Behavior of U-Zr Alloy Containing Simulated Fission Products during Anodic Dissolution in Molten Chloride Electrolyte

被引:23
作者
Iizuka, Masatoshi [1 ]
Omori, Takashi
Tsukada, Takeshi [1 ]
机构
[1] Cent Res Inst Elect Power Ind, Tokyo 2018511, Japan
关键词
metal fuel; pyrometallurgical reprocessing; molten salt; electrorefining; anodic dissolution; uranium; zirconium; noble metal; remaining ratio; decontamination factor; URANIUM; PLUTONIUM;
D O I
10.3327/jnst.47.244
中图分类号
TL [原子能技术]; O571 [原子核物理学];
学科分类号
0827 ; 082701 ;
摘要
To investigate the distribution of fission product elements in the electrorefining of spent metallic fuel, electrorefining tests were carried out using U-Zr alloy containing simulated fission products. An intermediate region was found between undissolved alloy and Zr-rich regions formed by the anodic dissolution of uranium. The composition of this region determined by wavelength-dispersive X-ray spectroscopy (WDS) analysis corresponded to that of delta-phase (63-78 at% Zr) in the U-Zr binary phase diagram. This region is expected to form in the course of the anodic dissolution sequence that begins from an undissolved U-Zr alloy and ends with a Zr-rich region. From the results of chemical and WDS analyses of anode residue samples, it was predicted that noble metals would stay in the anode residue as long as zirconium remains even after most of the uranium in the alloy was dissolved. Analytical results indicated no large difference between the noble metal behavior in simulated material and in irradiated EBR-II driver fuels. Decontamination factors of uranium from molybdenum and palladium were defined as ratios between their concentrations in the initial alloy loaded into an anode and those in cathode products, and evaluated from the analytical results. Although there was some scattering of data, decontamination factors of around 70 for molybdenum and 10 for palladium would be expected.
引用
收藏
页码:244 / 254
页数:11
相关论文
共 11 条
  • [1] Modeling of anodic dissolution of U-Pu-Zr ternary alloy in the molten LiCl-KCl electrolyte
    Iizuka, M
    Kinoshita, K
    Koyama, T
    [J]. JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2005, 66 (2-4) : 427 - 432
  • [2] Behavior of plutonium and americium at liquid cadmium cathode in molten LiCl-KCl electrolyte
    Iizuka, M
    Uozumi, K
    Inoue, T
    Iwai, T
    Shirai, O
    Arai, Y
    [J]. JOURNAL OF NUCLEAR MATERIALS, 2001, 299 (01) : 32 - 42
  • [3] Development of an Innovative Electrorefiner for High Uranium Recovery Rate from Metal Fast Reactor Fuels
    Iizuka, Masatoshi
    Uozumi, Koichi
    Ogata, Takanari
    Omori, Takashi
    Tsukada, Takeshi
    [J]. JOURNAL OF NUCLEAR SCIENCE AND TECHNOLOGY, 2009, 46 (07) : 699 - 716
  • [4] INOUE T, 1999, P INT C FUT NUCL SYS
  • [5] Separation behaviors of actinides from rare-earths in molten salt electrorefining using saturated liquid cadmium cathode
    Kato, Tetsuya
    Inoue, Tadashi
    Iwai, Takashi
    Arai, Yasuo
    [J]. JOURNAL OF NUCLEAR MATERIALS, 2006, 357 (1-3) : 105 - 114
  • [6] Koyama T, 1997, J NUCL SCI TECHNOL, V34, P384, DOI [10.3327/jnst.34.384, 10.1080/18811248.1997.9733678]
  • [7] Thermodynamic assessment of the Fe-U, U-Zr and Fe-U-Zr systems
    Kurata, M
    Ogata, T
    Nakamura, K
    Ogawa, T
    [J]. JOURNAL OF ALLOYS AND COMPOUNDS, 1998, 271 : 636 - 640
  • [8] Li SX, 2005, PROC GLOB 2005
  • [9] OGATA T, 2007, P GLOB 2007 BOIS ID
  • [10] URANIUM TRANSPORT TO SOLID ELECTRODES IN PYROCHEMICAL REPROCESSING OF NUCLEAR-FUEL
    TOMCZUK, Z
    ACKERMAN, JP
    WOLSON, RD
    MILLER, WE
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (12) : 3523 - 3528