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Journal Articles

Startup of superheavy element chemistry at RIKEN

Haba, Hiromitsu*; Akiyama, Takahiro*; Kaji, Daiya*; Kikunaga, Hidetoshi*; Kuribayashi, Takahiro*; Morimoto, Koji*; Morita, Kosuke*; Oe, Kazuhiro*; Sato, Nozomi*; Shinohara, Atsushi*; et al.

European Physical Journal D, 45(1), p.81 - 86, 2007/10

 Times Cited Count:11 Percentile:49.57(Optics)

A review is given on the startup of the superheavy element (SHE) chemistry at RIKEN. A gas-jet transport system for the SHE chemistry has been coupled to the gas-filled recoil ion separator GARIS at the RIKEN Linear Accelerator. The performance of the system was appraised using $$^{206}$$Fr and $$^{245}$$Fm produced in the $$^{169}$$Tm($$^{40}$$Ar,3${it n}$)$$^{206}$$Fr and $$^{208}$$Pb($$^{40}$$Ar,3${it n}$)$$^{245}$$Fm reactions, respectively. The $$alpha$$ particles of $$^{206}$$Fr and $$^{245}$$Fm separated with GARIS and transported by the gas-jet were identified with a rotating wheel system for $$alpha$$ spectrometry under desired low background condition. The high gas-jet efficiencies over 80% were independent of the beam intensities up to 2 particle $$mu$$A. A gas-jet coupled target system for the production of SHEs was also installed on the beam line of the RIKEN K70 AVF cyclotron. The gas-jet transport of $$^{255}$$No and $$^{261}$$Rf produced in the $$^{238}$$U($$^{22}$$Ne,5${it n}$)$$^{255}$$No and $$^{248}$$Cm($$^{18}$$O,5${it n}$)$$^{261}$$Rf reactions, respectively, was conducted for the future chemical studies of $$^{265}$$Sg via the $$^{248}$$Cm($$^{22}$$Ne, 5${it n}$)$$^{265}$$Sg reaction.

Oral presentation

TOPO reversed-phase extraction behavior of rutherfordium in HCl solutions

Toyoshima, Atsushi; Kasamatsu, Yoshitaka; Tsukada, Kazuaki; Haba, Hiromitsu*; Asai, Masato; Ishii, Yasuo; Tome, Hayato; Sato, Tetsuya; Nishinaka, Ichiro; Nagame, Yuichiro; et al.

no journal, , 

no abstracts in English

Oral presentation

Anion-exchange behavior of element 105, Db, in HF/HNO$$_{3}$$ media

Kasamatsu, Yoshitaka; Toyoshima, Atsushi; Asai, Masato; Tsukada, Kazuaki; Haba, Hiromitsu*; Ishii, Yasuo; Tome, Hayato; Nishinaka, Ichiro; Akiyama, Kazuhiko*; Kikunaga, Hidetoshi*; et al.

no journal, , 

Dubnium-262 was produced in the $$^{248}$$Cm($$^{19}$$F, 5${it n}$) reaction at the JAEA tandem accelerator. Adsorption of Db on the anion-exchange resin was investigated in 0.89 M HF/0.3 M HNO$$_{3}$$ solution. The anion-exchange behavior of Nb, Ta, and Pa as homologues of Db was also examined in details in HF/HNO$$_{3}$$ solutions. From the comparison of those results, we found that the adsorption of Db on the anion-exchange resin is considerably weaker than that of Ta and is relatively similar to those of Nb and Pa in the studied conditions.

Oral presentation

Chemical behavior of element-105, Db, in mixed HF/HNO$$_{3}$$ solutions

Kasamatsu, Yoshitaka; Tome, Hayato; Toyoshima, Atsushi; Tsukada, Kazuaki; Asai, Masato; Ishii, Yasuo; Nishinaka, Ichiro; Sato, Tetsuya; Shinohara, Nobuo; Nagame, Yuichiro; et al.

no journal, , 

Anion-exchange behavior of $$^{262}$$Db (half-life ${it T$_{1/2}$}$ = 34 s) produced in the $$^{248}$$Cm($$^{19}$$F, 5${it n}$) reaction at the JAEA tandem accelerator was investigated in the mixed 0.89 M HF/0.3 M HNO$$_{3}$$ solution ([F$$^{-}$$] = 3 $$times$$ 10$$^{-3}$$ M) with the automated ion-exchange separation apparatus coupled with the detection system for alpha-spectroscopy (AIDA). Anion-exchange behavior of its lighter homologues, Nb and Ta, was also studied under the same conditions using $$^{88}$$Nb (${it T$_{1/2}$}$ = 14.3 min) and $$^{170}$$Ta (${it T$_{1/2}$}$ = 6.76 min) produced in the $$^{nat}$$Ge($$^{19}$$F, ${it xn}$) and $$^{nat}$$Gd($$^{19}$$F, ${it xn}$) reactions, respectively. It was found that the adsorption probability on the anion-exchange resin is in the order of Ta $$>$$ Nb $$sim$$ Db under the present condition.

Oral presentation

Adsorption of element-105 (Db) on anion-exchange resin in HF/HNO$$_{3}$$ solutions

Kasamatsu, Yoshitaka; Toyoshima, Atsushi; Asai, Masato; Tsukada, Kazuaki; Haba, Hiromitsu*; Ishii, Yasuo; Tome, Hayato; Nishinaka, Ichiro; Akiyama, Kazuhiko*; Kikunaga, Hidetoshi*; et al.

no journal, , 

Dubnium-262 was produced in the nuclear reaction of $$^{248}$$Cm($$^{19}$$F,5n)$$^{262}$$Db using the JAEA Tandem accelerator. The reaction products were rapidly transported to the chemistry laboratory and the anion-exchange behavior of Db in HF/HNO$$_{3}$$ media was investigated with an on-line rapid ion-exchange apparatus. Based on the comparison of the behavior of Db with that of its homologues (Nb, Ta, and Pa), the fluoride complex formation of Db was discussed.

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