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Sr analysis of environmental samples by ion-laser interaction mass spectrometryHonda, Maki; Martschini, M.*; Marchhart, O.*; Priller, A.*; Steier, P.*; Golser, R.*; Sato, Tetsuya; Tsukada, Kazuaki; Sakaguchi, Aya*
Analytical Methods, 14(28), p.2732 - 2738, 2022/07
Times Cited Count：2 Percentile：56.45(Chemistry, Analytical)The sensitive Sr analysis with accelerator mass spectrometry (AMS) was developed for the advances of environmental radiology. One advantage of AMS is the ability to analyze various environmental samples with Sr/
Sr atomic ratios of 10
in a simple chemical separation. Three different IAEA samples with known Sr concentrations (moss-soil, animal bone, Syrian soil: 1 g each) were analyzed to assess the validity of the chemical separation and the AMS measurement. The Sr measurements were conducted on the AMS system combined with the Ion Laser InterAction MasSpectrometry (ILIAMS) setup at the University of Vienna, which has excellent isobaric separation performance. The isobaric interference of Zr in the Sr AMS was first removed by chemical separation. The separation factor of Zr in two-step column chromatography with Sr resin and anion exchange resin was 10
. The Zr remaining in the sample was removed by ILIAMS effectively. This simple chemical separation achieved a limit of detection 
0.1 mBq in the Sr AMS, which is lower than typical 
-ray detection. The agreement between AMS measurements and nominal values for the Sr concentrations of IAEA samples indicated that the new highly-sensitive Sr analysis in the environmental samples with AMS is reliable even for high matrix samples of soil and bone.
Uehara, Akihiro*; Matsumura, Daiju; Tsuji, Takuya; Yakumaru, Haruko*; Tanaka, Izumi*; Shiro, Ayumi*; Saito, Hiroyuki*; Ishihara, Hiroshi*; Homma-Takeda, Shino*
Analytical Methods, 14(24), p.2439 - 2445, 2022/06
Times Cited Count：2 Percentile：56.45(Chemistry, Analytical)Yomogida, Takumi; Esaka, Fumitaka; Magara, Masaaki
Analytical Methods, 9(44), p.6261 - 6266, 2017/11
Times Cited Count：8 Percentile：56.94(Chemistry, Analytical)A combination of micro-sampling, micro-Raman spectroscopy (MRS), and secondary ion mass spectrometry (SIMS) was applied to the characterization of individual uranium particles. Reference particles with U
O
(NBL CRM U010) and UO
were identified by scanning electron microscopy combined with energy dispersive X-ray detection (SEM-EDX) and transferred onto grassy carbon substrates by micro-sampling. The crystalline phases of the reference particles with diameters ranging from 1 
m to 5 m were determined non-destructively by using MRS thanks to the optimization of laser power at the measurement. Isotope ratios were also determined with SIMS after the MRS analysis and were consistent with values in the literature. These results indicate that chemical forms and isotope ratios of individual uranium particles as small as 1 m can be analyzed efficiently by using the proposed method.
Esaka, Fumitaka; Suzuki, Daisuke; Yomogida, Takumi; Magara, Masaaki
Analytical Methods, 8(7), p.1543 - 1548, 2016/02
Times Cited Count：7 Percentile：47.29(Chemistry, Analytical)The isotope ratio analysis of individual uranium particles in environmental samples taken at nuclear facilities is important to clarify their origins for nuclear safeguards. In the present study, automated particle screening was used to select uranium particles prior to precise isotope ratio analysis by thermal ionization mass spectrometry (TIMS). As a result, molecular ion interferences on the uranium mass region were able to be almost completely avoided in the analysis of real inspection samples using APM-TIMS. Therefore, the performance of APM-TIMS was sufficient for obtaining isotope ratio data of individual particles without molecular ion interferences.
Takagai, Yoshitaka*; Furukawa, Makoto*; Kameo, Yutaka; Suzuki, Katsuhiko*
Analytical Methods, 6(2), p.355 - 362, 2014/01
Times Cited Count：63 Percentile：97.2(Chemistry, Analytical)Radioactive strontium-90 (Sr) scattered by nuclear power plant accident was specifically determined by conventional inductively coupled plasma quadrupole mass-spectrometry (ICP-QMS) preceded by on-line chelate column separation and oxygen reaction. After implementing the cascade-step, the detection limit (DL) of quantitative ICP-QMS of Sr from spiked water samples was 2.85 Bq/L (equivalent to 0.56 ppq). Analysis of microwave-digested soil yielded a DL of 4.73 Bq/kg (equivalent to 0.93 ppq). The Sr from environmental contaminated soil samples ranged from 63 Bq/kg to 89 Bq/kg, with no statistical difference between the proposed and general methods at 98% confidence level.
