Activation of H(2)O(2) by nano zero-valent iron (nZVI) enables fast sulfadiazine degradation: mechanistic insights and process optimization

纳米零价铁(nZVI)活化H₂O₂可实现磺胺嘧啶的快速降解:机理研究及工艺优化

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Abstract

BACKGROUND: Antibiotic contamination in aquatic systems demands advanced oxidation solutions. This study develops a nano zero-valent iron (nZVI)-activated peroxide system to address sulfadiazine (SDZ) persistence and associated ecological risks. METHODS: Structural properties of nZVI were analyzed by TEM/XRD. Process parameters were optimized through Box-Behnken design. Degradation mechanisms were investigated via radical quenching experiments, HPLC-MS analysis, and acute toxicity bioassays. ‌. SIGNIFICANT FINDINGS: The system achieved complete SDZ (20 mg L⁻¹) removal within 5 min under optimal conditions (pH 2.44, 0.12 g L⁻¹ nZVI, 0.009% H₂O₂), showing strong agreement with pseudo-first-order kinetics (k = 0.637 min ⁻¹, R²=0.998). Hydroxyl radicals dominated SDZ degradation, generating 12 transformation products through amino oxidation, hydroxylation, and sulfonamide bridge cleavage. Toxicity reduction (60-90% EC50 improvement) confirmed effective detoxification. This work establishes nZVI-driven peroxide activation as a viable strategy for antibiotic wastewater remediation.

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