Page 52 - Pressure Swing Adsorption
P. 52

26   PRESSURE SWING ADSORPTION   FUNDAMENTALS OF ADSORPTION             27



 Favorable
 0.8               7
 ~                                                             193  K
 0.6
                    6
 qo- "o  0.4                                    0
                    5
 Unfavorable
              ""                   0
 0.2  0.4  0.6  0.8  1.0   :;                              N2   02
                    4                           Adsorption  D   0
               en        /
               C                                Desorption  Ill   •
              "D
               ro   3
 Figure 2.10  Dimcnsmnlcss  cquilibnum  isotherm  shi:.1wrng  the  mcanmg of the  terms   _,
               0
 "favorahle." "linear," and  "unfavorable."
                    2
 This form  may  be  denved from  s1mole  mass action considerations t)y consid-  273  K
 ering  the  balance  between  occupied  and  unoccupied  sites.  Equation  2.3
 clearly  shows  the  correct  asymptotic  behavior  since  1t  approaches  Hemys
 Law in  the low-concentrat1on  region ancl  the saturation limit {q  ......_.  qJ at high
 concentrations.  In  the onginal  Langmuir formulation  the saiurat1011  limit was   0   300   400   500   600   700   800
 assumed  to  coincide  with  saturation  of a  fixed  number  of identical  surface
                                           P(torr)
 sites and. as such. It  should he mdcncndcnt of tcmneraturc.  In  faci  a  modest
 decrease  of  q~  with  temperature  1s  generally  observed  and  1s  indeed  to  be   Figure  2.11  Euuilibnum  data  for  oxygen  and  nitrogen .on  carbon  molecular  sieve
 expected  if  the  saturation  limit  corresponds  with  filling  of  the  m,cropore   showmg  tile  s1milantv  between  the  1sot11erms  and  the:  effect  of  temperature  on
                       14
 voiume,  rather  than  with  the  saturation  of  a  set  of  surface  sites.  b  1s  an   isotherm shape.
 equilibnum constant that 1s  directly related to the Henry constant (K = bq).
 Since  adsorption  is  exothermic,  1t  follows  that  b,  like  K,  will  decrease  with
 temperature  so  at  higher  temperature  the  isotherms  become  less  sharply   2.2.5  Freundlich and  Langmuir - Freundlich Isotherms
 curved, as  illustrated in  Figure 2.11.
           An  alternative  expression  that  is  sometimes  used  to  represent  a  favorable
 The  1soster1c  enthalpy of sorpt1on  is  given  by:
           (type  I) isotherm  1s  the  Freundlich  eauat1on:
                a - bc:'I",   n >  1.0                                 (2.5)
 ( 2.4)
           This  form  of expression  can  be  derived  from  plau!->iblc  theoretical  arguments
           based on a distrihut10n of aflinity among the surface' adsomt1on sites, bur  1t  1s
 and it  follows  from  Eqs. 2.3  and 2.4  that if  q 1s  independent of temperature,
 5         probably  better  regarded  simply  as  an  empmcal  expression.  Both  the
 the  1sostenc  heat  will  be  independent of concentrat1on~a  well-known  fea-
           Freundlich and  Langmulf equations contain  two  parameters,  but,  unlike  the
 ture of idcai  Langmulf behavior.
           Langmutr expression, the Freundlich form  does not reduce to Henry·s Law m
 Although  there  are  relauveiy  few  systems  that  conform  accurately  io  the
           the low-concentration limit.  Nevertheless, Ea. 2.5  can  reoresent the behavior
 Langmuir  model,  there  are  a  great  many  systems  that  show  approximate
           of  several  systems  over  a  wide  range  of  condit10ns.  To  obtain  greater
 conformity,  and  this  model  has  the  further  advantage  that  It  reduces  to
           flexibility as an empmcal correlat1on  the  Langmuir and Freundlich forms  are
 Henry's  Law  m  the  low~concentration  limit,  which  ts  a  requirement  for
           sometimes combined:
 thermodynamic  consistency  in  any  physical  adsorpt10n  system.  For  these
 reasons  the  Langmuir  modci  has  hccl)nlc  widely  accented  as  the  basis  for   a   hc1111
 most  quc.1litat1vc  or sem1qu;inr1tat1ve  studies of PSA systems.   qs   I  + bc 11 "   (2.6)
   47   48   49   50   51   52   53   54   55   56   57