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Electrochemical Hydrogen Permeation in a Proton‐Hole Mixed Conductor and Its Application to a Membrane Reactor
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1994
Year
Materials ScienceChemical EngineeringElectrical EngineeringProton‐hole Mixed ConductionEngineeringElectrolyzer CellFormation RatesProton‐hole Mixed ConductorProton-exchange MembraneElectrochemical Hydrogen PermeationMembrane ReactorHydrogenChemistryElectrochemical CellElectrochemical ProcessElectrochemistryMixed Conductors
A proton‐hole mixed conduction in ceramic has been studied under an asymmetrical atmosphere with respect to hydrogen species. The following electrochemical cell was constructed; (I) 1% hydrogen, Pt | specimen ceramic | Pt, mixture (II) and electrochemical hydrogen permeation through this sample was examined under open‐ and closed‐circuit conditions. When the circuit was closed, the hydrogen or water vapor evolution rates at the cathode decreased with increasing partial pressure of oxygen in the cathode. From the conductivity measurement under various , it was confirmed that the main charge carrier except protons was a positive hole, and that this ceramic behaved as a proton‐hole mixed conductor under the asymmetrical condition. When the circuit was open, water vapor evolved spontaneously, and its formation rates were enhanced with increasing in compartment (II). These phenomena indicate that this cell is a self‐short‐circuited via hole conduction in the bulk, and that hydrogen permeates electrochemically from compartment (I) to (II). Further, based on the principle of hydrogen permeation due to the proton‐hole mixed conduction, dimerization was carried out at 1173 K using ceramic as a membrane reactor. Formation rates of were enhanced markedly by self‐short‐circuiting the electrochemical reactor due to the mixed conduction. To clarify the mechanism for the acceleration of dimerization, the electrolytic synthesis of ethane from was carried out at 948 K using ceramic as a membrane reactor.