Removal of oxytetracycline from water by S-doped MIL-53(Fe): Synergistic effect of surface adsorption and persulfate activation

过硫酸盐 过氧二硫酸盐 吸附 催化作用 化学 核化学 电子顺磁共振 土霉素 无机化学 有机化学 核磁共振 生物化学 物理 抗生素
作者
Chunyan Du,Yinchu Lv,Jian Cao,Hao Zhu,Yin Zhang,Yulv Zou,Huaiyuan Peng,Wei Dong,Lu Zhou,Guanlong Yu,Hanbo Yu,Jingyi Jiang
出处
期刊:Environmental Research [Elsevier BV]
卷期号:239 (Pt 1): 116842-116842 被引量:19
标识
DOI:10.1016/j.envres.2023.116842
摘要

In this study, a novel catalyst based on MIL-53(Fe) was synthesized and modified through sublimed sulfur (S-MIL-53(Fe)) to induce a synergistic effect of surface adsorption and persulfate activation. The S-doped modification not only increased the surface area but also accelerated the electron transfer process of the iron cycle. The performance of the newly synthesized S-MIL-53(Fe) adsorptive catalyst was evaluated by chemical adsorption and peroxydisulfate (PDS) activated removal of an emerging pollutants, oxytetracycline (OTC). The S-MIL-53(Fe) adsorptive catalyst was able to adsorb 61.7% of OTC after 120 min, and the removal efficiency reached 84.8% within 5 min after PDS dosing. The boosting effect of sulfur on the system was confirmed by characterization analysis and experimental testing. Even after 7 cycles, the removal efficiency of S-MIL-53(Fe) (69.0%) for OTC remained superior to that of pure MIL-53(Fe) (25.1%). Additionally, the adsorption kinetics and adsorption isotherm model of the material were investigated. The possible OTC degrading process was proposed based on radical quenching and electron paramagnetic resonance (EPR). This study provides a feasible way to fabricate an S-doped MIL-53(Fe) adsorptive catalyst for the remediation of antibiotics-containing wastewater.
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