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Tobita, Minoru*; Goto, Katsunori*; Omori, Takeshi*; Osone, Osamu*; Haraga, Tomoko; Aono, Ryuji; Konda, Miki; Tsuchida, Daiki; Mitsukai, Akina; Ishimori, Kenichiro
JAEA-Data/Code 2023-011, 32 Pages, 2023/11
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field as trench and pit. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until the beginning of disposal. In order to contribute to the study of radioactivity concentration evaluation methods for radioactive wastes generated from nuclear research facilities, we collected and analyzed concrete samples generated from JRR-3, JRR-4 and JAERI Reprocessing Test Facility. In this report, we summarized the radioactivity concentrations of 23 radionuclides (H, C, Cl, Ca, Co, Ni, Sr, Nb, Ag, Cs, Ba, Eu, Eu, Ho, U, U, U, Pu, Pu, Pu, Am, Am, Cm) which were obtained from radiochemical analysis of the samples in fiscal years 2021-2022.
Aono, Ryuji; Mitsukai, Akina; Tsuchida, Daiki; Konda, Miki; Haraga, Tomoko; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2023-002, 81 Pages, 2023/05
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field as trench and pit. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until the beginning of disposal. In order to contribute to this work, we collected and analyzed the samples generated from JRR-2, JRR-3 and Hot laboratory facilities. In this report, we summarized the radioactivity concentrations of 20 radionuclides (H, C, Cl, Co, Ni, Sr, Nb, Tc, Ag, I, Cs, Eu, Eu, U, U, Pu, Pu, Pu, Am, Cm) which were obtained from radiochemical analysis of the samples in fiscal year 2020.
Tobita, Minoru*; Konda, Miki; Omori, Takeshi*; Nabatame, Tsutomu*; Onizawa, Takashi*; Kurosawa, Katsuaki*; Haraga, Tomoko; Aono, Ryuji; Mitsukai, Akina; Tsuchida, Daiki; et al.
JAEA-Data/Code 2022-007, 40 Pages, 2022/11
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until the beginning of disposal. In order to contribute to this work, we collected and analyzed concrete, ash, ceramic and brick samples generated from JRR-3, JRR4 and JRTF facilities. In this report, we summarized the radioactivity concentrations of 24 radionuclides (H, C, Cl, Ca, Co, Ni, Sr, Nb, Tc, Ag, I, Cs, Ba, Eu, Eu, Ho, U, U, Pu, Pu, Pu, Am, Am, Cm) which were obtained from radiochemical analysis of the samples in fiscal years 2020-2021.
Tsuchida, Daiki; Mitsukai, Akina; Aono, Ryuji; Haraga, Tomoko; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2022-004, 87 Pages, 2022/07
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until by the beginning of disposal. In order to contribute to this work, we collected and analyzed samples generated from JPDR, JRR-3 and JRR-4. In this report, radioactivity concentrations of 20 radionuclides (H, C, Cl, Co, Ni, Sr, Nb, Tc, Ag, I, Cs, Eu, Eu, U, U, Pu, Pu, Am, Cm) were determined based on radiochemical analysis and summarized as basic data for the study of evaluation method of radioactive concentration.
Tobita, Minoru*; Haraga, Tomoko; Endo, Tsubasa*; Omori, Hiroyuki*; Mitsukai, Akina; Aono, Ryuji; Ueno, Takashi; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2021-013, 30 Pages, 2021/12
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until the beginning of disposal. In order to contribute to this work, we collected and analyzed concrete samples generated from JPDR facility. In this report, we summarized the radioactivity concentrations of 21 radionuclides (H, C, Cl, Ca, Co, Ni, Sr, Nb, Ag, Cs, Eu, Eu, Ho, U, U, Pu, Pu, Pu, Am, Am, Cm) which were obtained from radiochemical analysis of the samples in fiscal year 2018-2019.
Tsuchida, Daiki; Haraga, Tomoko; Tobita, Minoru*; Omori, Hiroyuki*; Omori, Takeshi*; Murakami, Hideaki*; Mitsukai, Akina; Aono, Ryuji; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2020-022, 34 Pages, 2021/03
Radioactive wastes generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried in the near surface disposal field. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes until the beginning of disposal. In order to contribute to this work, we collected and analyzed concrete samples generated from JRR-3 and JPDR. In this report, we summarized the radioactivity concentrations of 22 radionuclides(H, C, Cl, Ca, Co, Ni, Sr, Nb, Ag, Ba, Cs, Eu, Eu, Ho, U, U, Pu, Pu, Am, Am, Cm) which were obtained from radiochemical analysis of the samples.
Aono, Ryuji; Mitsukai, Akina; Haraga, Tomoko; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2020-006, 70 Pages, 2020/08
Radioactive wastes which generated from research and testing reactors in Japan Atomic Energy Agency are planning to be buried at the near surface disposal field. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes by the time it starts disposal. In order to contribute to this work, we collected and analyzed the samples generated from JPDR and JRR-4. In this report, we summarized the radioactivity concentrations of 19 radionuclides (H, C, Cl, Co, Ni, Sr, Nb, Tc, Ag, I, Cs, Eu, Eu, U, U, Pu, Pu, Am, Cm) which were obtained from radiochemical analysis of those samples.
Mitsukai, Akina; Haraga, Tomoko; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2019-012, 70 Pages, 2020/02
It is necessary to establish practical evaluation methods to determine radioactivity concentration of radioactive wastes which generated from research and testing reactors in Japan Atomic Energy Agency are planning to be buried for the near surface disposal. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes by the time it starts disposal. In order to contribute to this work, we collected and analyzed the samples generated from Post Irradiation Examination Facility. In this report, we summarized the radioactivity concentrations of 19 radionuclides which were obtained from radiochemical analysis of those samples.
Mitsukai, Akina; Haraga, Tomoko; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Technology 2019-015, 52 Pages, 2019/11
In the future, radioactive waste which generated from nuclear research facilities in Japan Atomic Energy Agency are planning to be buried for the near surface disposal. It is necessary to establish the method to evaluate the radioactivity concentrations of the radioactive wastes. In this work, we studied the evaluation method of radioactivity concentration based on radiochemical analysis data (H-3, C-14, Cl-36, Co-60, Ni-63, Sr-90, Mo-93, Nb-94, Tc-99, Ag-108m, Sn-126, I-129, Cs-137, Eu-152, Eu-154, U-233+234, U-238, Pu-238, Pu-239+240, Pu-241, Am-241, Am-243, Cm-244) which was generated from research facility Hot Laboratory. As a result of examining the application of the scaling factor method, the correlation with Key-nuclide in some nuclides which are Sr-90, I-129, Eu-154, U-233+234, Pu-238, Pu-239+240, Am-241, Cm-244 confirmed by the correlation coefficient and t-test. In the present radiochemical analysis data, the mean activity concentration method can be applied to all nuclides which could not be applied to the scaling factor method H-3, C-14, Cl-36, Ni-63, Mo-93, Nb-94, Tc-99, Ag-108m, Sn-126, Eu-152, U-238, Pu-241 and Am-243. Ni-63, Tc-99, Eu-152 and U-238 could be applied to the scaling factor method with getting several additional data, this study will be continued to review for the practical evaluation method.
Haraga, Tomoko; Shimomura, Yusuke; Mitsukai, Akina; Ishimori, Kenichiro; Kameo, Yutaka
JAEA-Data/Code 2019-004, 48 Pages, 2019/10
In the future, radioactive wastes which generated from research and testing reactors in Japan Atomic Energy Agency are planning to be buried for the near surface disposal. Therefore, it is required to establish the method to evaluate the radioactivity concentrations of radioactive wastes by the time it starts disposal. In order to contribute to this work, we collected and analyzed the samples generated from JRR-2 and JRR-3. In this report, we summarized the radioactivity concentrations of 19 radionuclides (H, C, Cl, Co, Ni, Sr, Nb, Tc, Ag, I, Cs, Eu, Eu, U, U, Pu, Pu, Am, Cm) which were obtained from radiochemical analysis of those samples.
Sato, Tetsuya; Asai, Masato; Borschevsky, A.*; Beerwerth, R.*; Kaneya, Yusuke*; Makii, Hiroyuki; Mitsukai, Akina*; Nagame, Yuichiro; Osa, Akihiko; Toyoshima, Atsushi; et al.
Journal of the American Chemical Society, 140(44), p.14609 - 14613, 2018/11
Times Cited Count:27 Percentile:69.82(Chemistry, Multidisciplinary)The first ionization potential (IP) yields information on valence electronic structure of an atom. IP values of heavy actinides beyond einsteinium (Es, Z = 99), however, have not been determined experimentally so far due to the difficulty in obtaining these elements on scales of more than one atom at a time. Recently, we successfully measured IP of lawrencium (Lr, Z = 103) using a surface ionization method. The result suggests that Lr has a loosely-bound electron in the outermost orbital. In contrast to Lr, nobelium (No, Z = 102) is expected to have the highest IP among the actinide elements owing to its full-filled 5f and the 7s orbitals. In the present study, we have successfully determined IP values of No as well as fermium (Fm, Z = 100) and mendelevium (Md, Z = 101) using the surface ionization method. The obtained results indicate that the IP value of heavy actinoids would increase monotonically with filling electrons up in the 5f orbital like heavy lanthanoids.
Toyoshima, Atsushi; Mitsukai, Akina; Tsukada, Kazuaki; Oe, Kazuhiro*; Haba, Hiromitsu*; Komori, Yukiko*; Murakami, Masashi; Kaneya, Yusuke*; Sato, Daisuke*; Asai, Masato; et al.
Journal of Radioanalytical and Nuclear Chemistry, 317(1), p.421 - 430, 2018/07
Times Cited Count:1 Percentile:11.6(Chemistry, Analytical)We have studied extraction behavior of group-6 elements Mo and W to search for suitable conditions for an on-line extraction experiment of their heavier homolog, seaborgium (Sg). Batch-wise extraction of carrier-free radiotracers Mo and W were carried out from 0.10 - 8.6 M HSO and 1.010 - 5.0 M HF/1.0 M HCl into toluene with a quaternary ammonium compound, Aliquat336. Anionic sulfate complexes of Mo and W with charge - 2 were extracted with Aliquat336 from HSO solutions with concentrations of [HSO] 2 M. In HF/1.0 M HCl, oxyfluoro complexes of Mo and W with charge - 1 were interpreted to be formed and extracted with Aliquat336. From these results, favorable conditions for the extraction of Sg are discussed.
Steinegger, P.*; Asai, Masato; Dressler, R.*; Eichler, R.*; Kaneya, Yusuke*; Mitsukai, Akina*; Nagame, Yuichiro; Piguet, D.*; Sato, Tetsuya; Schdel, M.; et al.
Journal of Physical Chemistry C, 120(13), p.7122 - 7132, 2016/04
Times Cited Count:21 Percentile:61.01(Chemistry, Physical)A new experimental method "vacuum chromatography" has been developed to measure adsorption enthalpy of superheavy elements, and its feasibility has been examined using short-lived thallium isotopes. The short-lived thallium isotopes were produced at the JAEA tandem accelerator. The thallium ion beam prepared with an on-line isotope separator which ionized and mass-separated the thallium isotopes was injected into an isothermal vacuum chromatography apparatus. A temperature-dependent adsorption property of thallium atom on SiO surface were measured. The adsorption enthalpy of thallium was determined to be 158 kJ/mol. The thallium is a homolog of element 113. Thus, the vacuum chromatography developed in this study enables us to perform chemical experiments for short-lived superheavy elements with half-lives of a order of one second.
Toyoshima, Atsushi; Miyashita, Sunao*; Oe, Kazuhiro*; Kitayama, Yuta*; Lerum, H. V.*; Goto, Naoya*; Kaneya, Yusuke; Komori, Yukiko*; Mitsukai, Akina*; Vascon, A.; et al.
no journal, ,
no abstracts in English
Sato, Tetsuya; Asai, Masato; Kaneya, Yusuke; Tsukada, Kazuaki; Toyoshima, Atsushi; Vascon, A.; Takeda, Shinsaku; Mitsukai, Akina*; Nagame, Yuichiro; Ichikawa, Shinichi; et al.
no journal, ,
In order to determine the IP of the heavy elements, we have developed a novel measurement method based on a surface ionization technique by using a surface ionization ion source coupled to a He/CdI gas-jet transport system for an Isotope Separator On-Line (ISOL) at the JAEA tandem accelerator facility. In this work, we have determined IP value of No by using the method. In a surface ionization process, an ionization efficiency of an atom depends on its IP. To obtain a relationship between IP and ionization efficiency in present system, we measured ionization efficiencies of various short-lived isotopes. Ionization efficiency of No produced in the Cm(C, 4n) reaction was also measured. Measured ionization efficiency of No was 0.8%, which yields IP value of No to be 6.6 eV. This value is in a good agreement with the value which has been evaluated by extrapolation from those of the lighter actinide elements, 6.65 eV.
Sato, Tetsuya; Asai, Masato; Kaneya, Yusuke; Tsukada, Kazuaki; Toyoshima, Atsushi; Takeda, Shinsaku; Mitsukai, Akina*; Nagame, Yuichiro; Ichikawa, Shinichi; Makii, Hiroyuki; et al.
no journal, ,
We successfully determined the first ionization energy (IE) of nobelium (No, = 102) using a short-lived No isotope, No produced in theCm(C, 4n) reaction, based on the IE dependence of the ionization efficiency in a surface ionization process. The IE value of No was evaluated to be 6.6 eV. This value is in a good agreement with the value which has been estimated by an extrapolation from those of the lighter actinide elements, 6.65 eV.
Toyoshima, Atsushi; Oe, Kazuhiro*; Asai, Masato; Attallah, M. F.*; Goto, Naoya*; Gupta, N. S.*; Haba, Hiromitsu*; Kaneko, Masashi*; Kaneya, Yusuke; Kasamatsu, Yoshitaka*; et al.
no journal, ,
Due to short half-lives less than 10 s and extremely low production rates, transactinide elements heavier than seaborgium (Sg) are produced on an atom per hour scale. Therefore, a continuous rapid chemistry assembly is required to study aqueous-phase chemistry of these heaviest elements. In the present study, we started developments of a continuous chemistry assembly. Our first attempt was made in on-line experiments with Mo and W, lighter homologs of Sg, to optimize a chemistry assembly consisting of a newly developed membrane degasser as an interface between gas-jet and aqueous phase, a flow electrolytic column apparatus utilized to control oxidation states of Mo and W ions, and the continuous liquid-liquid extraction apparatus of SISAK for separation. In the conference, present status of the developments will be presented.
Mitsukai, Akina; Toyoshima, Atsushi; Kaneya, Yusuke; Oe, Kazuhiro*; Sato, Daisuke*; Goto, Naoya*; Tsuto, Shohei*; Komori, Yukiko*; Murakami, Masashi*; Haba, Hiromitsu*; et al.
no journal, ,
We report on the extraction behavior of carrier-free radioisotopes Mo and W, which are lighter homologs of Sg, produced at the RIKEN K70 AVF cyclotron, in the HSO-Aliquat336 system. Results of the extraction experiments showed that the distribution ratios, , of Mo and W decrease up to 3 M as increasing [HSO]. This is probably due to protonation reactions of hydrolyzed Mo and W species. In 3 M HSO, the values of W and Mo showed sharp increases. Based on the slope analysis separately carried out, it was suggested that hydrolyzed species of [HMO] (M = Mo and W) are extracted in less than 3 M [HSO], while anionic sulphate complexes of [MO(SO)] are formed in more than [HSO]5 M.
Toyoshima, Atsushi; Mitsukai, Akina; Murakami, Masashi*; Sato, Daisuke*; Motoyama, Risa*; Oe, Kazuhiro*; Komori, Yukiko*; Haba, Hiromitsu*; Asai, Masato; Tsukada, Kazuaki; et al.
no journal, ,
The purpose of the present study is characterization of fluoride complexes of Db. In this study, we investigated anion-exchange behavior of Nb and Ta, lighter homologs of Db, in 1.0-24 M HF/2.0 M HNO solutions as a model experiment of Db. Nb and Ta produced at JAEA tandem accelerator and RIKEN AVF cyclotron, respectively, were prepared as non-carrier-added radiotracers by an ion exchange method. Batch experiments were performed with anion-exchange resin. As a result, distribution coefficients () of Nb showed a sharp increase at 6 M HF while those of Ta had a monotonic decrease as increasing HF concentration. This suggests that Nb forms fluoride complexes from oxy fluoride one at 6 M HF and Ta exists as fluoride complexes under the conditions. It is expected that chemical species of Db fluorides are characterized in its anion-exchange experiments under the present conditions.
Mitsukai, Akina; Toyoshima, Atsushi; Kaneya, Yusuke; Oe, Kazuhiro*; Sato, Daisuke*; Murakami, Masashi*; Komori, Yukiko*; Haba, Hiromitsu*; Asai, Masato; Tsukada, Kazuaki; et al.
no journal, ,
In the present study, extraction behavior of Mo and W was studied in the sulfuric acid - Aliquat336 system as model experiments for the sulfuric complexation of Sg. In the RIKEN AVF cyclotron, batch-wise extraction experiments were performed with Mo with a 6.8 h half-life. Similar batch experiments were carried out also with W produced in the JAEA tandem accelerator followed by chemical separation from a target material. As a result, both Mo and W form anionic sulfuric complexes at more than approximately 5 M HSO, which are extracted into the organic phase as RMO(SO) (R = Aliquat336, M = Mo, W). It is expected that sulfuric complexation of Sg would be clarified under the present conditions.