Mesoporous carbon framework supported Cu-Fe oxides as efficient peroxymonosulfate catalyst for sustained water remediation

煅烧 吸附 催化作用 碳纤维 化学工程 环境修复 介孔材料 活性炭 化学 材料科学 无机化学 氧化物 有机化学 污染 复合数 复合材料 工程类 生态学 生物
作者
Gen Wang,Weidong An,Yue Zhang,Zhuoyue Liu,Shengjiong Yang,Pengkang Jin,Dahu Ding
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:430: 133060-133060 被引量:79
标识
DOI:10.1016/j.cej.2021.133060
摘要

Mesoporous carbon framework enables highly spatial dispersion of nanosized Cu-Fe oxides, enhanced adsorption of BPA and improved electron transfer efficiency. Accordingly, BPA was efficiently degraded by PMS activated by mesoporous carbon framework supported Cu-Fe oxides. • Mesoporous carbon framework supported Cu-Fe oxides was prepared by calcination of metal-plant phenolic networks in air. • Nanosized Cu-Fe oxides were spatial monodispersed on mesoporous carbon framework providing high exposure of active sites. • Mesoporous carbon framework enables improved adsorption of pollutants and enhanced electron transfer efficiency. • Carbon supported Cu-Fe oxides exhibited efficient and sustained removal of BPA in flow-through test via PMS activation. Large-scale green synthesis of high-performance catalysts is desirable for practical application of peroxymonosulfate (PMS) based advanced oxidation process. In this study, mesoporous carbon framework supported Cu-Fe oxides (CuO/CuFe 2 O 4 ) was synthesized via calcination of cost-effective metal-plant phenolic networks for PMS activation to degrade organic pollutants. The mesoporous carbon framework enables highly spatial dispersion of nanosized Cu-Fe oxides, enhanced adsorption of organic pollutant (Bisphenol A, BPA) and improved electron transfer efficiency. Benefiting from the advantageous structure, the mesoporous carbon framework supported Cu-Fe oxides manifested excellent catalytic efficiency in PMS activation, enabling fast and sustained removal of BPA in simulated and actual contaminated water at neutral pH. Chemical scavenging experiments and electron paramagnetic resonance (EPR) tests revealed that reactive oxygen species (ROS) including SO 4 •− , OH • and 1 O 2 all participated in the degradation of BPA. The kinetic study and in situ characterization with ATR-FTIR indicated that PMS was activated by surface Cu(II) through an outer-sphere interaction, and a redox cycle of Cu(II)-Cu(I)-Cu(II) was responsible for the generation of ROS. This work demonstrates a reliable method for rational design of hybrid catalyst of metal oxide and carbon material for efficient wastewater remediation.
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