• 제목/요약/키워드: determination of lanthanum

검색결과 10건 처리시간 0.028초

Ion Chromatography-Inductively Coupled Plasma-Mass Spectrometry에 의한 $U_3Si/Al$ 사용후핵연료 중 La의 분리 및 정량 (Determination of La in $U_3Si/Al$ Spent Nuclear Fuel by Ion Chromatography-Inductively Coupled Plasma-Mass Spectrometry)

  • 한선호;최광순;김정석;전영신;박양순;지광용;김원호
    • 분석과학
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    • 제13권5호
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    • pp.601-607
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    • 2000
  • 란탄은 사용후핵연료의 연소도 지표원소들 중 하나로써 이용되고 있다. $U_3Si/Al$ 사용후핵연료는 다량의 U과 Al 속에 미량의 La이 포함되어 있어 정량시 매질의 영향을 줄이기 위해 화학적 분리가 요구된다. La의 분리 및 측정을 위해 IC-ICP-MS를 이용하였으며, 우선 방사성 시료를 취급하기 위하여 유도결합 플라스마 질량분석기의 플라스마 부분 및 분리관을 방사선 차폐 글로브박스 내에 설치하였다. CG10 분리관과 ${\alpha}$-HiBA 용리액을 사용하여 U, Al, La 및 몇 가지 핵분열생성물 (Sr, Zr, Y, Mo, Ru, Pd, Rh, Cs, Ba, Ce, Pr, Nd, Sm, Eu 및 Cd)의 머무름 거동을 살펴보았다. 0.2 M ${\alpha}$-HiBA 용리액에서 U과 Al이 초기에 용출되므로 분리관과 ICP-MS의 시료분무기 사이에 3방향 밸브를 연결하여 다량의 U과 Al이 ICP-MS로 유입되지 않도록 하므로써 매질의 영향을 줄일 수 있었다. 이 조건에서 La은 약 12분 정도에 분리 및 측정이 가능하였으며, $1-10{\mu}g/L$ (ppb)의 농도범위가 측청에 적합하였고 시료양을 $200{\mu}L$ 취할 경우 La의 검출한계는 $0.25{\mu}g/L$이었다.

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Sub-Micro Molar Monitoring of La3+ by a Novel Lanthanum PVC-Based Membrane Sensor Based on 3-Hydroxy-N'-(pyridin-2-ylmethylene)-2-naphthohydrazide

  • Ganjali, Mohammad Reza;Norouzi, Parviz;Yousefian, Nasrin;Faridbod, Farnoush;Adib, Mehdi
    • Bulletin of the Korean Chemical Society
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    • 제27권10호
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    • pp.1581-1586
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    • 2006
  • A La (III) ion-selective membrane sensor has been fabricated from poly vinyl chloride (PVC) matrix membrane, containing 3-hydroxy-N'-(pyridin-2-ylmethylene)-2-naphthohydrazide (HPMN) as a neutral carrier, potassium tetrakis (p-chlorophenyl) borate (KTpClPB) as an anionic excluder and ortho-nitrophenyloctyl ether (NPOE) as a plasticizing solvent mediator. The effects of membrane composition and pH as well as the influence of the anionic additive on the response properties were investigated. The sensor with 30% PVC, 62% solvent mediator, 6% ionophore and 2% anionic additive, shows the best potentiometric response characteristics. It displays a Nernstian behavior (19.2 mV per decade) across the range of $1.0{\times}10^{-2}-1.0{\times}10^{-7}$ M. The detection limit of the electrode is $7.0{\times}10^{-8}$ M ($\sim$10 ng/mL) and the response time is 15 s from $1.0{\times}10^{-2}$ up to $1.0{\times}10^{-4} $M and 30 s in the range of $1.0 {\times}10^{-5}-1.0{\times}10^{-7}$ M. The sensor can be used in the pH values of 3.0-9.0 for about seven weeks. The membrane sensor was used as an indicator electrode in the potentiometric titration of lanthanum ions with EDTA. It was successfully applied to the lanthanum determination in some mouth wash preparations.

X線螢光分析에 依한 珪酸鹽鑛物의 分析 (The X-Ray Fluorescent Spectrographic Analysis of Silicate Minerals)

  • 김찬국;상기남;김황암
    • 대한화학회지
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    • 제13권1호
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    • pp.49-55
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    • 1969
  • 螢光X線을 利用하여 珪酸鹽鑛物中의 主成分인 $SiO_2$, $Al_2O_3$, $Fe_2O_3$, CaO, MgO 및 $K_2O$를 迅速히 分析할 目的으로 試料의 處理 測定 및 各條件에 對하여 檢討하였다. 試料를 Lithium Tetraborate로 용융하여 300Mesh 以上의 微粉末로 한後 40,000Lb의 壓力으로 成型하여 Tungsten과 Chromium 對陰極의 X-線管과 LiF, EDDT, ADP의 分光結晶을 使用하여 測定하였다. 各成分에 對한 檢量曲線은 Matrix Effect를 고려하여 N.B.S 및 International Rock Standard를 選定 使用하였고 Lanthanum Oxide 및 Binder로서 Borie Acid를 첨가하여 얻었다. 各成分에 對하여 本法의 再現性 및 誤差를 檢討하기를 爲하여 I.R.S T-1을 使用하여 測定한 結果 0.47($SiO_2$), 0.85($Al_2O_3$), 0.05($Fe_2O_3$), 0.07(caO), 0.02($K_2O$), 0.13(MgO)의 標準偏差를 얻었다. 또한 化學分析植에 對한 偏差를 求하고져 Clay, Kaoline, Alunite, Wallastonite 및 Zeolite 等의 珪酸鹽鑛物을 選定하여 化學分析 및 本法에 依한 分析結果를 비교하였다.

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중성자 방사화에 의한 시료중의 크롬, 철, 란탄, 스칸듐 및 아연의 동시정량 (A Simultaneous Determination of Chromium, Iron, Lanthanum, Scandium and Zinc in River Water by Neutron Activation)

  • 이인종;김시중;이철
    • 대한화학회지
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    • 제21권6호
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    • pp.427-433
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    • 1977
  • 강물 시료속에 함유된 크롬, 철, 란탄, 스칸듐 및 아연의 함량을 방사화 분석법으로 동시정량하는 방법을 확립하였다. 10ml의 강물 시료를 사전 처리없이 석영관 속에 밀봉한 다음 열중성자속이 $1{\times}10^{13}n{\cdot}cm^{-2}{\cdot}sec^{-1}$인 곳에서 1주일간 조사하였다. 약 2일간 냉각시킨 후 시료 속에든 원소들을 0.1M 옥신의 클로로포름용액으로 여러 pH에서 연속적으로 추출하였다. 감마선 분광분석을 위하여 유기층을 800챈널 펄스높이 분석기에 연결된 $″3\;{\times}\;3″$ NaI (T1) 검출기로 계측하였다. 본분석법에 의하여 대부분의 강물 시료에 ppb 농도범위로 함유된 이들 원소들의 정량이 가능하였다. 추적자를 써서 이들 원소의 정량적 분리를 위한 연구를 수행하였다.

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Preconcentration and Determination of Trace Cd(II) and Pb(II) in a Water Sample by Organic Precipitate Flotation with 8-Hydroxyquinoline

  • 김영상;김기찬;이치우
    • Bulletin of the Korean Chemical Society
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    • 제20권4호
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    • pp.431-435
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    • 1999
  • An organic precipitate flotation of Cd(Ⅱ) and Pb(Ⅱ) was investigated by the coprecipitation with lanthanum 8-hydroxyquinolinate. Trace amounts of Cd(Ⅱ) and Pb(Ⅱ) with a significantly large amount of La(Ⅲ) were simultaneously precipitated in a 1,000 mL sample solution with the ethanolic 8-hydroxyquinoline solution. The pH was adjusted to 9.0 with 2 M ammonia solution. The precipitates were floated with the aid of tiny nitrogen bubbles and supported by the stable foam layer of sodium lauryl sulfate. The floats were collected on the fritted glass filter by a suction. The material collected was dissolved with 5.0 mL of ethanol and 1.5 mL of concentrated nitric acid, and then diluted to 25.0 mL with a deionized water. The analytes were determined by a flame atomic absorption spectrophotometry. The recoveries of the analytes spiked in the sample were 94.8% for Pb(Ⅱ) and 92.0% for Cd(Ⅱ). This flotation technique is simple and rapid, and also applicable to the determination of trace Cd(Ⅱ) and Pb(Ⅱ) at lew ppb levels.

Simultaneous Preconcentration and Determination of Trace Elements in Water Samples by Coprecipitation-Flotation with Lanthanum Hydroxide $[La(OH)_3]$

  • 김영상;김기찬
    • Bulletin of the Korean Chemical Society
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    • 제16권7호
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    • pp.582-588
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    • 1995
  • The preconcentration and determination of trace Cd(Ⅱ), Cu(Ⅱ), Pb(Ⅱ), Mn(Ⅱ) and Zn(Ⅱ) in water samples were studied by the precipitate flotation using La(OH)3 as a coprecipitant. The analytes were quantitatively coprecipitated by adding 3.0 mL of 0.1 M La(Ⅲ) solution in a 1,000 mL water sample and adjusting the pH to 9.5 with NaOH solution. After the addition of the 1:8 mixed surfactant solution of each 0.1% sodium oleate and sodium lauryl sulfate, the solution was stirred with a magnetic stirrer for 10 minutes. The precipitates were floated to the surface by bubbling with nitrogen gas and collected in a small sampling bottle. The precipitates were dissolved in nitric acid and then the solutions were diluted to 25.00 mL with a deionized water. The analytes were determined by flame atomic absorption spectrometry. This procedure was applied to the waste water analysis. This technique was simple, convenient and especially rapid for the analysis of a large volume of sample. And also, from the recoveries of better than 92% which were obtained from real samples, this method could be judged to be applicable to the preconcentration and quantitative determination of trace elements in water samples.

수소화물발생 유도결합플라즈마 원자방출분광법에 의한 머리카락 시료 중 미량의 Se와 Bi의 분석에 관한 연구 (A study on the Determination of Trace Se and Bi in the Scalp Hair by Hydride Generation- Inductively Coupled Plasma Atomic Emission Spectrometry)

  • 최범석;이동기
    • 분석과학
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    • 제9권1호
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    • pp.26-34
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    • 1996
  • 수소화물 발생장치를 사용한 유도결합플라즈마 원자방출분광법(ICP-AES)으로 머리카락 시료 중에 함유된 미량의 Se와 Bi의 분석에 관해 연구하였다. 기체상태의 수소화물 측정시 ICP의 최적 측정조건은 시료운반기체의 유속은 0.6~0.8L/min, 관측위치는 유도코일로부터 6mm 높이였다. 수소화물 생성효율이 최대를 나타내는 염산농도는 $NaBH_4$와 NaOH를 각각 2.5% 사용할 때 1.5M 이상일 때였으며, 2.5% $NaBH_4$와 0.1% $NaBH_4$를 사용할 때는 약 O.5M 이상일 때였다. 분석과정에서 Cu와 Ni 같은 전이금속으로부터의 심한 방해영향이 관찰되었고, lanthanum hydroxide로 Se와 Bi를 공침시켜 방해영향을 제거하였다.

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Determination of Individual Lanthanide Elements by Neutron Activation Using a New Comparator Technique

  • Lee, Chul;Yim, Yung-Chang;Chung, Koo-Soon
    • Nuclear Engineering and Technology
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    • 제4권2호
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    • pp.83-89
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    • 1972
  • 중성자 선속 모니타로써 단 수명 방사성 동위원소인 $^{56}$ Mn을 이용한 새로운 비교법을 사용하여 모나자이트중에 함유된 개개 희토류원소의 함량을 중성자 방사화법으로 정량하였다. 전회토류원소를 군으로 분리하고 난 다음 중성자 조사를 하였으며 개개 희토류 원소는 양이온 교환수지통을 통하여 알파 하이드록씨 부탈산으로 구배 용출시킴으로서 분리하였다. 루데슘으로 부터 란타늄까지 14개의 희토류원소를 정량하였다.

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Synthesis of a New Hexadendates Schiff's Base and Its Application in the Fabrication of a Highly Selective Mercury(II) Sensor

  • Ganjali, M.R.;Norouzi, P.;Alizadeh, T.;Salavati-Niasari, M.
    • Bulletin of the Korean Chemical Society
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    • 제28권1호
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    • pp.68-72
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    • 2007
  • A new PVC membrane potentiometric sensor that is highly selective to Hg2+ ions was prepared, using bis(2-hydroxybenzophenone) butane-2,3-dihydrazone (HBBD) as an excellent hexadendates neutral carrier. The sensor works satisfactorily in the concentration range of 1.0 × 10-6 to 1.0 × 10-1 mol L-1 (detection limit 4 × 10-7 mol L-1) with a Nernstian slope of 29.7 mV per decade. This electrode showed a fast response time (~8 s) and was used for at least 12 weeks without any divergence. The sensor exhibits good Hg2+ selectivity for a broad range of common alkali, alkaline earth, transition and heavy metal ions (lithium, sodium, potassium, magnesium, calcium, copper, nickel, cobalt, zinc, cadmium, lead and lanthanum). The electrode response is pH independent in the range of 1.5-4.0. Furthermore, the developed sensor was successfully used as an indicator electrode in the potentiometric titration of mercury ions with potassium iodide and the direct determination of mercury in some binary and ternary mixtures.

Extraction of La(III) by a nonionic microemulsion containing D2EHPA in hollow fiber contactor

  • Ou, Huilin;Gong, Fuzhong;Tang, Yanxia;Luo, Yan;Liu, Liheng
    • Membrane and Water Treatment
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    • 제12권2호
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    • pp.75-82
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    • 2021
  • This study aimed to prepare a W/O nonionic microemulsion system(MEs) consisting of OP-4[polyoxyethylene(4) nonylphenol], OP-7[polyoxyethylene(7) nonylphenol], 1-hexanol, D2EHPA, kerosene and HCl solution and applied to the extraction of La(III) from chloride aqueous solution within the polysulfone hollow fiber contactor (HFC),laboratory-scale experiments were carried out to investigate the recovery of La(III) using as-prepared microemulsion from the simulation wastewater containing La(III),Al(III) and Fe(III). The right weight ratio(Rs) of OP-4 to OP-7 was firstly confirmed through determination of the solubilization capacity of HCl solution(W0,HCl) in microemulsion, the effect of several factors such as the HCl concentration, temperature and effective extraction time on the extraction efficiency of La(III) was discussed. Results showed that the acceptable Rs was 4:6 to prepare the W/O MEs. The extraction yield of La(III) increased with the increasing of HCl concentration, temperature and effective extraction time and reaches to 97.3% while using five-stage modules. The recovery yield of La(III) from simulation La-bearing wastewater was 90.6%.