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Electrochemical oxidation of nobelium

Toyoshima, Atsushi; Kasamatsu, Yoshitaka; Tsukada, Kazuaki  ; Kitatsuji, Yoshihiro  ; Haba, Hiromitsu*; Ishii, Yasuo; Tome, Hayato; Asai, Masato  ; Akiyama, Kazuhiko*; Oe, Kazuhiro*; Sato, Wataru*; Shinohara, Atsushi*; Nagame, Yuichiro 

Electrochemical oxidation of nobelium (No) produced in the $$^{248}$$Cm($$^{12}$$C, 5n)$$^{255}$$No reaction was studied using a new electrochemistry apparatus combined with chromatographic separation technique. Chromatographic behaviour of $$^{255}$$No in 0.1 M $$alpha$$-hydroxyisobutyric acid ($$alpha$$-HIB) on the electrode surface was measured with verifying the difference in behaviour between divalent $$^{81}$$Sr$$^{2+}$$ and trivalent $$^{162}$$Yb$$^{3+}$$ ions. Independently of the applied potentials, Yb$$^{3+}$$ was eluted in the 0.1 M $$alpha$$-HIB while Sr$$^{2+}$$ was adsorbed on the electrode. At the low potential of 0.2 V, $$^{255}$$No was adsorbed on the electrode, indicating that No is bound in the most stable divalent state. On the other hand, at the higher potential of 1.2 V, $$^{255}$$No was unambiguously detected in the 0.1 M $$alpha$$-HIB, showing that No exists as a trivalent ion. These results demonstrate that the electrochemical oxidation of No$$^{2+}$$ to No$$^{3+}$$ is successfully performed.

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