• 제목/요약/키워드: Uranyl Ion

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Effective Uranyl Binding by a Dihydroxyazobenzene Derivative. Ionization of Uranium-Bound Water

  • 이관표;장보빈;서정훈
    • Bulletin of the Korean Chemical Society
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    • 제17권9호
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    • pp.814-819
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    • 1996
  • In search of simple host molecules for uranyl ion which form 1: 1-type complexes with high formation constants that can be used either in extraction of uranium from seawater or in catalysis of biologically important organic reactions, the uranophile activities of dihydroxyazobenzene derivative 1 were studied. Uranyl ion and 1 form a 1: 1-type complex with a very large formation constant. The formation constant was measured at pH 7-11.6 by competition experiments with carbonate ion. From the resulting pH dependence, ionization constants of the two aquo ligands coordinated to the uranium of the uranyl complex of 1 were calculated. The ionization constants were also measured by potentiometric titration of the uranyl complex of 1. Based on these results, the pKa values of the two aquo ligands were estimated as 7.1 and 11.0, respectively. At pH 7.5-9.5, therefore, the complex exists mostly as monohydroxo species. Under the conditions of seawater, 1 possesses greater affinity toward uranyl ion compared with other uranophiles such as carbonate ion, calixarene derivatives, or a macrocyclic octacarboxylate. In addition, complexation of 1 with uranyl ion is much faster than that of the calixarene or octacarboxylate uranophiles.

Sodium Alizarin Sulfonate-Uranyl 錯體의 組性에 對한 硏究 (A Study on the Composition of the Sodium Alizarin Sulfonate-Uranyl Complex)

  • 오상오
    • 대한화학회지
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    • 제7권1호
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    • pp.25-28
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    • 1963
  • Sodium alizarin sulfonate forms stable complex with uranyl ion, particularly over pH 3.85 condition. Spectrophotometric measurements have been used to study these complex. The continuous variation method and mole ratio method have been used to establish that the most stable complex contains one uranyl ion per sodium alizarin sulfonate.

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Salphen H2 as a Neutral Carrier for the Uranyl Ion-Selective PVC Membrane Sensor

  • Kim, Dong-Wan;Park, Kyeong-Won;Yang, Mi-Hyi;Kim, Jin-eun;Lee, Shim-Sung;Kim, Jae-Sang
    • Bulletin of the Korean Chemical Society
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    • 제27권6호
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    • pp.899-902
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    • 2006
  • The complexation of N,N'-4,5-(ethylenedioxy)benzenebis(salicylideneimine), (salphen$H_2$) with uranyl ion was studied in acetonitrile solution spectrophtometrically, and the formation constant of the resulting 1 : 1 complex was evaluated. The salphen$H_2$ ligand was used as an ionophore in plasticized poly(vinyl chloride) (PVC) matrix membrane sensor for uranyl ion. The prepared sensors exhibited a near Nernstian response, 28.0-30.9 mV/decade for uranyl ion over the concentration range $1.0\;{\times}\;10^{-2}$ to $1.0\;{\times}\;10^{-6}$M with a limit of detection of $3.2\;{\times}\;10^{-7}$ M. The proposed electrode could be used at a working pH range of 1.5 - 4.0.

산소-17 핵자기공명분광법을 이용한 디옥소우라늄(VI) 이온의 질산 이온과의 착물형성에 관한 연구 (Study of Complex Formation of Dioxouranium(VI) Ion with Nitrate Ion by 17O NMR Spectroscopy)

  • 정우식
    • 공업화학
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    • 제3권2호
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    • pp.312-317
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    • 1992
  • 디옥소우라늄(VI) (우라닐) 이온과 질산 이온과의 상호작용을 산소-17 핵자기공명분광법으로 연구하였다. $UO_2NO_3{^+}$의 우라닐 산소 원자(이후 우라닐 산소)의 산소-17 공명신호는 우라닐 이온의 그것보다 낮은 자기장에서 나타났다. $UO_2NO_3{^+}$의 안정도상수를 5, 15, 25, $35^{\circ}C$에서 질산 이온 농도에 따른 산소-17 화학적 이동의 변화로부터 구했으며, 그 값은 이온강도에 따라 달랐다. 안정도상수의 온도 의존성으로부터 계산한 열역학적 파라미터는 다음과 같다: ${\Delta}H=-(27.2{\pm}1.7)kJ\;mol^{-1}$${\Delta}S=-(110{\pm}7)JK^{-1}mol^{-1}$. 우라닐 이온과 여러가지 음이온의 배위자와의 1:1 착물형성 반응에 대한 엔탈퍼와 엔트로피 사이에는 직선관계가 있었다.

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염기성 수용액에서 우라닐이온의 전기화학적 환원 (Electrochemical Reduction of Uranyl Ion in Aqueous Basic Solutions)

  • 박종민
    • 대한화학회지
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    • 제29권2호
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    • pp.121-128
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    • 1985
  • 우라닐 이온의 염기성수용액에서의 전기화학적인 환원 반응을 폴라로그래피 및 순환전압 전류법을 써서 고찰하였다. 그 결과 0.1M 탄산수소나트륨 및 여기에 0.1M sodium tripolyphosphate를 섞은 혼합용액에서 첫째 환원파는 $UO_2^{2+}$로부터 $UO_2^+$로 환원반응이 일어난 결과로 볼 수 있다. 또한 우라닐이온은 이매질에서 상당한 정도의 가수분해가 일어난 것으로 안다. 이 가수분해 생성물인 $UO_2OH^+$는 첫째 환원파에서 환원이 일어나지 않고 둘째 환원파에서 $UO_2^+$와 함께 일어난다. 우라닐이온 농도 $7.5 {\times} 10^{-4}$에서 $3.75 {\times}10^{-3}$M까지의 범위에서 확산전류는 비례관계가 성립한다.

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Metal Sequestering by a Poly(ethylenimine)-Sephadex G-25 Conjugate Containing 2,2'-Dihydroxyazobenzene

  • 관원종;유창은;장원석;노영석;서정훈
    • Bulletin of the Korean Chemical Society
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    • 제21권4호
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    • pp.393-400
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    • 2000
  • 2,2¢-Dihydroxyazobenzene (DHAB) was attached to poly(ethylenimine) (PEI) to obtain DHAB-PEI. Spectral titration revealed that uranyl, Fe(III), Cu(II), and Zn(II) ion form 1 : 1-type complexes with DHAB attached to PEI. Formation constants for the metal complexes formed by the DHAB moieties of DHAB-PEI were mea-sured by using various competing ligands. The results indicated thatthe concentrations of uranyl, Fe(III), and Cu(II) ions can be reduced to 10 -16 -10 -23 M at p 8 with DHAB-PEI when the concentration of the DHAB moiety is 1 residue M. By using cyanuric chloride as the coupling reagent, DHAB-PEI was immobilized on Sephadex G-25 resin to obtain DHAB-PEI-Seph. Binding of uranyl,Fe(III), Cu(II), and Zn(II) ion by DHAB-PEI-Seph was characterized by using competing ligands. A new method has been developed for characteriza-tion of metal sequestering ability of a chelating resin. Formation constants and metal-binding capacity of two sets of binding sites on the resin were estimated for each metal ion. DHAB-PI-Seph was applied to recovery of metals such as uranium,Fe, Cu, Zn, Pb, V, Mn, and W from seawater. The uranium recovery from seawaterby DHAB-PEI-Seph does not meet the criterion for economical feasibility partlydue to interference by Fe and Zn ions. The seawater used in the experiment was contaminated by Fe and Zn and, therefore, the efficiency of uranium extractionfrom seawater with DHAB-PEI-Seph could be improved if the experiment is carried out in a cleaner sea.

Spectral and Thermal Properties of Some Uranyl Complexes of Some Schiff-Bases Derived from Glycylglycine

  • Sh. A. Sallam;M. I. Ayad
    • 대한화학회지
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    • 제47권3호
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    • pp.199-205
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    • 2003
  • 우라닐 이온, $UO^+_2$와 Schiff-base 와의 착화합물이 글리실글라이신과 살리실알데히드, 2-히드록시-1-나프트알데히드, 2,3-디히드록시 벤즈알데히드 그리고 2,4-디히드록시 벤즈알데히드와의 축합에 의해 합성되었으며 이들 착화합물의 특성을 원소분석, 전도도 측정, 자기화율 측정, UV, IR, NMR 스펙트라와 DTA, TG, DSC 결과를 이용하여 조사하였다. 구조와 열분해 메카니즘이 제안되었다.

우라늄의 분리 및 회수에 관한 연구 (A study on the separation and recovery of uranium)

  • 노기환;김준태
    • 환경위생공학
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    • 제12권1호
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    • pp.15-23
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    • 1997
  • The anionic exchange resins with the Dowex-1 and Amberlite CG-400 form were transformed into resin of sulfate and acetate acid form, respectively. The uranyl complex ions with SO$_{4}$$^{2-}$ and CH$_{3}$COO$^{-}$ were adsorbed on the anion exchange resion mentioned above, and these complex ions were eluted as mixture eluents of 0.7M HNO$_{3}$ - 0.5M NH$_{4}$NO$_{3}$ by anion exchange chromatography. The optimum adsorption conditions of uranyl anion complex ions adsorbed on the upper of the resin colmun were 1.5-2.0 ml/min of flow rates at pH 2.0 and adsorptive power of uranyl complex ion of sulfuric acid type were nearly consistent with the Caussion normal distribution curve, whereas the elution state of UO$_{2}$(Ac)$_{2}$$^{4-}$ with acetic acid type was departed. The weighing form obtained from resin of sulfuric acid and aceric acid type was U$_{3}$O$_{8}$ whose recovery was 91.7%. The possibility of recovering uranium from the monazite sulfate solution using a strong base anion resin, Amberlite CG-400(sulfate form), was successfully recovered more than 90%.

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