Sulfate radical-induced destruction of emerging contaminants using traces of cobalt ions as catalysts

Cobalt is part of vitamin B12, which is essential to maintain human health, and trace levels of cobalt ions are ubiquitous in water and soil environments. In this study, the destruction of 1,4-dioxane (1,4-D) by peroxymonosulfate (PMS) under the catalysis of trace levels of Co 2+ was investigated under buffered conditions. The results showed that near 100% removal of 1,4-D was achieved after reaction for 6 and 10 min with 50 and 25 μg/L Co 2+ , respectively, in the presence of 5 mM phosphate ions. Mechanism studies revealed that radicals mediated the destruction of 1,4-D and sulfate radicals were the primary reactive species. The traces of Co 2+ had the greatest reactivity for the catalysis of PMS in neutral environments (pH 7.0). However, pH 5.5 was observed to be the best condition for 1,4-D destruction, which was probably caused by the involvement of phosphate radicals. Common water components including chloride ions and bicarbonate ions were observed to have promoting and inhibiting effects, respectively, on the removal of 1,4-D. To further demonstrate the potential of Co 2+ -PMS in practical applications, we explored the simultaneous degradation of 20 antibiotics using trace levels of Co 2+ . The results showed that all the investigated antibiotics, except for lomefloxacin, could be efficiently degraded by Co 2+ -PMS with removal rates of greater than 97%. The findings from this study demonstrate the promise of using trace levels of cobalt for environmental remediation applications, even when high concentrations of phosphate ions are co-present.