Peroxydisulfate activation by atomically-dispersed Fe-Nx on N-doped carbon: Mechanism of singlet oxygen evolution for nonradical degradation of aqueous contaminants

被引:133
作者
Du, Ningjie [1 ,2 ]
Liu, Ying [1 ,2 ]
Li, Qiuju [1 ,2 ]
Miao, Wei [1 ,2 ]
Wang, Dandan [1 ,2 ]
Mao, Shun [1 ,2 ]
机构
[1] Tongji Univ, Shanghai East Hosp, Biomed Multidisciplinary Innovat Res Inst, Coll Environm Sci & Engn,State Key Lab Pollut Con, 1239 Siping Rd, Shanghai 200092, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
国家重点研发计划;
关键词
Single-atom iron; Peroxydisulfate oxidation; Singlet oxygen; Chloramphenicol; Organic contaminant removal; ZERO-VALENT IRON; PEROXYMONOSULFATE ACTIVATION; HETEROGENEOUS CATALYSIS; SELECTIVE DEGRADATION; BISPHENOL-A; CHLORAMPHENICOL; OXIDATION; NANOPARTICLES; PERSULFATE; NANOTUBES;
D O I
10.1016/j.cej.2020.127545
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Single-atom catalysts have drawn increasing attention in advanced oxidation due to their unique structure and significant promise in heterogeneous catalysis. Herein, single-atom iron anchored on nitrogen-doped carbon (SAFe-N-C) was synthesized with iron phthalocyanine (FePc) and metal-organic framework (ZIF-8). With thermal treatment and acid leaching, atomically-dispersed Fe-Nx sites were successfully formed on the surface of N-C support derived from ZIF-8. The prepared catalyst was demonstrated to activate peroxydisulfate (PDS) for chloramphenicol (CAP) degradation. Compared with N-C, the SAFe-N-C shows 6 times enhanced removal efficiency (from 15.3% to 93.1%) for CAP. Moreover, the catalyst shows high catalytic activity in a wide pH range of 5 to 9 and good resistance to inorganic anions, in which a singlet oxygen-dominated process is found. This study reveals the role of single-atom site in singlet oxygen evolution and offers a new catalytic approach for selective removal of organic pollutants in complex water matrix.
引用
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页数:12
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