Page 218 - Pressure Swing Adsorption
P. 218

194   PRESSURE SWING ADSORPTION   DYNAMIC MODELING OF A PSA SYSTEM   195

 is  assumed that  there  1s  no  nuxmg in  the midsectmns of the coiumns. The   Table 5.6.  Equations for PSA Simulation Using Pore Diffusion Model
 feed  and  the product ends-of the  high-pressure column  are connected to
 the  oroduct and feed  ends. respectively, of the  low-pressure column. The   Except  for  the  followmg  changes all  other equations m Table 5.2  a_pplv.  The subscnp!  i  has  the
 gas  from  the corresponding haivcs  1s  assumed to be uniformly mixed, with   same meaning as  rn  Tahle 5.2.
            Mass  transfer rale across  the  extern11l  Jilm:
 due  allowance  for  the  difference  in  initial  pressures  and  therefore  m  the
 number of moles of gas miHally present m each half-column. The resulting   iJci,-  3
              T, = 71k1( C, -d-R,)                                     (I)
 gas mixtures are then uniformly distributed through the relevant halves of   '
 the  two  columns.   Velocuv boundarv condition  tor  pressunzat1on:
 3.  Jn  the  particle  mass  balance  it  is  assumed  that the ~dsorbent  consists  of   vlz~L = 0   (2)
 uniform  microporous  spheres;  any  macropore  diffusional  resistance  1s
         Equation  2,  which  replaces  Eq.  IOa  1n  Table  5.2,  as  a  more  appropriate  ve1oc1tv  boundary
 negiected.  This  is  a  good  approximation,  since,  m  a  kinetically  selective
         condition  for  the  pressunzat1on  step.  Moreover.  with  this  boundarv  condition  1t  1s  no  longer
 adsorbent such as carbon molecular sieve, the diffusional  resistance of the   necessary IO  specify pressurization gas quantuy as  an  mpui.
 microoores  is  much  iarger  than  that  of  the  macrooores.  (The  relevant   Particle balance:
 particle radius m the  time constant 1s  that of the microparticles.)   aq, =""-[r .!1.(o' a,,,)]
 4.  The  gradient  of  chemical  potentiai  is  taken  as  the  ctnvmg  force  for   iJt   r2  Jr   '  Br   (3)
 rn1cropore  diffusion  with  a  constant  intrinsic  mobility.  This  leads  to  a
           Boundarv conditions:
 Fickian diffusion eauat1on 1n  which the diffusivity is a function only of the
 adsorbed-phase  concentrations.  Ideal Fickian  diffusion  with  constant dif-  -  -o
              ""'I  r-o -                                             ( 4)
              iJr
 fusivity  is also investigated for comparison.   aq, I
 5.  The  fluid  ·and  the  solid  phases  are  linked  through  an  external  film   D;a, r'""Rp =k1(c;-C;lr-Rp)   (5)
 resistance,  even  though  a  large  value  1s  usually  assigned  to  the  external
 film  mass  transfer  coefficient  to  approximate  equilibnum  at  the  particle   c,-1,~np  m  Ea. 5 is  related  to  q 1l,-n~  through  the equilibnum isotherm:
 surface.  In  conjunction  with  the  collocat1on  method  this  proves  s1moler   q,I;~•, = 0, = b,c,1,-•/( I+ I;h,,,1,-•,,)
 than  the  alternative  approach  involvmg  the  direct  application  of  the   (6)
 eouilibnum boundary condition at  the particle  surface.
         Equation  6,  written  for  the two components and  I hen solved s1mulfaneously,  v1elds
 The  model  equations  subject  to  these  assumottons  are  summanzed  m   c,1,-R, = 'o:•/( I -~•1)   (7)
 Table 5.6. Equations that are similar to those m Table 5.2 are not repeated in
 Table 5.6. Equations 1) 2a, 3, and 7-11  in Table 5.2 together with  Eqs.  1, 2, 7   Constanr  Diffus1vity.   If  the  m1cropore  diffusivity  (D;)  is  mdependem  of concc:ntraoon,  Eq.  J
 anct  the  approoriate  set  of  diffus10n  equations  (Eus.  4,  5,  and  8  for  the   becomes:
 constant-diffusivity case,  and  Eos.  11-14 and 4 for the concentration-depen-
 dent diffus1v1ty case) in Table 5.6 are rearranged and written m dimensionless   (8)
 form.  The  dimensionless  equal!ons  may  then  be  solved  by  the  method  of
         The  associated boundarv conditions, Eos. 4 and 5,  remam the same.
 orthogonal collocation  to obtain the gas-phase composition  as  a  function  of
         Concentration-dependent  dijfusidtY,  The  expressions  tor  the  diffusivities  m  a  binarv  Langmuir
 dimensmniess  bed  length  (zjL),  and  the  solid-phase  composition  as  a   system with consiant  mmns1c  mobilities (DAO• D 80 ) have  been  given  by  Habgood 54  and  Round
 functton of both the dimensionless bed length and  the dimensionless particle   et al.55a.
 radius (r/Rp) for various values of time.  Details of the collocation  form  are
 given In  Appendix B.  Starting from a given initial condition the computations   (9)
 are continued as usual  until cyclic steady state is  reached.
 The  air  separation  data  for  nitrogen  production  on  a  carbon  molecular   (10)
 18
 sieve  reported  by  Hassan  et al.  are  chosen  to  illustrate  the  importance  of
 the  concentration  deoendence  of  the  micropore  diffusivity  on  the  perfor-  (Conwwed)
 mance of the kinetically controlled PSA separation. The experiments, carried
 out m  a  two-bed  PSA unit  using the modified  cycle  with  pressure eaualiza-
 tion  and  no  purge,  were  conducted  over  a  wide  range  of  high  operating
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