<p>The increasing contamination of aquatic environments by antibiotics calls for efficient, economical, and environmentally sustainable remediation technologies. This study presents a zero-valent iron (ZVI)-activated periodate (IO<sub>4</sub><sup>−</sup>) advanced oxidation system for the degradation of oxytetracycline (OTC) in water. Under optimized conditions (pH = 3, ZVI = 1.64&#xa0;g/L, IO<sub>4</sub><sup>−</sup> = 1.97&#xa0;mM), the ZVI/IO<sub>4</sub><sup>−</sup> system achieved 81.16% OTC removal. Notably, coupling with UV irradiation enabled complete OTC degradation within 50&#xa0;min, demonstrating substantial enhancement over the standalone system. Mechanistic investigations revealed that IO<sub>3</sub><sup>•</sup>, <sup>1</sup>O<sub>2</sub>, and O<sub>2</sub><sup>•−</sup> were the dominant reactive species, and three degradation pathways were proposed based on LC–MS analysis. The system exhibited excellent performance in real water matrices, achieving 78.0% and 71.9% OTC removal in tap water and lake water, respectively, along with strong tolerance to coexisting ions and humic acid. Importantly, the ZVI catalyst retained 96.4% of its initial activity after five consecutive cycles, significantly reducing operational costs and secondary pollution risks. This work provides an efficient, stable, and cost-effective treatment strategy for antibiotic-contaminated water, holding strong promise for practical engineering applications.</p>

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Degradation of Oxytetracycline by Zero-Valent Iron Activated Periodate: Efficiency Optimization, Performance Improvement, Reaction Mechanisms, and Application Analysis

  • Yongbo Xiao,
  • Yanjiao Gao,
  • Fan Bai,
  • Jing Xiao

摘要

The increasing contamination of aquatic environments by antibiotics calls for efficient, economical, and environmentally sustainable remediation technologies. This study presents a zero-valent iron (ZVI)-activated periodate (IO4) advanced oxidation system for the degradation of oxytetracycline (OTC) in water. Under optimized conditions (pH = 3, ZVI = 1.64 g/L, IO4 = 1.97 mM), the ZVI/IO4 system achieved 81.16% OTC removal. Notably, coupling with UV irradiation enabled complete OTC degradation within 50 min, demonstrating substantial enhancement over the standalone system. Mechanistic investigations revealed that IO3, 1O2, and O2•− were the dominant reactive species, and three degradation pathways were proposed based on LC–MS analysis. The system exhibited excellent performance in real water matrices, achieving 78.0% and 71.9% OTC removal in tap water and lake water, respectively, along with strong tolerance to coexisting ions and humic acid. Importantly, the ZVI catalyst retained 96.4% of its initial activity after five consecutive cycles, significantly reducing operational costs and secondary pollution risks. This work provides an efficient, stable, and cost-effective treatment strategy for antibiotic-contaminated water, holding strong promise for practical engineering applications.