Ethanol is widely used as an additive in fuels, so its effect on the electrochemical oxidation of triethanolamine was investigated on a 25 μm platinum microelectrode. Ethyl acetate was applied as a cosolvent to increase the permittivity of the medium. A hydrocarbon n-heptane, typically present in gasohol samples as the main component, was studied, and its solutions prepared with ethanol in the entire concentration range (between 0 and 100 v/v% ethanol contents) were mixed with ethyl acetate. The as-prepared liquid mixtures were prepared separately, and they were mixed with ethyl acetate in uniform ratios. Triethanolamine, the selected redox-active compound, exhibited a sharp peak in ethyl acetate at the 15 mM concentration. The changes in the voltammograms served as a good template for quantitative analysis of ethanol content. The most suitable analytical signal used for it was the current minimum after the anodic peak, and this parameter proved more sensitive and reproducible than the anodic peak height itself. The scatterings of the current minimum values were typically within some nanoamperes. MTBE (methyl tert-butyl ether) was added to the apolar mixtures of ethanol, and this ether had a negligible interfering effect on the estimation of ethanol content.
Kiss et al. (Mon,) studied this question.