4.7 Article

Hofmann-MOF derived nanoball assembled by FeNi alloy confined in carbon nanotubes as a magnetic catalyst for activating peroxydisulfate to degrade an ionic liquid

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 295, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2022.120945

Keywords

MOFs; Hofmann; Sulfate radicals; Ionic liquids; FeNi

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With the increasing consumption of ionic liquids (ILs), the release of ILs into water environments poses risks to aquatic ecology. This study aims to develop a useful heterogeneous catalyst to activate peroxydisulfate (PDS) for degrading 1-Butyl-3-methylimidazolium chloride (BMIM). The FeNiC catalyst derived from a unique Hofmann-type MOF exhibits advantageous features and shows promising catalytic activity.
As ionic liquids (ILs) are increasingly consumed, release of ILs into water environment has posed risks to aquatic ecology due to their toxicities. Since 1-Butyl-3-methylimidazolium chloride (BMIMCl) represents the most typical IL, development of useful techniques to eliminate BMIM from water is urgent and critical. While SO4 center dot--based oxidation processes are useful for degrading BMIM, very few studies have been conducted using peroxydisulfate (PDS), and almost no studies exist for developing heterogeneous activation of PDS to degrade BMIM. Thus, the aim of this study is to develop a useful heterogeneous catalyst for the first time to activate PDS for degrading BMIM in water. Herein, a special catalyst is developed from a unique Hofmann-type MOF ([Fe]pyrazine[Ni (CN)(4)]) through carbonization to afford a nanoball assembled from carbon nanotubes (CNTs) with confinement of FeNi alloy nanoparticles. Such a FeNi@CNT (i.e., FeNiC) nanoball exhibits many advantageous features, including embedment of effective metals (Fe and Ni), strong magnetism, protection of FeNi by CNT, synergy of FeNi and CNT, and unique interwoven assembled structures, making FeNiC a promising heterogeneous catalyst for activating PDS to degrade BMIM. FeNiC is proven to exhibit a much higher catalytic activity (RSE = 0.0388) than Fe3O4 for PDS activation (RSE = 0.0155). FeNiC/PDS also shows a lower activation energy (i.e., 40.4 kJ/mol) for BMIM degradation then other reported values, revealing promising advantages of FeNiC. The activation mechanism as well as degradation pathway of BMIM degradation by FeNiC/PDS is also investigated here through theoretical DFT calculations and experimental evidences to provide valuable insights into degradation behaviors of BMIM using Hofmann MOF-derived catalysts.

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