Facile synthesis of Fe3O4-SiO2-EN@Zn-Al layered double hydroxide nanocomposites for degradation of amoxicillin under solar, visible and UV lights

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-05-01 Epub Date: 2025-01-16 DOI:10.1016/j.jphotochem.2025.116278
Huu-Tap Van , Mikhail Ivanov , Razzagh Rahimpoor , Nezamaddin Mengelizadeh , Marwah Mohammed hareeja , Neeti Misra , Saad Hayif Jasim Ali , Davoud Balarak
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Abstract

Antibiotics, categorized as emerging pollutants, present environmental challenges owing to their harmful and mutation-inducing properties, which hinder their removal. This study seeks to produce Fe3O4-SiO2-EN@Zn-Al layered double hydroxide (FSEZAL) nanocomposites for effectively degrading amoxicillin (AMX) through photocatalysis. The target nanocomposite was prepared using a sol–gel method and subsequently characterized in detail using SEM, XRD, FTIR, BET, PL, and VSM techniques. In this study, scavenger results showed that OH and O2 are both responsible for the AMX degradation. This study also showed that the energy consumed by visible light and UV light during 10–60 min was equal to 44.3 kWh/m3 to 18.5 and 10 to 20.6 kWh/m3, respectively. The reaction rate constant for the photocatalytic process with Fe3O4 and SiO2 nanoparticles, Fe3O4-SiO2-EN, and FSEZAL nanocomposite was 0.0045, 0.0059, 0.0084, and 0.116 1/min, respectively. Also, the half-life constant for nanocomposite was equal to 5.97 min. Ecotoxicity tests were performed using Daphnia magna, and the findings showed a significant reduction in the toxicity of AMX solution. In this study, three types of light were used, and the complete removal of AMX with UV and visible light required 40 min and 60 min, respectively. Also, using sunlight, 87.1 % of AMX was removed within one hour. The reaction rate constants for photocatalytic reactions with UV, visible, and solar lights were 0.116, 0.103, and 0.033 1/min, respectively. Biodegradability and mineralization tests also confirmed the efficacy of the photocatalytic system with synthesized nanocomposite. Therefore, the FSEZAL photocatalysts exhibit promising potential for use in water treatment, particularly in the mitigation of toxicity associated with antibiotic waste.

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太阳能、可见光和紫外光下降解阿莫西林的Fe3O4-SiO2-EN@Zn-Al层状双氢氧化物纳米复合材料的简易合成
抗生素被归类为新兴污染物,由于其有害和诱导突变的特性,阻碍了它们的去除,给环境带来了挑战。本研究旨在制备Fe3O4-SiO2-EN@Zn-Al层状双氢氧化物(FSEZAL)纳米复合材料,通过光催化有效降解阿莫西林(AMX)。采用溶胶-凝胶法制备了目标纳米复合材料,随后使用SEM, XRD, FTIR, BET, PL和VSM技术对其进行了详细的表征。在本研究中,清除剂结果表明,OH和O2−都是AMX降解的原因。本研究还表明,可见光和紫外光在10 - 60 min内消耗的能量分别为44.3 kWh/m3 ~ 18.5和10 ~ 20.6 kWh/m3。Fe3O4和SiO2纳米颗粒、Fe3O4-SiO2- en和FSEZAL纳米复合材料的光催化反应速率常数分别为0.0045、0.0059、0.0084和0.116 1/min。此外,纳米复合材料的半衰期常数为5.97 min。利用大水蚤进行生态毒性试验,结果表明AMX溶液的毒性显著降低。本研究使用了三种光,紫外线和可见光完全去除AMX分别需要40 min和60 min。此外,在阳光照射下,87.1%的AMX在一小时内被去除。紫外光、可见光和太阳光催化反应的反应速率常数分别为0.116、0.103和0.033 1/min。生物降解性和矿化试验也证实了合成的纳米复合材料光催化体系的有效性。因此,FSEZAL光催化剂在水处理,特别是减轻与抗生素废物有关的毒性方面显示出良好的潜力。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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