Page 29 - Radiochemistry and nuclear chemistry
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18                   Radiochemistry  and Nuclear Chemistry

                      difficult  problem  when  well  planned.  A  sample  is  then  withdrawn  from  the
                      mixture, containing M 1 atoms of isotope 1 and M 2 atoms of isotope 2. The sample
                      is measured by the mass spectrometer,  yielding  ~M = MI/M2"
               Since M 1 =  N 1 +  Pl  and M 2 =  N 2 +  P2 simple arithmetic gives


                                    NE = P(rP -  ~'M)/[(~P +  I)(~'M -rN)]          (2.12)
                Thus  from  3  mass  spectrometrically  determined  isotope  ratios  (~'N,  ~'P and  ~'M) and
               known standard amount P  =  PI  + P2, the unknown number of atoms N 2 in the sample is
               determined.  The precision of this technique is largest when sample and standard are added
               in such proportions that N ~  P.  Examples of the use of this technique are given in w   on
               geologic dating.
                Because  the  variables  in  these  equations  often  need  multiple  indexing  (e.g.  element,
               isotope and source) the amount of indexing can be reduced by using italic element symbols
               to  refer  to the  specific  radioactivity,  or concentration,  of that nuclide in the  sample;  e.g.
               238U  means  8238o  (radioactivity),  or  N238u (atoms)  per  unit  volume  or  weight  of  the
               sample.  Extensive use of this formalism will be found in  w   1.
                (d)  Analysis  of gas purity  (e.g.  in  plants  for  separation  of  235U and  238U) is  done
               conveniently  by  mass  spectrometry.  Not  only  are  the  ratios  of  the  uranium  isotopes
               determined,  but also the air and water vapor which leaks into the system can be measured.
               This  produces  such  ions as  O2 +,  N2 +,  CO2 +,  and  HF +,  which can be  measured easily
               because  mass  spectrometry  detects  the presence  of impurities  in parts  per  million  (ppm)
               concentration.
                (e) Instrumental chemical analysis  can be done by using mass spectrometers having ion
               sources  of the  inductively  coupled plasma  type (ICP-MS  systems),  sometimes  as on-line
               detectors for various chromatographic techniques. Due to the high resolution and sensitivity
               of this  technique it is widely used in analysis of pollutants in the environment.
                (f)  Measurement  of products from  nuclear  reactions can  be  made  with  special  mass
               spectrometers on line to the irradiated target.  With suitable arrangements both A and Z of
               the re, coiling reaction products can be determined.



                                       2.4.  Isotopic  ratios  in  nature

                Mass spectrometric investigations of geologic material has shown that isotopic ratios vary
               slightly in nature with the largest variations observed for the heaviest and lightest elements.
                For the heaviest dements the reason for the variation in the ratio of isotopes in an dement
               can  be  related  directly  to  the consequence  of naturally  occurring  radioactive  decay.  For
               example,  in a thorium mineral the decay sequence terminates in the formation of an isotope
               of lead with mass number 208.  By contrast,  in a uranium ore,  in which 238U is the most
               abundant  isotope,  the primary  end  product  of the  decay  is  an  isotope of lead  with  mass
               number 206 (see Fig.  1.2). This means that thorium minerals and uranium minerals contain
               lead  with  different  isotopic  composition.  In  fact,  one  of  the  best  conformations  of  the



               1 The  Student making notes may have difficulties in distinguishing between italics and normal letters and is
              therefore recommended to adhere to the use of multiple indexing.
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