Application of CoMn/CoFe layered double hydroxide based on metal–organic frameworks template to activate peroxymonosulfate for 2,4-dichlorophenol degradation

Author:

Liu Chenyu1,Wei Haitong1,Gao Yanhui1ORCID,Wang Ning1,Yuan Xiaoying1,Chi Zhilong23ORCID,Zhao Guangli23,Song Shuguang4,Song Jianjun1ORCID,Jin Xinghui1

Affiliation:

1. Shandong Provincial Key Laboratory of Molecular Engineering, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China

2. Kyiv College at Qilu University of Technology, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China

3. Kyiv National University of Technologies and Design, Kyiv 01011, Ukraine

4. School of Transportation Engineering, Shandong Jianzhu University, Jinan 250101, China

Abstract

Abstract Metal-organic frameworks (MOFs) have unique properties and stable structures, which have been widely used as templates/precursors to prepare well developed pore structure and high specific surface area materials. In this article, an innovative and facile method of crystal reorganization was designed by using MOFs as sacrificial templates to prepare a layered double hydroxide (LDH) nano-layer sheet structure through a pseudomorphic conversion process under alkaline conditions. The obtained CoMn-LDH and CoFe-LDH catalysts broke the ligand of MOFs and reorganized the structure on the basis of retaining a high specific surface area and a large number of pores, which had higher specific surface area and well developed pore structure compared with LDH catalysts prepared by traditional methods, and thus provide more active sites to activate peroxymonosulfate (PMS). Due to the unique framework structure of MOFs, the MOF-derived CoMn-LDH and CoFe-LDH catalysts could provide more active sites to activate PMS, and achieve a 2,4-dichlorophenol degradation of 99.3% and 99.2% within 20 minutes, respectively. In addition the two LDH catalysts displayed excellent degradation performance for bisphenol A, ciprofloxacin and 2,4-dichlorophenoxyacetic acid (2,4-D). X-ray photoelectron spectroscopy indicated that the valence state transformation of metal elements participated in PMS activation. Electron paramagnetic resonance manifested that sulfate radical () and singlet oxygen (1O2) were the main species for degrading pollutants. In addition, after the three-cycle experiment, the CoMn-LDH and CoFe-LDH catalysts also showed long-term stability with a slight activity decrease in the third cycle. The phytotoxicity assessment determined by the germination of mung beans proved that PMS activation by MOF-derived LDH catalysts can basically eliminate the phytotoxicity of a 2,4-D solution. This research not only developed high-activity LDH catalysts for PMS activation, but also expanded the environmental applications of MOF derivants.

Funder

Shandong Provincial Key Research and Development Program

Publisher

IWA Publishing

Subject

Water Science and Technology,Environmental Engineering

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