This study was performed to evaluate the separation of Sr, Cs, Ba, La, Ce, and Nd using gas pressurized extraction chromatography (GPEC) with anion exchange resin for the quantitation of Neodymium. GPEC is a micro-scaled column chromatography system that provides a constant flow rate by utilizing nitrogen gas. It is overcome the disadvantages of conventional column chromatography by reducing the volume of elution solvent and shortening the analysis time. Here, we compared the conventional column chromatography and the GPEC method. The whole analysis time was decreased by nine times and radioactive wastes were reduced by five times using the GPEC system. Anion exchange resin 1-X4 (200~400 mesh size) was used. The sample was prepared at a 0.8 M nitric acid in methanol solution. The elution solvent was used at a 0.01 M nitric acid in methanol solution. Finally the eluate was analyzed by ICP-MS to determine the identification and recovery. In this case, we applied the natural isotopes of LREEs (139La, 140Ce, and 144Nd) and high activity nuclides (88Sr, 133Cs, and 138Ba) instead of radioactive isotopes for the preliminary test; as a result, unnecessary radioactive waste was not produced. The recoveries were 93.9%, 105.9%, 91.9%, 47.6%, 35.9%, and 79.9% of Sr, Cs, Ba, La, Ce, and Nd, respectively. The reproducibility of recoveries by GPEC were in the range 2.8%–10.9%.

Liquid metal extraction (LME), a pyrometallurgical recycling method, is popular owing to its negligible environmental impact. LME mainly targets rare-earth permanent magnets having several rare-earth elements. Mg is used as a solvent metal for LME because of its selective and eminent reactivity with rare-earth elements in magnets. Several studies concerning the formation of Dy-Fe intermetallic compounds and their effects on LME using Mg exist. However, methods for reducing these compounds are unavailable. Fe reacts more strongly with B than with Dy; B addition can be a reducing method for Dy-Fe intermetallic compounds owing to the formation of Fe2B, which takes Fe from Dy-Fe intermetallic compounds. The FeB alloy is an adequate additive for the decomposition of Fe2B. To accomplish the former process, Mg must convey B to a permanent magnet during the decomposition of the FeB alloy. Here, the effect of Mg on the transfer of B from FeB to permanent magnet is observed through microstructural and phase analyses. Through microstructural and phase analysis, it is confirmed that FeB is converted to Fe2B upon B transfer, owing to Mg. Finally, the transfer effect of Mg is confirmed, and the possibility of reducing Dy-Fe intermetallic compounds during LME is suggested.

A new method for chemical separation of light rare-earth elements (LREEs) using gas-pressurized extraction chromatography (GPEC) is described. GPEC is a microscale column chromatography system that features a constant flow of solvents (0.1 mL/min), which is created by pressurized nitrogen gas. The separation column with a Teflon tubing was packed with LN resin. We evaluated the separation of Ba, La, Ce, and Nd using various elution solvents. Here, we applied the natural isotopes of LREEs (La-139, Ce-140, and Nd-144) and barium (Ba-138) instead of radioactive isotopes for the preliminary test and reducing unnecessary radioactive waste. The column reproducibility of the proposed GPEC system ranged from 2.4% to 4.9% with RSDs of recoveries, and the column-to-column reproducibility ranged from 3.1% to 6.3% with RSDs of recoveries. This proposed GPEC method provides robust analysis and facilitates production of lesser chemical wastes and faster separation owing to the use of low solvent volume compared to traditional column chromatography.

자기공명영상(MRI) 장비의 조영제로 흔히 사용되는 가돌리늄(Gd)은 매우 안정된 상태로 하수처리과정에서 거의 제거되지 않고 수환경으로 유입된다고 알려져 있다. 따라서 본 연구에서는 세 가지의 공법으로 하수처리를 하는 부산 수영 하수처리장에서 채취한 하수 시료의 공정별 용존 희토류 원소의 제거율 및 수환경으로 배출되는 인위적 기원 Gd (Gdanth)의 배출량을 평가하고자 하였다. 용존 희토류 원소는 공정별 처리 단계에 따라 무거운 희토류 원소(Tb-Lu)에 비 해 가벼운 희토류 원소(La-Eu)에서 농도가 감소하는 경향을 보였다. 또한 일부 시료에서 나타난 음의(negative) Sm anomaly (<1)는 생물학적 제거 과정에서 Sm이 입자나 인산염과 흡착되어 함께 제거되었을 가능성을 시사한다. 모든 시 료에서 양의(positive) Gd anomaly (149±50, n=9)를 보였으며, 공정별로 측정된 Gd의 총 농도 중 Gdanth은 약 97% 이 상을 차지하는 것으로 나타났다. 이는 하수처리과정에서 Gdanth 이 거의 제거되지 않고 수영강 하류로 배출된다는 것을 의미한다. 일별 처리용량을 고려하여 각 공정에서 배출되는 Gdanth의 배출량은 259 mmol/day로 추정할 수 있다. 본 연 구의 결과는 하수처리장을 통해 수영만 연안으로 Gdanth이 지속적으로 배출될 것으로 예상되며, 향후 Gd의 중장기적인 관측이 필요함을 시사한다.

Rare earth elements, which are important components of motors, are in high demand and thus constantly get more expensive. This tendency is driven by the growth of the electric vehicle market, as well as environmental issues associated with rare-earth metal manufacturing. TC 298 of the ISO manages standardization in the areas of rare-earth recycling, measurement, and sustainability. Korea, a resource-poor country, is working on international standardization projects that focus on recycling and encouraging the domestic adoption of international standards. ITU-T has previously issued recommendations regarding the recycling of rare-earth metals from e-waste. ISO TC 298 expands on the previous recommendations and standards for promoting the recycling industry. Recycling-related rare earth standards and drafts covered by ISO TC 298, as well as Korea’s strategies, are reviewed and discussed in this article.

Several studies investigating the behavior and environmental distribution of rare earth elements (REEs) have been reviewed to determine the geochemical processes that may affect their concentrations and fractionation patterns in groundwater and whether these elements can be used as tracers for groundwater-rock interactions and groundwater flow paths in small catchments. Inductively coupled plasma-mass spectrometry (ICP-MS), equipped with an ultrasonic nebulizer and active-film multiplier detector, is routinely used as an analytical technique to measure REEs in groundwater, facilitating the analysis of dissolved REE geochemistry. This review focuses on the distribution of REEs in groundwater and their application as tracers for groundwater geochemistry. Our review of existing literature suggests that REEs in ice cores can be used as effective tracers for atmospheric particles, aiding the identification of source regions.

희토류(Rare Earth) 함량이 높은 TRU 생성물 중의 RE 원소를 감소시키기 위하여 RE 원소와 UCl3의 산화반응을 이용한 RE 제거 공정의 타당성을 HSC Chemistry 코드를 이용하여 검토하였다. 사용후핵연료에 포함된 TRU 원소 및 RE 원소의 조성 및 열역학적 자료를 검토하였으며, UCl3와의 산화 반응에 따른 평형 자료를 계산하여 공정 가능성을 검토하였다. 실제 파이로 프로세싱 처리를 가정한 물질수지로부터 TRU 생성물의 RE 함량이 다른 두 가지 경우에 대하여 RE 원소 제거율과 TRU 회수율을 평가하였다. TRU 생성물을 산화제인 UCl3와 반응시켰을 때 각 원소의 Gibbs free energy의 차이에 의한 선택적 산화 반응이 일어났다. 투입된 UCl3 양을 조절하여 TRU 회수율을 최대로 유지하면서도 RE 원소를 제거하여 최종생성물의 TRU/ RE 비를 증가시킬 수 있는 가능성을 계산 결과로 확인하였다. 본 연구의 결과들은 열역학적 평형 자료에 기반한 결과이므로 실제 공정에 적용하기에는 많은 차이점이 존재한다. 그러나 TRU 물질을 취급하기 어려운 환경에서 파이로프로세싱의 TRU 생성물을 고속로의 핵연료로 공급하기 위한 공정 설계에 중요한 자료로 활용될 것으로 기대된다.

Since the ISO decided to deal with rare-earth elements at the 298th Technical Committee (TC) in 2015, Korea has participated in four plenary meetings and proposed four standards as of June 2019. The status of ISO TC 298, the standards covered by the TC, and the standardization strategies of Korea are summarized. Korean delegations are actively engaged in WG2, which deals with recycling, proposing four standards for fostering the rare-earth recycling industry. However, the participation of domestic experts is still low compared with the increase in the number of working groups and the number of standards in TC 298. The aim of this article is to summarize the current status of ISO international standards related to rare-earth elements, to encourage relevant experts to participate in standardization, and to develop international standards that accurately reflect the realities of the industry.

Layered LiNi0.83Co0.11Mn0.06O2 cathode materials single- and dual-doped by the rare-earth elements Ce and Nd are successfully fabricated by using a coprecipitation-assisted solid-phase method. For comparison purposes, nondoping pristine LiNi0.83Co0.11Mn0.06O2 cathode material is also prepared using the same method. The crystal structure, morphology, and electrochemical performances are characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) mapping, and electrochemical techniques. The XRD data demonstrates that all prepared samples maintain a typical α-NaFeO2-layered structure with the R-3m space group, and that the doped samples with Ce and/or Nd have lower cation mixing than that of pristine samples without doping. The results of SEM and EDS show that doped elements are uniformly distributed in all samples. The electrochemical performances of all doped samples are better than those of pristine samples without doping. In addition, the Ce/Nd dualdoped cathode material shows the best cycling performance and the least capacity loss. At a 10 C-rate, the electrodes of Ce/Nd dual-doped cathode material exhibit good capacity retention of 72.7, 58.5, and 45.2% after 100, 200, and 300 cycles, respectively, compared to those of pristine samples without doping (24.4, 11.1, and 8.0%).

Dianthus caryophyllus (carnation) is a globally important ornamental plant. Tissue culture techniques have been used for the commercial production of carnation; however, the micropropagation of carnation has been impeded due to the occurrence of hyperhydricity during the shoot multiplication process or micropropagation stage 2. In the present study, the effects of different concentrations of rare earth elements on the reduction of hyperhydricity in micropropagated carnation were investigated. Nodal explants of D. caryophyllus ‘13827’ were cultured on Murashige and Skoog medium containing 1.0 mg·L-1 6-benzyladenine and 0.5 mg·L-1 indole-3-acetic acid with 3.0% (w/v) sucrose and 0.8% (w/v) agar (control medium). The medium was supplemented with lanthanum nitrate, La(NO3)3, cerium nitrate, Ce(NO3)3, or neodymium chloride, NdCl3 at a concentration of 0.05, 0.1, or 0.15 mM. Hyperhydricity was observed in 68.9% of the cultures produced on the control medium. The lowest percentage (42.2%) of hyperhydricity was observed in plants propagated on the medium supplemented with 0.05 mM Ce(NO3)3. Furthermore, the soluble protein concentration was higher in both the non-hyperhydric and hyperhydric plants produced on the medium supplemented with 0.05 mM Ce(NO3)3, whereas the activity of catalase, guaiacol peroxidase, and ascorbate peroxidase was lower in comparison with the media lacking Ce3+. The results of this study suggest that supplementation of the culture medium with 0.05 mM Ce(NO3)3 alleviates oxidative stress and reduces hyperhydricity in carnation during the adventitious shoot multiplication stage.

산화물 사용후핵연료에 대한 전해환원의 금속전환체를 양극으로 한 전해정련공정에는 LiCl-KCl 공융염에 우라늄 원소뿐 아 니라 초우란 원소 및 희토류 원소들이 용해되므로 우라늄을 선택적으로 회수하기 위해서는 우라늄과 다른 원소들이 음극에 전착되는 거동에 대한 연구가 필요하다. LiCl-KCl 공융염 내 희토류 원소의 농도에 따른 음극에서의 전착거동을 고찰하기 위 해 U 및 Ce를 기준으로 한 U, Ce, Y 그리고 Nd 원소들의 분리계수에 대한 연구를 수행하였다. Ce 금속을 희생 양극으로 이용 하여 정전류 정련반응을 통해 용융염 상과 전착물 상의 U, Ce, Y 그리고 Nd 원소의 농도를 분석하여 이로부터 분리계수를 얻 었으며 UCl3 농도와 CeCl3/UCl3 농도비에 따른 분리계수로부터 우라늄을 선택적으로 회수할 수 있는 조건들을 고찰하였다.

Flat panel display devices are mainly used as information display devices in the 21st century. The worldwide waste flat panel displays are expected at 2-3 million units but most of them are land-filled for want of a proper recycling technology More specifically, rare earth metals of La and Eu are used as fluorescent materials of Cold Cathode Flourscent Lamp(CCFL)s in the waste flat panel displays and they are critically vulnerable and irreplaceable strategic mineral resources. At present, most of the waste CCFLs are disposed of by land-filling and incineration and proper recovery of 80-plus tons per annum of the rare earth fluorescent materials will significantly contribute to steady supply of them. A dearth of Korean domestic research results on recovery and recycling of rare earth elements in the CCFLs prompts to initiate this status report on overseas research trends and noteworthy research results in related fields.

본 연구는 희토류비료 시비가 8년생 '후지'/M.9 사과의 미량원소 변화 및 사과의 수확 품질과 5개월간 4 저장 후 과실 품질에 미치는 영향을 알아보기 위해 수행하였다. 1년차 희토류 비료의 시비는 '후지' 사과 과실내 란타늄, 프라세오디뮴, 가돌리늄 및 네오디뮴을 축적하였다. 또한 2년차 연구에서 높은 농도의 희토류비료 시비는 보다 많은 량의 희토류 성분을 과실에 축적하여 과실내 희토류의 축적은 희토류비료의 시비량에 비례하였다. 이러한 희토류비료의 시비는 과실내의 다른 미량원소인 칼슘, 마그네슘과 칼륨의 농도에는 영향을 미치지 않았다. 희토류비료 시비에 따른 과실 품질조사에 있어, 희토류비료 0.2%의 엽면살포는 수확기 사과 과피의 붉은 색을 증가시켰으나, '후지' 과실의 과중, 경도 및 산도는 변화가 없었다. 저장 사과의 희토류비료 시비효과를 조사한 결과, 희토류비료 처리된 사과의 경우 무처리에 비해 5개월 저장 후 과실의 연화 및 적정산도의 감소를 지연시키며, 호흡률과 에틸렌발생을 감소시켰다.

경기육괴 중부 의암 편마암 복합체에 분포하는 호상편마암에 대해 저어콘 연대 및 희유원소 분석을 진행했으며 분석 결과를 토대로 경기육괴 기반암류 모암의 퇴적시기와 이들의 변성작용 및 변성시기에 대해 검토하였다. 호상편마암의 쇄설성 저어콘은 신시생대와 고원생대 경계 부근(2500-2480Ma)에서 가장 두드러 진 연령 피크를 보이며 이들과 함께 고원생대 중기 시데로스기부터 라이악스기에 해당하는 다수의 연령이 확 인되었다. 쇄설성 저어콘의 가장 젊은 연령 피크는 2070Ma로 확인되었으며 이는 호상편마암 모암의 퇴적 시 기가 적어도 2070Ma 이후였음을 의미한다. 한편, 저어콘 외연부에서 1966 ± 39Ma ~ 1918 ± 13Ma에 해당하는 변성작용 연령이 확인되었으며 오차범위, 불일치도 그리고 평균 제곱 가중편차 값을 고려할 때 1918 ± 13 Ma 가 가장 합리적인 변성작용 시기를 지시하는 것으로 보인다. 이들 저어콘 외연부의 결정화 온도는 690-740℃ 로 확인되었다. 따라서 경기육괴에서는 1880-1860Ma에 일어난 광역변성작용 이전에도 고도의 변성작용이 있 었던 것으로 판단된다.