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Oral presentation

Extraction behavior of hexavalent and reduced Mo and W with 4-isopropyltropolone (Hinokitiol)

Miyashita, Sunao; Toyoshima, Atsushi; Oe, Kazuhiro*; Sato, Tetsuya; Asai, Masato; Tsukada, Kazuaki; Nagame, Yuichiro; Sch$"a$del, M.; Kaneya, Yusuke; Haba, Hiromitsu*; et al.

no journal, , 

The extraction behavior of hexavalent and reduced Mo and W were investigated when aqueous phase was 0.1 M HCl/0.9 M LiCl solution. The D value of Mo was changed from 10 to 1 when applied potential was near 0 to -0.2 V. On the other hand, the D value of W was not changed at all applied potentials in this experimental condition. Those results indicated that Mo was reduced by FEC, and the extraction behavior of reduced Mo was different from hexavalent Mo. In the case of W, W was not reduced or the D values of reduced W was same as hexavalent W.

Oral presentation

Electrolytic reduction of mendelevium using a flow electrolytic column

Toyoshima, Atsushi; Li, Z.*; Asai, Masato; Sato, Tetsuya; Kikuchi, Takahiro*; Kaneya, Yusuke*; Kitatsuji, Yoshihiro; Tsukada, Kazuaki; Nagame, Yuichiro; Sch$"a$del, M.; et al.

no journal, , 

The redox behavior of mendelevium (Md) was studied with flow electrolytic chromatography. The $$^{255}$$Md isotope produced in the $$^{248}$$Cm($$^{11}$$B, 4n)$$^{255}$$Md reaction at the JAEA tandem accelerator was used in the electrolytic reduction experiment with the flow electrolytic column apparatus in 0.1 M HCl. It was clearly observed that, applying appropriate potentials on the chromatography column, the most stable Md$$^{3+}$$ is reduced to Md$$^{2+}$$. The redox potential of the Md$$^{2+}$$ = Md$$^{3+}$$ + e$$^{-}$$ couple was determined to be -0.16 $$pm$$ 0.05 V vs. a normal hydrogen electrode.

Oral presentation

Nuclear structure of the heaviest elements revealed in $$alpha$$-spectroscopic studies

Asai, Masato

no journal, , 

Current status of spectroscopic studies for superheavy elements are reviewed. In particular, some of our experimental results on $$alpha$$-$$gamma$$ coincidence spectroscopy and $$alpha$$ fine-structure spectroscopy for odd-mass No, Lr, and Rf isotopes using a gas-jet transport technique are introduced, and what are revealed in the $$alpha$$-spectroscopic studies is presented.

Oral presentation

Ionization behavior of lawrencium (Lr, $$Z = 103$$) on surface ionization process

Sato, Tetsuya; Asai, Masato; Sato, Nozomi; Tsukada, Kazuaki; Toyoshima, Atsushi; Oe, Kazuhiro*; Miyashita, Sunao; Sch$"a$del, M.; Kaneya, Yusuke; Nagame, Yuichiro; et al.

no journal, , 

In order to determine the first ionization potential of lawrencium (Lr, $$Z = 103$$), we have developed a surface ionization type ion-source coupled to a He/CdI$$_2$$ gas-jet transport system for an Isotope Separator On-Line (ISOL) of the JAEA tandem accelerator experimental facility. We measured ionization efficiencies of short-lived Lr isotope and various short-lived lanthanide isotopes with our present system. We successfully ionized and mass-separated $$^{256}$$Lr ions for the first time and evaluated the first ionization potential of Lr based on a correlation between an effective ionization potential and ionization efficiencies of the lanthanide isotopes.

Oral presentation

Studies of ion-exchange chromatographic behavior of Rf and Db using automated rapid chemical separation apparatuses in JAEA

Tsukada, Kazuaki; Toyoshima, Atsushi; Asai, Masato; Kasamatsu, Yoshitaka*; Li, J.*; Ishii, Yasuo; Haba, Hiromitsu*; Sato, Tetsuya; Nagame, Yuichiro; Sch$"a$del, M.

no journal, , 

We will report studies of ion-exchange chromatographic behavior of element 104, rutherfordium (Rf), and element 105, dubnium (Db), in JAEA. The experiments based on an atom-at-a-time scale have been performed using an automated rapid ion-exchange separation apparatuses, AIDA and AIDA-II. We have found interesting information for the complex formations of Rf with chloride, nitrate, sulfate, and fluoride ions and Db with fluoride ions in aqueous solutions.

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