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Advanced oxidation is a very efficient method in wastewater treatment, but it is a waste of resources to directly oxide the high concentration of valuable organics into carbon dioxide and water. In this paper, the combination of persulfate and wet air oxidation was developed to recover organics from high concentration of wastewater, along with high mineralization of the residual organics. Nitrogen and sulfur co-doped hollow spherical polymers with narrow size distribution was recovered from the simulated benzothialzole (BTH) wastewater in this facile way, along with chemical oxygen demand (COD) removal rate higher than 90%. The formation route of the polymers was intensively studied based on detailed analysis of different kinds of reaction intermediates. The polymers can be further carbonized into co-doped hollow carbon microsphere, which showed better performance in organic contaminants removal than a commercial activated carbon both in adsorption or catalytic persulfate oxidation. This proposed a new strategy to simultaneously combine oxidation and polymerization for resource recovery from wastewater with high concentration of heterocyclic compounds., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Photocatalytic ozonation is an attractive advanced oxidation process for wastewater treatment, but highly active catalysts with strong response to visible light are urgently needed to push forward its practical application. In this study, a hierarchical biomimetic monoclinic bismuth vanadate (BiVO 4 ) with leaves morphology was synthesized by a hydrothermal method, and employed as catalyst for oxalic acid and penicillin degradation in photocatalytic ozonation. The results show that the organics degradation was more efficient using leaves shaped BiVO 4 as catalyst than the bulk shaped one in photocatalytic ozonation and the synergy index is ranged from 2.8 to 3.3, indicating a superior positive synergistic effect between photocatalysis and ozonation. The higher activity of the leaves shaped BiVO 4 was probably attributed to the distinctive biomimetic morphology and preferable band structure with more negative CB potential. Mechanism studies suggested that the main reactive species were h + and OH for the degradation of persistent oxalic acid in photocatalytic ozonation. In addition, the effect of ozone concentration and inorganic ions and reusability of the material were also intensively investigated., (Copyright © 2019 Elsevier Ltd. All rights reserved.)