ELECTROCATALYSIS OF ANODIC OXYGEN-TRANSFER REACTIONS - THE ELECTROCHEMICAL INCINERATION OF BENZOQUINONE

Citation
Jr. Feng et al., ELECTROCATALYSIS OF ANODIC OXYGEN-TRANSFER REACTIONS - THE ELECTROCHEMICAL INCINERATION OF BENZOQUINONE, Journal of the Electrochemical Society, 142(11), 1995, pp. 3626-3632
Citations number
27
Categorie Soggetti
Electrochemistry
ISSN journal
00134651
Volume
142
Issue
11
Year of publication
1995
Pages
3626 - 3632
Database
ISI
SICI code
0013-4651(1995)142:11<3626:EOAOR->2.0.ZU;2-6
Abstract
The electrochemical performance of several anode materials is compared for the electrochemical incineration of p-benzoquinone in acetate buf fer media (pH 5). The chemical oxygen demand (GOD) estimated for benzo quinone by titration with standard permanganate solution can be decrea sed to virtually zero by electrolysis at electrodes comprised of Fe(II I)-doped beta-PbO2 films on Ti substrates. Carbon dioxide is a product of the electrochemical process; however, the possibility of other vol atile products cannot be dismissed. Addition of solid benzoyuinone to acetate media is followed by slow formation of a brownish black color that is concluded to result from one or more humic compounds produced by condensation of benzoquinone; however, it cannot be concluded wheth er the condensation reaction is a necessary prerequisite to successful electrochemical incineration of benzoquinone. Optimal operating condi tions suggested for electrochemical incineration of benzoquinone in ac etate buffer include heating of the anode (e.g., 60 degrees C) to incr ease the rate of anodic discharge of H2O and, thereby, decrease the an odic overpotential. Evidence also is presented that the rate of electr ochemical incineration is enhanced slightly by the addition of a trace s of Fe(III) with reduction of dioxggen (O-2) to hydrogen peroxide (H2 O2) at a cooled stainless steel cathode (e.g., 15 degrees C) in an und ivided cell.