Page 577 - Bird R.B. Transport phenomena
P. 577

§18.4  Diffusion  with a Homogeneous Chemical Reaction  557
                                                                 Fig. 18.4-4.  Gas absorption
                                                                 accompanied by  an  irreversible
                                                                 first-order  reaction.










                                                    1
                                                      V/S8 = 0
                                                      I

                                                             10





                    Next we  use  assumption  (d) above  and equate the amount  of  A  entering  the main  body
                 of  liquid  at z  = 8 over  the total bubble  surface  S in the tank to the amount of A  consumed  in
                 the bulk  of the liquid  by  chemical reaction:
                                                                                    (18.4-16)
                                                      2 = 6
                 Substitution  of c  from  Eq. 18.4-15 into Eq. 18.4-16 gives an expression  for  B:
                              A
                                                       1
                                          B =                                       (18.4-17)
                                              cosh ф + (У/Б8)ф sinh ф
                 When  this result  is substituted  into Eq. 18.4-15, we  obtain an expression  for c /c  in terms of
                                                                              A  A0
                 ф and  V/SS.
                    From  this  expression  for  the concentration profile  we  can  then  get  the total rate  of  ab-
                 sorption with  chemical reaction from N  = -%b (dc /dz) evaluated  at z = 0, thus:
                                                Az     AB  A
                                             Ф                    1
                              N =                cosh ф                             (18.4-18)
                                   с ЯЬ АВ  sinh ф       cosh ф + (У/Б8)ф sinh ф
                                   А0
                 The result  is plotted in Fig.  18.4-4.
                    It  is  seen  here  that  the  dimensionless  absorption  rate  per  unit  area  of  interface,  N, in-
                 creases  with  ф for  all  finite  values  of  V/SS. At very low values  of ф—that is, for  very slow re-
                 actions—N  approaches  zero.  For this  limiting  situation  the  liquid  is  nearly  saturated  with
                 dissolved gas, and the "driving  force"  for absorption  is very small. At large values  of ф the di-
                 mensionless  surface  mass  flux  N increases  rapidly  with  ф and becomes very  nearly  indepen-
                 dent  of  V/S8.  Under  the latter  circumstances, the reaction  is  so  rapid  that almost  all  of  the
                 dissolving gas  is consumed within the film.  Then В is very nearly zero, and the bulk  of the liq-
                 uid plays no significant  role. In the limit as ф becomes very large, N approaches ф.
                    Somewhat  more interesting  behavior  is  observed  for  intermediate values  of  ф. It may  be
                 noted  that, for  moderately  large  V/S8,  there is  a considerable  range  of  ф for  which  N is very
                 nearly  unity.  In this region  the chemical reaction is  fast  enough  to keep  the bulk  of  the  solu-
                 tion  almost  solute  free,  but  slow  enough  to have  little  effect  on solute  transport  in  the  film.
                 Such a situation will arise when the ratio V/S8  of bulk  to film  volume is sufficient  to offset  the
                 higher  volumetric  reaction rate in the film.  The absorption  rate is  then  equal  to the  physical
                 absorption  rate (that is, the rate  for  k'" = 0) for  a solute-free  tank. This behavior  is  frequently
                 observed  in practice, and operation under such conditions has proven a useful  means  of char-
                 acterizing  the mass  transfer  behavior  of a variety  of gas  absorbers. 2
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