Electrochemical properties of uranyl ion and some other metal ions in ionic liquids

I&EC 168

Noriko Asanuma, nasanuma@keyaki.cc.u-tokai.ac.jp1, Masayuki Harada, mharada@nr.titech.ac.jp2, Masanobu Nogami, nogami@iri.or.jp3, Yoshiyuki Yasuike, yyasuike@iri.or.jp3, Kazunori Suzuki, k-suzuki@iri.or.jp3, and Yasuhisa Ikeda, yikeda@nr.titech.ac.jp2. (1) Department of Energy Science and Engineering, School of Engineering, Tokai University, 1117 Kitakaname, Hiratsuka-shi, Kanagawa, 259-1292, Japan, (2) Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology, 2-12-1-N1-34 O-okayama, Meguro-ku, Tokyo, 152-8550, Japan, (3) Nuclear Chemistry and Chemical Engineering Center, Institute of Research and Innovation, 1201 Takada, Kashiwa-shi, Chiba, 277-0861, Japan
We have proposed a new reprocessing process by using ionic liquids (ILs) instead of molten salts of alkali chlorides in pyrochemical reprocessing process, as shown in Fig. 1. In order to evaluate applicability of ILs as media of pyro-process, electrochemical properties of uranyl ion and some other metal ions in ILs have been examined by using cyclic voltammetry. A reversible redox couple was observed in a cyclic voltammogram of 1-butyl-3-methylimidazolium chloride containing uranyl chloride. It was supposed that the reaction corresponds to the redox couple of U(VI)/U(V). In 1-butyl-3-methylimidazolium nonafluorobutanesulfonate (BMINfO), irreversible reduction peaks and a sharp oxidation peak were observed in the voltammogram. The reduction peaks should be assigned to multi step reduction of U(VI) to U(IV) via U(V) and/or direct reduction of U(VI) to U(IV). As a result, the deposits including UO2 were found to be produced on a carbon electrode by electrochemical reduction of U(VI) in BMINfO.