Page 34 - Pressure Swing Adsorption
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9
 8   PRESSURE SWING ADSORPTION   INTRODUCTION

 Table 1.2.  Some Ma1or  PSA  Processes   devoted to a  cletai!ed  description of some current PSA processes, while some
           of the  future  trends  in  process development  are  discussed  in  Chapter 7 •
 Process   Product   Adsorbent   Type of SvsLern
 H  2  recove1v from   Ultrapure H ~   Act. C or zeolite   Multiple"bed svstem
 tuel gas   References
 J-leatless drier   Drv air (for   Act. Al O  3   Two-bed Skarstrom
 2
 1nstrumenrs)   cycle (or vacuum-  C.  w.  Skarstrom,  U.S.  Patent  2,944,627  (Feh.  1958)  to  Esso  Research  and  Engineering
 pressure swing cvde
             Companv.
 Air separation   0 2  (+Ar)   5A Zeolite   Two-bed Skarstrom   (Dec.  1957)  to  Air
           2.  p_  Guenn  de  Montgareuil  and  D.  Domme,  French  Patent  1,223,261
 cvcle
 Air separation   N (+Ar)   CMS   Two-bed self-  Liquide. See also U.S.  Patent 3,155,468 (1964)  to Air Liquide.
 2
 purgrng cvde
           .,.  H.  Kahle, Chemie  lnR.  Technik  23,  144 (1953).
 Air separation   N and 0  2   5A Zeolite   Vacuum swmg
 2
 ,  or CaX   sv::;tem   4.  H.  Kahle, Chemie  Jng.  Technik  26,  75  0954).
 ISOSJV   Linear /Branched   SA Zeolite   Molecular sieve separation   5.  R.  L. Hasche and W.  N.  Dargan, U.S.  Pateni  i,794,377  0931}
 hydrocarbons   with vacuum swing
 Landfill  gas   CO and CH  CMS   Vacuum swmg   6.  G. A.  Perley, U.S. Patent 1,896,916 (1933).
 2   4
 separation   7.  D.  Finlavson and A.  J. Sharp, U.K.  Pateni 365,092 (Oct.  15,  1930) to  British Celanese Corp.
              c  w  Skarsirom  "Heatless  Frac11onat1on  ot  Gases  over  Solid  Adsorbents,"  In  Recent
            8
            ·   ·   ·     '       .            95  1116  N  L.  d  CRC  Press  Cleveland
              Devetovments  In  Separatwn  Science,  Vol.  Il,  pp.   -  ,   ·   1  e  -,   ·
              (1972).
 misleading  since  the  inmunty  1s  almost  entirely  argon~which  1s  adsorbed
 with  the same affinity  as  oxygen  on  most  at1sorbents.
 The  largest-scale  PSA  processes  are  generally  to  be  found  m  petroleum
 refinery operat10ns-hydrogen purification  and  hydrocarbon seoaratt0n  pro-
 6
 cesses such as Isos1v.  In such processes product rates uo to 10 SCFH ( >  100
 tons/day) are not uncommon.  In the other mam areas of appiication (drying
 and  air separation) PSA  umts are generally economic only at  rat.her  smaller
 scales.  For  example,  for  large-scale  Oh-ygen  or  nitrogen  oroductmn  ( >  100
 tons/day)  it  1s  difficult  to  compete  economically  with  cryogenic  distillat1on.
 However, there are many small-scale uses for both oxygen and nitrogen (e.g.,
 home  oxygen  units  for  asthmatic  patients  and  nitrogen  units  for  purging
 the  fuel  tanks  of  fighter  aircraft  or  for  ourgmg  the  interiors  of  trucks
 and  warehouses  to  prolong  the  shelf  life  of  fruit  and  vegetables).  For
 such  applications  the  robustness  and  portability  of  a  PSA  system  provide
 addit1onai  advantages  that  reinforce  the  econom1c  considerations.  ln  these
 applications  the  most  direct  competition  comes  from  small-scale  membrane
 systems, which  offer  many  of the  same  advantages as  a PSA  system. A  bnef
 companson of these  two classes of process ts  included  in  Chapter 8.
 To  understand  the process options and  the factors  mvoived  m  design and
 optimization  of  PSA  systems,  some  background  m  the  fundamentals  of
 adsorption  and  the  ctynan11c  behavior  of  adsorption  columns  is  reouired.
 These aspects are considered m  Chapter 2.  A wide variety of different cycles
 have  been developed  in order to  mcrease energy efficiency,  1morove product
 ounty, and improve the flexibility of the operation. The basic cycles and a few
 of the more  advanced cycles are  reviewed  in  Chapter 3,  while  more  detailed
 aspects of process modeling are discussed  m  Chaoters 4  and 5.  Chaoter 6 1s
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