Phosphorus doping to enhance the peroxymonosulfate activation efficiency of carbon nitride for degrading tetracycline

化学 单线态氧 石墨氮化碳 氮化碳 电子顺磁共振 羟基化 热稳定性 光化学 兴奋剂 化学工程 有机化学 光催化 氧气 材料科学 催化作用 物理 光电子学 核磁共振 工程类
作者
Liquan Wang,Ruyi Li,Yimin Zhang,Baohua Tu,Yuan Zhao,Ting Chen,Yuexiang Gao
出处
期刊:Journal of water process engineering [Elsevier BV]
卷期号:54: 103916-103916 被引量:23
标识
DOI:10.1016/j.jwpe.2023.103916
摘要

Herein, a new type of peroxymonosulfate (PMS) activator—phosphorus-doped carbon nitride (P-C3N4)—was prepared using a one-step thermal shrinkage method. Material characterisation confirmed the successful doping of phosphorus in graphite-phase carbon nitride (g-C3N4) by replacing the carbon atoms in its triazine ring structure to form PN bonds. Phosphorus doping can regulate and re-organise the surface electronic structure of g-C3N4 without changing its structure. Moreover, phosphorus doping promotes varying degrees of optimisation of the g-C3N4 pore structure and electronic transport between the g-C3N4 sites. Batch experiments on tetracycline (TC) degradation revealed that 0.2 P-C3N4 showed the best physicochemical properties, the constructed P-C3N4/PMS system exhibited high TC removal efficiency and P-C3N4 exhibited good reusability and structural stability. Quenching experiments and electron paramagnetic resonance tests revealed that singlet oxygen was the primary active species in the P-C3N4/PMS system. The mechanism of PMS activation using P-C3N4 was then proposed. The analysis of TC and its intermediate products using liquid chromatography–mass spectroscopy demonstrated that TC was primarily degraded via ring-opening, hydroxylation, deamination and dealkylation reactions. Analysis using the toxicity estimation software tool demonstrated that most intermediate products were less toxic than TC. Thus, this study provides a feasible method for removing TC from aquatic environments.
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