Synthesis and characterization of amino functionalized bimetallic metal-organic frameworks as peroxymonosulfate activator for water purification: Performance and mechanistic studies

化学 双金属片 激活剂(遗传学) 金属有机骨架 吸附 表征(材料科学) 金属 组合化学 环境化学 纳米技术 有机化学 材料科学 生物化学 基因
作者
Huanxuan Li,Yucheng Lou,Junting Zheng,Liya Su,Shun Lu,Chen Xu,Jingang Huang,Qingwei Zhou,Junhong Tang,Mingzhi Huang
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:10 (5): 108272-108272 被引量:2
标识
DOI:10.1016/j.jece.2022.108272
摘要

The importance of new water purification technology for maintaining clean water resources and a high quality of life is self-evident. In this study, amino functionalized bimetallic metal-organic frameworks (NH 2 -MIL-101(FeCo)) were prepared to activate peroxymonosulfate (PMS) for removal of organic pollutants from water. The structure, morphology, and physicochemical properties of as-prepared NH 2 -MIL-101(FeCo) were comprehensively evaluated by X-ray diffraction, scanning electron microscopy, N 2 adsorption-desorption isotherms, and X-ray photoelectric spectroscopy. Degradation tests were performed to study effects of PMS concentration, catalyst dosage, initial pH, and common substances on the orange G (OG) removal. The acidic and alkaline conditions promoted the formation of mesoporous structures in NH 2 -MIL-101(FeCo) and enhanced the mass transfer processes to remove OG. 100% of OG was removed through a rate constant of 0.0711 min -1 within 45 min in NH 2 -MIL-101(FeCo)− 2/PMS/OG system, where 1 O 2 , SO 4 •− , and · OH played pivotal contributions in the OG removal. The catalytic activity of NH 2 -MIL-101(FeCo) originated from unsaturated metal sites of Fe(II) and Co(II). This work demonstrates a feasible strategy towards the synthesis of functional MOFs for removal of organic contaminants. • Acidic and alkaline conditions promoted formation of mesoporous structures. • NH 2 -MIL-101(FeCo) showed good activity to PMS and 100% of OG was removed. • 1 O 2 , SO 4 •− , and · OH were the major species responsible for OG removal. • Unsaturated metal sites of Fe(II) and Co(II) contributed to catalytic activity.

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