Jong-Il Yun
KAIST 방사화학 및 레이저 분광 연구실 · 화학
이 교수의 연구실은 주로 고준위 고체 폐기물의 안정적 처리를 위한 유리화 과정에서의 실시간 다성분 분석 기술을 핵심으로 연구하고 있습니다. 레이저 유도 분광법(LIBS)과 시간해상 분광법(TRLFS), X선 흡수 부동맥 분석(EXAFS)을 활용해 우라늄, 플루토늄, europium 등의 금속 이온이 수용액 및 고체 상에서 어떻게 복합체를 형성하는지 기초 화학적 거동을 규명하고 있습니다. 특히, 방사성 폐기물의 안정성 평가 및 환경 중 금속 이온의 이동성 예측에 기여할 수 있는 복합체 구조와 역학을 연구하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
The chemical behavior of ternary Ca-UO2-CO3 complexes was investigated by using time-resolved laser fluorescence spectroscopy (TRLFS) in combination with EDTA complexation at pH 7-9. A novel TRLFS revealed two distinct fluorescence lifetimes of 12.7 ± 0.2 ns and 29.2 ± 0.4 ns for uranyl complexes which were formed increasingly dependent upon the calcium ion concentration, even though nearly indistinguishable fluorescence peak shapes and positions were measured for both Ca-UO2-CO3 complexes. For
Laser-induced breakdown spectroscopy (LIBS) was applied to selectively analyze the aqueous suspension of Eu 2 O 3 (s) particles in the presence of the Eu 3+ aquo ion. A plasma was generated by focusing a pulsed Nd:YAG laser beam (λ = 532 nm) into the sample. The light emission from the plasma was detected by a spectrograph equipped with a gated intensified charge-coupled device (ICCD) in the wavelength range of 275–525 nm. The atomic emission intensity of the Eu 2 O 3 (s) suspension was about tw
The paper presents the application of laser-induced breakdown spectroscopy (LIBS) for the on-line multielement analyses of glass melts in a vitrification process of high level liquid waste (HLLW). The third harmonic pulse of an Nd:YAG laser is used for the generation of plasma on the molten glass surface and the plasma emission is monitored by an echelle spectrometer with an intensified charge-coupled device (ICCD), which simultaneously covers the wavelength range from 200 to 780 nm. Twelve diff
Laser-induced breakdown spectroscopy (LIBS) is presented for the on-line multielement analysis of molten radioactive glass at a simulated vitrification process of high level liquid waste (HLLW). A plasma plume is produced by focusing the third harmonic of a Nd: YAG laser (λ = 355 nm) onto the glass melt surface at 1200 °C, and the plasma emission is guided via optical fiber and is characterized by an echelle spectrometer for the spectral range from 200 to 780 nm with a resolution of ±0.01 nm. Co
Abstract The formation of ternary Mg-UO 2 -CO 3 complexes under weakly alkaline pH conditions was investigated by time-resolved laser fluorescence spectroscopy (TRLFS) and extended X-ray absorption fine structure (EXAFS) and compared to Ca-UO 2 -CO 3 complexes. The presence of two different Mg-UO 2 -CO 3 complexes was identified by means of two distinct fluorescence lifetimes of 17±2 ns and 51±2 ns derived from the multi-exponential decay of the fluorescence signal. Slope analysis in terms of fl
The hydrolysis of tetravalent plutonium in 0.5 M HCl/NaCl has been investigated by a combination of spectroscopy and redox potential measurements in the concentration range from 10 -5 to 4×10 -4 M and at pH c 0.3–2.1. Redox potentials were both measured and calculated from the plutonium oxidation state distributions using well-known equilibrium constants for the redox reactions of plutonium. The plutonium oxidation states in solution were quantified by spectroscopy. The p e values calculated fro
Electrochemical and spectroscopic properties of Tb(III) in molten LiCl–KCl eutectic at high temperature were investigated by cyclic voltammetry and time-resolved laser-induced fluorescence spectroscopy (TRLFS). The diffusion coefficient of Tb(III) and the formal standard potential of Tb(III)/Tb0 were determined to be 2.06 ± 0.4 × 10− 5 cm2 s− 1 and − 2.83 ± 0.03 V vs. Cl2/Cl− at 887 K, respectively. Additionally, visible fluorescence of Tb(III) due to the electronic transitions from 5D3 and 5D4
The ternary complexation of calcium uranyl tricarbonate species, CaUO<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub><sup>2-</sup> and Ca<sub>2</sub>UO<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub>(aq), which are the predominant U(vi) complexes in groundwater and seawater, was investigated at variable temperatures from 10 to 70 °C. Time-resolved laser fluorescence spectroscopy (TRLFS), calcium ion-selective electrode potentiometry, and ultraviolet/visible (UV/Vis) absorption spectroscopy were complementarily