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Nakanishi, Takumi*; Hori, Yuta*; Shigeta, Yasuteru*; Sato, Hiroyasu*; Kiyanagi, Ryoji; Munakata, Koji*; Ohara, Takashi; Okazawa, Atsushi*; Shimada, Rintaro*; Sakamoto, Akira*; et al.
Journal of the American Chemical Society, 145(35), p.19177 - 19181, 2023/08
Bersweiler, M.*; Sato, Hirokazu*; Adachi, Nozomu*; Todaka, Yoshikazu*; Peral, I.*; Kohlbrecher, J.*; Zaporozhets, V. D.*; Metlov, K. L.*; Michels, A.*; Oba, Yojiro
IUCrJ, 10(4), p.411 - 419, 2023/07
Times Cited Count:1 Percentile:87.7Kusaka, 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:0 Percentile:33.72(Nuclear Science & Technology)Nakanishi, Takumi*; Hori, Yuta*; Shigeta, Yasuteru*; Sato, Hiroyasu*; Wu, S.-Q.*; Kiyanagi, Ryoji; Munakata, Koji*; Ohara, Takashi; Sato, Osamu*
Physical Chemistry Chemical Physics, 25(17), p.12394 - 12400, 2023/05
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:0 Percentile:75.85(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 UO 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.
Akiyama, Daisuke*; Kusaka, Ryoji; Kumagai, Yuta; Nakada, Masami; Watanabe, Masayuki; Okamoto, Yoshihiro; Nagai, Takayuki; Sato, Nobuaki*; Kirishima, Akira*
Journal of Nuclear Materials, 568, p.153847_1 - 153847_10, 2022/09
Times Cited Count:2 Percentile:71.05(Materials Science, Multidisciplinary)FeUO, CrUO, and FeCrUO are monouranates containing pentavalent U. Even though these compounds have similar crystal structures, their formation conditions and thermal stability are significantly different. To determine the factors causing the difference in thermal stability between FeUO and CrUO, their crystal structures were evaluated in detail. A Raman band was observed at 700 cm in all the samples. This Raman band was derived from the stretching vibration of the O-U-O axis band, indicating that FeCrUO was composed of a uranyl-like structure in its lattice regardless of its "x"' value. Mssbauer measurements indicated that the Fe in FeUO and FeCrUO were trivalent. Furthermore, FeCrUO lost its symmetry around Fe with increasing electron densities around Fe, as the abundance of Cr increased. These results suggested no significant structural differences between FeUO and CrUO. Thermogravimetric measurements for UO, FeUO, and CrUO showed that the temperature at which FeUO decomposed under an oxidizing condition (approximately 800 C) was significantly lower than the temperature at which the decomposition of CrUO started (approximately 1250 C). Based on these results, we concluded that the decomposition of FeUO was triggered by an "in-crystal" redox reaction, i.e., Fe U Fe U, which would not occur in the CrUO lattice because Cr could never be reduced under the investigated condition. Finally, the existence of Cr in FexCrUO effectively suppressed the decomposition of the FeCrUO crystal, even at a very low Cr content.
Kirishima, Akira*; Akiyama, Daisuke*; Kumagai, Yuta; Kusaka, Ryoji; Nakada, Masami; Watanabe, Masayuki; Sasaki, Takayuki*; Sato, Nobuaki*
Journal of Nuclear Materials, 567, p.153842_1 - 153842_15, 2022/08
Times Cited Count:3 Percentile:80.29(Materials Science, Multidisciplinary)To understand the chemical structure and stability of nuclear fuel debris consisting of UO, Zr, and Stainless Steel (SUS) generated by the Fukushima Daiichi Nuclear Power Plant accident in Japan in 2011, simulated debris of the UO-SUS-Zr system and other fundamental component systems were synthesized and characterized. The simulated debris were synthesized by heat treatment for 1 to 12 h at 1600C, in inert (Ar) or oxidative (Ar + 2% O) atmospheres. Np and Am tracers were doped for the leaching tests of these elements and U from the simulated debris. The characterization of the simulated debris was conducted by XRD, SEM-EDX, Raman spectroscopy, and Mssbauer spectroscopy, which provided the major uranium phase of the UO -SUS-Zr debris was the solid solution of UO (s.s.) with Zr(IV) and Fe(II) regardless of the treatment atmosphere. The long-term immersion test of the simulated debris in pure water and that in seawater revealed the macro scale crystal structure of the simulated debris was chemically very stable in the wet condition for a year or more. Furthermore, the leaching test results showed that the actinide leaching ratios of U, Np, Am from the UO-SUS-Zr debris were very limited and less than 0.08 % for all the experiments in this study.
Kumagai, Yuta; Kusaka, Ryoji; Nakada, Masami; Watanabe, Masayuki; Akiyama, Daisuke*; Kirishima, Akira*; Sato, Nobuaki*; Sasaki, Takayuki*
Journal of Nuclear Science and Technology, 59(8), p.961 - 971, 2022/08
Times Cited Count:2 Percentile:56.43(Nuclear Science & Technology)We investigated potential degradation of fuel debris caused by HO, which is the oxidant of major impact from water radiolysis. We performed leaching experiments on different kinds of simulated debris comprising U, Fe, Cr, Ni, and Zr in an aqueous HO solution. Chemical analysis of the leaching solution showed that U dissolution was induced by HO. Raman analysis after the leaching revealed that uranyl peroxides were formed on the surface of the simulated debris. These results demonstrate that uranyl peroxides are possible alteration products of fuel debris from HO reaction. However, the sample in which the main uranium-containing phase was a U-Zr oxide solid solution showed much less uranium dissolution and no Raman signal of uranyl peroxides. Comparison of these results indicates that formation of an oxide solid solution of Zr with UO improves the stability of fuel debris against HO reaction.
Kumagai, Yuta; Kusaka, Ryoji; Nakada, Masami; Watanabe, Masayuki; Akiyama, Daisuke*; Kirishima, Akira*; Sato, Nobuaki*; Sasaki, Takayuki*
Hoshasen Kagaku (Internet), (113), p.61 - 64, 2022/04
The severe accident at TEPCO's Fukushima Daiichi Nuclear Power Station resulted in generation of fuel debris. The fuel debris is in contact with water and the radiolysis of water can accelerate degradation of the debris. The analysis of particles sampled from inside or near the damaged reactors indicates the complicated compositions of the fuel debris. It is challenging to estimate the effect of water radiolysis on such a complicated material. Therefore, in this study, we investigated the potential degradation process by leaching experiments of simulated fuel debris in aqueous HO solution. The results show that the reaction of HO induced uranium dissolution from most of the samples and then formation of uranyl peroxides. In contrast, a sample that had U-Zr oxide solid solution as the major phase exhibited remarkable resistance to HO. These findings revealed that the degradation of the simulated debris reflects the reactivity and stability of the uranium phase in the matrices.
Kusaka, Ryoji; Kumagai, Yuta; Yomogida, Takumi; Takano, Masahide; Watanabe, Masayuki; Sasaki, Takayuki*; Akiyama, Daisuke*; Sato, Nobuaki*; Kirishima, Akira*
Journal of Nuclear Science and Technology, 58(6), p.629 - 634, 2021/06
Times Cited Count:7 Percentile:67.5(Nuclear Science & Technology)Mori, Kazuhiro*; Okumura, Ryo*; Yoshino, Hirofumi*; Kanayama, Masaya*; Sato, Setsuo*; Oba, Yojiro; Iwase, Kenji*; Hiraka, Haruhiro*; Hino, Masahiro*; Sano, Tadafumi*; et al.
JPS Conference Proceedings (Internet), 33, p.011093_1 - 011093_6, 2021/03
no abstracts in English
Otaka, Toshiki*; Sato, Tatsumi*; Ono, Shimpei; Nagoshi, Kohei; Abe, Ryoji*; Arai, Tsuyoshi*; Watanabe, So; Sano, Yuichi; Takeuchi, Masayuki; Nakatani, Kiyoharu*
Analytical Sciences, 35(10), p.1129 - 1133, 2019/10
Times Cited Count:7 Percentile:41.13(Chemistry, Analytical)Oikawa, Kenichi; Su, Y.; Kiyanagi, Ryoji; Kawasaki, Takuro; Shinohara, Takenao; Kai, Tetsuya; Hiroi, Kosuke; Harjo, S.; Parker, J. D.*; Matsumoto, Yoshihiro*; et al.
Physica B; Condensed Matter, 551, p.436 - 442, 2018/12
Times Cited Count:5 Percentile:30.6(Physics, Condensed Matter)Oba, Yojiro; Shinohara, Takenao; Sato, Hirotaka*; Onodera, Yohei*; Hiroi, Kosuke; Su, Y.; Sugiyama, Masaaki*
Journal of the Physical Society of Japan, 87(9), p.094004_1 - 094004_5, 2018/09
Times Cited Count:1 Percentile:12.07(Physics, Multidisciplinary)no abstracts in English
Abe, Ryoji*; Nagoshi, Kohei*; Arai, Tsuyoshi*; Watanabe, So; Sano, Yuichi; Matsuura, Haruaki*; Takagi, Hideaki*; Shimizu, Nobutaka*; Koka, Masashi*; Sato, Takahiro*
Nuclear Instruments and Methods in Physics Research B, 404, p.173 - 178, 2017/08
Times Cited Count:5 Percentile:44.94(Instruments & Instrumentation)Oba, Yojiro*; Morooka, Satoshi; Oishi, Kazuki*; Suzuki, Junichi*; Takata, Shinichi; Sato, Nobuhiro*; Inoue, Rintaro*; Tsuchiyama, Toshihiro*; Gilbert, E. P.*; Sugiyama, Masaaki*
Journal of Applied Crystallography, 50(2), p.334 - 339, 2017/04
Times Cited Count:3 Percentile:29.42(Chemistry, Multidisciplinary)Toguri, Satohito*; Kobayashi, Shinji*; Tsuji, Masakuni*; Yahagi, Ryoji*; Yamada, Toshiko*; Matsui, Hiroya; Sato, Toshinori; Mikake, Shinichiro; Aoyagi, Yoshiaki
JAEA-Technology 2017-005, 43 Pages, 2017/03
The study on engineering technology in the Mizunami Underground Research Laboratory (MIU) project roughly consists of (1) development of design and construction planning technologies, (2) development of construction technology, (3) development of countermeasure technology, (4) development of technology for security, and (5) development of technologies regarding restoration and mitigating of the excavation effect. In FY2015, as a part of the important issues on the research program, water-tight grouting method has been developed. Grouting methods utilized in the MIU were evaluated and the post-excavation grouting at the -500m Access/Research Gallery-South was planned based on these evaluation results. Also, technology development from the viewpoint of geological disposal was summarized, and information on the alternative method to the grouting method was collected and organized.
Hirobe, Daichi*; Sato, Masahiro*; Kawamata, Takayuki*; Shiomi, Yuki*; Uchida, Kenichi*; Iguchi, Ryo*; Koike, Yoji*; Maekawa, Sadamichi; Saito, Eiji
Nature Physics, 13(1), p.30 - 34, 2017/01
Times Cited Count:91 Percentile:96.69(Physics, Multidisciplinary)Morooka, Satoshi; Kanata, Hiroyuki*; Oba, Yojiro*; Sato, Masugu*
Heisei-28-Nendo SPring-8 Sangyo Shinbunya Shien Kadai, Ippan Kadai (Sangyo Bunya) Jisshi Hokokusho, p.95 - 98, 2017/00
no abstracts in English
Oba, Yojiro*; Morooka, Satoshi; Sato, Hirotaka*; Sato, Nobuhiro*; Inoue, Rintaro*; Sugiyama, Masaaki*
Hamon, 26(4), p.170 - 173, 2016/11