SYNTHESIS AND THE STUDY OF PHOTOCATALYTIC ACTIVITY OF COBALT FERRITE (COFE2O4) NANOPARTICLES: SYNERGISTIC EFFECTS OF PHOTOCATALYSIS AND PHOTO-FENTON PROCESS

S. .
{"title":"SYNTHESIS AND THE STUDY OF PHOTOCATALYTIC ACTIVITY OF COBALT FERRITE (COFE2O4) NANOPARTICLES: SYNERGISTIC EFFECTS OF PHOTOCATALYSIS AND PHOTO-FENTON PROCESS","authors":"S. .","doi":"10.15623/ijret.2018.0709004","DOIUrl":null,"url":null,"abstract":"CoFe 2 O 4 was prepared by sol-gel combustion method. Powder X-ray diffraction (PXRD) studies confirmed the spinel structure for CoFe 2 O 4 . UV-Vis absorbance spectrum and the following Kubelka-Munk plot show the band gap of CoFe 2 O 4 to be 2.73eV. FTIR studies shows the existence of Co-O and Fe-O stretching vibrations. Raman spectroscopy gives the information pertaining to tetrahedral and octahedral sites. The activity of the catalyst was explored for the degradation of methyl orange in presence of peroxymonosulphate (PMS) as an oxidant which is dipolar, possessing unsymmetrical structure and higher oxidation potential and shows better oxidising reactions due to charge transfer to solvent molecule (CTTS) and PMS forms a charge transfer complex with CoFe 2 O 4 . The active roles of the hydroxyl and sulphate free radicals are confirmed. CoFe 2 O 4 catalyst shows synergistic effect between photocatalysis and photo- Fenton process especially even at higher pH values and the catalyst is found to be stable and can be reused for three consecutive cycles.","PeriodicalId":14258,"journal":{"name":"International Journal of Research in Engineering and Technology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Research in Engineering and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15623/ijret.2018.0709004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

CoFe 2 O 4 was prepared by sol-gel combustion method. Powder X-ray diffraction (PXRD) studies confirmed the spinel structure for CoFe 2 O 4 . UV-Vis absorbance spectrum and the following Kubelka-Munk plot show the band gap of CoFe 2 O 4 to be 2.73eV. FTIR studies shows the existence of Co-O and Fe-O stretching vibrations. Raman spectroscopy gives the information pertaining to tetrahedral and octahedral sites. The activity of the catalyst was explored for the degradation of methyl orange in presence of peroxymonosulphate (PMS) as an oxidant which is dipolar, possessing unsymmetrical structure and higher oxidation potential and shows better oxidising reactions due to charge transfer to solvent molecule (CTTS) and PMS forms a charge transfer complex with CoFe 2 O 4 . The active roles of the hydroxyl and sulphate free radicals are confirmed. CoFe 2 O 4 catalyst shows synergistic effect between photocatalysis and photo- Fenton process especially even at higher pH values and the catalyst is found to be stable and can be reused for three consecutive cycles.
纳米钴铁氧体(cofe2o4)的合成及光催化活性研究:光催化与光芬顿过程的协同效应
采用溶胶-凝胶燃烧法制备了cofe2o4。粉末x射线衍射(PXRD)研究证实了cofe2o4的尖晶石结构。紫外可见吸收光谱和Kubelka-Munk图显示,cofe2o4的带隙为2.73eV。FTIR研究表明Co-O和Fe-O拉伸振动的存在。拉曼光谱给出了有关四面体和八面体位点的信息。考察了该催化剂在双极性、结构不对称、氧化电位较高的过氧一元硫酸盐(PMS)作为氧化剂存在下降解甲基橙的活性,PMS由于向溶剂分子(CTTS)的电荷转移而表现出较好的氧化反应,PMS与cofe2o4形成电荷转移配合物。证实了羟基和硫酸盐自由基的活性作用。在较高的pH值下,CoFe 2o4催化剂在光催化和光Fenton工艺之间表现出协同作用,且催化剂性能稳定,可连续重复使用3次。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信