Nonradical induced degradation of bisphenol AF by NaBiO3 coupled peroxymonosulfate process: Performance and mechanism

• A heterogeneous catalytic system of NaBiO 3 for PMS without light irradiation was investigated. • Both radical (SO 4 −• and • OH) and non-radical ( 1 O 2 ) were contributed to BPAF degradation. • The contribution rate of 1 O 2 , · SO- 4, and · OH was calculated as 80.4%, 8.7%, and 9.9%, respectively. It has been shown previously that the NaBiO 3 (NBO) could efficiently photocatalytically degrade organic contaminants because of its excellent photocatalytic property. In this study, we proposed a heterogeneous catalytic system of NBO for peroxymonosulfate (PMS) without light irradiation. The results showed that NBO/PMS exhibited excellent performance toward bisphenol AF (BPAF) degradation and mineralization. The effectiveness of the NBO/PMS system was also investigated in different multicomponent systems. The effects of initial pH, NBO dosages, and PMS concentration for BPAF degradation were also investigated. Radical quenching experiments combined with electron spin resonance analysis indicated that singlet oxygen ( 1 O 2 ) was the main reactive oxygen species, and · SO 4 - and · OH – radicals participated in the process. X-ray photoelectron spectroscopy revealed the main catalytic mechanism: lattice oxygen (O vac ) was extruded during the transformation of Bi(V) to Bi(III) to form and activate oxygen (O*), and the generated O* between the [BiO 6 ] regular octahedral layers reacted with PMS on the NBO surface to form 1 O 2 . Based on the results of the Bi element, it is suggested that the activation process proceeded through electron transfer from NBO to PMS. The stability of NBO and applicability of the NBO/PMS system in a natural water environment were explored. This work provides a novel approach to PMS activation and the potential use of NBO for the decontamination of organic pollutants.