摘要
Mesoporous carbon materials are promising catalysts for peroxydisulfate (PDS) activation for degrading aqueous organic pollutants but limited by the intrinsic inertness. Herein, co-doping of iron and nitrogen into the mesoporous carbon framework was performed via thermal conversion of metal-polyphenol coordination polymers (Fe-TA) to synthesize Fe/N co-doped mesoporous carbon for efficient PDS activation. Owing to the large surface area, high graphitization degree and defective configurations, the Fe/N co-doped mesoporous carbon (Fe/N-MCs) exhibited superior catalytic performance toward the degradation of organic pollutants . Electron paramagnetic resonance tests, chemical quenching experiments, electrochemical analysis and spectra measurements revealed that the degradation of organic pollutants over the Fe/N-MCs followed a nonradical oxidation pathway based on electron transfer process. Graphite nitrogen and hydroxyl (C-OH) groups on the defective edges of Fe/N-MCs were proved to be possible active sites for PDS activation. PDS catalyzed by the Fe/N-MCs exhibited strong anti-interference capability to surrounding inorganic ions (such as Cl – , CO 3 2– , NO 3 – and SO 4 2– ) and natural organic matters, making it a promising candidate for the degradation of organic pollutants. This work provides a new prospect for developing highly active mesoporous carbon materials via heteroatom doping for PDS activation for wastewater decontamination .
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