{"title":"MgFeTi-LDH/g-C3N4 composites promote sodium persulfate activation through Fe3+/Fe2+ cycles for efficient tetracycline degradation under visible light irradiation†","authors":"Zihan Wei, Xiaoqian Ren, Tianhong Mei, Rongcheng Xiang, Wugan Wei, Xiaorui Yang, Yan Fang, Wenlong Xu, Jianliang Zhu and Jinhua Liang","doi":"10.1039/D5NJ00442J","DOIUrl":null,"url":null,"abstract":"<p >In this study, various MgFeTi-LDH/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> photocatalytic materials were successfully synthesized through self-assembly, and their physicochemical and photoelectric properties were thoroughly characterized. Optical performance characterization of band gaps and VB-XPS spectra revealed that the <em>E</em><small><sub>VB</sub></small> and <em>E</em><small><sub>CB</sub></small> alignments of MgFeTi(3 : 1)-LDH/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> composites are consistent with the fundamental characteristics of S-type heterojunctions. MgFeTi(3 : 1)-LDH/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> coupled with sodium persulfate activation for TCH degradation achieved nearly 100% removal efficiency under visible light, surpassing previously reported catalysts. Moreover, five repeated tests of MgFeTi(3 : 1)-LDH/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> showed negligible change in the removal rate of TCH, indicating its potential value for industrial applications. Furthermore, the catalytic degradation pathway and mechanism for MgFeTi(3 : 1)-LDH/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> have been elucidated through LC-MS analysis, radical capture, and characterization. In addition, the high efficiency of TCH degradation is attributed to the synergy of Fe<small><sup>3+</sup></small>, Fe<small><sup>2+</sup></small>, SPS, and active species such as ˙OH, SO<small><sub>4</sub></small>˙<small><sup>−</sup></small>, and ˙O<small><sub>2</sub></small><small><sup>−</sup></small>. Finally, the QSAR analysis and OD<small><sub>600</sub></small> values suggest that the degradation pathway and time lead to a reduction in toxicity and the potential risk to the degradation liquid. This study offers a simple and economical approach to completely degrade TCH, also providing practical application prospects in wastewater treatment.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 22","pages":" 9079-9095"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj00442j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, various MgFeTi-LDH/g-C3N4 photocatalytic materials were successfully synthesized through self-assembly, and their physicochemical and photoelectric properties were thoroughly characterized. Optical performance characterization of band gaps and VB-XPS spectra revealed that the EVB and ECB alignments of MgFeTi(3 : 1)-LDH/g-C3N4 composites are consistent with the fundamental characteristics of S-type heterojunctions. MgFeTi(3 : 1)-LDH/g-C3N4 coupled with sodium persulfate activation for TCH degradation achieved nearly 100% removal efficiency under visible light, surpassing previously reported catalysts. Moreover, five repeated tests of MgFeTi(3 : 1)-LDH/g-C3N4 showed negligible change in the removal rate of TCH, indicating its potential value for industrial applications. Furthermore, the catalytic degradation pathway and mechanism for MgFeTi(3 : 1)-LDH/g-C3N4 have been elucidated through LC-MS analysis, radical capture, and characterization. In addition, the high efficiency of TCH degradation is attributed to the synergy of Fe3+, Fe2+, SPS, and active species such as ˙OH, SO4˙−, and ˙O2−. Finally, the QSAR analysis and OD600 values suggest that the degradation pathway and time lead to a reduction in toxicity and the potential risk to the degradation liquid. This study offers a simple and economical approach to completely degrade TCH, also providing practical application prospects in wastewater treatment.