Crystal structure, photomagnetic and dielectric properties of a cyanido-bridged Cu-Mo assembly film

Ikeda, Yusuke*; Matsumura, Daiju; Tsuji, Takuya; Namai, Asuka*; Imoto, Kenta*; Tokoro, Hiroko*; Nakabayashi, Koji*; Okoshi, Shinichi*

Inorganica Chimica Acta, 550, p.121434_1 - 121434_8, 2023/03

https://doi.org/10.1016/j.ica.2023.121434

Thermally altered subsurface material of asteroid (162173) Ryugu

Kitazato, Kohei*; Milliken, R. E.*; Iwata, Takahiro*; Abe, Masanao*; Otake, Makiko*; Matsuura, Shuji*; Takagi, Yasuhiko*; Nakamura, Tomoki*; Hiroi, Takahiro*; Matsuoka, Moe*; et al.

Nature Astronomy (Internet), 5(3), p.246 - 250, 2021/03

https://doi.org/10.1038/s41550-020-01271-2

Here we report observations of Ryugu's subsurface material by the Near-Infrared Spectrometer (NIRS3) on the Hayabusa2 spacecraft. Reflectance spectra of excavated material exhibit a hydroxyl (OH) absorption feature that is slightly stronger and peak-shifted compared with that observed for the surface, indicating that space weathering and/or radiative heating have caused subtle spectral changes in the uppermost surface. However, the strength and shape of the OH feature still suggests that the subsurface material experienced heating above 300 C, similar to the surface. In contrast, thermophysical modeling indicates that radiative heating does not increase the temperature above 200 C at the estimated excavation depth of 1 m, even if the semimajor axis is reduced to 0.344 au. This supports the hypothesis that primary thermal alteration occurred due to radiogenic and/or impact heating on Ryugu's parent body.

Measurement of neutron scattering cross section of nano-diamond with particle diameter of approximately 5 nm in energy range of 0.2 meV to 100 meV

Teshigawara, Makoto; Tsuchikawa, Yusuke*; Ichikawa, Go*; Takata, Shinichi; Mishima, Kenji*; Harada, Masahide; Oi, Motoki; Kawamura, Yukihiko*; Kai, Tetsuya; Kawamura, Seiko; et al.

Nuclear Instruments and Methods in Physics Research A, 929, p.113 - 120, 2019/06

https://doi.org/10.1016/j.nima.2019.03.038

A nano-diamond is an attractive neutron reflection material below cold neutron energy. The total neutron cross section of a nano-diamond was derived from a neutron transmission measurement over the neutron energy range of 0.2 meV to 100 meV because total neutron cross section data were not available. The total cross section of a nano-diamond with particle size of approximately 5 nm increased with a decrease in neutron energy to 0.2 meV. It was approximately two orders of magnitude larger than that of graphite at 0.2 meV. The contribution of inelastic scattering to the total cross section was to be shown negligible small at neutron energies of 1.2, 1.5, 1.9, 2.6, and 5.9 meV in the inelastic neutron scattering measurement. Moreover, small-angle neutron scattering measurements of the nano-diamond showed a large scattering cross section in the forward direction for low neutron energies.

Applicability of polyvinylpolypyrrolidone adsorbent to treatment process of wastes containing uranium

Ohashi, Yusuke; Harada, Masayuki*; Asanuma, Noriko*; Ando, Shion; Tanaka, Yoshio; Ikeda, Yasuhisa*

Journal of Radioanalytical and Nuclear Chemistry, 311(1), p.491 - 502, 2017/01

https://doi.org/10.1007/s10967-016-5017-9

In order to assess the feasibility of method for recovering U from wastes containing uranium (scrap uranium) using polyvinylpolypyrrolidone (PVPP) adsorbent, we have examined the adsorption and desorption behavior of metal species in HCl aqueous solutions dissolving scrap uranium. It was found that the U(VI) species are selectively adsorbed onto PVPP regardless of the presence of a large amount of Na(I) and Al(III), that the adsorbed U(VI) species are desorbed from PVPP column selectively by water. Pure uranium was efficiently recovered from the eluates. From these results, the PVPP resin is expected to be used as the adsorbent in the treatment process of scrap uranium.

Science from the initial operation of HRC

Ito, Shinichi*; Yokoo, Tetsuya*; Masuda, Takatsugu*; Yoshizawa, Hideki*; Soda, Minoru*; Ikeda, Yoichi*; Ibuka, Soshi*; Kawana, Daichi*; Sato, Taku*; Nambu, Yusuke*; et al.

JPS Conference Proceedings (Internet), 8, p.034001_1 - 034001_6, 2015/09

https://doi.org/10.7566/JPSCP.8.034001

Photophysical property of -bis(thiocyanato)aurate(I) complexes in ionic liquids

Aoyagi, Noboru; Shinha, Yusuke*; Ikeda, Atsushi*; Haga, Yoshinori; Shimojo, Kojiro; Brooks, N. R.*; Izuoka, Akira*; Naganawa, Hirochika; Kimura, Takaumi; Binnemans, K.*

Crystal Growth & Design, 15(3), p.1422 - 1429, 2015/03

https://doi.org/10.1021/cg501792m

The photochemistry of a gold(I) thiocyanate complex has been investigated to determine the coordination structure in both the solid and liquid states. The coordination geometries of the supramolecular complex and the concomitant exciplex have mainly been analyzed by crystallographic analysis and X-ray absorption spectroscopy. The Au-S bond distance and Au-Au separation of the compound in the ground state and in the phosphorescent excited state were compared. Upon irradiation with UV light, the excimeric interactions were enhanced, resulting in a contraction of the Au-Au aurophilic distance. A broad luminescence spectrum was observed for the one-dimensional chain suprastructure. The time-resolved luminescence spectra indicated the entity of several oligomeric species in the crude liquid without neutral solvent molecules. In addition, EXAFS spectroscopy exhibited a slight change in the nearest Au-S distance due to the photo-switched transformation. The deformation of the (Au-Au)* exciplexes was not apparently promoted in the liquid state with the asymmetrical imidazoium cations having a non-local charge distribution in the present observation. This is plausibly due to a flexible molecular structure and a property in the liquid state. In conclusion, the photo-excited nature of the pseudo-one dimensional complexes is emerged in controlling bond distances among the supramolecular networks.

Annual report of Nuclear Emergency Assistance and Training Center (April 1, 2012 - March 31, 2013)

Sato, Takeshi; Muto, Shigeo; Okuno, Hiroshi; Katagiri, Hiromi; Akiyama, Kiyomitsu; Okamoto, Akiko; Koie, Masahiro; Ikeda, Takeshi; Nemotochi, Toshimasa; Saito, Toru; et al.

JAEA-Review 2013-046, 65 Pages, 2014/02

JAEA-Review-2013-046.pdf:11.18MB

When a nuclear emergency occurs in Japan, the Japan Atomic Energy Agency (JAEA) has the responsibility of providing technical support to the National government, local governments, police, fire stations and nuclear operators etc., because the JAEA has been designated as the Designated Public Institution under the Basic Act on Disaster Control Measures and the Act on Response to Armed Attack Situations, etc.. The Nuclear Emergency Assistance and Training Center (NEAT) of JAEA provides a comprehensive range of technical support activities to an Off-Site Center in case of a nuclear emergency. Specifically, NEAT gives technical advice and information, dispatches specialists as required, and supplies the National Government and local governments with emergency equipments and materials. NEAT provides various exercise and training courses concerning nuclear disaster prevention to those personnel taking an active part in emergency response organizations at normal times. The tasks of NEAT, with its past experiences as a designated public institution including the responses to TEPCO's Fukushima Accident, have been shifted to technical supports to the national government for strengthening its abilities to emergency responses; the NEAT therefore focused on maintenance and operation of its functions, and strengthening its response abilities in cooperation with the national government. This annual report summarized these activities of JAEA/NEAT in the fiscal year 2012.

Magnetic-field-induced metallic state in -US

Sugiyama, Kiyohiro*; Hirose, Yusuke*; Enoki, Kentaro*; Ikeda, Shugo*; Yamamoto, Etsuji; Tateiwa, Naoyuki; Haga, Yoshinori; Kida, Takanori*; Hagiwara, Masayuki*; Kindo, Koichi*; et al.

Journal of the Physical Society of Japan, 80(Suppl.A), p.SA104_1 - SA104_3, 2011/07

https://doi.org/10.1143/JPSJS.80SA.SA104

Identified charged hadron production in collisions at = 200 and 62.4 GeV

Adare, A.*; Afanasiev, S.*; Aidala, C.*; Ajitanand, N. N.*; Akiba, Yasuyuki*; Al-Bataineh, H.*; Alexander, J.*; Aoki, Kazuya*; Aphecetche, L.*; Armendariz, R.*; et al.

Physical Review C, 83(6), p.064903_1 - 064903_29, 2011/06

https://doi.org/10.1103/PhysRevC.83.064903

Transverse momentum distributions and yields for , and in collisions at = 200 and 62.4 GeV at midrapidity are measured by the PHENIX experiment at the RHIC. We present the inverse slope parameter, mean transverse momentum, and yield per unit rapidity at each energy, and compare them to other measurements at different collisions. We also present the scaling properties such as and scaling and discuss the mechanism of the particle production in collisions. The measured spectra are compared to next-to-leading order perturbative QCD calculations.

Magnetic and dielectric study of RSrMnO (R = Gd, Tb and Dy)

Yoshii, Kenji; Hiramitsu, Yusuke*; Okajima, Yuka*; Yoneda, Yasuhiro; Nishihata, Yasuo; Mizuki, Junichiro; Nakamura, Akio; Shimojo, Yutaka; Ishii, Yoshinobu*; Morii, Yukio; et al.

Materials Research Bulletin, 45(11), p.1574 - 1580, 2010/10

https://doi.org/10.1016/j.materresbull.2010.07.024

Magnetic and dielectric properties of perovskite manganites RSrMnO (R = Gd, Tb and Dy) have been investigated. DC and AC magnetic measurements showed short-range glassy magnetic ordering at Tg about 40 K. Such ordering was observed by neutron diffraction and is ascribable to the size mismatch of R and Sr settled randomly at the same crystallographic site. Dielectric constants for each material were about 1000-10000 between about 50 K and 300 K and showed broad maximums above Tg. Dielectric dispersion showed poor coherency of the motion of polar regions, plausibly because of the size-mismatch effect; both the magnetic and dielectric properties of this system are governed by the randomness at the R/Sr site. The tan and EXAFS data suggest that the dielectric response is rooted in a transfer of the Mn-3d electrons.