Page 309 - Modelling in Transport Phenomena A Conceptual Approach
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8.4. MASS TRANSPORT WITHOUT CONVECTION                              289


            Therefore, the initial molar flow rate of  species A is
                             (41)(3 x 10-5)(0.9 - 0.25)
                        hA =                        = 1.88 x     mol/s
                                     4244.1
                           an
           b) Fbm Eq.  (0) Table 8.8
                  .    C~AB(XA, - ~AL)A
                 nA  =
                               L
                     - (41)(3 x 10-5)(0.9 - 0.25) [~(0.008)~/4]
                     -                                     = 2.01 x 10-~ mol/ s
                                       0.2

           8.4.1.1  Electrical circuit analogy

           The molar transfer rate of  species A is given by &. (D) in Table 8.8 as

                                                                            (8.414)

                                               'DABA
           Comparison of  Q.  (8.414) with Eq. (8.2-10) indicates that

                                    Driving force = CA,  - CA~              (8.415)

                                   L
                     Resistance = - -            Thickness                  (8.416)
                                 VABA - ('lkansport property)(Area)


           8.4.1.2  Transfer rate in terms of bulk fluid properties

           Since it is much easier to measure the bulk concentrations of  the adjacent solu-
           tions to the surfaces at  z  = 0 and  z  = L,  it  is necessary to relate the surface
           concentrations,  XA, and XA~, to the bulk concentrations.
              For  energy  transfer,  the  assumption of  thermal  equilibrium at  a solid-fluid
           boundary leads to  the  equality of  temperatures  and  this  condition  is  generally
           stated  as, "temperature is continuous at  a  solid-fluid boundary."  In the case of
           mass transfer, the condition of  phase equilibrium for a nonreacting multicomp+
           nent system at a solid-fluid boundary implies the equality of  chemical potentials
           or  partial  molar  Gibbs free energies.  Therefore, concentrations at a solid-fluid
           boundary are not necessarily equal to each other with a resulting discontinuity in
           the concentration distribution.  For example, consider a homogeneous membrane
           which is chemically different from the solution it is separating.  In that case, the
           solute may be more (or, less) soluble in the membrane than in the bulk solution.
           A typical distribution of concentration is shown in Figure 8.28. Under these condi-
           tions, a thermodynamic property H, called the partition  coeficient, is introduced
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