The performance of the long lasting sessile drop mercury electrode (lfsdme) as a working electrode for various electrochemical techniques was studied . Dimethylpyrmlydinium [E" 2 a -2.7 V (see)] and 2,4,6-trimethylpyridine [E, 12 al -2.85 V (see)] were used as substrates in DMF as the solvent and te
The desorption of n-decyltriethylammonium ion at negative potentials at a mercury electrode
β Scribed by J.B. Hayter; M.W. Humphreys; R.J. Hunter; Roger Parsons
- Publisher
- Elsevier Science
- Year
- 1974
- Weight
- 233 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0022-0728
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β¦ Synopsis
The adsorption of long chain quaternary ammonium ions at a mercury electrode was studied recently by the capacity and drop-time methods 1-s. An unusual feature of this system was the behaviour of the capacity peak at negative potentials. In many other systems 6 this peak corresponds to the desorption-adsorption (desad) process of the surface active species. However, a careful study of the system containing long chain quaternary ammonium ions suggested that in this case the peak could be ascribed to a re-orientation rather than a desad process. To test this explanation more rigorously we have investigated this system by the ellipsometric method 7 as well as measuring interfacial tensions by the maximum bubble pressure method s .
π SIMILAR VOLUMES
The orientation of coumarin molecqles adsorbed at a mercury surface depends on potential, coumarin concentration and ionic strength of the electrolyte. At positive potentials the adsorbed molecules are arranged with the plane of the ring parallel to the mercury surface; as the potential is made more