Substitution at a carbon atom of the pyridine ring was shown to cause a ris
e in the surface activity and a change in the molecular orientation of pyri
dine compounds at the interface. High-molecular-weight pyridinium salts had
especially high surface activities that correlated with their antistatic p
roperties. Adsorption parameters of the compounds investigated were calcula
ted, and the results obtained indicated segmental adsorption of the polymer
compounds. It was disclosed that the surface activity of the pyridinium sa
lts was increased at the bismuth electrode-solution interface in comparison
with the free surface of the solution.