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Sato, Tatsuhiko; Furuta, Takuya; Sasaki, Hidetaka*; Watabe, Tadashi*
EJNMMI Physics (Internet), 12, p.28_1 - 28_16, 2025/03
Times Cited Count:0 Percentile:0.00(Radiology, Nuclear Medicine & Medical Imaging)Inoue, Rintaro*; Oda, Takashi; Nakagawa, Hiroshi; Tominaga, Taiki*; Ikegami, Takahisa*; Konuma, Tsuyoshi*; Iwase, Hiroki*; Kawakita, Yukinobu; Sato, Mamoru*; Sugiyama, Masaaki*
Biophysical Journal, 124(3), p.540 - 548, 2025/02
Times Cited Count:2 Percentile:0.00(Biophysics)Yoshigoe, Akitaka; Tsuda, Yasutaka; Kobata, Masaaki; Okane, Tetsuo; Satou, Yukihiko; Okochi, Takuo*
e-Journal of Surface Science and Nanotechnology (Internet), 23(1), p.16 - 21, 2025/02
Tsutsui, Satoshi; Higashinaka, Ryuji*; Mizumaki, Masaichiro*; Kobayashi, Yoshio*; Nakamura, Jin*; Ito, Takashi; Yoda, Yoshitaka*; Matsuda, Tatsuma*; Aoki, Yuji*; Sato, Hideyuki*
Interactions (Internet), 245(1), p.9_1 - 9_10, 2024/12
Oikawa, Kenichi; Matsumoto, Yoshihiro*; Watanabe, Kenichi*; Sato, Hirotaka*; Parker, J. D.*; Shinohara, Takenao; Kiyanagi, Yoshiaki*
Scientific Reports (Internet), 14, p.27990_1 - 27990_11, 2024/11
Times Cited Count:0 Percentile:0.00(Multidisciplinary Sciences)Kobayashi, Taishi*; Sato, Yutaro*; Tonna, Ryutaro*; Matsumura, Daiju; Sasaki, Takayuki*; Ikeda, Atsushi
Dalton Transactions (Internet), 53(46), p.18616 - 18628, 2024/10
Times Cited Count:0 Percentile:0.00(Chemistry, Inorganic & Nuclear)Matsumoto, Yoshihiro*; Oikawa, Kenichi; Watanabe, Kenichi*; Sato, Hirotaka*; Parker, J. D.*; Shinohara, Takenao; Kiyanagi, Yoshiaki*
Journal of Archaeological Science; Reports, 58, p.104729_1 - 104729_10, 2024/10
Lan, Z.*; Arikawa, Yasunobu*; Mirfayzi, S. R.*; Morace, A.*; Hayakawa, Takehito*; Sato, Hirotaka*; Kamiyama, Takashi*; Wei, T.*; Tatsumi, Yuta*; Koizumi, Mitsuo; et al.
Nature Communications (Internet), 15, p.5365_1 - 5365_7, 2024/07
Times Cited Count:7 Percentile:82.88(Multidisciplinary Sciences)Tonna, Ryutaro*; Sasaki, Takayuki*; Okamoto, Yoshihiro; Kobayashi, Taishi*; Akiyama, Daisuke*; Kirishima, Akira*; Sato, Nobuaki*
Journal of Nuclear Materials, 589, p.154862_1 - 154862_10, 2024/02
Times Cited Count:2 Percentile:40.17(Materials Science, Multidisciplinary)The dissolution behavior of FeUO compounds formed by a high-temperature reaction of UO
with iron, a stainless-steel component of reactor structural materials, was investigated under atmospheric conditions. The compounds were prepared in an electric furnace using U
O
and Fe
O
as starting materials, and their solid states were analyzed using X-ray diffraction, scanning electron microscopy energy dispersive X-ray spectroscopy, and X-ray absorption fine structure spectroscopy. The concentration of nuclides dissolved in water was examined by performing static leaching tests of FeUO
compounds for up to three months. A redox reaction was proposed to occur between trivalent Fe and pentavalent U ions in the early stage of FeUO
dissolution. It was thermodynamically deduced that the reduced divalent Fe ion was finally oxidized into a trivalent ion in the presence of dissolved oxygen, and iron hydroxide limited the solubility of Fe. Meanwhile, the concentration of hexavalent U (i.e., uranyl ion) was limited owing to the presence of secondary minerals such as metaschoepite and sodium uranate and subsequently decreased, possibly owing to sorption on Fe oxides, for example. The concentrations of multivalent ions of fission products, such as Ru and Ce, also decreased, likely for the reason above. By contrast, the concentration of soluble Cs ions did not decrease. The validity of this interpretation was supported by comparing the results with the dissolution behavior of a reference sample (Fe-free U
O
).
Sato, Nobuaki*; Kirishima, Akira*; Sasaki, Takayuki*; Takano, Masahide; Kumagai, Yuta; Sato, Soichi; Tanaka, Kosuke
Current Location of Fuel Debris Chemistry, 178 Pages, 2023/11
Considerable efforts have been devoted to the decommissioning of the TEPCO's Fukushima Daiichi Nuclear Power Station (1F) and now the retrieval of fuel debris is being proceeded on a trial basis. It can be said that the succession of science and technology related to debris, that is, human resource development, is important and indispensable. For that reason, we thought that a specific textbook on decommissioning is necessary. Regarding the 1F fuel debris, we still do not know enough, and it would be difficult to describe the details. However, 12 years have passed since the accident, and we have come to understand the situation of 1F to a certain extent. At this stage, it is essential for future development to organize the current situation by combining examples of past severe accidents. Therefore, we presented in this book the current state of fuel debris chemistry research from the perspectives of solid chemistry, solution chemistry, analytical chemistry, radiochemistry, and radiation chemistry.
Oikawa, Kenichi; Sato, Hirotaka*; Watanabe, Kenichi*; Su, Y. H.; Shinohara, Takenao; Kai, Tetsuya; Kiyanagi, Yoshiaki*; Hasemi, Hiroyuki
Journal of Physics; Conference Series, 2605, p.012013_1 - 012013_6, 2023/10
Machida, Masahiko; Yamada, Susumu; Kim, M.; Okumura, Masahiko; Miyamura, Hiroko; Shikaze, Yoshiaki; Sato, Tomoki*; Numata, Yoshiaki*; Tobita, Yasuhiro*; Yamaguchi, Takashi; et al.
RIST News, (69), p.2 - 18, 2023/09
The contamination of radioactive materials leaked from the reactor has resulted in numerous hot spots in the Fukushima Daiichi Nuclear Power Station (1F) building, posing obstacles to its decommissioning. In order to solve this problem, JAEA has conducted research and development of the digital technique for inverse estimation of radiation source distribution and countermeasures against the estimated source in virtual space for two years from 2021 based on the subsidy program "Project of Decommissioning and Contaminated Water Management" performed by the funds from the Ministry of Economy, Trade and Industry. In this article, we introduce the results of the project and the plan of the renewal project started in April 2023. For the former project, we report the derivative method for LASSO method considering the complex structure inside the building and the character of the source and show the result of the inverse estimation using the method in the real reactor building. Moreover, we explain the platform software "3D-ADRES-Indoor" which integrates these achievements. Finally, we introduce the plan of the latter project.
Kondo, Yosuke*; Achouri, N. L.*; Al Falou, H.*; Atar, L.*; Aumann, T.*; Baba, Hidetada*; Boretzky, K.*; Caesar, C.*; Calvet, D.*; Chae, H.*; et al.
Nature, 620(7976), p.965 - 970, 2023/08
Times Cited Count:32 Percentile:95.15(Multidisciplinary Sciences)no abstracts in English
Wang, H.*; Yasuda, Masahiro*; Kondo, Yosuke*; Nakamura, Takashi*; Tostevin, J. A.*; Ogata, Kazuyuki*; Otsuka, Takaharu*; Poves, A.*; Shimizu, Noritaka*; Yoshida, Kazuki; et al.
Physics Letters B, 843, p.138038_1 - 138038_9, 2023/08
Times Cited Count:5 Percentile:71.35(Astronomy & Astrophysics)Detailed -ray spectroscopy of the exotic neon isotope
Ne has been performed using the one-neutron removal reaction from
Ne. Based on an analysis of parallel momentum distributions, a level scheme with spin-parity assignments has been constructed for
Ne and the negative-parity states are identified for the first time. The measured partial cross sections and momentum distributions reveal a significant intruder p-wave strength providing evidence of the breakdown of the N = 20 and N = 28 shell gaps. Only a weak, possible f-wave strength was observed to bound final states. Large-scale shell-model calculations with different effective interactions do not reproduce the large p-wave and small f-wave strength observed experimentally, indicating an ongoing challenge for a complete theoretical description of the transition into the island of inversion along the Ne isotopic chain.
Takahatake, Yoko; Watanabe, So; Arai, Tsuyoshi*; Sato, Takahiro*; Shibata, Atsuhiro
Applied Radiation and Isotopes, 196, p.110783_1 - 110783_5, 2023/06
Times Cited Count:2 Percentile:40.17(Chemistry, Inorganic & Nuclear)Kusaka, Ryoji; Kumagai, Yuta; Watanabe, Masayuki; Sasaki, Takayuki*; Akiyama, Daisuke*; Sato, Nobuaki*; Kirishima, Akira*
Journal of Nuclear Science and Technology, 60(5), p.603 - 613, 2023/05
Times Cited Count:6 Percentile:64.86(Nuclear Science & Technology)Tonna, Ryutaro*; Sasaki, Takayuki*; Kodama, Yuji*; Kobayashi, Taishi*; Akiyama, Daisuke*; Kirishima, Akira*; Sato, Nobuaki*; Kumagai, Yuta; Kusaka, Ryoji; Watanabe, Masayuki
Nuclear Engineering and Technology, 55(4), p.1300 - 1309, 2023/04
Times Cited Count:6 Percentile:81.68(Nuclear Science & Technology)Simulated debris was synthesized using UO, Zr, and stainless steel and a heat treatment method under inert or oxidizing conditions. The primary U solid phase of the debris synthesized at 1473 K under inert conditions was UO
, whereas a (U,Zr)O
solid solution formed at 1873 K. Under oxidizing conditions, a mixture of U
O
and (Fe,Cr)UO
phases formed at 1473 K whereas a (U,Zr)O
solid solution formed at 1873 K. The leaching behavior of the fission products from the simulated debris was evaluated using two methods: the irradiation method, for which fission products were produced via neutron irradiation, and the doping method, for which trace amounts of non-radioactive elements were doped into the debris. The dissolution behavior of U depended on the properties of the debris and aqueous medium the debris was immersed in. Cs, Sr, and Ba leached out regardless of the primary solid phases. The leaching of high-valence Eu and Ru ions was suppressed, possibly owing to their solid-solution reaction with or incorporation into the uranium compounds of the simulated debris.
Pohl, T.*; Sun, Y. L.*; Obertelli, A.*; Lee, J.*; Gmez-Ramos, M.*; Ogata, Kazuyuki*; Yoshida, Kazuki; Cai, B. S.*; Yuan, C. X.*; Brown, B. A.*; et al.
Physical Review Letters, 130(17), p.172501_1 - 172501_8, 2023/04
Times Cited Count:15 Percentile:88.36(Physics, Multidisciplinary)We report on the first proton-induced single proton- and neutron-removal reactions from the neutron deficient O nucleus with large Fermi-surface asymmetry at
100 MeV/nucleon. Our results provide the first quantitative contributions of multiple reaction mechanisms including the quasifree knockout, inelastic scattering, and nucleon transfer processes. It is shown that the inelastic scattering and nucleon transfer, usually neglected at such energy regime, contribute about 50% and 30% to the loosely bound proton and deeply bound neutron removal, respectively.
Sato, Rika*; Nishi, Tsuyoshi*; Ota, Hiromichi*; Hayashi, Hirokazu; Sugawara, Takanori; Nishihara, Kenji
Dai-43-Kai Nihon Netsu Bussei Shimpojiumu Koen Rombunshu (CD-ROM), 3 Pages, 2022/10
no abstracts in English
Ito, Daisuke*; Sato, Hirotaka*; Odaira, Naoya*; Saito, Yasushi*; Parker, J. D.*; Shinohara, Takenao; Kai, Tetsuya; Oikawa, Kenichi
Journal of Nuclear Materials, 569, p.153921_1 - 153921_6, 2022/10
Times Cited Count:6 Percentile:64.86(Materials Science, Multidisciplinary)