Heterogeneous photocatalytic activation of electrogenerated chlorine for the production of reactive oxygen and chlorine species: A new approach for Bisphenol A degradation in saline wastewater

Abstract

UV-E-chlorination/hematite nanoparticles (UV/E-Cl/HNs) as a heterogeneous photocatalytic activation of electrogenerated chlorine was assessed for the degradation of bisphenol A (BPA) as a new approach based on the generation of reactive chlorine and oxygen species. The prepared sample was characterized using multiple techniques, such as XRD, FTIR, FESEM, EDS, and BET-BJH. An excellent decontamination efficiency of 99.4% was achieved within 40 min of electrolysis under optimum conditions (pH of 5, HNs dosage 100 mg/L, current density of 20 mA/cm², and NaCl concentration of 50 mM). The HOCl content was reduced more swiftly in the presence of ultraviolet (UV) irradiation and hematite, resulting in the production of oxidative radicals (i.e., ^•OH, Cl^•, and Cl₂^•-). The scavenging experiments also verified the vital role of these radicals in oxidative treatment. The UV/E-Cl/HNs process is readily supplied with hydroxyl radicals through several mechanisms. Bicarbonate ions showed a noticeable inhibitory impact, whereas nitrate and sulfate anions only slightly affected BPA degradation. The HNs were a recoverable and stable catalyst for six cycles. Furthermore, the ECOSAR program predicted that the UV/E-Cl/HNs can be labeled as an environmental-friendly process. Eventually, reasonable degradation pathways were proposed based on the identified by-products through experimental and theoretical approaches.

Keywords: Bisphenol A; Electro-photocatalytic degradation; Reactive oxygen and chlorine species; Saline wastewater; Toxicity assessment.