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Membrane technology  45


           adapted for cross-flow operation if the proportion of  undeposited solute material
           can be calculated.
             The  expressions  listed  in  Table  2.10  illustrate  a  common  difficulty  in
           describing filtration behaviour.  Even  for a  supposedly generic matrix  (mixed
           liquor), the innate heterogeneity and diversity in composition of  real feedwater
           matrices  forbids  the  formulation  of  general  equations  describing  filtration
           behaviour,  even  under  steady-state  conditions.  Different  key  water  quality
           determinants (chemical oxygen demand, dissolved organic carbon and mixed
           liquor  (volatile)  suspended  solids)  have  been  identified  as  the  basis  for
           quantifying  fouling  propensity  and  dynamic  behaviour.  Most  recent
           publications of  experimental studies of MBR processes make little or no reference
           to dynamic modelling, with  data interpretation being substantially  limited to
           reporting of  hydraulic resistance values (Choo and Lee, 1996; Chang and Lee,
           1998; Defrance and Jaffrin, 1999b). The more global semi-empirical models that
           have been developed (Nagaoka et d., 1998), as with many other semi-empirical
           models in this area, rely on specific hydraulic resistance data which is likely to be
           specific to the system under investigation.
             Dead-end filtration theory is thus to a very large extent limited by the accuracy
           of  the representation of  the interaction between the solids and the membrane
           material.  The  same also  applies to  cross-flow  filtration.  However, for  dense
           membrane processes where the water can be considered to be a continuum with
           no complicating solid-liquid  interactions, modelling from first principles of  the
           resistance  offered by the membrane-solution  interface, due to  concentration
           polarisation, is possible.

           Classical concentration polarisation model
           As  already  stated  (Section  2.2.3), concentration  polarisation  describes the
           tendency of  the solute to build up in the membrane solution interfacial region,
           and the extent to which this occurs depends on:



           Table 2.8  Empirical dead-end filtration equations (from Chang et al.. 2002)
           Approach         Physical cause   Description           Equationa
           Cake filtration   Boundary layer   Deposit of particles larger than   t/V = AV i
                                                                           R
                            resistance    the membrane pore size  onto
                                          the membrane surface
           Complete         Pore blocking   Occlusion of pores by particles   -ln(J/]o)  = At + I3
           blocking                       with no particle
                                          superimposition
           Intermediate     Long-term     Occlusion ofpores by particles   1/J = At + R
           blocking         adsorption    with particle superimposition
           Standard         Direct        Deposit of particles smaller than   t/V = At + B
           blocking         adsorption    the membrane pore size onto
                                          the pore walls, reducing the
                                          pore size
           a  A,  B, constants  (value dependent  upon cake and system characteristics): R  cumulative volume of
           permeate at time t; Jo 1, flux initially and at timet respectively.
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