Hydroxylamine enhanced FeOOH-mediated advanced oxidation processes for the treatment of norfloxacin

IF 2.8 4区 工程技术 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Xueru Huang, Beiyu Xin, Huan Ma, Yanyan Wang, Yajing Sun, Dandan Wang, Jing Li, Mintao Zhang, Jifeng Guo
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引用次数: 0

Abstract

In recent years, advanced oxidation processes (AOPs) based on persulfate (PDS) and hydrogen peroxide (H2O2) have become widely used for removing antibiotics from water. However, the formation of iron sludge limits the practical application of homogeneous iron-based catalysts for activating H2O2 and PDS. Therefore, heterogeneous catalysis offers a promising alternative. This study compares the degradation of norfloxacin (NOR) using FeOOH-activated PDS and H2O2 in a photocatalytic system. Hydroxylamine (HA) was employed to assist the activation process to further optimize the degradation process and improve the degradation efficiency. Without the presence of HA, the findings revealed that the degradation rates of NOR were merely 31.2% in the PDS system and 24.8% in the H2O2 system. The introduction of HA markedly improved NOR degradation efficiency, achieving removal rates of 89.7% in the PDS system and 56.3% in the H2O2 system. Key operational parameters including pH, HA concentration, oxidant dosage, and the presence of HA were systematically evaluated for their influence on degradation performance. Scavenging experiments revealed that ⋅OH, SO4⋅, and ⋅O2 served as the dominant reactive species in the PDS system, whereas h+ and ⋅OH were the primary drivers in the H2O2 system. Based on these findings, a plausible reaction mechanism was proposed. Additionally, the stability of the FeOOH catalyst in the presence of HA and its effectiveness in degrading NOR across various water matrices were investigated. This study offers an innovative strategy for visible-light-assisted activation of H2O2 and PDS, demonstrating considerable potential for antibiotic degradation in water treatment applications.

羟胺增强feooh介导的高级氧化过程治疗诺氟沙星
近年来,基于过硫酸盐(PDS)和过氧化氢(H2O2)的高级氧化工艺(AOPs)已被广泛用于去除水中的抗生素。然而,铁污泥的形成限制了均相铁基催化剂活化H2O2和PDS的实际应用。因此,多相催化提供了一个很有前途的选择。本研究比较了feooh活化PDS和H2O2在光催化体系中对诺氟沙星(NOR)的降解效果。采用羟胺(HA)辅助活化,进一步优化降解过程,提高降解效率。在没有HA的情况下,研究结果显示,在PDS系统中,NOR的降解率仅为31.2%,在H2O2系统中,NOR的降解率仅为24.8%。HA的引入显著提高了NOR的降解效率,在PDS体系中去除率为89.7%,在H2O2体系中去除率为56.3%。系统评价了pH、HA浓度、氧化剂用量和HA存在等关键操作参数对降解性能的影响。清除实验表明,在PDS体系中,⋅OH、SO4−⋅和⋅O2−是主要的反应物质,而在H2O2体系中,h+和⋅OH是主要的驱动物质。在此基础上,提出了一种合理的反应机理。此外,研究了FeOOH催化剂在HA存在下的稳定性及其在不同水基质中降解NOR的有效性。该研究提供了一种可见光辅助活化H2O2和PDS的创新策略,显示了在水处理应用中抗生素降解的巨大潜力。
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来源期刊
Journal of Materials Science: Materials in Electronics
Journal of Materials Science: Materials in Electronics 工程技术-材料科学:综合
CiteScore
5.00
自引率
7.10%
发文量
1931
审稿时长
2 months
期刊介绍: The Journal of Materials Science: Materials in Electronics is an established refereed companion to the Journal of Materials Science. It publishes papers on materials and their applications in modern electronics, covering the ground between fundamental science, such as semiconductor physics, and work concerned specifically with applications. It explores the growth and preparation of new materials, as well as their processing, fabrication, bonding and encapsulation, together with the reliability, failure analysis, quality assurance and characterization related to the whole range of applications in electronics. The Journal presents papers in newly developing fields such as low dimensional structures and devices, optoelectronics including III-V compounds, glasses and linear/non-linear crystal materials and lasers, high Tc superconductors, conducting polymers, thick film materials and new contact technologies, as well as the established electronics device and circuit materials.
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