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CoFe2O4/CuO活化过氧乙酸高效降解磺胺甲恶唑(英文)
引用本文:刘振中,万思文,吴阳,王波延,季宏亮.CoFe2O4/CuO活化过氧乙酸高效降解磺胺甲恶唑(英文)[J].物理化学学报,2023,39(5):2211019-0.
作者姓名:刘振中  万思文  吴阳  王波延  季宏亮
作者单位:1 南昌大学资源与环境学院, 南昌 3300312 南昌大学工程建设学院, 南昌 330031
摘    要:利用化学沉淀法和溶胶凝胶法,通过两步法成功制备出含有尖晶石钴铁氧体和氧化铜的复合催化剂CoFe2O4/CuO,通过扫描电子显微镜(SEM)、X射线光电子能谱(XPS)和X射线衍射(XRD)对制备出的CoFe2O4/CuO进行表征,探究不同高级氧化体系对磺胺甲恶唑(SMX)去除能力,考察过氧乙酸(PAA)浓度、催化剂投加量、水体中常见干扰物质(Cl-,HCO-3,SO42-,HA)和不同自由基捕获剂对SMX去除的影响。分析结果表明CoFe2O4/CuO同时具有CoFe2O4与CuO的特征,对比单独CoFe2O4与CuO,CoFe2O4/CuO对PAA展现出极高的活化性能,在最佳反应条件下(催化剂投加量=20mg·L-1,c(PAA)=200μ...

关 键 词:尖晶石钴铁氧体  氧化铜  高级氧化  磺胺甲恶唑  过氧乙酸  有机自由基
收稿时间:2022-11-12

Highly Efficient Degradation of Sulfamethoxazole Using Activating Peracetic Acid with CoFe2O4/CuO
Zhenzhong Liu,Siwen Wan,Yang Wu,Boyan Wang,Hongliang Ji.Highly Efficient Degradation of Sulfamethoxazole Using Activating Peracetic Acid with CoFe2O4/CuO[J].Acta Physico-Chimica Sinica,2023,39(5):2211019-0.
Authors:Zhenzhong Liu  Siwen Wan  Yang Wu  Boyan Wang  Hongliang Ji
Institution:1. School of Resources and Environment, Nanchang University, Nanchang 330031, China;2. School of Infrastructure Engineering, Nanchang University, Nanchang 330031, China
Abstract:Advanced oxidation processes (AOPs), especially AOPs that use transition metals as catalyst activated oxidants, are extremely effective in removing organic pollutants; they can completely degrade pollutants into CO2 and H2O. Thus, they have been widely studied in the field of water treatment. However, owing to the low catalytic efficiency and metal leakage, their applicability is currently limited. In this paper, the composite catalyst CoFe2O4/CuO containing spinel cobalt ferrite and copper oxide was successfully prepared by the chemical precipitation and sol-gel methods with two steps. The prepared CoFe2O4/CuO was characterized using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD), and its ability to remove sulfamethoxazole (SMX) with different AOPs was evaluated. Characterization results show that CoFe2O4 and CuO are well-complexed together, and the catalyst has good crystallinity. The effects of peracetic acid (PAA) concentration, catalyst dosage, common interfering substances (Cl?, HCO3?, SO42?, and HA) in water, and different radical scavengers on SMX removal were also investigated. The results show that CoFe2O4/CuO has the characteristics of both CoFe2O4 and CuO. Compared with CoFe2O4 or CuO alone, CoFe2O4/CuO exhibits an excellent activation performance for PAA. Under the optimal reaction conditions (catalyst dosage = 20 mg·L?1, c(PAA) = 200 μmol·L?1, c(SMX) = 10 μmol·L?1), the degradation rate of SMX reaches 92% within 90 s. The existence of Cu+/Cu2+ electron pairs can convert Co from the high valence to low valence state and accelerate the conversion of Co2+/Co3+, thereby improving the catalytic performance. An increase in the PAA concentration increases the removal efficiency of SMX; however, too high a concentration lowers removal efficiency. Compared to acidic or alkaline conditions, the CoFe2O4/CuO reaction system exhibits a better removal rate of SMX under neutral conditions. The common interfering substances in the environment have different effects on the CoFe2O4/CuO reaction system. Cl? promotes the degradation of SMX by producing Cl?, HCO3? and HA inhibit the removal of SMX because of their quenching effect on free radicals, and SO42? has no significant effect on the progress of the reaction. The XPS characterization results before and after the reaction show that the valence state of Co changes, indicating that Co is the main element involved in the activation of PAA. Radical quenching experiments demonstrate that the organic radical (R―O?) plays a dominant role in the removal of SMX. Further, the removal rate of SMX decreases after the catalyst is subjected to 3 recycle; nevertheless, it achieves a relatively rapid degradation of SMX (85% within 10 min).
Keywords:Spinel cobalt ferrite  Copper oxide  Advanced oxidation  Sulfamethoxazole  Peracetic acid  Organic radical  
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