Highly efficient catalyst of Crednerite CuMnO2 for PMS activation: Synthesis, performance and mechanism

催化作用 氧化还原 热液循环 可重用性 电子转移 浸出(土壤学) 化学 过渡金属 金属 激进的 羟基自由基 无机化学 材料科学 光化学 化学工程 有机化学 环境科学 软件 计算机科学 土壤科学 工程类 土壤水分 程序设计语言
作者
Hang Chen,Xiangyu Zhang,Ying Zhao,Shuo Wang,Yueming Ren,X Wang
出处
期刊:Surfaces and Interfaces [Elsevier]
卷期号:42: 103522-103522 被引量:11
标识
DOI:10.1016/j.surfin.2023.103522
摘要

Exploring highly efficient and stable transition metal-based catalysts is significant for the heterogeneous catalysis of peroxymonosulfate (PMS) in contaminants removal during water purification. Herein, we developed a series of Crednerite CuMnO2 catalysts by tuning the hydrothermal synthesis conditions and applied them to catalyze PMS to degrade Orange I (OI). Hydrothermal temperature, hydrothermal reaction time, and NaOH dosage had a great influence on the catalytic performance of catalysts, but different synthetic raw materials had little diversity. Amongst, CMO-160°C-110mmol-24h exhibited the optimal PMS activation effect due to the promoted surface oxygen mobility and electron conduction. Regardless of the wide pH range of 5-9, the coexistence of Inorganic anions and humic acid, the inhibition of OI removal was not significant. Additionally, CMO-160°C-110mmol-24h showed low metal ion leaching and noticeable reusability, implying a great potential application of the CMO-160°C-110mmol-24h/PMS system in practical wastewater engineering. Mechanism studies indicated that surface hydroxyl groups, Cu+/Cu2+ and Mn2+/Mn3+ redox couples were key active sites for PMS activation. Both free radical pathways (•OH, SO4•−, O2•−) and non-free radical pathways (1O2 and electron transfer) were detected in the oxidation reaction, with non-free radical pathways as major contributors. The possible degradation pathway of OI was proposed, and the toxicity of intermediates was assessed. Overall, this study provided an important strategy for the construction of efficient and stable PMS catalysts in wastewater treatment.
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