经铈基金属有机框架 (Ce-MOF) 衍生物改性的碳布阴极上的电活性过硫酸钠降解左氧氟沙星

Xinbiao Mao, Mingyu Ou, Wenjun Zhao, Shuangting Yu, Hao Xu
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引用次数: 0

摘要

左氧氟沙星(LFX)因其分子稳定性难以有效降解,已成为亟待解决的问题。过硫酸盐的高级氧化技术越来越受到研究人员的关注。本研究通过水热合成和煅烧制备了一种 Ce-MOF 衍生物(Ce-MOF-T),该衍生物与电活化协同反应生成硫酸根自由基,可高效降解 LFX。实验证明,电活化和 Ce-MOF 衍生物共同作用生成硫酸根自由基,有效降解 LFX。以 Ce-MOF-550 改性碳布为阴极,铂电极为阳极,LFX 的浓度为 20 mg-L-1,Ce-MOF-550 的负载量为 15 mg,pH = 5,过硫酸钠(PMS)的浓度为 0.3 g-L-1,电流密度为 100 A-m-2,反应 1 h 后降解率为 82.05%,反应 3 h 后降解率为 95%。经过五个循环测试后,降解率仍高于 75.00%,表明该材料具有良好的稳定性。此外,LFX 的降解符合准一级动力学反应,表观速率常数为 2.26 × 10-2 min-1。
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Degradation of Levofloxacin by Electroactivated Sodium Persulfate on Carbon Cloth Cathode Modified with Cerium-Based Metal Organic Frameworks (Ce-MOF) Derivatives
Levofloxacin (LFX), which is difficult to degrade effectively due to its molecular stability, has become an problem that needs to be solved urgently. The advanced oxidation technology of persulfate has received increasing attention from researchers. In this study, a Ce-MOF derivative (Ce-MOF-T) was prepared by hydrothermal synthesis and calcination, which synergistically responded to electroactivation to generate sulfate radicals for the efficient degradation of LFX. It has been proven that electrical activation and the Ce-MOF derivatives work together to generate sulfate radicals and effectively degrade LFX. Ce-MOF-550-modified carbon cloth was used as the cathode and a platinum electrode as the anode, the concentration of LFX was 20 mg·L−1, the loading of Ce-MOF-550 was 15 mg, pH = 5, the concentration of sodium persulfate (PMS) was 0.3 g·L−1, the current density was 100 A·m−2, and the degradation rate was 82.05% after 1 h of reaction and 95% after 3 h of reaction. After five cycle tests, the degradation rate was still higher than 75.00%, indicating that the material had good stability. In addition, the degradation of LFX was consistent with a quasi-primary kinetic reaction with apparent rate constants of 2.26 × 10−2 min−1.
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