A low maintenance, “self-cleaning” electrochemical approach is evaluated for regeneration of dye-loaded granular activated carbon (GAC). To do so, batch experiments were conducted using a low-cost granular activated carbon/stainless steel mesh (GACSS) composite cathode and a stable Ti/mixed metal oxides (Ti/MMO) anode without the addition of oxidants or iron catalysts. The GACSS cathode supports simultaneous H₂O₂ electrogeneration via the in situ supplied O₂ from Ti/MMO anode and the subsequent H₂O₂ activation for ·OH generation, thus enabling the cracking of dye molecules adsorbed on GAC and regenerating the GAC’s sorption capacity. Results show that a prolonged electrochemical processing for 12h will achieve up to 88.7% regeneration efficiency (RE). While RE decreases with multi-cycle application, up to 52.3% could still be achieved after 10 adsorption-regeneration cycles. To identify the mechanism, experiments were conducted to measure H₂O₂ electrogeneration, H₂O₂ activation, and ·OH generation by various GAC samples. The dye-loaded GAC and GAC treated after 10 adsorption-regeneration cycles were still capable of ·OH generation, which contributes to effective “self-cleaning” and regeneration over multi-cycles.

Synergistic effects of alkali metals and nitrogen doping on CO ₂ adsorption in coal-based carbon materials.