纳米片
降级(电信)
尖晶石
四环素
多孔性
化学
机制(生物学)
化学工程
材料科学
计算机科学
生物化学
冶金
工程类
物理
有机化学
电信
量子力学
抗生素
作者
Yuan Pan,Xiansheng Zhang,Ting Wu,Binbin Shao,Teng Li,Qingyun He,Zehua Chen,Lingfeng Zhou,Sheng Liu,Xinyi Huang,Zhifeng Liu
摘要
The rational design of bimetallic-based heterogeneous Fenton-like catalyst derived from metal-organic-frameworks (MOFs) for peroxymonosulfate (PMS) activation via a non-radical pathway is attractive but challenging. Herein, a spinel-type 3D hierarchical porous NiCo2O4 nanosheet array for the activation of PMS is rationally designed by surfactant-assisted interfacial engineering. The NiCo2O4/PMS system demonstrated remarkable oxidative degradation of tetracycline (TC) through 1O2 attack and electron transfer process, which was different from previous reports where the free radicals also play a role in the degradation. The synergy between surface Co and Ni enhances electron transfer efficiency and peroxyl bond cleavage, laying the foundation for subsequent radical conversion to 1O2, which was the dominant catalytic mechanism. The system also possessed a broad spectrum for degrading other typical contaminants, and maintained decent degradation performance in actual water matrix, wide pH range and in the presence of anions and organic matter. Furthermore, the robust stability of the structure and catalytic activity make it promising for practical water treatment. It can be expected that this proposal will provide insights for the delicate structural design and the understanding of its PMS activation mechanism of bimetallic-based Fenton-like catalysts, as well as for the efficient degradation of emerging organic pollutants.
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