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利用迷迭香叶提取物生物合成的磁性尖晶石镍铁氧体(NiFeO)纳米颗粒在紫外光下对双氯芬酸钠进行光催化降解。

Photocatalytic degradation of diclofenac sodium under UV light by a biosynthesized magnetic spinel nickel ferrite (NiFeO) nanoparticles using rosemary leaf extract.

作者信息

Bouchenak Meriem, Boutemak Khalida, Haddad Ahmed, Boutra Belgassim

机构信息

Laboratory of Functional Analysis of Chemical Processes (LAFPC), Process Engineering Department, Faculty of Technology, University Blida 1, Blida, Algeria.

Corrosion, Protection and Durability of Materials Division, Research Centre in Industrial Technologies - CRTI, Cheraga, Algiers, Algeria.

出版信息

Environ Sci Pollut Res Int. 2025 May;32(25):15359-15373. doi: 10.1007/s11356-025-36587-x. Epub 2025 Jun 9.

DOI:10.1007/s11356-025-36587-x
PMID:40488980
Abstract

In this study, we report the first successful biosynthesis of magnetic nickel ferrite nanoparticles NiFeO NPs via a sono-chemical method, employing ultrasonic assistance and using rosemary leaves extract as a multifunctional capping, reducing, and stabilizing agent. This approach was undertaken with the aim of developing a catalyst for the photodegradation of the nonsteroidal anti-inflammatory drug diclofenac sodium (DS), which not only represents an environmentally benign alternative to conventional chemical methods but also results in NiFeO NPs with enhanced structural, optical, and magnetic properties. Characterization by XRD and FESEM-EDX analysis indicated the formation of NiFeO NPs with quasi-spherical morphology. TEM/HR-TEM analysis revealed its spinel phase structure, with particle sizes ranging from 4 to 20 nm. FT-IR was utilized to elucidate molecular vibrations, while VSM revealed the superparamagnetic behavior of these NPs; this property enables their efficient recovery after the photocatalytic process. The photocatalytic degradation of DS by NiFeO NPs with a band gap energy of 2.7-3.32 eV was examined under ultraviolet light (UV-A) irradiation. Various operating parameters, including solution pH, DS concentration, and NiFeO catalyst dose, were studied. The degradation kinetics were monitored using a UV-Visible spectrophotometer. The biosynthesized NiFeO NPs demonstrated a high degradation efficiency of 95% for DS in acidic pH conditions within only 140 min. The NiFeO NPs exhibited excellent recyclability and maintained structural and photocatalytic stability over three consecutive photodegradation cycles.

摘要

在本研究中,我们报告了首次通过声化学方法成功生物合成磁性镍铁氧体纳米颗粒NiFeO NPs,该方法采用超声辅助,并使用迷迭香叶提取物作为多功能封端、还原和稳定剂。采用这种方法的目的是开发一种用于光降解非甾体抗炎药双氯芬酸钠(DS)的催化剂,这不仅是一种比传统化学方法更环保的替代方法,而且还能得到具有增强的结构、光学和磁性的NiFeO NPs。XRD和FESEM-EDX分析表明形成了具有准球形形态的NiFeO NPs。TEM/HR-TEM分析揭示了其尖晶石相结构,粒径范围为4至20 nm。利用FT-IR阐明分子振动,而VSM揭示了这些NPs的超顺磁性行为;这一特性使它们在光催化过程后能够有效回收。在紫外光(UV-A)照射下,研究了带隙能量为2.7-3.32 eV的NiFeO NPs对DS的光催化降解。研究了各种操作参数,包括溶液pH值、DS浓度和NiFeO催化剂剂量。使用紫外可见分光光度计监测降解动力学。生物合成的NiFeO NPs在酸性pH条件下仅140分钟内对DS的降解效率就高达95%。NiFeO NPs表现出优异的可回收性,并且在连续三个光降解循环中保持结构和光催化稳定性。

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