Adsorption and Condensation of Xanthine at the Mercury/Solution Interface

1998 ◽  
Vol 63 (12) ◽  
pp. 1977-1993 ◽  
Author(s):  
Viktor Dražan ◽  
Vladimír Vetterl

The adsorption and two-dimensional condensation of xanthine at the mercury electrode in 0.2 and 2 M NaCl was studied by electrode double layer capacity measurements. The condensation of xanthine molecules adsorbed at the electrode was observed at pH 6.0 and 7.4, but not at 9.0. The standard Gibbs energy of adsorption, energy of lateral interactions and the surface occupied by one xanthine molecule in a compact layer were calculated from the temperature dependence of the capacity pit using the Frumkin and Ising lattice gas models. The orientation of xanthine molecules in a compact layer at the electrode surface was estimated. At higher bulk concentrations of xanthine, the double layer capacity decreases to a very low value of about 1.5 mF cm-2, which might be an indication of the formation of a xanthine multilayer at the electrode surface.


1998 ◽  
Vol 63 (6) ◽  
pp. 749-760 ◽  
Author(s):  
Grażyna Dalmata

A two-step reduction of Zn(II) ions at the dropping mercury electrode in 1 M NaClO4/0.001 M HClO4 in the presence of N,N'-dialkylthioureas was examined in wide potential and frequency ranges, using the impedance method. The rate constant of the first electron transfer increases with increasing concentration of N,N'-dialkylthioureas, whereas that of the second electron transfer depends largely on the double layer effects, particularly, on the orientation of molecules on the electrode surface.



1982 ◽  
Vol 60 (13) ◽  
pp. 1643-1647 ◽  
Author(s):  
Ernesto R. Gonzalez

The adsorption of sulfamate ions on mercury electrodes has been studied by measuring the double layer capacity in constant ionic strength solutions of composition xM NH4SO3NH2 + (1−x)M NH4F. It was found that sulfamate ions are weakly adsorbed on mercury, the amount adsorbed being significant only for x > 0.1 at positive charges on the electrode. Because of this, the properties of the inner layer were found to be strongly dependent on the adsorbed water molecules and the structure of the diffuse layer. It was determined that the adsorption of sulfamate ions can be described by an isotherm based on the electrostatic model of the double layer. The possible effects of the activity coefficient variation with solution composition are discussed.



1982 ◽  
Vol 47 (1) ◽  
pp. 190-195
Author(s):  
Valerii Kozlov ◽  
Valentina Vilinskaya ◽  
Gurami Tedoradze

The double layer capacity has been measured in dilute 1,1-valent electrolyte solutions (HCl, KCl, NaF) at infrasonic frequencies. The results obtained confirm the validity of the Gouy-Chapman theory for electrolyte solutions in the concentration range 10-3 - 10-5 mol/dm3.



1991 ◽  
Vol 56 (1) ◽  
pp. 90-95 ◽  
Author(s):  
Libuše Kišová ◽  
Libor Reichstädter ◽  
Jaro Komenda

The rate constants for the reduction of V(III) and oxidation of V(II) were measured on a mercury electrode in water and water-dimethylsulphoxide mixtures. Their dependance on the concentration of DMSO differs from that in mixtures of water with an organic solvent of lower basicity. This can be attributed to the existence of different solvates of vanadium in solutions and to different values of the rate constant for these solvates on the electrode surface at different coverages with the organic component. The influence of DMSO both in the primary solvation sphere and in the electrode double layer on the electrode reaction rate is discussed.





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