Treatment of bisphenol pollutant in water by N,P-co-doped carbon nanosheet: Fast degradation, toxicity elimination and reaction mechanism investigation

Abstract

Metal-free carbon catalysts perform well in peroxymonosulfate-based advanced oxidation process for the treatment of organic pollutant-containing wastewater. Herein, a natural biomolecule of adenosine triphosphate (ATP), containing abundant N and P elements, served as sole precursor to prepare N,P-co-doped carbon through one-step anoxic pyrolysis, which was applied as peroxymonosulfate activator to treat bisphenol-contaminated water. Owing to the endogenous N and P elements in ATP, in-situ doping was achieved for the prepared carbon material with excellent doping effect, such as high doping amount and numerous defects. During pyrolysis process, the generated gases facilitated the exfoliation of carbon structure, resulting in a nanosheet-like morphology with large specific surface area, e.g., 852.75 m² g^-1 for NPCN-900 sample obtained at 900 °C. Benefiting from the structural modulation brought by N,P co-doping, typical sample of NPCN-900 presented excellent catalytic performance towards bisphenol AF (BPAF) degradation through PMS activation. An apparent reaction rate constant of 0.4115 min^-1 was calculated under the investigated reaction conditions. Further studies indicated that ¹O₂, surface-bound •OH and SO₄^-• worked together in NPCN-900/PMS system for BPAF degradation. Graphitic N, pyrrolic N, CO groups, defect structure and the doped P atoms in NPCN-900 contributed to PMS activation. It was also important that the toxicity of BPAF solution could be preliminarily eliminated after treatment by NPCN-900/PMS system, which was verified by ecotoxicity assessments through ECOSAR program and green algae growth experiments.

Keywords: ATP; Bisphenol AF; Carbon; Ecotoxicity; In-situ doping; Peroxymonosulfate activation.