Page 130 - Pressure Swing Adsorption
P. 130

,I .I.
 104   PRESSURE SWING ADSORPTION   EQUILIBRIUM THEORY                  105

 i .0     cations  are  possible  due  to  mult1ole  conceivable values  of the  velocities  and
 ~        the  parameters  8,  and  8.  The  compositions  bounding  the  shock  front  are
 o.~,.,
 0.9   0.5~  ,-
 0.171    constramed  by  the  influent  and  effluent  compositions,  but  due  to  entropic
 o.,~2
 0.#6
 0.8      effects they may  tend  to lie  somewhere  between  those.  For multrcomponent
          systems,  the  phenomenon  of "rollup" can  cause  Joe.al  maxima  of the  lighter
 0.7   -
          comoonents,  resulting  in  a  shock  velocity  slower  or  faster  than  expected.
 0.6   -  Subtleties  anse  because  the  choice  1s  suhject  to  :a  uniqueness  condition.
                                                                4
 <O       Applications to PSA  have been discussed by  Kayser and Knaebel. When the
 0.5   -  curvature of the isotherms 1s not too severe (i.e., at Jew  partial pressures), the
 0.'4   -  umoueness  condition  will  be  automatically  satisfied,  and  the  shock  velocity
           predicted  by  Eo.  4.9  will  be  valid  for  YA,~ YA,  (i.e.,  the  feed  comoositron).
 0.3   -
 0.2
 0.1   '   '   '   '
 0   10   20   30   40   50   4.4  Cycle Analysis
 Re
           Certam  orelirnmanes  are  essential  for  predicting  PSA  performance.  First,
 Figure 4.3  Effect of Re on adsorption selectivitv parameter, 0, for  air-0 on zeolite   one must determine basic properties, and  among these, for  the local  equilib-
 2
 5
 5A (Ball ), and N .and He on activated carbon, and N and CH on activated carbon.   rium  theory  to  be  accurate,  mass  transfer  resistances  must  be  small.  One
 4
 2
 2
           must  then  decide  on  the  steps  comprising  the  PSA  cycle,  and  choose
           operating conditmns, such as  feed  comoositmn, pressures, and step times.  At
 results  are  piotted  as  O versus  Reynolds  number (Re= pEvdp/µ, where  p   that  point  material  balances  and  thermodynamic  relatmnships  can  predict
 and  µ.  are the gas density and v1scos1ty,  eo  1s  the gas superficial  vcioc1ty,  and   over;ll  p;rformance  m  terms  of:  flow  rates,  product  recovery,  byproduct
 d p  1s  the particle diameter) in  Figure 4.3.  In that figure,  absolute  pressure is   comoosit10n, and  power reamrements.
 shown as a parameter, and results for a1r (A)-oxygen (B) on zeolite SA, and   The key concept involved  in  applymg eauilibnurn :models is  that each step
 mtrogen (A)-helium (B) on acuvated carbon are also  mcluded. Some of the   is  intended to accomplish  a soecific change. For steps such  as  pressurization
 pressures  were  suffictently  low  for  the  isotherms  to  be  nearly  linear,  while   and countercurrent blowctown,  the specific change is .obvious. Other steps are
 others were at pressures ·high enough for 1Sotherm curvature to be significant.   more  subtle  because  they  may  proceed  until  breakthrough  1s  1mmment,
 Furthermore,  the  dependence  of  0  (or  (3)  on  Re  is  similar  among  the   complete,  or  some  fractron  thereof.  Such  operating  policres  link  the  flow
 different cases, reflecting the tmpact of dissipative effects. For each data set,   rates,  step times,  bed size,  etc.  of those  steps,  and  depending on  mitial  and
 the  mmunum  value  of  O corresponds  to  conditions  m which  the  combined   final states, may impact other steps in  the cycle. ln that sense the goals of the
 effects of diffusion  and  dispersion  are  mmimaL  At  that oomt,  8  1s  typically   steps are not at all  open ended.
 found to be iarger (worse) than the vaiue predicted from isotherm data alone   As  an  example  of  stepwise  matenai  balances"  the  number  of  moles
 by  about 0.02  to 0.05.  The optimal  Reynolds number (Re) for  all  the cases,   '  I!   contained in an influent or effluent stream cturmg any step can be determined
 except  mtrogen-helium,  1s  in  the  range  of  9  to  18.  The  elapsed  time  per   from  appropnate  velocities,  as  grven  by  Eqs.  4.5,  4.7,  4.9,  and  4. 10.  The
 breakthrough expenment is  on  the  order of a  few mmutes, while  batchwise   I   ch01ce  depends  on the nature of the  step.  The  rnol'es  added  to  or removed
 isotherm measurements are much more time consuming.   from  the  column m  each step can  be  expressed  as  the  integral over  time  of
 For certam comoositions,  when  the  isotherms  are  Quite  nonlinear,  there   the  mstantaneous  molar  flow  rate(s),  or as  the  difference  between  the  finai
 may  be  a  selec1tv1ty  reversal,  mdicated  by  0 >  I.  This  can occur  when  the   and  initial contents of the column. Generai exoress1bns are:
 partial  pressure of the  heavy  component  1s  so  large  that O A  becomes greater
 than  8 •  In  that case,  if a shock front  existed,  1t  would  begin  to  dismtegrate
 11                                                                  ( 4.13)
 and  a  simple  wave  would  form.  The  resulting  breakthrough  pattern  would
 have  a  tail  (at high partial  oressures)  that  might  be  falsely  diagnosed  as  an
 effect of mass  transfer resistance (see  Figure 2.23).  Generally, other compli-  (4.14)
   125   126   127   128   129   130   131   132   133   134   135