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在类芬顿反应中,通过简便方法将铁纳米颗粒的涂层从碳化铁调整为氮化铁,以实现不同性能。

Facilely tuning the coating layers of Fe nanoparticles from iron carbide to iron nitride for different performance in Fenton-like reactions.

作者信息

Li Ningyuan, Wang Jun, Liao Tao, Ma Biao, Chen Ying, Li Yang, Fan Xiaobin, Peng Wenchao

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China.

Department of Chemical Engineering, Tianjin Renai College, Tianjin 301636, China.

出版信息

J Colloid Interface Sci. 2024 Oct 15;672:688-699. doi: 10.1016/j.jcis.2024.06.029. Epub 2024 Jun 6.

Abstract

In this study, a series of Fe-based materials are facilely synthesized using MIL-88A and melamine as precursors. Changing the mass ratio of melamine and MIL-88A could tune the coating layers of generated zero-valent iron (Fe) particles from FeC to FeN facilely. Compared to Fe/FeN@NC sample, Fe/FeC@NC exhibits better catalytic activity and stability to degrade carbamazepine (CBZ) with peroxymonosulfate (PMS) as oxidant. Free radical quenching tests, open-circuit potential (OCP) test and electron paramagnetic resonance spectra (EPR) prove that hydroxyl radicals (OH) and superoxide radical (O) are dominant reactive oxygen species (ROSs) with Fe/FeC@NC sample. For Fe/FeN@NC sample, the main ROSs are changed into sulfate radicals (SO) and high valent iron-oxo (Fe (IV)=O) species. In addition, the better conductivity of FeC is beneficial for the electron transfer from Fe to the FeC, thus could keep the activity of the surface sites and obtain better stability. DFT calculation reveals the better adsorption and activation ability of FeC than FeN. Moreover, PMS can also be adsorbed on the Fe sites of FeN with shorter FeO bonds and longer SO bonds than on FeC, the Fe (IV)=O is thus present in the Fe/FeN@NC/PMS system. This study provides a novel strategy for the development of highly active Fe-based materials for Fenton-like reactions and thus could promote their real application.

摘要

在本研究中,以MIL-88A和三聚氰胺为前驱体,简便地合成了一系列铁基材料。改变三聚氰胺与MIL-88A的质量比能够轻松地将生成的零价铁(Fe)颗粒的包覆层从FeC调整为FeN。与Fe/FeN@NC样品相比,Fe/FeC@NC对以过一硫酸盐(PMS)为氧化剂降解卡马西平(CBZ)表现出更好的催化活性和稳定性。自由基猝灭试验、开路电位(OCP)测试和电子顺磁共振光谱(EPR)证明,对于Fe/FeC@NC样品,羟基自由基(OH)和超氧自由基(O)是主要的活性氧物种(ROSs)。对于Fe/FeN@NC样品,主要的ROSs转变为硫酸根自由基(SO)和高价铁氧(Fe(IV)=O)物种。此外,FeC较好的导电性有利于电子从Fe转移到FeC,从而能够保持表面位点的活性并获得更好的稳定性。密度泛函理论(DFT)计算表明,FeC比FeN具有更好的吸附和活化能力。此外,与FeC相比,PMS也能以较短的FeO键和较长的SO键吸附在FeN的Fe位点上,因此Fe(IV)=O存在于Fe/FeN@NC/PMS体系中。本研究为开发用于类芬顿反应的高活性铁基材料提供了一种新策略,从而能够促进其实际应用。

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