As. Baranski et A. Moyana, USE OF HIGH-FREQUENCY AC VOLTAMMETRY TO STUDY KINETICS OF PHYSICAL ADSORPTION AT MERCURY ULTRAMICROELECTRODES, Langmuir, 12(13), 1996, pp. 3295-3304
Adsorption kinetics of small organic molecules was studied by ac volta
mmetry with mercury ultramicroelectrodes in the frequency range 0.22-6
.25 MHz. It was found that the activation energy of the adsorption pro
cess can be expressed as a linear combination of the electrical compon
ent of the standard free energy of adsorption (a major contribution) a
nd the energy of lateral interactions (a minor contribution). The resu
lts suggest that, during the adsorption process, work against an elect
rical field must be performed before excess energy (due to the change
in the hydrophobic interactions) is released. The final state is reach
ed by a rotational and translational motion of the surfactant molecule
. At the zero charge potential the rate constant reaches the maximum v
alue of (4.6 +/- 0.3) x 10(9) s(-1). This value indicates that the vis
cosity of interfacial water at mercury near the zero charge potential
is about 1.7 times higher than the bulk viscosity.