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Nomoto, Yasunobu; Mizuta, Naoki; Morita, Keisuke; Aoki, Takeshi; Okita, Shoichiro; Ishii, Katsunori; Kurahayashi, Kaoru; Yasuda, Takanori; Tanaka, Masato; Isaka, Kazuyoshi; et al.
Proceedings of 30th International Conference on Nuclear Engineering (ICONE30) (Internet), 7 Pages, 2023/05
Mizuta, Naoki; Morita, Keisuke; Aoki, Takeshi; Okita, Shoichiro; Ishii, Katsunori; Kurahayashi, Kaoru; Yasuda, Takanori; Tanaka, Masato; Isaka, Kazuyoshi; Noguchi, Hiroki; et al.
Proceedings of 30th International Conference on Nuclear Engineering (ICONE30) (Internet), 6 Pages, 2023/05
Shimokita, Keisuke*; Yamamoto, Katsuhiro*; Miyata, Noboru*; Nakanishi, Yohei*; Shibata, Motoki*; Takenaka, Mikihito*; Yamada, Norifumi*; Seto, Hideki*; Aoki, Hiroyuki; Miyazaki, Tsukasa*
Soft Matter, 19(11), p.2082 - 2089, 2023/03
Times Cited Count:0 Percentile:0(Chemistry, Physical)Uchino, Seiko*; Narita, Hirokazu*; Kita, Keisuke*; Suzuki, Hideya*; Matsumura, Tatsuro; Naganawa, Hirochika*; Sakaguchi, Koichi*; Oto, Keisuke*
Solvent Extraction Research and Development, Japan, 30(1), p.39 - 46, 2023/00
The extraction of trivalent rare earth ions (RE) from HNO solution using a triamide amine, tris(N,N-di-2-ethylhexyl-ethylamide)amine (DEHTAA), was conducted, and the extraction mechanism was estimated from extraction behavior of HNO and RE and the relationship between atomic number and extraction percentages (E%) for RE. A DEHTAA molecule dominantly formed a DEHTAA HNO at 1.0 M HNO and a DEHTAA(HNO) at 6.0 M HNO in the acid-equilibrated organic phase. This would provide the unique dependence of E% for the light RE on the HNO concentration, in which the E% value had a minimum and maximum at 0.5 M and 2 M HNO, respectively. The results of the slope analyses for the distribution ratios for RE suggested that the dominant RE complex was RE(NO)DEHTAA(DEHTAA HNO) at 1.0 M HNO. The E% for RE decreased from La to Lu at 1.0 M HNO; on the other hand, those increased from La to Nd at 0.25 M and from La to Sm and 6.0 M HNO.
Shimokita, Keisuke*; Yamamoto, Katsuhiro*; Miyata, Noboru*; Arima-Osonoi, Hiroshi*; Nakanishi, Yohei*; Takenaka, Mikihito*; Shibata, Motoki*; Yamada, Norifumi*; Seto, Hideki*; Aoki, Hiroyuki; et al.
Langmuir, 38(41), p.12457 - 12465, 2022/10
Times Cited Count:0 Percentile:0(Chemistry, Multidisciplinary)Tanaka, Hirohisa*; Masaki, Sayaka*; Aotani, Takuro*; Inagawa, Kohei*; Iwata, Sogo*; Aida, Tatsuya*; Yamamoto, Tadasuke*; Kita, Tomoaki*; Ono, Hitomi*; Takenaka, Keisuke*; et al.
SAE Technical Paper 2022-01-0534 (Internet), 10 Pages, 2022/03
Ueda, Yuki; Morisada, Shintaro*; Kawakita, Hidetaka*; Wenzel, M.*; Weigand, J. J.*; Oto, Keisuke*
Separation and Purification Technology, 277, p.119456_1 - 119456_8, 2021/12
Times Cited Count:5 Percentile:29.15(Engineering, Chemical)no abstracts in English
Ueda, Yuki; Morisada, Shintaro*; Kawakita, Hidetaka*; Oto, Keisuke*
Separations (Internet), 8(9), p.139_1 - 139_15, 2021/09
Times Cited Count:9 Percentile:62.42(Chemistry, Analytical)no abstracts in English
Reinecke, E.-A.*; Takenaka, Keisuke*; Ono, Hitomi*; Kita, Tomoaki*; Taniguchi, Masashi*; Nishihata, Yasuo; Hino, Ryutaro; Tanaka, Hirohisa*
International Journal of Hydrogen Energy, 46(23), p.12511 - 12521, 2021/03
Times Cited Count:5 Percentile:21.34(Chemistry, Physical)The safe decommissioning as well as decontamination of the radioactive waste resulting from the nuclear accident in Fukushima Daiichi represents a huge task for the next decade. At present, research and development on long-term safe storage containers has become an urgent task with international cooperation in Japan. One challenge is the generation of hydrogen and oxygen in significant amounts by means of radiolysis inside the containers, as the nuclear waste contains a large portion of sea water. The generation of radiolysis gases may lead to a significant pressure build-up inside the containers and to the formation of flammable gases with the risk of ignition and the loss of integrity. In the framework of the project "R&D on technology for reducing concentration of flammable gases generated in long-term waste storage containers" funded by the Japanese Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), the potential application of catalytic recombiner devices inside the storage containers is investigated. In this context, a suitable catalyst based on the so-called intelligent automotive catalyst for use in a recombiner is under consideration. The catalyst is originally developed and mass-produced for automotive exhaust gas purification, and is characterized by having a self-healing function of precious metals (Pd, Pt and Rh) dissolved as a solid solution in the perovskite type oxides. The basic features of this catalyst have been tested in an experimental program. The test series in the REKO-4 facility has revealed the basic characteristics of the catalyst required for designing the recombiner system.
Miyazaki, Tsukasa*; Shimokita, Keisuke*; Yamamoto, Katsuhiro*; Aoki, Hiroyuki; Yamada, Norifumi*; Miyata, Noboru*
Langmuir, 36(49), p.15181 - 15188, 2020/12
Times Cited Count:6 Percentile:31.01(Chemistry, Multidisciplinary)Ono, Hitomi*; Takenaka, Keisuke*; Kita, Tomoaki*; Taniguchi, Masashi*; Matsumura, Daiju; Nishihata, Yasuo; Hino, Ryutaro; Reinecke, E.-A.*; Takase, Kazuyuki*; Tanaka, Hirohisa*
E-Journal of Advanced Maintenance (Internet), 11(1), p.40 - 45, 2019/05
Asari, Keisuke*; Hetland, O. S.*; Fujita, Satoshi*; Itakura, Mitsuhiro; Okita, Taira*
Journal of Nuclear Materials, 442(1), p.360 - 364, 2013/11
Times Cited Count:21 Percentile:83.7(Materials Science, Multidisciplinary)Molecular dynamics simulations were conducted using a set of six interatomic potentials for FCC metals that differed only in stacking fault energy (SFE), to clarify the effect of SFE on interactions between a dissociated edge dislocation and a void. There are two different types of interaction mechanism: separate depinning of the individual partial dislocations and almost simultaneous depinning of the combined partial dislocations. The interaction mechanism depends on both the SFE and void size, and changes the absolute value of the critical resolved shear stress (CRSS) and its dependence on the SFE. In the separate depinning case, the CRSS is relatively low and is almost independent of the SFE, while in the simultaneous case, the CRSS is increases with SFE. The void size for which the change in interaction mechanism occurs increases with decreasing SFE.
Parajuli, D.; Khunathai, K.*; Adhikari, C. R.*; Inoue, Katsutoshi*; Oto, Keisuke*; Kawakita, Hidetaka*; Funaoka, Masamitsu*; Hirota, Koichi
Minerals Engineering, 22(13), p.1173 - 1178, 2009/10
Times Cited Count:44 Percentile:88.07(Engineering, Chemical)Xu, P. G.; Suzuki, Tetsuya*; Yamanaka, Keisuke*; Akita, Koichi
no journal, ,
Ueda, Yuki; Sugita, Tsuyoshi; Okamura, Hiroyuki; Shimojo, Kojiro; Naganawa, Hirochika; Morisada, Shintaro*; Kawakita, Hidetaka*; Oto, Keisuke*
no journal, ,
Platinum group metals (PGMs) are indispensable metals in modern industries and are used for example as active components in automobile gas catalysts, jewellery goods, electronic devices and dental materials. In order to meet the growing demand, high efficient receptors for liquid-liquid extraction of the respective anionic chloro-complexes are required in order to enhance capable winning from either pour geological deposits or complex secondary sources within the Urban Mining. The ligand containing urea or amide groups can form the hydrogen bond with anionic species. The novel urea or amide containing extractants were synthesized and its extraction behavior and mechanism were investigated in this work.
Ueda, Yuki; Sugita, Tsuyoshi; Okamura, Hiroyuki; Shimojo, Kojiro; Naganawa, Hirochika; Morisada, Shintaro*; Kawakita, Hidetaka*; Oto, Keisuke*
no journal, ,
Platinum group metals (PGMs) are indispensable metals in modern industries and are used for example as active components in automobile gas catalysts, jewelry goods, electronic devices and dental materials. In order to meet the growing demand, high efficient extraction reagents for liquid-liquid extraction of the respective anionic chloro-complexes are required in order to enhance capable winning from either pour geological deposits or complex secondary sources within the Urban Mining. The ligand containing urea or amide groups can form the hydrogen bond with anionic species. The novel urea or amide containing extraction reagents were synthesized and its extraction behavior and mechanism were investigated in this work.
Ueda, Yuki; Morisada, Shintaro*; Kawakita, Hidetaka*; Omi, Kentaro*; Fujita, Mitsuharu*; Weigand, J.*; Shimojo, Kojiro; Naganawa, Hirochika; Oto, Keisuke*
no journal, ,
Platinum group metals (PGMs) are indispensable metals in modern industries and are used for example as active components in automobile gas catalysts, jewelry goods, electronic devices and dental materials. In order to meet the growing demand, high efficient extraction reagents for liquid-liquid extraction of the respective anionic chloro-complexes are required in order to enhance capable winning from either pour geological deposits or complex secondary sources within the Urban Mining. The ligand containing urea or amide groups can form the hydrogen bond with anionic species. The novel urea or amide incorporating extraction reagents were synthesized and its extraction behavior and mechanism were investigated in this work.
Matsumura, Daiju; Tsuji, Takuya; Nishihata, Yasuo; Hino, Ryutaro; Taniguchi, Masashi*; Takenaka, Keisuke*; Ono, Hitomi*; Kita, Tomoaki*; Tanaka, Hirohisa*
no journal, ,
no abstracts in English
Adachi, Sadia*; Sueki, Keisuke*; Toyoshima, Atsushi*; Tsukada, Kazuaki; Haba, Hiromitsu*; Komori, Yukiko*; Yokokita, Takuya*; Mori, Taiki*
no journal, ,
Anion exchange behavior of group-5 elements, Nb, Ta, and their pseudo homologue Pa in HF and HF/HNO solution was investigated to understand chemical properties of Db. Adsorption behavior of Db is clearly different from that of Ta and is similar to those of Nb and Pa. In the present study, anion exchange experiments of Nb, Ta and Pa were carried out with HF/HNO aqueous solution as basic experiments for estimating the species of Db fluoride complex. Adsorption behavior was investigated by changing the fluoride ion concentration for each HNO concentration. Based on the observed distribution coefficients of these elements, we discuss the formation reaction of the anionic fluoride complex and chemical species of Db.
Kato, Mizuho*; Adachi, Sadia*; Toyoshima, Atsushi*; Tsukada, Kazuaki; Asai, Masato; Haba, Hiromitsu*; Yokokita, Takuya*; Komori, Yukiko*; Shigekawa, Yudai*; Sueki, Keisuke*
no journal, ,
A few studies have been so far performed on aqueous chemistry of Db, the group-5 superheavy element, by anion-exchange experiments in HF and HF/HNO mixture solutions. Although the distribution coefficient (Kd) of Db was shown to trend to Ta Nb Db Pa in the group-5 homologs and pseudo-homolog elements, its chemical species has not been clarified. In this work, for identification of fluoride species of Db, we performed anion-exchange experiments of Nb, Ta, and Db in HF/1.0 M HNO mixture solutions by using an automated rapid chemistry apparatus, ARCA.