THE ENHANCED TRANSPORT OF THE CADMIUM ACETYLACETONE COMPLEX ACROSS THE ADSORBED ALIPHATIC ALCOHOL MONOLAYER DURING ELECTROREDUCTION ON MERCURY-ELECTRODES
R. Schmidt et al., THE ENHANCED TRANSPORT OF THE CADMIUM ACETYLACETONE COMPLEX ACROSS THE ADSORBED ALIPHATIC ALCOHOL MONOLAYER DURING ELECTROREDUCTION ON MERCURY-ELECTRODES, Journal of electroanalytical chemistry [1992], 456(1-2), 1998, pp. 131-137
The electrode reaction of the Cd2+ complex with acetylacetone (Acac) w
as studied on mercury electrodes in the absence and in the presence of
n-pentanol and n-octanol. In the inhibitor free solution and under co
nditions where Cd(Acac), complex predominated, the standard rate const
ant of the cadmium reaction was found to be 6.2 x 10(-2) cm s(-1). In
the presence of inhibitors, it was determined from cathodic and anodic
reaction orders with respect to Acac, that the Cd(I)(Acac) species re
acted directly with the electrode. In the presence of n-pentanol and n
-octanol adsorbed on electrodes, the electrode reaction of the Cd-aq(2
+) \ Cd(Hg) system with hydrated Cd2+ ions proceeds more than one orde
r of magnitude slower than the reaction of Cd-acetylacetone complexes.
The ionophoretic effect of Acac is postulated to he due to the intera
ction of the reactant with the adsorbed surface layer. (C) 1998 Elsevi
er Science S.A. All rights reserved.