Oxygen doped graphite carbon nitride as efficient metal-free catalyst for peroxymonosulfate activation: Performance, mechanism and theoretical calculation
Chemosphere, ISSN: 0045-6535, Vol: 338, Page: 139539
2023
- 6Citations
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Article Description
In this study, oxygen-doped graphitic carbon nitride (g-C 3 N 4 ), named O-g-C 3 N 4, was successfully fabricated and characterized, and its performance in activating peroxymonosulfate (PMS, HSO 5 − ) for the removal of phenol, 2,4-dichlorophenol (2,4-DCP), bisphenol A (BPA), rhodamine B (RhB), reactive brilliant blue (RBB) and acid orange 7 (AO7) was evaluated. The catalytic performance of O-g-C 3 N 4 for AO7 removal increased by 14 times compared to g-C 3 N 4. In the presence of 0.2 g L −1 O-g-C 3 N 4, 3.5 mM PMS at natural pH 5.8, 96.4% of AO7 could be removed in 60 min, reduced toxicity of the treated AO7 solution was obtained, and the mineralization efficiency was 47.2% within 120 min. Density functional theory (DFT) calculations showed that the charge distribution changed after oxygen doping, and PMS was more readily adsorbed by O-g-C 3 N 4 with the adsorption energy (E ads ) of −0.855 kcal/mol than that of the pristine g-C 3 N 4 (E ads : −0.305 kcal/mol). Mechanism investigation implied that AO7 was primarily removed by the sulfate radicals (SO 4 •− ) and hydroxyl radicals ( • OH) on the surface of O-g-C 3 N 4, but the role of singlet oxygen ( 1 O 2 ) to AO7 elimination was negligible. The results of cyclic experiments and catalyst characterization after reaction confirmed the favorable catalytic activity and structural stability of O-g-C 3 N 4 particles. Furthermore, the O-g-C 3 N 4 /PMS system was very resistant to most of the environmental impacts, and AO7 removal was still acceptable in natural water environment. This study may provide an efficient metal-free carbonaceous activator with low dosage for PMS activation to remove recalcitrant organic pollutants (ROPs).
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0045653523018064; http://dx.doi.org/10.1016/j.chemosphere.2023.139539; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85165329199&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37474028; https://linkinghub.elsevier.com/retrieve/pii/S0045653523018064; https://dx.doi.org/10.1016/j.chemosphere.2023.139539
Elsevier BV
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