Page 49 - Radiochemistry and nuclear chemistry
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38                   Radiochemistry and Nuclear Chemistry





















                        FIG. 2.11. Section through a separation nozzle arrangement showing stream lines.



               stages for a 3 % 235U enrichment (with 0.2 % tails),  the nozzle technique will require only
               about  500  stages.  However,  the  power  consumption  is  said  to  be  larger,  ~  3000  kWh
               SWU-l  at a capacity of 10 MSWU/y, as compared to  ~ 2500 kWh SWU-l  for a diffusion
               plant of the same size.  The operating cost is said to be higher than  for both the diffusion
               and the centrifuge methods.  A plant based on the original German design is being built in
               Brazil (10 kSWU/y). A 0.3 MSWU/y separation plant at Valindaba,  South Africa, used its
               own version of the nozzle technique (Helikon process),  but is now shut down.
                A  number  of photoionization  and photoexcitation  processes  are  being  investigated  for
               isotopic separation,  especially of uranium.  In one such process UF 6 is irradiated by a laser
               beam,  producing  selective  vibrational  excitation  in  the  235UF6 molecule  (of.  w   By
               irradiation  with  ultraviolet  (possibly,  but  not  necessarily,  by  laser)  light  the  excited
               molecule  is  caused  to  dissociate,  leaving  238UF 6 undissociated.  It  is  important  that  the
               ultraviolet pulse follows quite rapidly after the laser pulse,  so that the vibrationally excited
               235UF6 molecule  does  not  lose  its  excitation  energy  through  collision  with  surrounding
               molecules.  It  is  obvious  that  this  necessitates  gas  phase  reactions.  The  235UFn 6-n  ion
               formed through the dissociation (n  <  6) is then collected by the action of electromagnetic
               fields.  This  technique  is  not  limited  to  UF6;  pure  uranium  metal  vapor  and  plutonium
               compounds  have  been  separated  into  their  isotopic  constituents  by  two  or  three  photon
               ionization  with  laser  light  (e.g.  the US  AVLIS process  and  the French  SILVA process).
               Another alternative is to selectively excite 235UF 6 molecules by laser light in the presence
               of a  reactive  gas  (the CRISLA process).  The excited molecules  then reacts preferentially
               with the gas forming molecules with lower vapor pressure than UF 6. Although research in
               these areas has indicated a large scale feasibility of several similar processes, no predictions
               can  yet  be  made  of their  technological  value.  The  energy consumption  for  the  quantum
               processes  discussed  above  are  in  the  range  10  -  40  kWh  SWU-1.  However,  economic
               estimates indicate that their enrichment cost falls in the same price range as for centrifuge
              based  plants.  Hence,  the interest  in  these methods  has decreased  and development  of the
               ALVIS and SILVA processes has been terminated. Finally, it should be pointed out that the
               general  concept  of separative work breaks down  for very high  separation  factors  leading
               to very  few units  in a cascade (and always for mixtures of more than two isotopes).
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