モリブデンとＮａ２Ｏ・２Ｂ２Ｏ３ガラス融液との分極下における反応について

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タイトル別名
  • Interaction between Molybdenum and Molten Sodium Diborate Glass under Electric Field
  • モリブデン ト Na2O 2B2O3 ガラス ユウエキ ト ノ ブンキョクカ

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説明

In the previous papers, the authors investigated the electrochemical phenomena of some electric conductive materials such as Pt, Ni, Co, graphite etc. in molten sodium diborate glass. In this paper, molybdenum was chosen as the object of study since molybdenum is a particularly interesting electrode material used in electric melting of glass. Anodic dissolution, passivation and catholic deposition of molybdenum were investigated by linear potential sweep voltammetry in Na2O·2B2O3 at 900°C in N2 gas atmosphere. Moreover, the metal-glass interface after polarization was analyzed by EPMA.<br>On cathodic polarization of Mo electrode, a relatively narrow residual current region appeared first and then a steep current increase followed at higher cathodic potential than ca. -0.7V (vs. Pt reference). Borate anions were easily reduced to boron element and the molybdenum boride layer having close texture covered the electrode surface. Sodium oxide layer was formed outside the boride layer at ca. -2.5V, and this layer moved toward molybdenum metal at higher cathodic polarization. Sodium ions were not seemed to be reduced readily till -5V. Ni electrode also formed nickel boride before sodium deposition like in the case of Mo.<br>The anodic voltammogram of Mo electrode showed three current peaks due to the formation of passive films made of molybdenum oxides. At a lower anodic potential than ca. 1V, MoO2 and Mo2O5 films were likely to be formed, but both films re-dissolved at higher anodic polarization. Anodic current increased up to ca. 4V due to dissolution of Mo oxides and Mo metal. Passivation phenomenon at ca. 4V could be attributed to the formation of MoO3 layer. The MoO3 layer looked remarkably porous and was readily sublimed at 900°C, so that Mo electrode was consumed acceleratedly. Ni electrode was revealed to form passive NiO layer.

収録刊行物

  • 材料

    材料 32 (352), 101-107, 1983

    公益社団法人 日本材料学会

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