Page 124 - Pressure Swing Adsorption
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 98   PRESSURE SWING ADSORPTION   EQUILIBRIUM THEORY                    99

 PRESSURIZATION   FEED   SLOWDOWN   PURGE
          assumed mdeoendent m the  adsorbed  ohase:
                aPy    avPv  )           aq.
               (  e Tt +  az"  + RT( l  - e) a/  - O                 ( 4.1)
  i
 •I         The subscript  ,  refers  to  component  A  or  B.  Shendalrnan  and  Mitchell2
  i                    3
          and  Chan  et  al. considered  the  case  of  a  trace  amount  of component  A
          bemg adsorbed  from  a  earner,  B.  Shcndalman and Mitchell  took the earner
          to be nonactsorbing, while Chan et al. accounted for adsorotmn of the earner.
          In  both  cases,  the  mterst1tiai  veioc1ty,  v,  was  taken  to  be  independent  of
          composition (and of both  time and axial  position  at constant  pressure)_  As 1t
          1s  written, however, Ea. 4.1  applies to bulk separations as well  as removal of
          a  dilute contaminant.
            An important detail is  the definition of the void fraction  e.  If the adsorbed
 Y•D   y .. 0
          phase concentratwns are expressed on a particle volume basis (i.e., including
          mtraparticle  porosity),  then  e  1s  simply  the  extra-particle  or  interstitial  bed
 Feed     voidage.  Such  a  defimtron  JS  Jog1cal  where  mass tran~fer rates  are finite  and
 1.0
 End      when  the  mass  transfer  resistance  JS  associateO  with  external  film  diffusion,
 -  0.8   l   rnacropore  diffusion,  or  solid-side  mass  transfer  resistance  at  the  part1cie
 _J
          surface.  With  this definition,  the  bed density (p ),  particle density (pp),  and
                                                  8
 N
  {       the solid  or m1crooarhcle  density (pc),  and  the corresponding void  fractions
 C
 0   0.6   [   are related by:
 :e   '
 (/)
 0
 Cl.   0.4
          When m1cropore  resistance  1s  dommant,  or mcteed  under  the assumption  of
 al
 ·x       local  equilibrium  on which  this chapter 1s  based,  it  is' more  logical  to regard
 <(       the external void  fraction  as  the sum  of the  particle  macroooros1ty  and  the
          bed voidage  (i.e.,  all  gas  space  outside  the  m1cropores).  The  dens1t1es  and
 Product
 End     void  fraction  are then related by:
 Pressun-  Feed
 zation
         Pc  corresponds  to  the  density  determmed  with  a  Huid  that  penetrates  the
 Figure  4.1  Steps  in  a  convcnt1onal  PSA  cycje;  onentatlon  of column  ~~d streams.
 (Top)  Flows  and  compositions  associated  with  each step.  (Bottom)  Pos1tmns-versus-  external  voidage  and  the  macropores  but  not  the  m1cropores.  Since  these
 iimc representation of each step. Shaded  regions depict pcnetratmn of heavy comoo-  definitions affect  the  magnitude of the  isotherm  parameters,  it is  essential  to
 nent.    maintam  consistency  when  equilibrium  data  are  incorporated  into  a  PSA
          model.
            The  balance  equations  are  modified  by  subst1tut1ng  adsorption  isotherm
          expresstons for each component in  the form,
                                                                     ( 4.2)
          Examples are given in Chapter 2.  Following assumption 6 above,  the temper-
          ature is fixed,  so the second term of Eq. 4.1  can be detenmned from  Ea. 4.2.
          as:
              aq.    1
              Tt =  RTf'(PY;)                                        ( 4.3)
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