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Preliminary Treatment
(Combustion, grinding, open digestion)


        Chemical Separation
          (Ion exchange)


         Source preparation
    (Microprecipitation/filtration)
Weigh sample 1-2 g to Teflon evaporation dish;

                        Add radioactive tracers: Th-229 and U-232

                   Add 20 mL HNO3 and evaporate to dryness (3 times)
Open Digestion


                     Add 20 mL HF and evaporate to dryness (2 times)

                   Add 20 mL HClO4 and evaporate to dryness (2 times)

                      Dissolve the residue with 20 mL 9 M HCl and
                         transfer the solution to a centrifuge tube

                     Separate the residue by centrifugation and decant

                       Wash the precipitate with 5 mL 9 M HCl and
                 separate the residue by centrifugation and decant (3 times)

                 Save the supernatant for the chemical separation process
 Load sample
                                                    Rinse Th: 35 mL 9M HCl
                                                    Elute Pu: 50-60 mL
                                                              6M HCl + 0.26M HF
                                                    Elute U+Fe: 50 mL 0.1M HCl
Main Column



                   Main column
                    (Cl- column)
              Biorad AG1-X8 12 mL
                   Prewash with
                 50-60 mL 9M HCl


                                                                       Save for
                                                                          Th
                                         +  Th, Am, Ac, Al         processing
                        Save for
                           U                Pu
                       processing           U+Fe            Evaporate to dryness
                                                                  and dissolve
              Evaporate to dryness and dissolve                  with 5mL HNO3
                with 2mL HNO3 + 2mL H2O                             + 5mL H2O
 Load U fraction solution
                                            Elute Fe & other contamination:
                                             25 mL 8M HNO3
                                            Elute U: 50 mL 0.1M HCl

                  U column
U Column



                (NO3- column)
           Biorad AG1-X8 12 mL
                 Prewash with
             50-60 mL 8M HNO3



                                 +  Fe & other contaminations
                                  U              Evaporate
                                                     to dryness
                  Repeat if
                 evidence of
                                                Source preparation for
                  Fe present
                                                 alpha spectrometry
 Load Th fraction solution
                                             Elute contamination:
                                             35-50 mL 8M HNO3
                                             Elute Th: 50-60 mL 9M HCl

                   Th column
Th Column



                 (NO3- column)
            Biorad AG1-X8 12 mL
                  Prewash with
              50-60 mL 8M HNO3



                                  +  Other contaminations
                                     Th           Evaporate
                                                      to dryness
                   Repeat if
                  evidence of
                                                 Source preparation for
                 contamination
                                                  alpha spectrometry
Final U/Th acidic fraction
Counting Source Preparation
                                                   Add 10 mL Ce carrier
                              (Cerous nitrate carrier in 0.1M HNO3 = 0.5 g Ce/mL solution)

                                         Add 1-2 drops of Safranin O indicator

                                 Add of 20% TiCl3 dropwise until solution becomes clear

                                                   Add 1mL conc. HF

                                        Allow to precipitate for    20-30 minutes

                                            Filter with 0.1 m Metricel filter

                                               Dry at 60 C for 10 minutes

                                         Mount the filter on a stainless steel disc

                                              Ready for Alpha spectrometry
Uranium and Thorium analysis method at CU

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Uranium and Thorium analysis method at CU

  • 1.
  • 2. Preliminary Treatment (Combustion, grinding, open digestion) Chemical Separation (Ion exchange) Source preparation (Microprecipitation/filtration)
  • 3. Weigh sample 1-2 g to Teflon evaporation dish; Add radioactive tracers: Th-229 and U-232 Add 20 mL HNO3 and evaporate to dryness (3 times) Open Digestion Add 20 mL HF and evaporate to dryness (2 times) Add 20 mL HClO4 and evaporate to dryness (2 times) Dissolve the residue with 20 mL 9 M HCl and transfer the solution to a centrifuge tube Separate the residue by centrifugation and decant Wash the precipitate with 5 mL 9 M HCl and separate the residue by centrifugation and decant (3 times) Save the supernatant for the chemical separation process
  • 4.  Load sample  Rinse Th: 35 mL 9M HCl  Elute Pu: 50-60 mL 6M HCl + 0.26M HF  Elute U+Fe: 50 mL 0.1M HCl Main Column Main column (Cl- column) Biorad AG1-X8 12 mL Prewash with 50-60 mL 9M HCl Save for Th +  Th, Am, Ac, Al processing Save for U   Pu processing   U+Fe Evaporate to dryness and dissolve Evaporate to dryness and dissolve with 5mL HNO3 with 2mL HNO3 + 2mL H2O + 5mL H2O
  • 5.  Load U fraction solution  Elute Fe & other contamination: 25 mL 8M HNO3  Elute U: 50 mL 0.1M HCl U column U Column (NO3- column) Biorad AG1-X8 12 mL Prewash with 50-60 mL 8M HNO3 +  Fe & other contaminations U Evaporate to dryness Repeat if evidence of Source preparation for Fe present alpha spectrometry
  • 6.  Load Th fraction solution  Elute contamination: 35-50 mL 8M HNO3  Elute Th: 50-60 mL 9M HCl Th column Th Column (NO3- column) Biorad AG1-X8 12 mL Prewash with 50-60 mL 8M HNO3 +  Other contaminations   Th Evaporate to dryness Repeat if evidence of Source preparation for contamination alpha spectrometry
  • 7. Final U/Th acidic fraction Counting Source Preparation Add 10 mL Ce carrier (Cerous nitrate carrier in 0.1M HNO3 = 0.5 g Ce/mL solution) Add 1-2 drops of Safranin O indicator Add of 20% TiCl3 dropwise until solution becomes clear Add 1mL conc. HF Allow to precipitate for 20-30 minutes Filter with 0.1 m Metricel filter Dry at 60 C for 10 minutes Mount the filter on a stainless steel disc Ready for Alpha spectrometry