4.8 Article

Enhanced Direct Electron Transfer Mediated Contaminant Degradation by Fe(IV) Using a Carbon Black-Supported Fe(III)-TAML Suspension Electrode System

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AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c08467

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Fe-TAML; suspension anode reactor; organic oxidation; electrochemical activation; high valent iron

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Iron complexes of tetra-amido macrocyclic ligands (Fe-TAML) are effective catalysts for the degradation of organic contaminants, with the high valent Fe(IV) and Fe(V) species generated by activation with hydrogen peroxide (H2O2). This study explores the use of an electrode attached Fe-TAML complex to generate high valent iron species at the anode, resulting in enhanced stability and improved oxidation rates. The application of this carbon black-supported Fe-TAML suspension anode reactor shows significantly higher oxidation rates and lower energy consumption compared to alternate technologies.
Iron complexes of tetra-amido macrocyclic ligands (Fe-TAML) are recognized to be effective catalysts for the degradation of a wide range of organic contaminants in homogeneous conditions with the high valent Fe(IV) and Fe(V) species generated on activation of the Fe-TAML complex by hydrogen peroxide (H2O2) recognized to be powerful oxidants. Electrochemical activation of Fe-TAML would appear an attractive alternative to H2O2 activation, especially if the Fe-TAML complex could be attached to the anode, as this would enable formation of high valent iron species at the anode and, importantly, retention of the valuable Fe-TAML complex within the reaction system. In this work, we affix Fe-TAML to the surface of carbon black particles and apply this suspension anode process to oxidize selected target compounds via generation of high valent iron species. We show that the overpotential for Fe(IV) formation is 0.17 V lower than the potential required to generate Fe(IV) electrochemically in homogeneous solution and also show that the stability of the Fe(IV) species is enhanced considerably compared to the homogeneous Fe-TAML case. Application of the carbon black-supported Fe-TAML suspension anode reactor to degradation of oxalate and hydroquinone with an initial pH value of 3 resulted in oxidation rate constants that were up to three times higher than could be achieved by anodic oxidation in the absence of Fe-TAML and at energy consumptions per order of removal substantially lower than could be achieved by alternate technologies.

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