Page 228 - Pressure Swing Adsorption
P. 228

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 204   PRESSURE SWING ADSORPTION   DYNAMIC MODELING OF A  PSA SYSTEM   205

 '
 Table 5.9.  Continuous Countercurrent Flow Model Equations for   ;,   Table 5.9.  (Contmued)
 a Bulk PSA Separation Process"
 '         From Eqs.  4 and 8 we  get:
 Assumptmns  I-7 discussed  in connection with  the  LDF model  apply.
             _   akmq 1 j. 1 +(1-a)k;1.qti
 C'ompo£lent  mass balance:   q;=   ak  +(1-a)k;1.  .                 ('I)
 d(vic 1 J   1- 8  dii;j   111
 m -----az + -e- -di= 0   (1)   I   Substituting Eo. 9 into 4 and  rearranging yields:
             dQ,'f
                      m
 Commuuy condition:   '   -=  (n-l+ma)  e,   iH-  q*)                (10)
                           k  -(q*
 '
              dt
                                   d.
 I      where n.  = 1 for  high-pressure flow  and 2 for  purge flow;  and
 Lc 1 =C; (constant)   (2)
 Overall mass  balance:                                              (11)
                 l/ak11- 1  + 1/(1- a)k,1.
 . d,•,  I-£" dQ;j
 mC 1 7z +-e- L, dt ... 0   (3)   Combinmg Eqs.  i, 3, and  J()  gives:
              deli   1-e   I
 Mass transfer rates:   V1dz+  e   (n-I~ma)(ke;(qfH-q;*L)
 dif;;  _   *  _
 dl-k;iCq,.i-q;)   (4)
             - X;1 ~kei(qfH - qf'd) = 0                              ( 12)
 Adsorption  equilibrium:
                                                                     /13)
 (5)
         Equation 12  for  i = A  and Eq.  13  are simultaneously m!egrated for high- and  low-pressure flow
 In  lhese equa11ons, = A  for component  A  and  8  for component  8, J =Hor L, and  m =+I or   usmg the fourth-order  Runge-Kutta method  to obtatn  cA; and  tr;  at differem  axial  Jocanons  m
 - L  The vaiues  _,  = H fl,lld  m = + I  represent  high-pressure  flow,  J =  L  and  m = - l  represent   the bed. The boundary conditions for  high-pressure flow  are knoWn at  z = 0 and those for  purge
 purge flow.   are given at z = L;  therefore, the soiuhon procedure requires 1terahon. Values of the dependent
 BoundatY conditions: high-pressure flow   variables for purge flow  are guessed at  z = 0. The integration 1s  then  performed  from  z = 0 to
         L, which  1s  repeated  until  known  boundarv  conditions  for  purge !flow  at  z =  L  are  satisfied.
 (6)
         Jacobian  analysis  1s  performed  to  update  the  trial  vaiues,  which  accelerates  the  speed  of
 purge fl.ow   convergence. Values of c i  a1  different  locations are obtamed bv difference from  total  concen•
                          8
         tration. Steady-state adsorbed-phase concentrat1ons are then calculated from Eq. 9.
 (7)
         "  The material  balance  Eqs.  J  and  3  should  acmallv be  wrmen  m terms  of equivalent  velocities  in
 The  concentration  boundary  condition  for  purge  flow  represents  the  fact  that  part  of  the   order to ensure  that  the  total  volume of feed  and purge used  in  actual operalion are  the same  m  the
 high-pressure product is expanded to low pressure and used for  purge. v 0 1.  and v 0 H  are relatecl   steady-stare  represent-allon.  However,  such  a  restriction  on  the  mass  balance  leads  lo an  equivalent
 hy  the  purge to feed veioc1ty  ratio, G.   purge  to  reed  velocity  ratm  given  by  G[(l-a)/a).  For  a=0.5 G[(l,a)/orl=G,  but  when  a--1,
 The assumption of zero net accumulation in the solid  phase leads to:   G  .... 0, and when o -,. O,  G  .... w, and therefore  the CCF model  fails  for Cycles  in which the adsorption
         and  desorption  steps  are  unequal  (i.e.,  a  ,,..0.5).  The  present  form  of  material  baiancc  equations,
         although iess accurate  from  the  paint of mass balance  between the  act1,1al  operation and steadv-st!lle
 Ct dii;!! + (1- •)· dq._  IL= 0   (8)
 dt   dl   approx1mat10n (except when  a= 0.5), extends the  usefulness of the CCF model  to the cvcles  m  which
         a 'F 0.5.
 ln this equation  a - i . j(t + 11,). The factors  a  and (1- a) with  the solid  phase accumulat1on
 11   11
 terms  for  the  high- and  low-pressure  steps.  respectively,  have  been  mtroduced  to  mamtam
 consistency m mass  transfer raies between the CCF apprmumat1on and the transient simulation.
 (Contmued)
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