Highly efficient electro-cocatalytic Fenton-like reactions for the degradation of recalcitrant naphthenic acids: Exploring reaction mechanisms and environmental implications

In this study, an electrochemical/peroxymonosulfate/Fe(III) (EC/PMS/Fe(III)) system was established for efficient degradation of four naphthenic acids (NAs) compounds including cyclohexanecarboxylic (CHA), heptanoic (HPA), benzoic (BA) and 2-methylhexanoic acids (2-MHA). The introduction of electric field enhances the redox cycle of Fe(III)/Fe(II) to activate PMS for degredation of NAs. Complete degradation of NAs compounds (5 mg/L) has been achieved within 30 min in the EC/PMS/Fe(III) system. The results of electron paramagnetic resonance (EPR) analysis, scavenging experiment, and chemical probe experiments indicated hydroxyl radical ((OH)-O-center dot), sulfate radical (SO4 center dot-) and singlet oxygen (O-1(2)) are primary reactive oxygen species (ROS) in the EC/PMS/Fe(III) system. NAs compounds with different structures exhibit inconsistent degradation efficiency in current system (k(CHA) > k(BA) > k(HPA) > k2( MHA)), depending on the selectivity of the different ROS and stability of respective intermediate organic radicals. Besides, multiple degradation pathways of CHA, mainly including hydroxylation and carbonylation, were proposed by combining the results of mass spectrometry analysis with the calculated Fukui index based on density functional theory (DFT) calculation. In addition, the EC/PMS/Fe(III) system exhibited robust performance with the addition of co-existing ions. This work provides a novel strategy for efficient degradation of NAs for future remediation of petroleum wastewater.

Automated summary

In this study, an electrochemical/peroxymonosulfate/Fe(III) system was established for efficient degradation of four naphthenic acids (NAs) compounds. The primary reactive oxygen species (ROS) in this system were identified as hydroxyl radical, sulfate radical, and singlet oxygen. The degradation efficiency of different NAs compounds varied depending on the selectivity of ROS and stability of intermediate organic radicals. Additionally, the system showed robust performance in the presence of co-existing ions.