Spallation and fragmentation cross sections for 168 MeV/nucleon Xe ions on proton, deuteron, and carbon targets

Sun, X. H.*; Wang, H.*; Otsu, Hideaki*; Sakurai, Hiroyoshi*; Ahn, D. S.*; Aikawa, Masayuki*; Fukuda, Naoki*; Isobe, Tadaaki*; Kawakami, Shunsuke*; Koyama, Shumpei*; et al.

Physical Review C, 101(6), p.064623_1 - 064623_12, 2020/06

https://doi.org/10.1103/PhysRevC.101.064623

The spallation and fragmentation reactions of Xe induced by proton, deuteron and carbon at 168 MeV/nucleon were studied at RIKEN Radioactive Isotope Beam Factory via the inverse kinematics technique. The cross sections of the lighter products are larger in the carbon-induced reactions due to the higher total kinetic energy of carbon. The energy dependence was investigated by comparing the newly obtained data with previous results obtained at higher reaction energies. The experimental data were compared with the results of SPACS, EPAX, PHITS and DEURACS calculations. These data serve as benchmarks for the model calculations.

Nuclear structure of Ni from the (,) reaction

Elekes, Z.*; Kripk, *; Sohler, D.*; Sieja, K.*; Ogata, Kazuyuki*; Yoshida, Kazuki; Doornenbal, P.*; Obertelli, A.*; Authelet, G.*; Baba, Hidetada*; et al.

Physical Review C, 99(1), p.014312_1 - 014312_7, 2019/01

https://doi.org/10.1103/PhysRevC.99.014312

The nuclear structure of the Ni nucleus was investigated by (,) reaction using a NaI(Tl) array to detect the deexciting prompt rays. A new transition with an energy of 2227 keV was identified by and coincidences. Our shell-model calculations using the Lenzi, Nowacki, Poves, and Sieja interaction produced good candidates for the experimental proton hole states in the observed energy region, and the theoretical cross sections showed good agreement with the experimental values. Although we could not assign all the experimental states to the theoretical ones unambiguously, the results are consistent with a reasonably large Z = 28 shell gap for nickel isotopes in accordance with previous studies.

Shell evolution beyond =28 and =50; Spectroscopy of Zn

Shand, C. M.*; Podolyk, Zs.*; Grska, M.*; Doornenbal, P.*; Obertelli, A.*; Nowacki, F.*; Otsuka, T.*; Sieja, K.*; Tostevin, J. A.*; Tsunoda, T.*; et al.

Physics Letters B, 773, p.492 - 497, 2017/10

https://doi.org/10.1016/j.physletb.2017.09.001

decay of unbound neutron-hole states in Sn

Vaquero, V.*; Jungclaus, A.*; Doornenbal, P.*; Wimmer, K.*; Gargano, A.*; Tostevin, J. A.*; Chen, S.*; Ncher, E.*; Sahin, E.*; Shiga, Yoshiaki*; et al.

Physical Review Letters, 118(20), p.202502_1 - 202502_5, 2017/05

https://doi.org/10.1103/PhysRevLett.118.202502

Type II shell evolution in isobars from the island of inversion

Morales, A. I.*; Benzoni, G.*; Watanabe, H.*; Tsunoda, Yusuke*; Otsuka, T.*; Nishimura, Shunji*; Browne, F.*; Daido, R.*; Doornenbal, P.*; Fang, Y.*; et al.

Physics Letters B, 765, p.328 - 333, 2017/02

https://doi.org/10.1016/j.physletb.2016.12.025

Low-lying excitations in Ni

Morales, A. I.*; Benzoni, G.*; Watanabe, H.*; Nishimura, Shunji*; Browne, F.*; Daido, R.*; Doornenbal, P.*; Fang, Y.*; Lorusso, G.*; Patel, Z.*; et al.

Physical Review C, 93(3), p.034328_1 - 034328_14, 2016/03

https://doi.org/10.1103/PhysRevC.93.034328

Hydrophobic platinum honeycomb catalyst to be used for tritium oxidation reactors

Iwai, Yasunori; Kubo, Hitoshi*; Oshima, Yusuke*; Noguchi, Hiroshi*; Edao, Yuki; Taniuchi, Junichi*

Fusion Science and Technology, 68(3), p.596 - 600, 2015/10

https://doi.org/10.13182/FST14-921

We have newly developed the hydrophobic platinum honeycomb catalysts applicable to tritium oxidation reactor since the honeycomb-shape catalyst can decrease the pressure drop. Two types of hydrophobic honeycomb catalyst have been test-manufactured. One is the hydrophobic platinum catalyst on a metal honeycomb. The other is the hydrophobic platinum catalyst on a ceramic honeycomb made of silicon carbide. The fine platinum particles around a few nanometers significantly improve the catalytic activity for the oxidation tritium at a tracer concentration. The hydrogen concentration in the gaseous feed slightly affects the overall reaction rate constant for hydrogen oxidation. Due to the competitive adsorption of hydrogen and water molecules on platinum surface, the overall reaction rate constant has the bottom value. The hydrogen concentration for the bottom value is 100 ppm under the dry feed gas. We have experimentally confirmed the activity of these honeycomb catalysts is as good as that of pellet-shape hydrophobic catalyst. The results support the hydrophobic honeycomb catalysts are applicable to tritium oxidation reactor.

Hydrophobic Pt catalyst for combustion of hydrogen isotopes at low temperatures

Iwai, Yasunori; Kubo, Hitoshi*; Sato, Katsumi; Oshima, Yusuke*; Noguchi, Hiroshi*; Taniuchi, Junichi*

Proceedings of 7th Tokyo Conference on Advanced Catalytic Science and Technology (TOCAT-7) (USB Flash Drive), 2 Pages, 2014/06

Hydrophobic platinum catalysts have been developed especially for combustion of hydrogen isotopes released in a nuclear facility. A new type of hydrophobic hydrogen combustion catalyst commercially named TKK-KNOITS catalyst is hardly susceptible to water mist and water vapor in the atmosphere and water produced by hydrogen combustion. It is capable of maintaining the activity even at relatively low temperatures. The TKK-KNOITS catalyst is superior to other previous hydrophobic catalysts in applicability to wide range of hydrogen concentration from very thin to dense. The catalyst which carrier is composed of inorganic oxide has thermal stability up to 873 K.

Room-temperature reactor packed with hydrophobic catalysts for the oxidation of hydrogen isotopes released in a nuclear facility

Iwai, Yasunori; Sato, Katsumi; Taniuchi, Junichi*; Noguchi, Hiroshi*; Kubo, Hitoshi*; Harada, Nobuo*; Oshima, Yusuke*; Yamanishi, Toshihiko

Journal of Nuclear Science and Technology, 48(8), p.1184 - 1192, 2011/08

https://doi.org/10.3327/jnst.48.1184

The inorganic-based hydrophobic Pt-catalyst named H1P has been developed especially for efficient oxidation of a tracer level of tritium in the ambient temperature range even in the presence of saturated water vapor. The overall reaction rate constant for H1P catalyst in the ambient temperature range was considerably larger than that for traditionally applied Pt/AlO catalyst. Moreover, the decrease in reaction rate for H1P in the presence of saturated water vapor compared with in the absence of water vapor was slight due to its excellence in hydrophobic performance. Oxidation reaction on the catalyst surface is the rate-controlling step in the ambient temperature range and diffusion in a catalyst substratum above 313 K due to its fine porosity. The overall reaction rate constant in the ambient temperature range was dependent on the space velocity and hydrogen concentration in carrier.

Tritium oxidation performance of hydrophobic regular Pt catalyst

Iwai, Yasunori; Sato, Katsumi; Kubo, Hitoshi*; Oshima, Yusuke*; Noguchi, Hiroshi*; Taniuchi, Junichi*

no journal, , 

To enhance the reliability of tritium handling technologies for a fusion reactor, hydrophobic catalysts are strongly required for sufficient tritium oxidation at the room temperature without additional heating, considering the loss of electronic supply accident in the event of a fire. Traditional hydrophilic catalysts have lost its activity at room temperature due to the formation of water layer on the surface of the catalysts. JAEA and TKK have jointly researched and developed some inorganic-based hydrophobic catalysts for tritium oxidation at room temperature. The tritium oxidation performance of newly developed Hydrophobic Regular Pt Catalyst was independent on the moisture concentration in atmosphere. The reaction on the surface was the rate-controlling step at the room temperature. The tritium (hydrogen) concentration affected strongly the overall reaction rate coefficient. Research to improve catalyst activity is the next step for Hydrophobic Regular Pt Catalyst.