Dynamic control of pentachlorophenol photodegradation process using P25/PDA/BiOBr through regulation of photo-induced active substances and chemiluminescence

Abstract

Photodegradation is a new approach for the removal of pentachlorophenol (PCP). Photooxidation degradation (using hydroxyl radicals) exhibits better performance to remove PCP than photoreduction degradation, but the former will lead to an increase in the production of toxic by-products such as tetrachloro-1,4-benzoquinone (TCBQ). Thus, a new strategy is required to enhance PCP photodegradation and simultaneously inhibit toxic intermediates production. Herein, TiO2 (P25)/polydopamine (PDA)/BiOBr was synthesized and used to photodegrade PCP. Based on the relative position of the CB and VB of P25 and BiOBr, and PDA as an electron transfer mediator, a high number of holes, electrons, and superoxide anions were produced instead of hydroxyl radicals. The photocatalytic activity of P25/PDA/BiOBr exhibited the best performance among as-prepared samples, reaching a k(pcp) value of 0.4 min−1 (20 μM PCP) under UV light irradiation within 10 min. According to chemiluminescence and acute toxicity assays, relative to P25, the toxic intermediates of TCBQ and trichlorohydroxy-1,4-benzoquinone (OH-TrCBQ) generation was greatly reduced over P25/PDA/BiOBr, with a lack of toxic product generation during PCP photodegradation process. These findings provide an alternative strategy to achieve greener and more efficient organic pollutant photodegradation.