Page 711 - Bird R.B. Transport phenomena
P. 711

§22.4  Definition  of Transfer  Coefficients  in Two Phases  691

                               The  solubility  of  O  in water  at  20°C is  1.38  X  10  3  moles  per  liter  at an  oxygen  partial
                                              2
                           pressure  of  760 mm Hg, the vapor pressure  of  water  is  17.535  mm Hg, and the total pressure
                           in  the solubility  measurements  is  777.5  mm  Hg.  At  20°C,  the diffusivity  of  O 2  in  water  is
                                                                                                  2
                                            2
                                        5
                           ЯЬ  = 2.1  X 10~  cm /s, and in the gas  phase the diffusivity  for O 2  -  N  is ЯЬ  = 0.2 cm /s.
                                                                                     2
                             АВ
                                                                                          АС
                           We  can then  write
                                                        i^    f[  &i                             .
                                                             =                                ( 2 2 4  1 5 )
                           Into this we must substitute
                                                                  1000/18        =  1308      (22.4-16)
                                                          (77751760) / (0.08206) (293.5)
                                                            =  0.01                           (22.4-17)
                                                       0.2
                                                          3
                                                  1.38  X  10" /55.5
                                                    760/777.5                                 (22.4-18)
                           It follows that

                                                   =  (1308X0.01X2.54  x  10" )  = 3.32  x  10  (22.4-19)
                                                                      5
                           Therefore,  only  the liquid-phase  resistance  is  significant,  and  the assumption  of penetration
                           behavior  in the gas  phase  is  not critical  to the determination of  liquid-phase  control. It may
                           also be seen that the dominant factor is the low solubility  of oxygen  in water. One may gener-
                           alize and state that absorption  or desorption  of  sparingly  soluble  gases  is  almost always  liq-
                           uid-phase controlled. Correction of  the gas-phase  coefficient  for  net mass  transfer  is  clearly
                           not  significant,  and the correction for the liquid phase is  negligible.


       EXAMPLE 22.4-2      There are many situations  for  which  the one-phase transfer  coefficients  are not available  for
                           the  boundary conditions of  the two-phase mass  transfer  problem, and it is common practice
     Interaction  of Phase  to  use  one-phase models  in which  interfacial  boundary  conditions are assumed, without re-
     Resistances           gard  to the interaction of the diffusion  processes  in the two phases. Such a simplification  can
                           introduce  significant  errors.  Test  this  approximate procedure  for  the leaching  of  a  solute  A
                           from a solid  sphere of В of radius R in an incompletely stirred  fluid  C, so large in volume that
                           the  bulk fluid concentration of A  can be neglected.

      SOLUTION             The  exact  description  of  the leaching  process  is  given  by  the solution  of  Fick's  second  law
                           written  for the concentration of A  in the solid  in the region 0 <  r < R:


                                                                                               (22.4-20)
                                                             AB
                                                       dt   -" idrY   dr
                                                               r
                           The  boundary and initial conditions are:
                           B.C.I:  atr  = 0,                c As  is  finite                   (22.4-21)
                           B.C. 2:  at r = R,               c  =  mc  + b                      (22.4-22)
                                                             As   AI
                           I.C.:  at t  = 0,                c  = c                             (22.4-23)
                                                             As  0
                           The  diffusional  process on the liquid side  of the solid-liquid  interface is described  in terms of
                           a  mass transfer  coefficient,  defined  by
                                                       r^  dC As  =  k (c  -  0)               (22.4-24)
                                                           dr       c  Al
                           in  which c (t) is the concentration in the liquid phase adjacent to the interface. The behavior  of
                                   Al
                           the  diffusion  in the two phases is coupled through Eq. 22.4-22, which describes the equilibrium
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