Wang Jun, Lv Hao, Tong Xiandong, Ren Wei, Shen Yi, Lu Lun, Zhang Yang
State Key Laboratory of Separation Membranes and Membrane Processes, School of Environmental Science and Engineering, Tiangong University, Tianjin 300387, China.
Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063, China.
J Hazard Mater. 2023 Oct 5;459:132334. doi: 10.1016/j.jhazmat.2023.132334. Epub 2023 Aug 16.
In order to minimize the knowledge gap between single and binary pollutants degradation by persulfate-based advanced oxidation processes (PS-AOPs), iron-loaded N-doped carbon nanotubes (Fe-NCNT) and its acid-washing sample (Fe-NCNT-W) were synthesized as peroxymonosulfate (PMS) activator for simultaneous oxidation of acid orange 7 (AO7) and electron-rich (phenol/ibuprofen) or electron-deficient pollutants (nitrobenzene/benzoic acid). Mechanistic studies revealed that both radical (HO•, SO) and nonradical (electron-transfer, high-valent iron) pathways involved for organic oxidation in Fe-NCNT/PMS system, while electron-transfer pathway (ETP) and high-valent iron-oxo species accounted for pollutant degradation at the surface and inner space of Fe-NCNT-W, respectively. The oxidation performances in single or binary systems were systematically investigated. In comparison to benchmark radical-based (Fe/PMS), nonradical ETP (NCNT/PMS) and mixed (Fe-NCNT/PMS) systems, Fe-NCNT-W/PMS outperformed superior performance toward oxidation of binary pollutants with little inference from solution pH or background substances, which could also be fabricated into membrane reactor for actual dyeing sewage treatment. Such superiorities should be mainly ascribed to the particular selectivity and intensive treatment of nonradical pathways in Fe-NCNT-W/PMS system with nanoconfinement effect. This work affords novel insights into the treatment of combined pollution via PMS activation by engineered nanomaterials.
为了缩小基于过硫酸盐的高级氧化工艺(PS-AOPs)在单一和二元污染物降解方面的知识差距,合成了负载铁的氮掺杂碳纳米管(Fe-NCNT)及其酸洗样品(Fe-NCNT-W)作为过一硫酸盐(PMS)活化剂,用于同时氧化酸性橙7(AO7)和富电子(苯酚/布洛芬)或缺电子污染物(硝基苯/苯甲酸)。机理研究表明,Fe-NCNT/PMS体系中有机氧化涉及自由基(HO•、SO)和非自由基(电子转移、高价铁)途径,而电子转移途径(ETP)和高价铁氧物种分别在Fe-NCNT-W的表面和内部空间导致污染物降解。系统研究了单一或二元体系中的氧化性能。与基于自由基的基准体系(Fe/PMS)、非自由基ETP体系(NCNT/PMS)和混合体系(Fe-NCNT/PMS)相比,Fe-NCNT-W/PMS对二元污染物的氧化表现出卓越的性能,几乎不受溶液pH值或背景物质的影响,还可制成膜反应器用于实际印染污水处理。这些优势应主要归因于Fe-NCNT-W/PMS体系中具有纳米限域效应的非自由基途径的特殊选择性和强化处理。这项工作为通过工程纳米材料活化PMS处理复合污染提供了新的见解。