The rapidly dropping mercury electrode in direct current and alternating current polarography

1959 ◽  
Vol 20 ◽  
pp. 573-580 ◽  
Author(s):  
Nobuyuki Tanaka ◽  
Reita Tamamushi ◽  
Mutsuo Kodama
1955 ◽  
Vol 8 (4) ◽  
pp. 480 ◽  
Author(s):  
B Breyer ◽  
HH Bauer

The behaviour of perinaphthenone at the dropping mercury electrode has been investigated by the combined techniques of conventional (D.C.) and alternating current (A.C.) polarography. Two D.C. steps were observed, but an A.C. polarographic wave was found only at the potential of the more positive D.C. step. Two tensammetric waves were also seen, one of which appears to be the outcome of multilayer adsorption or of a change in state of the adsorbed film.


1988 ◽  
Vol 66 (5) ◽  
pp. 1053-1058 ◽  
Author(s):  
A. Anastopoulos ◽  
A. Christodoulou ◽  
I. Moumtzis

The effect of adsorbed propargyltriphenyl- and vinyltriphenylphosphonium cations on the discharge of Cd2+ and Zn2+ at dropping mercury electrode is studied by direct current polarographic measurements. Adsorption characteristics are determined by capacitance measurements. The size parameters of the activated complex and the surfactant particles are derived and an elucidation of the mechanism of the inhibited reaction is attempted.


1954 ◽  
Vol 7 (3) ◽  
pp. 225 ◽  
Author(s):  
B Breyer ◽  
S Hacobian

An equation for the A.C. polarographic current is derived from considerations of concentration changes produced at the dropping mercury electrode in virtue of the superposition of a small sinusoidal alternating voltage onto the direct potential, for the case of reversibly reduced inorganic ions. The equation predicts the magnitude of the A.C. polarographic current at any point on the polarogram.


1956 ◽  
Vol 9 (1) ◽  
pp. 1 ◽  
Author(s):  
B Breyer ◽  
HH Bauer

Equations are derived to express the adsorption equilibrium subsisting at an adsorbent surface in the presence of two adsorbable species. These equations are applied to the case of the reduction of organic compounds at the dropping mercury electrode. It is well known that adsorption at the electrode can produce irreversibility in the D.C. step, and a qualitative explanation is provided. The same treatment is used to explain the shape of the A.C. calibration curves.


1955 ◽  
Vol 8 (4) ◽  
pp. 472 ◽  
Author(s):  
B Breyer ◽  
HH Bauer

The behaviour of chloranilic acid at the dropping mercury electrode has been techniques of ordinary and of alternating current polarography. A new type of tensammetric wave has been encountered, which is probably an outcome either of multilayer adsorption and/or of a change in state of the adsorbed film. At the same time, a new tensammetric phenomenon, the exchange of one species of surface-active molecules against another, has been observed. Alternating current polarography can be used for estimating chloranilic acid at concentrations as low as 10-7M, whereas conventional polarography does not permit analysis at concentrations below 10-5M.


1954 ◽  
Vol 7 (4) ◽  
pp. 312 ◽  
Author(s):  
GS Buchanan ◽  
RL Werner

The superposition of a small alternating voltage on the normal D.C. voltage applied at the dropping mercury electrode (D.M.E.) results in the case of irreversible systems in a marked displacement of the entire D.C. wave, in contradistinction to those cases known to be reversible. Such a displacement has been interpreted in terms of an ionic picture. The cases examined were ZnO2--, Fe++, Ni++, Sb+++ in the presence of varying concentrations of Cl-, and Cd++ in the presence of varying concentrations of cyclohexanol. The effect of frequency was investigated.


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