Sol–gel synthesis and characterization of Ni-doping enhanced NixCd0.8−XZn0.2Al0.3Fe1.7O4 nanoparticles with exceptional photocatalytic activity for ciprofloxacin degradation

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL Reaction Kinetics, Mechanisms and Catalysis Pub Date : 2024-05-28 DOI:10.1007/s11144-024-02665-3
Muhammed Yasar, Khalid Javed, Muhammad Ibrahim, Fozia Noreen
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Abstract

In this study, the sol–gel synthesis of Ni-doped cadmium zinc aluminum ferrite Ni-doped NixCd0.8−XZn0.2Al0.3Fe1.7O4 (X = 0,0.4) nanoparticles and their photocatalytic activity for ciprofloxacin degradation under visible-light irradiation were investigated. The nanoparticles were characterized using XRD, FTIR, SEM, EDX, and BET analyses. XRD revealed cubic spinel structures with crystallite sizes of 39 (undoped) and 30 nm (Ni-doped). FTIR spectra showed peak shifts upon Ni doping, indicating Ni2+ ion substitution in the spinel lattice. SEM images showed that the nickel-free sample was porous and had larger, loosely packed grains, whereas the nickel-doped sample was denser and featured smaller, uniformly distributed grains. The Ni-doped sample exhibited a higher BET surface area (37.85 m2/g) and pore volume (1.836 cm3/g) than those of the undoped sample. The photocatalytic degradation of ciprofloxacin was significantly enhanced by Ni doping, achieving 97.88% in 60 min under visible light, which was attributed to the narrowed bandgap (2.1 eV), improved visible light absorption, and increased charge separation. Scavenger studies have identified hydroxyl radicals as primary reactive species. The addition of H2O2 (up to 6 mM) enhanced the degradation rate, but higher concentrations decreased the rate. The catalyst exhibited gradual deactivation upon reuse, with the degradation efficiency decreasing from 97.88 (first cycle) to 90.93% (fifth cycle), owing to loss, deactivation, and fouling.

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具有卓越光催化活性的 NixCd0.8-XZn0.2Al0.3Fe1.7O4 纳米粒子的溶胶-凝胶合成及其在降解环丙沙星方面的表征
本研究考察了溶胶凝胶合成掺杂镍的镉锌铝铁氧体 Ni-doped NixCd0.8-XZn0.2Al0.3Fe1.7O4 (X = 0,0.4) 纳米粒子及其在可见光照射下降解环丙沙星的光催化活性。采用 XRD、FTIR、SEM、EDX 和 BET 分析对纳米颗粒进行了表征。XRD 显示了立方尖晶石结构,晶粒大小分别为 39 纳米(未掺杂)和 30 纳米(掺杂镍)。傅立叶变换红外光谱显示掺入镍后的峰值移动,表明尖晶石晶格中的镍2+离子被取代。扫描电镜图像显示,无镍样品多孔,晶粒较大且松散,而掺镍样品密度较大,晶粒较小且分布均匀。掺镍样品的 BET 表面积(37.85 m2/g)和孔隙率(1.836 cm3/g)均高于未掺镍样品。掺杂镍后,环丙沙星的光催化降解能力显著增强,在可见光下 60 分钟内达到 97.88%,这归因于带隙变窄(2.1 eV)、可见光吸收能力增强以及电荷分离能力增强。清除剂研究发现羟基自由基是主要的活性物种。加入 H2O2(最高 6 mM)可提高降解率,但浓度越高,降解率越低。由于损耗、失活和堵塞,催化剂在重复使用时逐渐失活,降解效率从 97.88%(第一个循环)降至 90.93%(第五个循环)。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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