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Journal Articles

Challenging studies by accelerator mass spectrometry for the development of environmental radiology; Status report on the analysis of $$^{90}$$Sr and $$^{135}$$Cs by AMS

Honda, Maki; Martschini, M.*; Wieser, A.*; Marchhart, O.*; Lachner, J.*; Priller, A.*; Steier, P.*; Golser, R.*; Sakaguchi, Aya*

JAEA-Conf 2022-001, p.85 - 90, 2022/11

Accelerator mass spectrometry (AMS) is an analytical method that combines mass spectrometry with a tandem accelerator, which has been used mainly in nuclear physics experiments. AMS is used to measure radionuclides with half-lives of 10$$^{3}$$-10$$^{8}$$ years. For radionuclides with half-lives of this order, the method of measuring their mass is 10$$^{3}$$-10$$^{6}$$ times more sensitive than measuring their activity. Because of this advantage, AMS has been widely applied in Earth and planetary sciences, atomic energy research, and other fields. Among the various studies, Wallner et al. (2021, 2016) have achieved excellent work in Earth and planetary sciences. For example, they have attained the ultra-sensitive analysis of $$^{60}$$Fe and $$^{244}$$Pu in environmental samples. These are radionuclides produced by rapid-neutron-capture (r-process) nucleosynthesis. Our recent work shows that a new AMS system (VERA, University of Vienna), which combines laser isobaric separation and a typical AMS system, has been successfully applied to the ultra-sensitive determination of $$^{90}$$Sr and $$^{135}$$Cs in environment. For $$^{90}$$Sr in environmental samples, the $$beta$$-ray measurement by the milking of the daughter nuclide $$^{90}$$Y is still the principal method, which takes 3-6 weeks. The new AMS method has a detection limit of $$<$$ 0.1 mBq, which is comparable to that of $$beta$$-ray measurement, with a more straightforward chemical treatment than $$beta$$-measurement. Our achievement demonstrates that AMS can be a practical new method for determining $$^{90}$$Sr in the environment.

Journal Articles

Developing accelerator mass spectrometry capabilities for anthropogenic radionuclide analysis to extend the set of oceanographic tracers

Hain, K.*; Martschini, M.*; G$"u$lce, F.*; Honda, Maki; Lachner, J.*; Kern, M.*; Pitters, J.*; Quinto, F.*; Sakaguchi, Aya*; Steier, P.*; et al.

Frontiers in Marine Science (Internet), 9, p.837515_1 - 837515_17, 2022/03

 Times Cited Count:12 Percentile:95.34(Environmental Sciences)

Recent major advances in accelerator mass spectrometry (AMS) at the Vienna Environmental Research Accelerator (VERA) regarding detection efficiency and isobar suppression have opened possibilities for the analysis of additional long-lived radionuclides at ultra-low environmental concentrations. These radionuclides, including $$^{233}$$U, $$^{135}$$Cs, $$^{99}$$Tc and $$^{90}$$Sr, will become important for oceanographic tracer application due to their generally conservative behavior in ocean water. In particular, the isotope ratios $$^{233}$$U/$$^{236}$$U and $$^{137}$$Cs/$$^{135}$$Cs have proven to be powerful fingerprints for emission source identification as they are not affected by elemental fractionation. Improved detection efficiencies allowed us to analyze all major long-lived actinides, i.e. $$^{236}$$U, $$^{237}$$Np, $$^{239, 240}$$Pu, $$^{241}$$Am as well as the very rare $$^{233}$$U, in the same 10 L water samples of an exemplary depth profile from the northwest Pacific Ocean. Especially for $$^{90}$$Sr analysis, our new approach has already been validated for selected reference materials (e.g. IAEA-A-12) and is ready for application in oceanographic studies. We estimate that a sample volume of only (1-3) L ocean water is sufficient for $$^{90}$$Sr as well as $$^{135}$$Cs analysis, respectively.

Oral presentation

Pioneering applications in AMS for the development of environmental radiology; Studies towards the implementation of $$^{90}$$Sr and $$^{135}$$Cs AMS

Honda, Maki; Martschini, M.*; Lachner, J.*; Marchhart, O.*; Wieser, A.*; Priller, A.*; Steier, P.*; Golser, R.*; Sakaguchi, Aya*

no journal, , 

We have developed new analytical methods for$$^{90}$$Sr (28.79 yr) and $$^{135}$$Cs (2.3x10$$^{6}$$ yr) by accelerator mass spectrometry (AMS) for the further development of the research on the environmental fate of artificial radionuclides$$^{90}$$Sr and $$^{137}$$Cs (30.1 yr). The AMS method enables the analysis of trace amounts of$$^{90}$$Sr and $$^{135}$$Cs with a simple chemical separation procedure. Having a longer half-life $$^{135}$$Cs applies as a proxy for $$^{137}$$Cs. For $$^{90}$$Sr, SrF$$_{2}$$ targets were prepared from radioactive environmental reference materials with known $$^{90}$$Sr concentrations (IAEA) by a chemical separation procedure that takes about two days to complete. $$^{90}$$Sr measured by AMS at VERA, University of Vienna. As a result, a limit of detection of $$<$$0.1 mBq was obtained, which is comparable to the $$beta$$ ray measurement. The detection of $$^{90}$$Sr in environmental samples was also successful, indicating that the $$^{90}$$Sr AMS can apply to environmental samples. On the other hand, there are still some technical challenges in the $$^{135}$$Cs AMS. Therefore, the experimental measurements are in progress.

Oral presentation

Frontiers of challenging studies in geoscience utilizing accelerator mass spectrometry

Honda, Maki; Martschini, M.*; Lachner, J.*; Wieser, A.*; Marchhart, O.*; Steier, P.*; Golser, R.*; Sakaguchi, Aya*

no journal, , 

The effective isobar suppression system based on the interaction between accelerated ions and lasers (photons) has been introduced into conventional AMS systems, allowing an increasing number of nuclides to be measured by AMS. This presentation will give an overview of the analytical technique, the measurement results, and the remaining challenges as examples of world-leading successful AMS of $$^{90}$$Sr and $$^{135}$$Cs in environmental samples obtained from the IAEA and others. Moreover, the applicability of the AMS method in geoscience (e.g., studies of $$^{90}$$Sr distribution in the hydrosphere and the range of applicable environmental samples) will also be discussed.

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