降级(电信)
催化作用
镍
化学
基质(水族馆)
兴奋剂
化学工程
猝灭(荧光)
氧气
激进的
光化学
核化学
材料科学
荧光
有机化学
计算机科学
电信
光电子学
海洋学
物理
地质学
工程类
量子力学
作者
Jiadian Wang,Min Wang,Jin Kang,Yiwu Tang,Zhenqi Xu,Qing Dong,Taizhuo Ma,Jiangwei Zhu
标识
DOI:10.1016/j.seppur.2023.123584
摘要
In this work, to promote the catalytic efficiency of Fe2O3 and achieve the facile retrieve and recycle from the solution, Ni2+ doped Fe2O3 in-situ growing on a nickel foam (NF) (Ni-Fe2O3/NF) was fabricated using NF as the Ni2+ internal doping source and the substrate support and used in the peroxymonosulfate (PMS) assisting visible-light photoelectrochemical oxidation (EC + Photo + catalyst + PMS) system for sulfamethoxazole (SMX) degradation. Benefiting from more Fe2+ and oxygen vacancies generation after Ni2+, and the enhanced electrical conductivity owing to NF substrate, the optimum Ni-Fe2O3/NF(II) exhibited excellent catalytic efficiency. 100% of SMX was removed in 10 min in the EC + Photo + Ni-Fe2O3/NF(II) + PMS system and the pseudo-first order kinetic constant (kobs) was 45.10 × 10-2 min−1, being about 9.80 folds of powder Fe2O3. Meantime, due to the employed loading method benefits in the Ni-Fe2O3 uniformly and steady loading on NF, Ni-Fe2O3/NF(II) demonstrated the excellent stability and recycle ability. Reactive oxygen species (ROSs) quenching and electron paramagnetic resonance evidenced that photo-induced hole (h+), hydroxy radical (•OH) and superoxide radical (•O2−) contributed to SMX degradation. And the SMX degradation pathways were deduced according to the determined degraded products and density functional theory (DFT) calculation. This study developed one convenient separation and recovery catalyst suitable for EC + Photo + catalyst + PMS system for efficient and environmentally friendly antibiotics removal in water.
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