Highly efficient and selective organic pollutants degradation via peroxymonosulfate activation over micron-sized Co-MOF: Nearly 100% singlet oxygen mechanism

单线态氧 化学 催化作用 罗丹明B 降级(电信) 污染物 双酚A 光降解 苯甲酸 光化学 猝灭(荧光) 氧气 无机化学 光催化 有机化学 荧光 电信 物理 量子力学 计算机科学 环氧树脂
作者
Mengyu Wang,Fei Wang,Peng Wang,Hong-Yu Chu,Huifen Fu,Chen Zhao,Chong‐Chen Wang,Yijiang Zhao
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:326: 124806-124806 被引量:44
标识
DOI:10.1016/j.seppur.2023.124806
摘要

Singlet oxygen-based advanced oxidation processes (1O2-AOPs) have attracted extensive interest in selective removal of organic pollutants in the complicated water matrices. However, both the highly efficient 1O2 production and selective pollutants oxidation degradation are challenging. In this work, a 2D Co-MOF (Co-tib) was synthesized and applied to accomplish nearly 100% 1O2 production during peroxymonosulfate (PMS) activation, which exhibited excellent selective catalytic oxidation performance toward multiple organic pollutants. More importantly, >99% selective removal efficiencies for rhodamine B (RhB), bisphenol A (BPA) and sulfamethoxazole (SMX) are achieved in the mixed RhB/BPA/SMX/Benzoic acid (BA) solutions, and >90% selective removal efficiencies for RhB, BPA and SMX are achieved in the mixed RhB/BPA/SMX/P-nitrobenzoic acid (NBA) solutions. The influences of PMS dosage, pH, pollutant concentrations and inorganic ions for pollutants degradation were investigated. The reaction mechanisms were proposed via active species quenching tests, probe experiments and electron spin resonance (ESR). This work will provide new inspiration for 1O2 production and selective degradation toward multiple pollutants in a complicated aqueous matrix via the catalytic PMS activation over MOFs catalysts.
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