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Enhancement of Fe@porous carbon to be an efficient mediator for peroxymonosulfate activation for oxidation of organic contaminants: Incorporation NH2-group into structure of its MOF precursor

化学 催化作用 电子顺磁共振 多孔性 碳纤维 水溶液 化学工程 光化学 无机化学 有机化学 材料科学 核磁共振 物理 复合材料 工程类 复合数
作者
Chao Liu,Yiping Wang,Yuting Zhang,Ruoyu Li,Wei‐Dong Meng,Zilong Song,Fei Qi,Bingbing Xu,Wei Chu,Donghai Yuan,Bin Yu
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:354: 835-848 被引量:148
标识
DOI:10.1016/j.cej.2018.08.060
摘要

Metal-organic frameworks (MOFs) derived [email protected] carbon showed good performance in peroxymonosulfate (PMS) activation for refractory organic chemical degradation from aqueous. However, the effect of structure and physical-chemical properties of [email protected] carbon on PMS activation and its involved reaction mechanism were still unclear. Herein, [email protected] carbon derived from MOF MIL-53(Fe) was used as target, to discuss the role of NH2-group incorporation on the development of structure and physical-chemical properties of obtained [email protected] carbon, and reaction mechanism for PMS activation. The incorporation of NH2-group significantly decreased the synthesis temperature of [email protected] carbon and increased the encapsulation of Fe0 in the porous carbon. Furthermore, the addition of nitrogen in porous carbon and rigid encapsulation structure reduced the defects of the [email protected] carbon. These improvements of the structure and chemical properties were favored for enhancement of the catalytic activity and stability of the obtained [email protected] carbon in the activation of PMS. Electron paramagnetic resonance (EPR) experiments indicated that SO4−, OH and 1O2 were involved. The radical pathway involving SO4− and OH was the prevailing pathway while the nonradical pathway involving 1O2 was the recessive pathway. Based on intermediate identification, the degradation pathway of acyclovir (ACV) was proposed as SO4− and OH derived process, and eight of intermediates were first reported. It was interesting to note that iron species, carbon structure, and nitrogen element in the catalysts derived from MIL-53(Fe) or NH2-MIL-53(Fe) clearly showed different role and reaction pathway. This work not only provided an efficient [email protected] porous carbon for activation PMS to degrade refractory organic chemicals for water purification, but also suggested a valuable insight for the design of [email protected] carbon derived from MOF.
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