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72                   Radiochemistry  and Nuclear  Chemistry



               where we again have to consider the net atomic charge.
                Part of the nuclear excitation energy is required to overcome the binding energy Ebe,  of
               the  electron  in  its  electronic  orbital. 1 The  remaining  excitation  energy  is  distributed
               between the recoiling daughter nucleus and the ejected electron E e. The relationship is given
               by the equation

                                           0,-  ebo  =  ed  +  eo                  (4.36)

                The ejected electron, known as the conversion electron, normally originates from an inner
               orbital,  since their wave functions have greater overlap with the nucleus.  It is to be noted
               that the conversion electrons are mono-energetic.  Inasmuch as the binding energies of the
               atomic  orbitals  are  different,  the  values  of  E e  reflect  the  differences  in  the  electronic
               binding energies.  In Figure 4.1  two sharp peaks are observed just beyond Ema x.  The  first
               peak,  designated  as  K,  is  due  to  conversion  electrons  originating  in  the  K  atomic  shell,
               while  the peak labeled L  is due to conversion electrons originating  in the L  atomic  shell.
               Both of these groups of conversion electrons arise from the decay of 137tuBa. Figure 4.5(f)
               shows schematically the decay process of 137Cs --, 137Ba +/3-  for the principal decay path;
               IT  is  an  abbreviation  for  isomeric  transition.  The  decay  of  137tuBa proceexls both  by
               emission of a 0.66  MeV -y-ray and by the competitive process of internal conversion.  The
               ratio between the number of conversion electrons and the number of 'y-rays emitted in this
               competition  is called the conversion  coefficient.  The  amount of internal  conversion  is not
               indicated  in simplified  decay schemes like Figure 4.5.
                If we denote the conversion coefficient as ai,  it is equal to the ratio of K-electrons ejected
               (which we may denote with leK) to that of gamma quanta emitted (Iv):

                                               a K  =  leK/l v                     (4.37)

               Usually  a K  <  0.1.  Also  a K  >  0%  >  OeM, etc.  For  137mBa the  ratio  of K-electrons  to
               L-electrons emitted is about 5 while the value of o~ K is 0.094.
                It can be shown that the energy of the recoiling nucleus (E d, eqn.  (4.36)) is much smaller
               than  the kinetic energy of the ejected electron E e and may be ignored.  The mathematical
               expression  to use is (4.32).
                A note on terminology.  Consider Figure 4.5(f).  Though the 'y is emitted from an exited
               state of 137Ba, in  common  language we nevertheless  talks of  "137Cs-'y" (of 0.662  MeV),
               i.e.  as  if the 'y was emitted  from the  137Cs nucleus.  The quotation  is  to be interpreted  as
               "137Cs (decay through/3-  followed by) 'y(-emission)".



                                         4.6.  Spontaneous fission

                As  the  nuclear  charge  increases  to  large  values,  nuclei  become  more  unstable.  This  is
              reflected by decreasing half-lives for nuclei heavier than uranium.  In  1940 K.  Petrzak and




               1  Electron-binding  energies are tabulated  in standard physics tables.
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