Page 246 - Radiochemistry and nuclear chemistry
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230                  Radiochemistry and Nuclear Chemistry

                In nuclear installations like uranium mines, nuclear reactors,  reprocessing plants,  etc.,  it
               is  necessary  to  continuously  monitor  gas  and  liquid  effluents.  Figure  8.21  shows  an
               arrangement  for  monitoring  of radioactive aerosols  (e.g.  Tc,  Ru,  actinides  in  air).  Two
               detectors  are used,  so  that  some  activity  (e.g.  mother  or daughter  activity)  is allowed  to
               dezay between the two detectors.  The delay time is adjusted by  varying the length of the
               paper strip between the detector and the rate of movement of the paper strip.  The detector
               may be energy sensitive or simple GM, proportional or scintillation devices.  In monitoring
               of water the detectors (e.g.  GM tubes) may dip into the streaming water,  or the water may
               flow around  the detector as in Figure 8.8(a).
                Radioactive gas flows can be measured by using capillaries or packed columns of 2  -  20
               ml volume containing scintillating material, either for monitoring purposes or, commonly,
               combined  with  a  gas  chromatograph  for obtaining  "radio-chromatograms"  of 3H  or  14C
               labeled organic substances.  These detectors, which are commercially available, are viewed
               by  PMTs  connected to Personal-Computer (PC) based analysis and display  systems.
                Radioactive liquidflows can be monitored in several ways depending on the decay mode,
               energy and liquid film thickness.  Liquid flow GM-counters (Fig.  8.8.a),  or other types of
               flow cells  combined with  solid  state detectors,  are used  at high/3-  and "y-energies.  Glass
               scintillators embedded in tubings (alternatively tubings containing scintillators) are used for
               low-energy B-emitters (e.g. 3H,  14C, 35S). The flow cells have typically volumes from 0.01
               to 5 ml.  By using peak analysis (i.e.  analyzing each scintillation intensity versus time,  so-
               called "time-resolved technique") it is possible to measure cx-emitters in high/3-~ fluxes and
               even to obtain crude a-spectra,  as well as to discriminate different B-emitters and to reduce
              background.  A weakness of this technique is the memory effect in the detectors caused by
               radionuclide  sorption.  Therefore,  the  commercial  systems have easily exchangeable  flow
              cells.  This  demand  is  circumvented  in  the  LISOL-system,  in  which  the  liquid  flow  is



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                      FIG. 8.21. Monitor for radioactive aerosols with prompt and delayed measurements. (From
                      H. Kiefer and R. Maushardt.)
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