Cobalt (II)-intercalated layered double hydroxide as an efficient activator for catalytic oxidation of organic contaminants

被引:7
|
作者
Wang, Rongyao [1 ]
Chen, Fanli [2 ]
Gao, Lijuan [3 ]
Ren, Xiaohua [1 ]
Guo, Weilin [1 ]
机构
[1] Univ Jinan, Sch Water Conservancy & Environm, Jinan 250022, Peoples R China
[2] Jinan Tianzheng Environm Technol Co LTD, Jinan 250014, Peoples R China
[3] Shandong Acad Environm Planning, Jinan 250013, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Cobalt (II)-intercalated LDH; Topological transformation; Peroxymonosulfate activation; Contaminants degradation; PEROXYMONOSULFATE; DEGRADATION; CO; PERSULFATE; NANOSHEETS; WATER; MECHANISM; LDH; ELECTROCATALYST; INTERCALATION;
D O I
10.1016/j.jece.2022.108361
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The simultaneous optimization and design of catalysts' structure or components are extremely significant ap-proaches to further enhancing the catalytic activity. Herein, cobalt (II)-intercalated Ni-Fe layered double hy-droxide (Co-NiFe-LDH) was fabricated via a novel topological transformation process and employed as an efficient activator on peroxymonosulfate (PMS) activation for simulated sewage decontamination. Character-izations with state-of-the-art spectroscopies demonstrated Co (II) was successfully embedded in the interlayer of NiFe-LDH after reconstruction. Meanwhile, experiments manifested that the Co-NiFe-LDH possessed an enhanced catalytic performance relative to neither pristine NiFe-LDH nor ternary CoNiFe-LDH. The maximum Orange II sewage degradation (30 mg L-1, 99.5 %) could be obtained under the optimal conditions (30 min, 120 mg L-1 Co-NiFe-LDH, and 1 mM PMS) with the first-order up to 0.216 min(-1). Encouragingly, the Co-NiFe-LDH/PMS system exhibited stable performance over a wide pH range and low dissolution. It was also found that the superior performance of Co-NiFe-LDH was attributed to the clusters of Co in the interlayer, which can improve electro-chemical characteristics, thereby accelerating interfacial electron transfer. Moreover, on the basis of redox cycles of Ni (II)/Ni (III) and Fe (II)/Fe (III), a new redox cycle of Co (II)/Co (III) was discovered in Co-NiFe-LDH, therefore promoting the utilization efficiency of oxidants. Besides, quenching experiments and electron para-magnetic resonance spectroscopy (EPR) demonstrated that SO4 center dot- and center dot OH acted as the dominant active radicals for Orange II degradation. It's also encouraging that the Co-NiFe-LDH/PMS system could efficiently decompose other typical contaminants, and its catalytic activity remained unchanged after five uses. Ultimately, a reason-able catalytic mechanism of the Co-NiFe-LDH/PMS system was proposed by the comprehensive analysis. This work sheds light on the elegantly designed LDH with high performance toward activating PMS in water decontamination.
引用
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页数:11
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