Electrochemical oxidation and mechanism of sulfanilamide from groundwater in a flow-through system using carbon fiber (CF) anode

Metal-based anodes have been used for a long time in the electrochemical oxidation processes to remediate groundwater. However, the high cost of this technique as well as the release of potentially toxic metals (ex, lead), are major barriers being fully implemented. As an alternative of metal-based anodes, in recent years, carbon-based anodes have been paid attention due to their eco-friendliness and cost-effectiveness. This study evaluated the oxidation performance of carbon fiber (CF) anode in a flow-through system. The CF anode degraded 45–87% of the target pollutant (sulfanilamide), depending on the current intensity applied. However, no further degradation of sulfanilamide was observed after the cathode, indicating that sulfanilamide degradation occurred mainly at the anode. This study also determined the effect of electrolytes on electrochemical oxidation using chloride (Cl−), sulfate (SO42−), bicarbonate (CO3−), and synthetic groundwater. Cl− and SO42− electrolytes were converted electrochemically into active species, thereby enhancing sulfanilamide degradation, while the bicarbonate and groundwater electrolytes inhibited oxidation performance by scavenging hydroxyl radicals. A series of scavenger tests and characterization showed that the direct oxidation and hydroxyl radicals involved the sulfanilamide degradation. Especially, the production of hydroxyl radicals is more favorable in high currents than in low currents. That is, CF anode contributed to the degradation by direct oxidation of carbon-based electrodes and generation of hydroxyl radicals. In summary, this study highlights how a CF anode is capable of effectively degrading organic pollutants via anodic oxidation. [Display omitted] •CF anode is efficient degradation for sulfanilamide in a groundwater environment.•Anodic reaction is more effective than cathodic reaction in a flow-through reactor.•The production of hydroxyl radicals is determined according to current intensity.•Hydroxyl radicals and oxygenated functional groups were dominant oxidants.