Homolytic cleavage C-C bond in the electrooxidation of ethanol and bioethanol

  • J. Barroso*
  • , A. R. Pierna
  • , T. C. Blanco
  • , E. Morallón
  • , F. Huerta
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

Nowadays, the studies are focused on the search of better electrocatalysts that promote the complete oxidation of ethanol/bioethanol to CO2. To that end, amorphous bi-catalytic catalysts of composition Ni59Nb 40Pt1-xYx (Y = Cu, Ru, x = 0.4% at.) have been developed, obtained by mechanical alloying, resulting in higher current densities and an improvement in tolerance to adsorbed CO vs. Ni 59Nb40Pt1 catalyst. By using voltammetric techniques, the appearance of three oxidation peaks can be observed. The first peak could be associated with the electrooxidative process of ethanol/bioethanol to acetaldehyde, the second peak could be the oxidation of acetaldehyde to acetic acid, and the last peak might be the final oxidation to CO2. Chrono-amperometric experiments show qualitative poisoning of catalytic surfaces. However, the in situ Fourier Transformed Infrared Spectroscopy, FTIR, is used for the quasi-quantitative determination with which can be observed the appearance and evolution of different vibrational bands of carbonyl and carboxylic groups of different species, as it moves towards anodic potential in the electrooxidative process.

Original languageEnglish
Pages (from-to)4193-4199
Number of pages7
JournalJournal of Power Sources
Volume196
Issue number9
DOIs
Publication statusPublished - 1 May 2011
Externally publishedYes

Keywords

  • Acetic acid
  • Bi-catalytic catalysts
  • Bioethanol
  • CO
  • Electrooxidation
  • Ethanol

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