• Title/Summary/Keyword: 희토류 침전물

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Characteristic of Oxidation Reaction of Lanthanide Chlorides in Oxygen-Eutectic Salt Bubble Column (산소-공융염 기포탑에서 희토류염화물의 산화반응 특성)

  • Cho, Yung-Zun;Yang, Hee-Chul;Lee, Han-Soo;Kim, In-Tae
    • Korean Chemical Engineering Research
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    • v.47 no.4
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    • pp.465-469
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    • 2009
  • Characteristics of oxidation reaction of four lanthanide chlorides(Ce, Nd, Pr and $EuCl_3$) in a oxygen-eutectic(LiCl-KCl) salt bubble column was investigated. From the results obtained from the thermochemical calculations by HSC chemistry software, the most stable lanthanide compounds in the oxygen-used rare earth chlorides system were oxychlorides(EuOCl, NdOCl, PrOCl) and oxides($CeO_2$, $PrO_2$), which coincide well with results of the Gibbs free energy of the reaction. In this study, similar to the thermochemical results, regardless of the sparging time and molten salt temperature, oxychlorides for Eu, Nd and Pr and oxides for Ce and Pr were formed as a precipitant by a reaction with oxygen. The structure of the rare earth precipitates was divided into two shapes : small cubic(oxide) and large tetragonal (oxychloride) structures. The conversion efficiencies of the lanthanide elements to their molten salt-insoluble precipitates(or compound) were increased with the sparging time and temperature, and Ce showed the best reactivity. In the conditions of $650^{\circ}C$ of the molten salt temperature and 420 min of the sparging time, the conversion efficiencies were over 99% for all the investigated lanthanide chlorides.

A study on recovery of rare earth oxide powders from waste NiMH batteries (폐니켈수소전지로부터 희토류 산화물 분말의 회수에 대한 연구)

  • Ahn, Nak-Kyoon;Kim, Dae-Weon;Shim, Hyun-Woo;Park, Jae-Hun;Park, Jeung-Jin
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.28 no.2
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    • pp.85-90
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    • 2018
  • For the recovering rare earths in the spent nickel-metal hydride batteries, 10 M NaOH is added to the solution leached with sulfuric acid. The rare earth powders were precipitated at rate of 98 % at the condition of pH 2.0 or less. The recovered rare earth complex precipitate increased the leaching rate to nitric acid by heat treatment at $800^{\circ}C$ for 4 hours. Subsequently secondary precipitation was performed by adding oxalic acid to the solution in which the rare earth complex precipitate was dissolved. The re-precipitated rare earth powders were converted into oxide form through heat treatment at $800^{\circ}C$ for 4 hours with purity of 99.5 %.

Recovery of Residual LiCl-KCl Eutectic Salts in Radioactive Rare Earth Precipitates (방사성 희토류 침전물내 잔류하는 LiCl-KCl 공융염의 회수)

  • Eun, Hee-Chul;Yang, Hee-Chul;Kim, In-Tae;Lee, Han-Soo;Cho, Yung-Zun
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.8 no.4
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    • pp.303-309
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    • 2010
  • For the pyrochemical process of spent nuclear fuels, recovery of LiCl-KCl eutectic salts is needed to reduce radioactive waste volume and to recycle resource materials. This paper is about recovery of residual LiCl-KCl eutectic salts in radioactive rare earth precipitates (rare earth oxychlorides or oxides) by using a vacuum distillation process. In the vacuum distillation test apparatus, the salts in the rare earth precipitates were vaporized and were separated effectively. The separated salts were deposited in three positions of the vacuum distillation test apparatus or were collected in the filter and it is difficult to recover them. To resolve the problem, a vacuum distillation and condensation system, which is subjected to the force of a temperature gradient at a reduced pressure, was developed. In a preliminary test of the vacuum distillation/condensation recovery system, it was confirmed that it was possible to condense the vaporized salts only in the salt collector and to recover the condensed salts from the salt collector easily.

탄산수와 탄산침전물 및 침전잔류물에서의 희토류원소(REEs)의 분배 및 거동 특성

  • 최현수;고용권;윤성택;배대석
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2004.04a
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    • pp.384-387
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    • 2004
  • 강원도 지역 탄산수에 대해 혼합에 의한 용존 희유원소의 거동특성 및 탄산염 침전물 형성에 따른 REE 분별작용을 살펴보았다. 탄산수들은 화학적으로 $Na-HCO_3형,\; Ca-Na-HCO_3형\; 및\; Ca-HCO_3$형으로 구분되며, 동위원소조성도 유형에 따라 명확히 구분되는 특징을 보인다. 지화학 및 동위원소 자료의 해석 결과, $Na-HCO_$형 탄산수는 지하심부에서 심부 기원 $CO_2$의 공급에 의해 형성된 반면, 다른 두 유형의 탄산수들은 $Na-HCO_$ 형 탄산수와 천부지하수 간의 혼합에 의해 생성되었음을 지시하였다. 탄산수 내 용존 REE 함량은 물 유형에 따라 변화하지만, ∑REE 함량은 TDS, pH, alkalinity, $\delta^{18}O$$\delta^{18}O$ 및 tritium 함량과 좋은 상관성을 보여주어, 천부 지하수와의 혼합된 특징을 나타내었다. Na-HCO$_3$형 탄산수의 용존 REE 패턴은 강한 HREE 부화를 보여주어 이른바 'S-shape'을 나타내는 반면, $Na-HCO_$ 형은 분산되어 있으며 LREE 부화를 보여주었다. $Ca-Na-HCO_3$형은 약한 HREE 분화 패턴을 보여주었다. 탄산수로부터 침전된 침전물과 침전물을 제거한 잔류물의 REE 패턴은 원 탄산수와 거의 유사한 형태를 보여주어, 탄산염 침전물과 잔류물 간의 REE 분별작용은 일어나지 않았음을 나타낸다.지 않았음을 나타낸다.

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