Page 191 - Introduction to Colloid and Surface Chemistry
P. 191

180  Charged  interfaces

             \lt  =  (l/ 0  exp[-»o:]                           (7.7)

        which  shows that  at  low potentials the  potential  decreases  exponen-
        tially  with  distance  from  the  charged  surface.  Close  to  the  charged
        surface,  where  the  potential  is  likely  to  be  relatively high  and  the
        Debye-Hiickel approximation inapplicable, the potential is predicted  to
        decrease  at a greater  than exponential  rate.
          The  potential  fa  can  be  related  to  the  charge  density  cr 0  at  the
        surface  by equating the  surface charge with  the  net  space  charge in


        the diffuse  part of the double layer  i.e.  cr 0 =  -  pdr  j and applying
                                       \         Jo    /
        the  Poisson-Boltzmann  distribution. The  resulting expression is

             ob =  (SnackTf*  sinh  —                           (7.8)
                                 2*7
        which  at  low potentials reduces  to

                =  eKfa                                         (7.9)
             cr 0
          The  surface potential  fa,  therefore,  depends  on  both  the  surface
        charge  density  cr 0  and  (through  K) on  the  ionic composition  of  the
        medium.  If  the  double  layer  is compressed  (i.e.  K increased),  then
        either  cr 0 must increase,  or  fa  must decrease,  or  both.
          In  many  colloidal  systems,  the  double  layer  is  created  by  the
        adsorption  of potential-determining  ions;  for example, the  potential
        fa  at  the  surface  of  a/silver  iodide  particle  depends  on  the
        concentration  of silver (and iodide) ions in solution. Addition of inert
        electrolyte  increases  K and  results  in  a  corresponding  increase  of
        surface  charge  density  caused  by  the  adsorption  of  sufficient
        potential-determining  silver  (or  iodide)  ions to  keep  fa  approximately
        constant.  In  contrast,  however,  the  charge  density  at  an  ionogenic
        surface  remains constant  on  addition  of  inert electrolyte  (provided
        that  the  extent  of ionisation  is unaffected) and  fa  decreases.
          From equation  (7.9)  it can be seen that, at low potentials, a  diffuse
        double  layer has the  same capacity  as a parallel plate  condenser with
        a distance  I/K  between  the plates. It is customary  to refer to  l/*c (the
        distance  over  which the  potential  decreases by an exponential factor
        at  low potentials)  as the  'thickness' of  the  diffuse  double layer.
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