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Electrochemical Ferrate(VI) Synthesis: A Molten Salt Approach

  • M. Benová
    M. Benová
    Department of Inorganic Technology, Slovak University of Technology in Bratislava, 812 37 Bratislava, Slovakia
    More by M. Benová
  • J. Híveš
    J. Híveš
    Department of Inorganic Technology, Slovak University of Technology in Bratislava, 812 37 Bratislava, Slovakia
    More by J. Híveš
  • K. Bouzek
    K. Bouzek
    Department of Inorganic Technology, Institute of Chemical Technology Prague, 166 28 Prague, Czech Republic
    More by K. Bouzek
  • , and 
  • V. K. Sharma
    V. K. Sharma
    Florida Institute of Technology, Melbourne, FL 32901
    More by V. K. Sharma
DOI: 10.1021/bk-2008-0985.ch003
    Publication Date (Print):July 25, 2008
    Copyright © 2008 American Chemical Society
    Ferrates
    Chapter 3pp 68-80
    ACS Symposium SeriesVol. 985
    ISBN13: 9780841269613eISBN: 9780841221284

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    Abstract

    The electrochemical synthesis of ferrate(VI) was studied for the first time in a molten salt environment. An eutectic NaOH-KOH melt at the temperature of 200 °C was selected as a most appropriate system for the synthesis. Cyclic voltammetry was used to characterize the processes taking place on the stationary platinum (gold) or iron electrodes. The identified anodic current peak corresponding to the ferrate(VI) production was close to the potential region at which oxygen evolution begins. During the reverse potential scan, well defined cathodic current peak corresponding to the ferrate(VI) reduction appears. However, the peak was shifted to less cathodic potential than that of potential corresponding to the electrolysis in aqueous solutions. This indicates less progressive anode inactivation in a molten salts environment.

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