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Influence of anions on methylpyridinium ion adsorption on the mercury electrode in aqueous solutions

Journal Article · · Sov. Electrochem. (Engl. Transl.); (United States)
OSTI ID:6450387
The adsorption behavior of aromatic and heterocyclic cations is known to be determined by image forces on one hand and by pi-electron interaction on the other. The first factor is effective at the negatively charged surface of the mercury electrode whereas the second factor is effective at the positively charged surface where the forces of pi-electron interaction are in opposition to the electrostatic repulsion forces of the cations. The authors of this paper study the adsorption of methylpyridinium as the aromatic cation in combination with persulfate, chlorine, bromine, and iodine as the anions. The potential range studied was limited on the anodic side by a potential of -0.1 eV, since the values of interfacial tension were poorly reproducible at more positive potentials, and on the cathodic side by a potential of -1.1 eV, since methylpyridinium is reduced at more negative potentials. It is found that the halide ions, owing to the possible formation of charge transfer complexes, have an even stronger effect on the adsorption behavior of organic cations than that observed previously for tetraalkylammonium ions.
Research Organization:
M.V. Lomonosov State Univ., Moscow, USSR
OSTI ID:
6450387
Journal Information:
Sov. Electrochem. (Engl. Transl.); (United States), Journal Name: Sov. Electrochem. (Engl. Transl.); (United States) Vol. 22:8; ISSN SOECA
Country of Publication:
United States
Language:
English

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