MgO-supported CuO with encapsulated structure for enhanced peroxymonosulfate activation to remove thiamphenicol

催化作用 浸出(土壤学) 化学 自来水 甲砜霉素 矿化(土壤科学) 分解 核化学 无机化学 降级(电信) 有机化学 环境工程 土壤科学 土壤水分 工程类 电信 抗生素 氮气 生物化学 计算机科学 氯霉素 环境科学
作者
Jiabin Dan,Pinhua Rao,Qiongfang Wang,Lei Dong,Wenhai Chu,Min Zhang,Zedi He,Naiyun Gao,Jing Deng,Juxiang Chen
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:280: 119782-119782 被引量:26
标识
DOI:10.1016/j.seppur.2021.119782
摘要

Copper-base catalysts with high load content of CuO were commonly utilized to activate peroxymonosulfate (PMS) for removal of contaminants but limited catalytic efficiency and increased risk of copper ion leaching restricted their use. In this paper, Cu-Mg mixed metal oxides with highly dispersed minute quantities of CuO were successfully prepared by one-pot synthesis for efficiently activating PMS to remove thiamphenicol (TAP), which was economical and environmentally friendly. The catalytic activities of catalysts with different molar ratios of Cu and Mg for PMS and their characteristics were evaluated, illustrating the optimal molar ratio of Cu and Mg (1:15, named CuMg-MMO) in the catalyst. For the CuMg-MMO catalyst, MgO widely dispersed and wrapped CuO nanoparticles, minimized the copper ion leaching and promoted the generation of Cu-OH complex and non-radical species. In the CuMg-MMO/PMS system, the influence factors for TAP degradation were analyzed, including different systems, catalyst dosages, PMS concentrations, temperatures, initial pH values, TAP concentrations, anions (NO3-, HCO3-, Cl-, HPO42- and H2PO4-) and natural organic matter (NOM) concentrations. Under the optimal conditions (i.e., [catalyst]: 75 mg/L, [PMS]: 0.3 mM, temperature: 30 °C and initial pH: 6.5), TAP removal efficiency obtained by this system was 99.9%. SO4·-, ·O2- and 1O2 played more important roles than HO· in TAP degradation. Four successive repeated experiments indicated that CuMg-MMO possessed good reusability and stability. PMS decomposition, mineralization of TAP, the activation mechanism of PMS and possible degradation pathways of TAP were analyzed.

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