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Publication
Featured researches published by Jeong Lee.
Korean Journal of Chemical Engineering | 2016
Min Ku Jeon; Eun-Young Choi; Sung-Wook Kim; Sang-Kwon Lee; Hyun Woo Kang; Sun Seok Hong; Jeong Lee; Jin-Mok Hur; Sang-Chae Jeon; Ju Ho Lee; Yung-Zun Cho; Do-Hee Ahn
The electrolytic reduction rate of porous UO2 pellets in a LiCl salt was investigated for various applied charges. The degree of reduction (α) value was evaluated from the ratios of cross-sectional areas of the reduced and oxide parts. An analysis of the experimental results revealed that the first-order reaction model is the best geometry function to describe the reduction reaction. An electrolytic reduction rate equation was proposed using the first-order model, although it was available in a limited region of (0≤α≤0.56). A power law based reaction rate equation was also suggested for the whole range of α, and the reaction time for a complete reduction, estimated using the power law equation, was confirmed through the experimental results. Changes in the Li-Li2O concentration around the reduced pellets for various applied charges were also measured, which increased up to 23 wt% with increasing α.
Science and Technology of Nuclear Installations | 2017
Eun-Young Choi; Jeong Lee; Dong Hyun Heo; Jin-Mok Hur
We demonstrated that the metallic product obtained after electrolytic reduction (also called oxide reduction (OR)) can be simply separated from a stainless steel wire mesh cathode basket only by using a salt drain. First, the OR run of a simulated oxide fuel (0.6 kg/batch) was conducted in a molten Li2O–LiCl salt electrolyte at 650°C. The simulated oxide fuel of the porous cylindrical pellets was used as a cathode by loading a stainless steel wire mesh cathode basket. Platinum was employed as an anode. After the electrolysis, the residual salt of the cathode basket containing the reduction product was drained by placing it at gas phase above the molten salt using a holder. Then, at a room temperature, the complete separation of the reduction product from the cathode basket was achieved by inverting it without damaging or deforming the basket. Finally, the emptied cathode basket obtained after the separation was reused for the second OR run by loading a fresh simulated oxide fuel. We also succeeded in the separation of the metallic product from the reused cathode basket for the second OR run.
Journal of The Korean Chemical Society | 2015
Eun-Young Choi; Jeong Lee; Min Ku Jeon; Sang-Kwon Lee; Sung-Wook Kim; Sang-Chae Jeon; Ju Ho Lee; Jin-Mok Hur
The platinum anode for the electrolytic reduction process is generally surrounded by a nonporous ceramic shroud with an open bottom to offer a path for O2 gas produced on the anode surface and prevent the corrosion of the electrolytic reducer. However, the O 2- ions generated from the cathode are transported only in a limited fashion through the open bottom of the anode shroud because the nonporous shroud hinders the transport of the O 2- ions to the anode surface, which leads to a decrease in the current density and an increase in the operation time of the process. In the present study, we demonstrate the electrolytic reduction of 1 kg-uranium oxide (UO2) using the porous shroud to investigate its long-term stability. The UO2 with the size of 1~4 mm and the den-
Science and Technology of Nuclear Installations | 2017
Eun-Young Choi; Jeong Lee; Dong Hyun Heo; Jin-Mok Hur
Quantitative analysis by in situ measurement of oxygen gas evolved from an anode was employed to monitor the progress of electrolytic reduction of simulated oxide fuel in a molten Li2O–LiCl salt. The electrolytic reduction of 0.6 kg of simulated oxide fuel was performed in 5 kg of 1.5 wt.% Li2O–LiCl molten salt at 650°C. Porous cylindrical pellets of simulated oxide fuel were used as the cathode by loading a stainless steel wire mesh cathode basket. A platinum plate was employed as the anode. The oxygen gas evolved from the anode was exhausted to the instrumentation for in situ measurement during electrolytic reduction. The instrumentation consisted of a mass flow controller, pump, wet gas meter, and oxygen gas sensor. The oxygen gas was successfully measured using the instrumentation in real time. The measured volume of the oxygen gas was comparable to the theoretically calculated volume generated by the charge applied to the simulated oxide fuel.
Journal of The Korean Chemical Society | 2015
Jeong Lee; Sung-Wook Kim; Sang-Kwon Lee; Jin-Mok Hur; Eun-Young Choi
Experiments using a metal oxide of a non-nuclear material as a fuel are very useful to develop a new electrolytic reducer for pyroprocessing. In this study, the titanium oxides (TiO and ) were selected and investigated as the non-nuclear fuel for the electrolytic reduction. The immersion tests of TiO and in a molten 1.0 wt.% -LiCl salt revealed that they have solubility of 156 and 2100 ppm, respectively. Then, the Ti metals were successfully produced after the separate electrolytic reduction of TiO and in a molten 1.0 wt.% -LiCl salt. However, Ti was detected on the platinum anode used for the electrolytic reduction of unlike TiO due to the dissolution of into the salt.
Journal of Nuclear Materials | 2017
Eun-Young Choi; Jeong Lee; Dong Hyun Heo; Sang Kwon Lee; Min Ku Jeon; Sun Seok Hong; Sung-Wook Kim; Hyun Woo Kang; Sang-Chae Jeon; Jin-Mok Hur
Journal of Nuclear Materials | 2017
Eun-Young Choi; Min Ku Jeon; Jeong Lee; Sung-Wook Kim; Sang Kwon Lee; Sung-Jai Lee; Dong Hyun Heo; Hyun Woo Kang; Sang-Chae Jeon; Jin-Mok Hur
Electrochemistry Communications | 2016
Min Woo Lee; Eun-Young Choi; Sang Chae Jeon; Jeong Lee; Sung Bin Park; Seungwoo Paek; Michael F. Simpson; Sang Mun Jeong
Journal of Nuclear Materials | 2016
Eun-Young Choi; Jeong Lee; Sung-Jai Lee; Sung-Wook Kim; Sang-Chae Jeon; Soo Haeng Cho; Seung Chul Oh; Min Ku Jeon; Sang Kwon Lee; Hyun Woo Kang; Jin-Mok Hur
Journal of Nuclear Materials | 2017
Eun-Young Choi; Jeong Lee