Cu2O-promoted degradation of sulfamethoxazole by α-Fe2O3-catalyzed peroxymonosulfate under circumneutral conditions: synergistic effect, Cu/Fe ratios, and mechanisms

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ABSTRACTTo promote the application of iron oxides in sulfate radical-based advanced oxidation processes, a convenient approach using Cu2O as a catalyst additive was proposed. Composite catalysts based on α-Fe2O3 (CTX%Cu2O, X = 1, 2.5, 5, and 10) were prepared for peroxymonosulfate (PMS) activation, and sulfamethoxazole was used as a model pollutant to probe the catalytic reactivity. The results show that a synergistic catalytic effect exists between Cu2O and α-Fe2O3, which was explained by the promoted reduction of Fe(III) by Cu(I). Iron K-edge X-ray absorption spectroscopy investigations indicated that the promoted reduction probably occurred with PMS acting as a ligand that bridges the redox centers of Cu(I) and Fe(III). The weight ratio between Cu2O and α-Fe2O3 influenced the degradation of sulfamethoxazole, and the optimal ratio depended on the dosage of PMS and catalysts. With 40 mg L–1 PMS and 0.6 g L–1 catalyst, a pseudo-first-order constant of ∼0.019 min–1 was achieved for CT2.5%Cu2O, whereas only 0.004 min–1 was realized for α-Fe2O3. Nearly complete degradation of the sulfamethoxazole was achieved within 180 min under the conditions of 40 mg L–1 PMS, 0.4 g L–1 CT2.5%Cu2O, and pH 6.8. In contrast, less than 20% degradation was realized with α-Fe2O3 under similar conditions. The CT2.5%Cu2O catalyst had the best stoichiometric efficiency of PMS (0.317), which was 4.5 and 5.8 times higher than those of Cu2O (0.070) and α-Fe2O3 (0.054), respectively. On the basis of the products identified, the cleavage of the S–N bond was proposed as a major pathway for the degradation of sulfamethoxazole.