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218                  Radiochemistry and Nuclear Chemistry


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                           FIG.  8.16.  Well-type  scintillation  detector  with  photomultiplier  circuitry.

                                        8.5.  Scintillation  detectors

                In  1908  Rutherford  and  Geiger  established  the  reliability  of  a  method  of  counting
               a-particles  by observing  visually the flashes  of luminescence I produced in  a thin  layer of
               ZnS by the a-particles.  Since the development of reliable photomultiplier tubes  (PMT)  in
               1946, scintillating counting techniques have played an important role in nuclear science.  A
               scintillation  detector  consists  of a  scintillator,  or phosphor optically  coupled  to  a  PMT
               which  produces  a pulse of electric current when  light  is transmitted  to  the tube  from the
               scintillator  (see  Fig.  8.16).  The  scintillating  material  can  be  an  inorganic  crystal  or  an
               organic  solid,  liquid,  or  gas.  Detectors  with  sandwiched  scintillators  of  different  kind,
               phoswich-detectors,  can,  with  suitable  electronics,  use  the  difference  in  scintillator
               properties  (light  output  and  decay  time),  thickness  and  position  in  the  sandwich  to
               differentiate  between  radiation  types and  radiation  energies  permitting  e.g.  simultaneous
               separate counting  of ce- and 3,7-radiation.
                In organic substances  the absorbtion  of energy raises the organic molecule  to one of the
               vibrational  levels  of  an  excited  electronic  state  (see  {}{}7.5 and  7.8).  Through  lattice
               vibrations  some of the excitation  energy  is dissipated  as heat and  the molecule  decays to
               lower vibrational  levels of the exited electronic state.  After approximately  10 -8  s,  a time
               sufficient for many molecular vibrations,  the molecule may return to the ground electronic
               state  with  emission  of light  photons.  Since  the  energy  which  excites  the  molecule  is  in
               general  larger  than  that emitted  in any  single  step  in  the decay back  to  the ground  state,
               reabsorption of these emitted photons is unlikely, and the crystal is consequently transparent
               to the emitted photon.  This transparency is necessary if the scintillations  are to escape the
               scintillator  and  reach  the  PMT.  Aromatic  hydrocarbons  such  as  anthracene  and  stilbene
              which  have  resonance  structures  are excellent  scintillators.  Liquid  and  solid  solutions  of
               such  organic  substances  as p-terphenyl are also used as scintillators.  In  these systems  the



               1  Luminescence  includes  both  fluorescence  and  phosphorescence  (w167  and  7.8).
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