Page 142 - Introduction to Colloid and Surface Chemistry
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132  The solid-gas  interface























        Figure 5.11  BET  isotherms



        Adsorption energies
        A  most  important  feature  of  the  models  upon  which  adsorption
        isotherm equations,  such as those  above, are based  is a characteristic
        assumption  relating  to  heat  of  adsorption  and  surface  coverage.
        Several factors  merit consideration  in this  respect.
          Solid  surfaces are  usually heterogeneous;  therefore,  since  adsorp-
        tion  at  the  more  active  sites  is favoured,  heats  of  both  monolayer
        physical  adsorption  and  chemisorption  might,  in  this  respect,  be
        expected  to  become  significantly  less  exothermic  as  the  surface
        coverage  increases,  as,  for  example,  shown  at  low  pressures  in
        Figures 5.12a and 5.12b. This, in turn would cause the initial slope of
        an adsorption isotherm  to be steeper than that predicted  according to
        the  Langmuir equation or  the BET equation.
          Chemisorption  might involve the  adsorbate  gas  molecules  either
        giving up electrons  to or receiving electrons from  the adsorbent  solid.
        As  either  of these  processes continues,  further  adsorption  becomes
        more  and  more  difficult  and  monolayer  coverage  is  not  as  readily
        attained as would be predicted  according to the Langmuir equation.
        The  heat  of  adsorption  becomes  less  exothermic  as  monolayer
        coverage  is approached,  as,  for example, shown in Figure 5.12b.
          When  a  gas  molecule  is  adsorbed  on  to  a  solid  surface  which  is
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