Abstract

Adsorption of tyrosine and serine at the Hg/solution and air/solution interface was studied by means of differential capacity and surface tension measurements. In the case of Hg/solution interface, the experimental data were analysed to obtain the surface excess and adsorption parameters as a function of the electrode charge density and the bulk concentration of the adsorbate. In the case of the free surface, only qualitative analysis was provided due to very small adsorption effects at this interface. The role of the π electrons of the benzene ring in the adsorption process is discussed.

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