Synthesis of novel zeolite-supported zinc-cobalt bimetallic catalyst by co-precipitation-calcination method for efficient activation of persulfate to degrade tetracycline hydrochloride

Author:

Tang Chengjiao1,Ren Dajun1,Zhang Shuqin1,Zhang Xiaoqing1

Affiliation:

1. a College of Resource and Environmental Engineering, Wuhan University of Science and Technology, Wuhan, 430081, China

Abstract

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.

Publisher

Springer Science and Business Media LLC

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