Electrochemical degradation of nanoplastics in water: Analysis of the role of reactive oxygen species

Microplastics and nanoplastics (NPs) are emerging water contaminants which have recently gained lots of attention because of their effects on the aquatic systems and human life. Most of the previous works on the treatment of plastic pollution in water have been focused on microplastics and a very limited study has been performed on the NPs treatmenL In this work, the role of main reactive oxygen species (ROSs) in the electrooxidation (EO) and electro-peroxidation(EO-H2O2) of NPs in water is investigated. In-situ generation of hydroxyl radicals ((OH)-O-center dot), persulfates (S2O82-), and hydrogen peroxide (H2O2) were performed using boron-doped diamond (BDD) as the anode, whereas titanium (in EO process) and carbon felt (CF, in EO-H2O2 process) were used as cathode. In the EO process, NPs were mainly oxidized by two types of ROSs on the BDD surface (i) (OH)-O-center dot from water discharge and (ii) SO4 center dot- via S2O82- reaction with (OH)-O-center dot. In EO-H2O2 process, NPs were additionally degraded by (OH)-O-center dot formed from H2O2 decomposition as well as SO4 center dot- generated from direct or indirect reactions with H2O2. Analysis of the degradation of NPs showed that EO-H2O2 process was around 2.6 times more effective than EO process. The optimum amount of NPs degradation efficiency of 86.8% was obtained using EO-H2O2 process at the current density of 36 mA.Cm-2, 0.03 M Na2SO4, pH of 2, and 40 min reaction time. In addition, 3D EEM fluorescence analysis confinned the degradation of NPs. Finally, the economic analysis showed the treatment of NPs using EO-H(2)O(2 )process had an operating cost of 2.3 $US.m(-3), which was around 10 times less than the EO process. This study demonstrated that the in-situ generation of ROSs can significantly enhance the degradation of NPs in water.