Abstract
Oxygen reduction in molten NaOH at 623 K has been studied by the use of an Ni rotating disk electrode and a porous O2 gas electrode. It was clarified that the diffusing species to the electrode surface is molecular oxygen itself, and not an oxygen-containing anion, such as O2- 2, by limiting current measurements. Kinetic studies show that the following reaction mechanism is more probable: {A figure is presented} where the latter is rate determining. Since H2O transport to the electrode surface is rate determining, pO2- control is especially important, taking into account the following equilibrium; {A figure is presented}.
| Original language | English |
|---|---|
| Pages (from-to) | 149-153 |
| Number of pages | 5 |
| Journal | Electrochimica Acta |
| Volume | 28 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 1983 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemical Engineering(all)
- Analytical Chemistry
- Electrochemistry
Cite this
Studies on oxygen reduction in molten NaOH. / Hayashi, Hidetaka; Yoshizawa, Shiro; Ito, Yasuhiko.
In: Electrochimica Acta, Vol. 28, No. 2, 1983, p. 149-153.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Studies on oxygen reduction in molten NaOH
AU - Hayashi, Hidetaka
AU - Yoshizawa, Shiro
AU - Ito, Yasuhiko
PY - 1983
Y1 - 1983
N2 - Oxygen reduction in molten NaOH at 623 K has been studied by the use of an Ni rotating disk electrode and a porous O2 gas electrode. It was clarified that the diffusing species to the electrode surface is molecular oxygen itself, and not an oxygen-containing anion, such as O2- 2, by limiting current measurements. Kinetic studies show that the following reaction mechanism is more probable: {A figure is presented} where the latter is rate determining. Since H2O transport to the electrode surface is rate determining, pO2- control is especially important, taking into account the following equilibrium; {A figure is presented}.
AB - Oxygen reduction in molten NaOH at 623 K has been studied by the use of an Ni rotating disk electrode and a porous O2 gas electrode. It was clarified that the diffusing species to the electrode surface is molecular oxygen itself, and not an oxygen-containing anion, such as O2- 2, by limiting current measurements. Kinetic studies show that the following reaction mechanism is more probable: {A figure is presented} where the latter is rate determining. Since H2O transport to the electrode surface is rate determining, pO2- control is especially important, taking into account the following equilibrium; {A figure is presented}.
UR - http://www.scopus.com/inward/record.url?scp=0020705148&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0020705148&partnerID=8YFLogxK
U2 - 10.1016/0013-4686(83)85101-9
DO - 10.1016/0013-4686(83)85101-9
M3 - Article
AN - SCOPUS:0020705148
VL - 28
SP - 149
EP - 153
JO - Electrochimica Acta
JF - Electrochimica Acta
SN - 0013-4686
IS - 2
ER -