mof衍生的Co/CeO2@GC活化过氧单硫酸酯降解盐酸四环素

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Shenghui Tu, Peng Zhou, Mingming Dong, Wenbin Wu and Lu Sun
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引用次数: 0

摘要

本研究以Co@Ce-MOF为前驱体,煅烧合成了高效磁性Co/CeO2@GC催化剂。考察了不同催化剂用量、四环素(TC)浓度、pH值、过氧单硫酸根(PMS)浓度、温度和共存阴离子对催化性能的影响。采用20 mg催化剂和20 mg PMS,对100 mL 40 mg L−1四环素的降解率可达95.7%。该催化剂在较宽的pH范围内(5-11)保持有效的PMS活化,连续4次循环后仍保持79.2%的活性。电子顺磁共振波谱和自由基猝灭实验证实了自由基途径和非自由基途径在体系中共存,其中非自由基途径在降解过程中占主导地位。液相色谱-质谱联用分析进一步阐明了氧化条件下TC转化机理。这项工作提出了一种mof衍生的材料作为一种有效的PMS活化剂,用于一种简单的TC降解方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MOF-derived Co/CeO2@GC for the activation of peroxomonosulfate for the degradation of tetracycline hydrochloride

MOF-derived Co/CeO2@GC for the activation of peroxomonosulfate for the degradation of tetracycline hydrochloride

In this study, an efficient and magnetic Co/CeO2@GC catalyst was synthesized by calcination using Co@Ce-MOF as a precursor. The effects of different catalyst dosages, tetracycline (TC) concentrations, pH values, peroxomonosulfate (PMS) concentrations, temperatures, and coexisting anions on the catalytic performance were investigated. Using 20 mg of catalyst and 20 mg of PMS, the degradation rate of 100 mL of 40 mg L−1 tetracycline could reach 95.7%. The catalyst maintained effective PMS activation across a broad pH range (5–11), retaining 79.2% activity after four consecutive cycles. Electron paramagnetic resonance spectroscopy and radical quenching experiments confirmed the coexistence of both radical pathways and non-radical pathways in the system, with the latter identified as the dominant contributor to the degradation process. Reaction pathway analysis via liquid chromatography-mass spectrometry further elucidated TC transformation mechanisms under these oxidative conditions. This work proposes a MOF-derived material as an efficient PMS activator for a simple method of TC degradation.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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