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Preparetion of Rare-earth Metal Films by Electrochemical Deposition from Non-aqueous Madia with High-purity

Research Project

Project/Area Number 09650808
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Metal making engineering
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

HIRATO Tetsuji  Kyoto University, Faculty of Engineering, Associate Professor, 工学研究科, 助教授 (70208833)

Co-Investigator(Kenkyū-buntansha) MURASE Kuniaki  Kyoto University, Faculty of Engineering, Research Associate, 工学研究科, 助手 (30283633)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 1998: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1997: ¥2,400,000 (Direct Cost: ¥2,400,000)
Keywordselectrodeposition / rare earths / neodymium / europium / nonaqueous solvent / redox behavior / triflate / room temperature molten salts / 常温溶融塩 / 電気めっき / 希土類元素 / 銅 / 酸化還元反応 / ユウロピウム
Research Abstract

Triflate-type rare earth salts, Ln(TfO)_3 or Ln(Tf_2N)_3 (Ln = Nd, Eu), were dissolved in imidazolium-type room temperature molten salts with corresponding anion, 1-ethyl-3-methylimidazolium trifluoromethanesulfonate (EMITfO) and 1-ethyl-3-methylimidazoium bis((trifluoromethyl)sulfonyl)amide (EMILTf_2N), in order to investigate redox behavior of rare earth ions in the nonaqueous ionic liquids. EMITfO was prepared by the reaction of 1-ethylimidazol with Methyl trifluoromethanesulfonate in dried 1,1,1-trichloroethane. EMITf_2N was prepared by the reaction of 1-ethyl-3-methylimidazolium bromide (EMIBr) with lithium bis((trifluoromethyl)sulfonyl)amide (LiTf_2N) in deionized water followed by extraction with dichloromethane ; the EMIBr was obtained by the reaction of 1-methylimidazol with bromoethane in 1,1,1-trichioroethane. The resulting molten salts were dried in vacuo at 120-150 。C for more than 3 days.
Solubility of the rare earth salts into the corresponding molten salts exceeds 0.1 mol dm^<-3>. Ln(TfO)_3 is not soluble in EMITf_2N, whereas Ln(Tf_2N)_3 soluble in both EMIITfO and EMITf_2N.Cyclic voltammograms show that the redox potentials of Eu^<2+>/Eu^<3+> were ca. -0.9 V in EMITfO, +0.3 V in EMITf_2N, and ca.. -0.9 V vs. I_3^-/I^- in 1/1 mixture (in volume) of EMJTfO and EMITf_2N.These phenomena are explained by a lower Lewis basicity of Tf_2N^- anion compared to TfO, suggesting Tf_2N^--type room temperature molten salts are promising solvents for cathode electrolysis of rare earth ions.
A new ammonium-type room temperature molten salt, trimethylhexylammonium bis((trifluoromethyl)sulfonyl)amide (TMHATf_2N), was also prepared by the reaction of trimethylhexylammonium bromide (TMHABr) with LiTf_2N.Solubility of Nd(Tf_2N)_3 into the TMHATf_2N was more than 0.1 mol dm^<-3>. Since the electrochemical window of TMHATf_2N exceeds 5.5 V, the molten salt is also a promising solvent for electrodeposition of rare earths at ambient temperature.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] 平藤哲司: "トリフラート系室温溶媒塩中における希土類イオンの酸化還元挙動" 希土類. 32. 270-271 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] T.Hirato: "Redox Behavior of Rare Earth Ions in Triflate-type Room Temperature Molten Salts" Kidorui. 32. 270-271 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 新田 耕司 ほか: "トリフラート系室温溶融塩中における希土類イオンの酸化還元挙動" 希土類. 32巻. 270-271 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 新田 耕司: "トリフラート系室温溶融塩浴中における希土類イオンの酸化還元挙動" 希土類. 32(印刷中). (1998)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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