{"title":"Mechanism of TMB Discoloration Catalyzed by Layered CoNi@CN Nanozymes: Application Based on Smart Phone for Resorcinol Detection","authors":"Qingyong Guo, Rongsheng Xiao, Haifeng Chen, Meishuo Bao, Jingwen Qi, Qian-qian Jia, Wuxiang Zhang","doi":"10.1002/cjoc.202400841","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Real-time on-site monitoring of resorcinol (RS) concentrations is crucial for detecting hazardous levels, enabling prompt response measures to mitigate potential environmental and health risks. In this study, we developed an innovative method using CoNi@CN-2 nanozymes to activate peroxymonosulfate (PMS) for oxidizing 3,3',5,5'-tetramethylbenzidine (TMB). Our results show that the formation of Ni<sup>2+</sup> through the oxidation of Ni<sup>0</sup> on the CoNi@CN-2 surface significantly enhances the electron-donating capacity of Co<sup>0</sup>. The catalytic reaction of TMB is mediated by redox active species (SO<sub>4</sub><sup>•−</sup>, •O<sub>2</sub><sup>−</sup>, •OH and <sup>1</sup>O<sub>2</sub>). RS drives colorimetry by transferring electrons to the benzene ring and specific nitrogen atoms in ox-TMB, reducing ox-TMB to TMB. Furthermore, the colorimetric assay shows a robust linear correlation between RS concentration and absorbance (Abs), described by Abs = –0.44[RS] + 0.886 (0—200 μmol/L, R<sup>2</sup> = 0.983). Also, we introduce a novel smartphone-integrated autonomous detection software that can analyze RS concentration and grayscale values (GSV), yielding GSV = 0.327[RS] + 63.601 (0—200 μmol/L, <i>R</i><sup>2</sup> = 0.990) with a detection limit of 5.29 μmol/L. Additionally, excess PMS leads to ROS attacking specific sites in ox-TMB, forming secondary oxidation products. This study has enabled rapid and accurate detection of RS, making a significant contribution to environmental safety and protection.</p>\n <p>\n </p>\n </div>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"43 3","pages":"281-291"},"PeriodicalIF":5.5000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202400841","RegionNum":1,"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
Real-time on-site monitoring of resorcinol (RS) concentrations is crucial for detecting hazardous levels, enabling prompt response measures to mitigate potential environmental and health risks. In this study, we developed an innovative method using CoNi@CN-2 nanozymes to activate peroxymonosulfate (PMS) for oxidizing 3,3',5,5'-tetramethylbenzidine (TMB). Our results show that the formation of Ni2+ through the oxidation of Ni0 on the CoNi@CN-2 surface significantly enhances the electron-donating capacity of Co0. The catalytic reaction of TMB is mediated by redox active species (SO4•−, •O2−, •OH and 1O2). RS drives colorimetry by transferring electrons to the benzene ring and specific nitrogen atoms in ox-TMB, reducing ox-TMB to TMB. Furthermore, the colorimetric assay shows a robust linear correlation between RS concentration and absorbance (Abs), described by Abs = –0.44[RS] + 0.886 (0—200 μmol/L, R2 = 0.983). Also, we introduce a novel smartphone-integrated autonomous detection software that can analyze RS concentration and grayscale values (GSV), yielding GSV = 0.327[RS] + 63.601 (0—200 μmol/L, R2 = 0.990) with a detection limit of 5.29 μmol/L. Additionally, excess PMS leads to ROS attacking specific sites in ox-TMB, forming secondary oxidation products. This study has enabled rapid and accurate detection of RS, making a significant contribution to environmental safety and protection.
期刊介绍:
The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.