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

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
{"title":"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","authors":"Muhammed Yasar,&nbsp;Khalid Javed,&nbsp;Muhammad Ibrahim,&nbsp;Fozia Noreen","doi":"10.1007/s11144-024-02665-3","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, the sol–gel synthesis of Ni-doped cadmium zinc aluminum ferrite Ni-doped Ni<sub>x</sub>Cd<sub>0.8−X</sub>Zn<sub>0.2</sub>Al<sub>0.3</sub>Fe<sub>1.7</sub>O<sub>4</sub> (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 Ni<sup>2+</sup> 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 m<sup>2</sup>/g) and pore volume (1.836 cm<sup>3</sup>/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 H<sub>2</sub>O<sub>2</sub> (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.</p></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"137 5","pages":"2847 - 2866"},"PeriodicalIF":1.7000,"publicationDate":"2024-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sol–gel synthesis and characterization of Ni-doping enhanced NixCd0.8−XZn0.2Al0.3Fe1.7O4 nanoparticles with exceptional photocatalytic activity for ciprofloxacin degradation\",\"authors\":\"Muhammed Yasar,&nbsp;Khalid Javed,&nbsp;Muhammad Ibrahim,&nbsp;Fozia Noreen\",\"doi\":\"10.1007/s11144-024-02665-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this study, the sol–gel synthesis of Ni-doped cadmium zinc aluminum ferrite Ni-doped Ni<sub>x</sub>Cd<sub>0.8−X</sub>Zn<sub>0.2</sub>Al<sub>0.3</sub>Fe<sub>1.7</sub>O<sub>4</sub> (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 Ni<sup>2+</sup> 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 m<sup>2</sup>/g) and pore volume (1.836 cm<sup>3</sup>/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 H<sub>2</sub>O<sub>2</sub> (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.</p></div>\",\"PeriodicalId\":750,\"journal\":{\"name\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"volume\":\"137 5\",\"pages\":\"2847 - 2866\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11144-024-02665-3\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-024-02665-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

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)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Sol–gel synthesis and characterization of Ni-doping enhanced NixCd0.8−XZn0.2Al0.3Fe1.7O4 nanoparticles with exceptional photocatalytic activity for ciprofloxacin degradation

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
期刊最新文献
Editorial. Special issue papers presented at the International Conference on Recent Trends in Materials and Devices 2023 Visible light active bismuth chromate/curcuma longa heterostructure for enhancing photocatalytic activity Influence of electron-donating groups on the aniline oxidative coupling reaction with promethazine: a comprehensive experimental and theoretical investigation Xanthan gum templated hydrothermal synthesis of Bi2O3 nano-photocatalyst for the mineralization of chlorophenols prevalent in paper pulp mill Innovative CO2 conversion: harnessing photocatalytic activity in polyvinylidene fluoride/TiO2 electrospun nanofibers for environmental sustainability
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1