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Synthesis of Co-doped Fe metal–organic framework MIL-101(Fe,Co) and efficient degradation of organic dyes in water.

Authors :
Xiao, Ziyi
Wu, Rui
Shu, Tingting
Wang, Yingxi
Li, Ling
Source :
Separation & Purification Technology. Jan2023, Vol. 304, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

[Display omitted] • Co doped MIL-101(Fe, Co) with different degrees was synthesized by a simplified benign method. • MIL-101(Fe, Co) presented higher activity than MIL-101(Fe) for peroxymonsulfate(PMS) activation. • MIL-101(Fe, Co)/PMS exhibited excellent degradation performance for organic dyes. • MIL-101(Fe, Co 20%) have good structural stability and recyclability.. In order to further improve the catalytic performance of MIL-101, cobalt-doped MIL-101(Fe,Co) was synthesized by solvothermal method. By adjusting the ratio of cobalt doping, the MIL-101(Fe,Co 20%) with the best catalytic activity was obtained. The activation performance of MIL-101(Fe,Co 20%) for peroxymonosulfate (PMS) was studied using Rhodamine B (RhB) as a pollutant model. The experimental results proved MIL-101(Fe,Co 20%) with much better catalytic performance than MIL-101(Fe), which can degrade more than 99% of RhB within 15 min. The effects of initial solution pH and coexisting anions in water on the degradation of RhB were further discussed. The results showed that MIL-101(Fe,Co 20%) was with excellent stability and degradation efficiency can still keep above 90% after five cycles. The free radical quenching experiments were further studied to explore the degradation mechanism. It can be concluded that SO 4 -· was the main active free radical for the degradation of RhB. The possible intermediate products in the degradation process of RhB were analyzed by LC-MS. Combined with the comparison of XPS before and after the reaction, the possible reaction mechanism of RhB degradation process was inferred. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13835866
Volume :
304
Database :
Academic Search Index
Journal :
Separation & Purification Technology
Publication Type :
Academic Journal
Accession number :
159908594
Full Text :
https://doi.org/10.1016/j.seppur.2022.122300