Weak magnetic field for enhanced degradation of sulfamethoxazole by the CoFe2O4/PAA system: Insights into performance and mechanism

被引:0
|
作者
Lv, Xinyuan [1 ]
Yu, Miao [1 ]
Guo, Yali [1 ]
Sui, Minghao [1 ,2 ,3 ]
机构
[1] Tongji Univ, Coll Environm Sci & Engn, 1239 Siping Rd, Shanghai 200092, Peoples R China
[2] Tongji Univ, State Key Lab Pollut Control & Resource Reuse, 1239 Siping Rd, Shanghai 200092, Peoples R China
[3] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
关键词
Peracetic acid; Cobalt ferrite; Weak magnetic field; Sulfamethoxazole; Oxygen vacancy; ZERO-VALENT IRON; WASTE-WATER TREATMENT; UV/PERACETIC ACID; REMOVAL; RADICALS; KINETICS; OXYGEN; PHARMACEUTICALS; PERSULFATE; GENERATION;
D O I
10.1016/j.seppur.2024.130017
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this work, a novel approach coupling a heterogeneous weak magnetic field (WMF) with the CoFe2O4/peroxyacetic acid (PAA) system was employed to enhance the degradation of sulfamethoxazole (SMX). Under the optimized conditions of 50 mT WMF, 0.1 g/L CoFe2O4, 0.2 mM PAA, and initial pH 6.0, a complete degradation of 10 mu M SMX was achieved in 25 min, exhibiting a high synergistic coefficient of 1.61. This result indicates a significant synergistic effect among WMF, CoFe2O4, and PAA in effectively degrading SMX. The introduction of WMF did not alter the pH application range of the CoFe2O4/PAA system. Furthermore, the degradation efficiency of SMX by the CoFe2O4/PAA/WMF system was significantly reduced in the presence of humic acid (HA) and bicarbonate ions (HCO3-), while chloride ions (Cl-) exhibited a minor inhibitory effect. Quenching experiments and electron paramagnetic resonance (EPR) analysis reveal that WMF did not alter the types of reactive oxygen species (ROS) generated in the CoFe2O4/PAA system. The degradation of SMX in the CoFe2O4/PAA/WMF system involved both radical (CH3C(O)O center dot and CH3C(O)OO center dot) and non-radical (O-1(2)) oxidation pathways, driven by the redox cycling between equivalent to Co2+/equivalent to Co3+ and PAA, as well as the rapid adsorption and transformation of oxygen (O-2) at oxygen vacancies (OV), respectively. The presence of WMF enhanced the utilization of PAA by CoFe2O4 by improving the convection and mass transport in the solution, facilitating the formation of superoxide anion (O-2(center dot-)) and supplemented lattice oxygen (O2-) through the directional migration of paramagnetic O-2 towards the CoFe2O4 surface, thus significantly promoting ROS formation. Additionally, the degradation pathways of SMX in the CoFe2O4/PAA/WMF system were proposed based on density functional theory (DFT) calculations and the detected transformation products (TPs). The toxicity of SMX was effectively reduced, as verified by predictions from the Ecological Structure-Activity Relationship Model (ECOSAR) procedure. The excellent catalytic performance, reusability, and effective degradation of various organic pollutants demonstrated by the CoFe2O4/PAA/ WMF system suggest its potential as a promising strategy for water treatment.
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页数:12
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