• 제목/요약/키워드: Copper(II)

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황산용액에서 용매추출에 의한 코발트(II), 니켈(II) 및 구리(II) 분리 (Separation of Co(II), Ni(II), and Cu(II) from Sulfuric Acid Solution by Solvent Extraction)

  • 문현승;송시정;;이만승
    • 자원리싸이클링
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    • 제31권1호
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    • pp.21-28
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    • 2022
  • 폐리튬이온배터리를 고온에서 용융환원시키면 코발트, 니켈 및 구리 금속합금상을 얻을 수 있다. 이러한 금속합금상으로부터 금속을 분리회수하기 위한 공정을 개발하기 위해 코발트, 니켈 및 구리 금속을 혼합한 금속혼합물을 3% 과산화수소를 함유한 2 M 황산용액으로 침출하면 9.6%의 구리와 함께 코발트와 니켈이 모두 침출된다. 침출용액에서 Cyanex 301로 구리(II)가 선택적으로 추출되었으며, 30% 왕수로 구리(II)를 탈거했다. 구리가 분리된 여액에서 이온성액체인 ALi-SCN으로 Co(II)를 선택적으로 추출했으며, 15%의 암모니아용액으로 3단의 교차식 탈거를 통해 모두 탈거했다. 본 연구를 통해 코발트, 니켈 및 구리 금속혼합물의 황산침출액에서 용매추출로 세 금속을 분리할 수 있는 공정을 제안했다.

Delicate Difference in Coordinating Nature between Copper(II) and Nickel(II) Ions. Structural Properties of Copper(II) and Nickel(II) Nitrate Containing 1,2-Bis(dimethyl-3-pyridylsilyl)ethane

  • Kim, Shin-A;Kim, Chi-Won;Noh, Tae-Hwan;Lee, Young-A;Jung, Ok-Sang
    • Bulletin of the Korean Chemical Society
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    • 제31권8호
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    • pp.2158-2162
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    • 2010
  • Studies on the molecular construction and structures of $M(NO_3)_2$ (M = Cu(II), Ni(II)) complexes with 1,2-bis(dimethyl-3-pyridylsilyl)ethane (L) have been carried out. Formation of each molecular skeleton appears to be primarily associated with a suitable combination of bidentate N-donors of L and coordinating nature of octahedral metal(II) ions: [$Cu(NO_3)_2(L)_2$] yields a 2-dimensional sheet structure consisting of 44-membered $Cu_4L_4$ skeleton whereas $[Ni(L)_2(H_2O)_2](NO_3)_2$ produces an interpenetrated 3-dimensional structure consisting of 66-membered cyclohexanoid ($M_6L_6$) skeleton. The Cu(II) ion prefers nitrate whereas the Ni(II) ion prefers water molecules as the fifth and the sixth ligands.

Determination and Preconcentration of Copper(Ⅱ) after Adsorption of Its Cupferron Complex onto Benzophenone

  • Lee, Taik-Jin;Choi, Hee-Seon
    • Bulletin of the Korean Chemical Society
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    • 제23권6호
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    • pp.861-865
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    • 2002
  • A sensitive method for the determination of trace copper(II) after the preconcentration by adsorbing its cupferron complex onto microcrystalline benzophenone was developed.Several experimental conditions such as the pH of sample solution,concentration of cupferron, amount of benzophenone and atirring time were optimized. Trace compper(II) in 100mL solution was chelated with $3.0\;{\times}\;10^3$ M cupferron at pH 5.0. After 0.20g benzophenone, The benzophenone adsorbing Cu-cupferron complex was filtered and then Cu-cupferron complex was desorbed in 10 mL ethanol. Copper was determined by a flame atomic absorption spectrophotomethry. The interfering effects of diverse concomitant ions were investigated. Fe(III) interfered seriously with, but the interference by Fe(III) was completely eliminated by adjusting the concentration of copferron to $5.0\;{\times}\;10^3$ M. The detection limit of this method was 8.6${\times}$10 M(5.5 ngmL$^1$). Recoveries of 97% and 96% were obtained for Cu(II) in a stream water and a brass sample, respectively. Based on the results from the experiment. this proposed technique could be applied to the determination of copper(II) in real samples.

Voltammetric Determination of Copper(II) at Chemically Modified Carbon Paste Electrodes Containing Alga

  • Bae, Zun-Ung;Kim, Young-Lark;Chang, Hye-Young
    • 분석과학
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    • 제8권4호
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    • pp.611-615
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    • 1995
  • The design of appropriate chemically modified electrodes should allow development of new voltammetric measurement schemes with enhanced selectivity and sensitivity. Microorganism like algae has high ability to trap toxic and heavy metal ions and different affinities for metal ions. A copper(II) ion-selective carbon paste electrode was constructed by incorporating alga Anabaena into a conventional carbon paste mixture, and then the film of 10% Nafion was coated to avoid the swelling of the electrode surface. Copper ion could be deposited at the 25% algamodified electrode for 15 min without the applied potential while stirring the solution by only immersing the electrode in a buffer (pH 4.0) cot1taining copper(II). Temperature was controlled at $35^{\circ}C$. After preconcentration was carried out the electrode was transferred to a 0.1 M potassium chloride solution and was reduced at -0.6 volt at $25^{\circ}C$. The differential pulse anodic stripping voltammetry was employed. A well-defined oxidation peak could be obtained at -0.1 volt (vs SCE). In five deposition / measurement / regeneration cycles, the responses were reproducible and relative standard deviations were 3.3% for $8.0{\times}10^{-4}M$ copper(II). Calibration curve for copper was linear over the range from $2.0{\times}10^{-4}M$ to $1.0{\times}10^{-3}M$. The detection limit was $7.5{\times}10^{-5}M$. Studies of the effect of diverse ions showed that the coexisting metal ions had little or no effect for the determination of copper. But anions such as cyanide. oxalate and EDTA seriously interfered.

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액상프리커서법에 의한 산화구리(CuO) 나노 입자의 합성 (Synthesis of CuO nanoparticles by liquid phase precursor process)

  • 신성환
    • 문화기술의 융합
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    • 제9권6호
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    • pp.855-859
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    • 2023
  • 질산구리삼수화물염(copper(II) nitrate trihydrate) 수용액을 공업용 전분(starch)에 함침 시킨 전구체를 이용하여 산화구리(CuO) 나노 입자를 합성하였다. 주사전자현미경(SEM)을 통하여 질산구리삼수화물염 수용액이 함침된 전구체에 대한 구조를 분석하였고, 전구체에 대한 열처리 온도를 증가 시킴에 따라 생성되는 산화구리 입자의 입자 크기와 결정 구조를 X선회절분석법(XRD)과 주사전자현미경(SEM)으로 분석하였다. 분석 결과에 따르면, 전구체에서 유기물질이 완전히 열분해 되어지는 온도는 450-490℃이며, 열처리하는 온도가 증가함에 따라 생성되는 산화구리 입자의 크기와 결정성이 증가하는 것을 확인할 수 있었고, 또한 500-800℃에서 1시간씩 열처리하여 얻은 산화구리 입자의 크기는 100nm-2㎛인 것으로 나타났다. 하소 온도 400℃에서 산화구리 결정상이 형성되고, 800℃까지는 산화구리 단일상만 존재하며, 하소 온도의 증가에 따라 생성되는 입자의 크기가 커지는 것을 확인하였다.

Sphagnum 피트모스에서의 카드뮴, 구리, 납의 흡착 (Adsorption of Cadmium, Copper, and Lead on Sphagnum Peat Moss)

  • 방선백;이상우;김주용;유동일;강용곤;김경웅
    • 자원환경지질
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    • 제39권2호
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    • pp.103-109
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    • 2006
  • Sphagnum 피트모스에서의 Cd(II), Cu(II) Pb(II)의 흡착에 대한 회분식 실험을 수행하였다. 실험결과 10-50 mg/L의 Cd(II), Cu(II), Pb(II)이 1.0 g/L의 sphagnum 피트모스에 1시간 내에 흡착되어 효과적으로 제거되었다. 초기농도에 따라 sphagnum 피트모스에 홉착된 Cd(II), Cu(II), Pb(II)의 반응속도는 유사이차 반응모델을 적용하여 설명하였다. 또한 Langmuir 등온흡착으로부터 Cd(II), Cu(II), Pb(II)에 대한 최대흡착량을 계산하여, 각각 33.90, 29.15, 91.74 mg/g가 sphagnum 피트모스에 흡착될 수 있음을 알아내었다. Sphagnum 피트모스가 Cd(II), Cu(II), Pb(II)를 흡착하는데 매우 효과적인 흡착제임을 실험결과를 통해 나타내었다.

Water treatment sludge for removal of heavy metals from electroplating wastewater

  • Ghorpade, Anujkumar;Ahammed, M. Mansoor
    • Environmental Engineering Research
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    • 제23권1호
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    • pp.92-98
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    • 2018
  • Suitability of aluminium-based water treatment sludge (WTS), a waste product from water treatment facilities, was assessed for removal of heavy metals from an electroplating wastewater which had high concentrations of copper and chromium along with other heavy metals. Batch tests with simulated wastewater in single- and multi-metal solutions indicated the influence of initial pH and WTS dose on removal of six metals namely Cu(II), Co(II), Cr(VI), Hg(II), Pb(II) and Zn(II). In general, removal of cationic metals such as Pb(II), Cu(II) and Zn(II) increased with increase in pH while that of anionic Cr(VI) showed a reduction with increased pH values. Tests with multi-metal solution showed that the influence of competition was more pronounced at lower WTS dosages. Column test with diluted (100 times) real electroplating wastewater showed complete removal of copper up to 100 bed volumes while chromium removal ranged between 78-92%. Other metals which were present in lower concentrations were also effectively removed. Mass balance for copper and chromium showed that the WTS media had Cu(II) and Cr(VI) sorption capacities of about 1.7 and 3.5 mg/g of dried sludge, respectively. The study thus indicates that WTS has the potential to be used as a filtration/adsorption medium for removal of metals from metal-bearing wastewaters.

Synthesis and Crystal Structures of Copper(II) Complexes with Schiff Base Ligands: [Cu2(acpy-mdtc)2(HBA)(ClO4)]·H2O and [Cu2(acpy-phtsc)2(HBA)]·ClO4

  • Koo, Bon Kweon
    • Bulletin of the Korean Chemical Society
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    • 제34권11호
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    • pp.3233-3238
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    • 2013
  • Two new Cu(II) complexes, $[Cu_2(acpy-mdtc)_2(HBA)(ClO_4)]{\cdot}H_2O$ (1) (acpy-mdtc- = 2-acetylpyridine S-methyldithiocarbamate and $HBA^-$ = benzilic acid anion) and $[Cu_2(acpy-phtsc)_2(HBA)]{\cdot}ClO_4$ (2) (acpy-$phtsc^-$ = 2-acetylpyridine 4-phenyl-3-thiosemicarbazate) have been synthesized and characterized by elemental analysis, infrared spectroscopy, thermogravimetric analysis, and single crystal X-ray diffraction. The X-ray analysis reveals that the structures of 1 and 2 are dinuclear copper(II) complexes bridged by two thiolate sulfur atoms of Schiff base ligand and bidentate bridging $HBA^-$ anion. For 1, each of the two copper atoms has different coordination environments. Cu1 adopts a five-coordinate square-pyramidal with a $N_2OS_2$ donor, while Cu2 exhibits a distorted octahedral geometry in a $N_2O_2S_2$ manner. For 2, two Cu(II) ions all have a five-coordinate square-pyramidal with a $N_2OS_2$ donor. In each complex, the Schiff base ligand is coordinated to copper ions as a tridentate thiol mode.

정사면체 구조를 갖는 Cu (II) 및 Co (II) 착화물들의 아쿠오화반응에 관한 연구 (Kinetic Studies on the Aquation of Tetrahedral Copper (II) and Cobalt (II) Complexes)

  • 김영인;최성락;김정숙;김해경
    • 대한화학회지
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    • 제32권2호
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    • pp.122-129
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    • 1988
  • $Co(sp)X_2P$(sp=sparteine, $C_{15}H_{26}N_2$, X=Cl, Br)과 Cu(sp)$X_2$의 아쿠오화반응이 메카니즘을 규명하기 위하여 pH~5인 조건에서 속도론적 연구를 실시하였다. Co(sp)$Cl_2$$Co(sp)Br_2$는 halide 이온들에 의해 촉매 효과를 나타내지 않았으며 $Cu(sp)Cl_2$$Cu(sp)Br_2$에 비해 매우 빠르게 아쿠오화가 진행되었다. $Cu(sp)Cl_2$$Cu(sp)Br_2$는 halide cyanide의 존재에 의해 반응속도가 크게 증가하였으며 pH = 2~5인 범위에서 pH가 증가함에 따라 반응속도가 증가하였다. 본 연구에서 얻어진 실험결과, $Co(sp)X_2$의 아쿠오화반응이 D-메카니즘으로 진행되는 반면 $Cu(sp)X_2$의 경우는 $I_d$ 메카니즘으로 진행되는 것으로 믿어진다.

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New Unsymmetric Dinuclear Copper(II) Complexes of Trans-disubstituted Cyclam Derivatives: Spectral, Electrochemical, Magnetic, Catalytic, Antimicrobial, DNA Binding and Cleavage Studies

  • Prabu, R.;Vijayaraj, A.;Suresh, R.;Jagadish, L.;Kaviyarasan, V.;Narayanan, V.
    • Bulletin of the Korean Chemical Society
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    • 제32권5호
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    • pp.1669-1678
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    • 2011
  • Six new binuclear copper(II) complexes have been prepared by template condensation of the dialdehydes 1,8-[bis(3-formyl-2-hydroxy-5-methyl)benzyl]-l,4,8,11-tetraazacyclotetradecane (PC-a) and 1,8-[bis(3-formyl-2-hydroxy-5-bromo)benzyl]-l,4,8,11-tetraazacyclotetradecane (PC-b) with appropriate aliphatic diamines, and copper(II) perchlorate. The structural features of the complexes have been confirmed by elemental analysis, IR, UV-vis and mass spectra etc. The electrochemical behavior of all the copper(II) complexes show two irreversible one electron reduction process. The room temperature magnetic moment studies depict the presence of an antiferromagnetic interaction in the binuclear complexes. The catechol oxidation and hydrolysis of 4-nitrophenylphosphate were carried out by using the complexes as catalyst. The antimicrobial screening data show good results. The binding of the complexes to calf thymus DNA (CT DNA) has been investigated with absorption and emission spectroscopy. The complex [$Cu_2L^{1a}$] displays significant cleavage property of circular plasmid pBR322 DNA in to linear form. Spectral, electrochemical, magnetic and catalytic studies support the distortion of the copper ion geometry that arises as the macrocyclic ring size increases.