorption:
                             A,su~,r= 4.r- ~8
   and the integral molar entropy of adsorption:

                             Aa&sT,r=s;,r-                       (2.60)
   We may  derive the relation between these integral molar quantities of adsorption
   from Equations (2.20) using the expression of surface excess chemical potential y"
   given by Equation (2.41) and assuming the gas to be ideal:




   Then, from Equation (2.40), the transformed integral molar enthalpy of adsorption is
    obtained:
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