The Limiting Dissolution Current of a Spherical Electrode in Acid

2004 ◽  
Vol 40 (3) ◽  
pp. 300-302
Author(s):  
A. P. Grigin ◽  
A. D. Davydov
1983 ◽  
Vol 48 (6) ◽  
pp. 1571-1578 ◽  
Author(s):  
Ondřej Wein

Theory has been formulated of a convective rotating spherical electrode in the creeping flow regime (Re → 0). The currently available boundary layer solution for Pe → ∞ has been confronted with an improved similarity description applicable in the whole range of the Peclet number.


1980 ◽  
Vol 45 (1) ◽  
pp. 169-178 ◽  
Author(s):  
František Opekar ◽  
Karel Holub

The galvanostatic dissolution of mercury from the surface of glassy carbon into a thiocyanate solution proceeds in accord with theoretical assumptions, as manifested by the constant product of the dissolution current and transition time. Under certain relations between the amount of oxidised mercury and concentration of thiocyanate at the electrode surface, however, a small part of the mercury dissolves at more positive potentials than correspond to the Nernst equation. This dissolution can be accompanied by potential oscillations. The anomalous behaviour is elucidated by the concept about coverage of a certain part of mercury with a film of sparingly soluble compounds of SCN- ions with mercury. This film is formed at the end of the galvanostatic dissolution on certain places of the electrode surface covered with mercury droplets, where SCN- ions are much exhausted as a result of a high current density.


1992 ◽  
Vol 4 (12) ◽  
pp. 3847-3855 ◽  
Author(s):  
E. Ahedo ◽  
M. Martínez‐Sánchez ◽  
J. R. Sanmartín

1982 ◽  
Vol 43 (3) ◽  
pp. 1020-1026
Author(s):  
O. Vain ◽  
N. A. Pokryvailo

1966 ◽  
Vol 19 (6) ◽  
pp. 923 ◽  
Author(s):  
CM Gorden ◽  
RF Matlak

An expression has been derived for the concentration of oxidant and reductant at the surface of an expanding spherical electrode as a function of time and the polarizing potential in the case where a slow irreversible chemical reaction follows a reversible electron transfer reaction under the conditions of a somewhat idealized polarographic system.


1.—Several investigators have claimed that electrons are emitted from metals under the influence of chemical action, but the only claim which seems well substantiated is that of Haber and Just, who found that when drops of cæsium or of the liquid alloy of sodium and potassium are attacked, at a low pressure, by a number of chemically active gases, the drops lose a negative but not a positive electric charge. The electric currents set up with the drops negatively charged are stopped by the application in a suitable manner of relatively small magnetic fields. This shows that the currents are carried by electrons emitted from the drops. The object of the present investigation has been to obtain quantitative information about this interesting phenomenon, and, more especially, to ascertain the magnitude of the kinetic energy of the emitted electrons and the mode of its distribution among them. The importance of the subject lies in the fact that it is the only way, so far as I am aware, in which any information at all can be made available as to the distribution of energy among the individual products—molecular, atomic, ionic or electronic—of a chemical reaction. The majority of the experiments have been directed towards obtain­ing the curves showing the relation between the chemical electron current and the applied electromotive force for the case of a small spherical source concentric with a large spherical electrode.


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