ELECTROCHEMICAL EXTRACTION OF OXYGEN FROM AIR VIA HYDROPEROXIDE ION

Citation
E. Brillas et al., ELECTROCHEMICAL EXTRACTION OF OXYGEN FROM AIR VIA HYDROPEROXIDE ION, Journal of Applied Electrochemistry, 27(1), 1997, pp. 83-92
Citations number
17
Categorie Soggetti
Electrochemistry
ISSN journal
0021891X
Volume
27
Issue
1
Year of publication
1997
Pages
83 - 92
Database
ISI
SICI code
0021-891X(1997)27:1<83:EEOOFA>2.0.ZU;2-W
Abstract
A novel electrochemical method for the extraction of pure oxygen from air is described. The system consists of an undivided cell with a nick el anode, a carbon-polytetrafluoroethylene (CP) air-fed cathode and a KOH+HO2- solution as electrolyte. In such a Ni-CP cell, oxygen from th e air is reduced in the cathode to form HO2- via a two-electron proces s, whereas anodic generation of oxygen gas can take place by the two-e lectron oxidation of HO2- and/or the four-electron oxidation of OH- of the medium. Gas chromatography confirmed that the oxygen produced fro m cells operating up to 190 mA cm(-2) does not contain hydrogen, as ex pected if cathodic reduction of H2O does not take place. The presence of HO2- causes a decrease in energy consumption of the cell, since it is easier to oxidize than OH-. Ni-CP cells containing solutions with c oncentrations of OH- to 2.4 mol dm(-3) and HO2- from 0.1 to 0.5 mol dm (-3) are stable at 25 degrees C for voltages to about 1.0 V. These cel ls work in a steady state in which the same number of moles of HO2- io ns electrogenerated at the cathode are also anodically decomposed at t he anode, without OH- oxidation. In this state, the oxygen consumed in the cathode,is anodically generated and extraction of oxygen from air occurs by a two-electron process. Energy consumptions between 1.710kW hkg(-1) O-2 and 1.224kWhkg(-1) O-2 are obtained for bielectronic stabl e cells operating at 100 mA cm(-2) and at temperatures between 25 degr ees C and 45 degrees C, which are significantly lower than those repor ted for previous electrochemical oxygen generators based on the anodic decomposition of OH-.