It is found that the differential capacity of the dropping mercury electrode is affected mainly in two ways by added surface-active substances. At about the electrocapillary zero there is a strong lowering of the capacity due to adsorption of surface-active substances. At some higher cathodic potential there is enormous increase in differential capacity leading to a maximum and is followed by a sharp fall in the capacity; the latter is due to the desorption taking place more or less sharply at the higher cathodic potentials. The theory of the phenomenon has been formulated
The double layer theory is one of the fundamentals of electrochemical kinetics. At the present time ...
In this research, the effect of surface-active substances (CMC and DFP) on the electrolysis of coppe...
[[abstract]]©1991 Elsevier - The electrochemical reduction of Pd(II)-ethanolamine complex on mercury...
PAST and JOFAJ),2) have recently studied the decay curve, i. c. the abrupt change of overvoltage wit...
The adsorption behaviour of the condensation polymers of ethylene oxides and lauryl alcohol was stud...
A general approach to the theory of ionic adsorption at the mercury electrode (mobile adsorption) is...
The hanging drop electrode devised in this laboratory is an improvement over those used elsewhere by...
The potential range of polarization of the twin dropping mercury electrodes, over which the coalesce...
The effect of the change in the supporting electrolyte (from KCI to Kl) on the nature of the capacit...
The differential double layer capacities at mercury-0.1 N salt solution interfaces are meas-ured by ...
PhDAnalytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://de...
The kinetic study of various electrode reactions shows, in agreement with previous Russian work, tha...
An electrochemical approach has been used to switch adsorbate monolayers on a mercury surface betwee...
Present work was devoted to the experimental study of absence of cathodic saturation current of hydr...
We demonstrate that the interfacial energy between mercury and mica is a function of charge on the m...
The double layer theory is one of the fundamentals of electrochemical kinetics. At the present time ...
In this research, the effect of surface-active substances (CMC and DFP) on the electrolysis of coppe...
[[abstract]]©1991 Elsevier - The electrochemical reduction of Pd(II)-ethanolamine complex on mercury...
PAST and JOFAJ),2) have recently studied the decay curve, i. c. the abrupt change of overvoltage wit...
The adsorption behaviour of the condensation polymers of ethylene oxides and lauryl alcohol was stud...
A general approach to the theory of ionic adsorption at the mercury electrode (mobile adsorption) is...
The hanging drop electrode devised in this laboratory is an improvement over those used elsewhere by...
The potential range of polarization of the twin dropping mercury electrodes, over which the coalesce...
The effect of the change in the supporting electrolyte (from KCI to Kl) on the nature of the capacit...
The differential double layer capacities at mercury-0.1 N salt solution interfaces are meas-ured by ...
PhDAnalytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://de...
The kinetic study of various electrode reactions shows, in agreement with previous Russian work, tha...
An electrochemical approach has been used to switch adsorbate monolayers on a mercury surface betwee...
Present work was devoted to the experimental study of absence of cathodic saturation current of hydr...
We demonstrate that the interfacial energy between mercury and mica is a function of charge on the m...
The double layer theory is one of the fundamentals of electrochemical kinetics. At the present time ...
In this research, the effect of surface-active substances (CMC and DFP) on the electrolysis of coppe...
[[abstract]]©1991 Elsevier - The electrochemical reduction of Pd(II)-ethanolamine complex on mercury...