Synergistic degradation of phenols using peroxymonosulfate activated by CuO-Co3O4@MnO2 nanocatalyst

催化作用 浸出(土壤学) 降级(电信) 化学 氧化还原 过渡金属 金属 反应性(心理学) 苯酚 结晶度 化学工程 无机化学 有机化学 地质学 病理 替代医学 土壤水分 土壤科学 结晶学 工程类 电信 医学 计算机科学
作者
Aimal Khan,Zhuwei Liao,Yong Liu,Jawad Ali,Jerosha Ifthikar,Zhuqi Chen
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:329: 262-271 被引量:196
标识
DOI:10.1016/j.jhazmat.2017.01.029
摘要

The development of transition metal based heterogeneous catalysts with efficient reactivity and intensive stability is of great demand in peroxymonosulfate based AOPs in water treatment. Herein, we present a novel approach of creating stable and effective nano-rod catalyst of CuCo@MnO2 with tetragonal structure. A remarkable synergetic effect was found between bi-metallic oxides of Cu and Co: 0.5%Cu-2%Co-MnO2 can efficiently degrade 100% of 30ppm phenol, while 0.5%Cu@MnO2 or 2%Co@MnO2 alone is apparently sluggish for the degradation of organic contaminants. The nanocatalyst retained good stability in recycling tests, during which little leaching of Co and Cu ions can be detected and crystallinity of support α-MnO2 remained unchanged. Mechanism study indicated that SO4- and OH are accounted to participate the degradation, and the generation of radicals is originated from the interaction of CuCo@MnO2 and PMS through metal site with peroxo species bond. The redox cycle among the active metals (M2+↔M3+↔M2+) and Cu enhanced generation of Co(II)-OH complex are critical for the remarkable performance in CuCo@MnO2/PMS system. Both the synergetic acceleration of catalyst activity and instinct mechanism are highly suggestive to the design of heterogeneous catalysts for the degradation of organic contaminants in PMS based advanced oxidation processes.
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