Analytical determination of radioactive strontium and cesium by Thermal Ionization Mass Spectrometry

Abstract Thermal Ionization Mass Spectrometry (TIMS) has been evaluated for the detection of the radioactive isotopes of Sr and Cs. The commercial instrument (i.e., a Thermo Scientific Triton) was investigated for the analysis of isotopic ratios of 89Sr/90Sr and 135Cs/137Cs in the presence of atomic isobars (89Y and 90Zr for 89,90Sr analysis and 135,137Ba for 135,137Cs analysis). The decontamination achievable instrumentally was examined by isotopic ratio measurements of 89Y/88Sr and 90Zr/88Sr for Sr and 135Ba/133Cs and 137Ba/133Cs for Cs. The decontamination found was at or above 2.0E+8 for 90Zr from 88Sr, while the Y demonstrated a temperature dependence as it sublimed from the filament but remained better than ≈ 5E+7. The decontamination of Ba from Cs did not show any temperature dependence and remained above 5E+6 and 8E+6 for 135Ba and 137Ba from 133Cs, respectively. Two standard fusion procedures one with sodium hydroxide (NaOH) plus sodium peroxide (Na2O2) flux, and the second used lithium tetraborate (Li2B4O7) plus lithium metaborate (LiBO2) flux were evaluated for preparation of sample matrices prior to performing chemical separations. Ammonium molybdophosphate-polyacrylonitrile (AMP-PAN) and Sr-spec resin were used to isolate the Cs and Sr, respectively from a prepared background matrix (i.e., Montana Soil). A graded approach, increasing in stable background isotopes, was performed to monitor the chemical and instrumental response. The radioisotopes of Sr and Cs were produced by thermal neutron irradiation of a highly enriched uranium foil. Even though the irradiated sample was not a certified standard it does provide accurate expectation values via the published cumulative fission yield nuclear data in the Evaluated Nuclear Data Files (ENDF) [ 1 ]. The intra-element isotopic ratio results presented in this work for 89Sr/90Sr and 135Cs/137Cs agree with the published data at 1σ. Furthermore, the uncertainty of the isotopic ratio measurements with TIMS was a factor of 5–10 improved compared to these published values.