Abstract Addressing the challenges posed by the high cost and limited efficiency of traditional Chinese medicine wastewater treatment, the development of a cost-effective and highly efficient catalyst for activating persulfate (PMS) to degrade organic pollutants holds significant practical importance. This research successfully synthesized a zinc-cobalt bimetallic catalyst supported on sepiolite (Zn-Co@SEP) using a straightforward co-precipitation-calcination method. Various characterization techniques, including scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy, validated the synthesis process. The introduction of sepiolite as a carrier provided additional active sites, facilitating the redox cycling of Co²⁺/Co³⁺ and Zn²⁺/Zn³⁺, which continuously generated reactive species. Zn-Co@SEP exhibited remarkable catalytic activity towards PMS, achieving a degradation efficiency of over 93% for TC (50 mg/L) within just 30 minutes in the Zn-Co@SEP/PMS system. The study systematically investigated the influence of Zn-Co@SEP dosage, PMS dosage, TC concentration, pH, and temperature on the degradation efficiency of the catalytic system. Notably, the Zn-Co@SEP/PMS system maintained high degradation rates for TC across a wide pH range (3–11) and demonstrated robust stability and recyclability, retaining a degradation rate of 89.56% after four cycles of reuse. Further experimental evidence from free radical quenching studies, electron paramagnetic resonance (EPR) experiments, and oxidative capacity potential (OCPT) results underscored the involvement of multiple radicals (¹O₂, SO₄⁻•, O₂⁻•, •OH) and electron transfer pathways in promoting TC degradation. In conclusion, this research contributes new insights into the synthesis of efficient PMS catalysts tailored for the degradation of antibiotic wastewater, addressing a critical need in environmental remediation.
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Tang et al. (2024) studied this question.
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