Ruthenium based DSA in chlorate electrolysis–critical anode potential and reaction kinetics

• Ruthenium based DSA®s have been investigated in chlorate electrolyte using rotating discs made from commercial electrodes. Measurements of the voltammetric charge, q*, and of iR-corrected polarisation curves up to current densities of 40 kA/m2 were recorded on new anodes and on aged anodes from 3 years of production in a chlorate plant. Anodic polarisation curves in chloride containing electrolytes bend towards a higher slope at approximately 1.2 V versus Ag/AgCl, likely due to oxidation of ruthenium. The potential and current density at which the curves bend have been defined as the critical potential, Ecr, and the critical current density, icr. New anodes that operate at a relatively high potential, >Ecr, obtain an increase in real surface area and thereby a decrease in anode potential and in the selectivity for oxygen formation during the first months of operation. Experiments at constant ionic strength under chlorate process conditions showed that Ecr decreased with increasing chloride concentration with a factor of −0.09 V/log Cl−, whereas icr increased with increasing chloride concentration. The chlorine evolution reaction was of the first order with respect to chloride concentration. A possible reaction mechanism for chlorine formation is suggested.

Keyword

Chlorate electrolysis

DSA

RuO2

Critical potential

Reaction kinetics

Publication and Content Type

ref (subject category)

art (subject category)