Oxidizing
an organic solute at the anode of an electrolysis cell
can enhance the overall cell current, I, by supplementing
the applied cell potential by an amount, E
boost, the difference in potential required to achieve the observed rate
in the presence and absence of the organic. We have found that, when
the organic solute is methanol at concentrations, C, corresponding to a chemical oxygen demand of <25 g/L (in the
range of that of wastewater or process water from hydrothermal liquefaction),
then the effect of the anode-boosting becomes a strong function of
the product of C and the cell current, I. Empirically, the boosting follows Hill–Langmuir kinetics,
consistent with the cooperativity in the transport of the organic
into the double layer of the anode or adsorption on the oxidation
site.