Available oxidation processes for removing Cr(III) complexes from water/wastewater usually encounter the formation of highly toxic Cr(VI) and the generation of Cr enriched waste sludge, posing challenges on the subsequent disposal. Herein, we achieve efficient removal of Cr(III)-organic complexes and simultaneous recovery of Cr from wastewater with enhanced curtailment of intermediate Cr(VI), by using an electrochemically driven peroxone (i.e., electro-peroxone) process with activated carbon fiber (ACF) electrodes. For Cr(III)-EDTA, electro-peroxone could remove ∼90% total Cr from 11.50 mg/L to 1.20 mg/L and ∼80% total organic carbon, with a strong curtailment of Cr(VI) to less than 0.2 mg/L. Additionally, the process could obtain a complete recovery of the removable Cr, of which 78.3% are enriched at ACF cathode as amorphous Cr(OH)3 deposits and the remaining 21.7% are adsorbed at the anode, thus avoiding the generation of Cr laden sludge. Mechanism studies show the electro-generated H2O2 reacts with O3 to generate abundant HO· for decomplexation, which sequentially oxidizes Cr(III) to Cr(VI), and degrades the released EDTA via stepwise decarboxylated process, as confirmed by HPLC analysis. Multiple pathways including electro-reduction, H2O2 reduction and electro-adsorption synergistically curtail and immobilize the formed intermediate Cr(VI). ACF characterizations and continuous 5-cycle experiments substantiate the excellent reusability of the ACF electrodes. Moreover, this process exhibits satisfactory effectiveness to Cr(III) complexed with other ligands (e.g., citrate and oxalate), and complexed Cr(III) in the real electroplating wastewater. We believe this study would provide an efficient and eco-friendly alternative for Cr(III) complexes removal from wastewater.
Keywords: Cr recovery; Cr(III)-organic complexes; Decomplexation; Electro-peroxone; Intermediate Cr(VI).
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