{"title":"低成本电化学传感器用于同时检测和估计二羟基苯异构体","authors":"N. T. Tonu, M. A. Yousuf","doi":"10.4152/pea.2022400105","DOIUrl":null,"url":null,"abstract":"An ionic liquid (IL) based pencil graphite electrode (PGE) sensor was electrochemically fabricated for hydroquinone (HQ), catechol (CC) and resorcinol (RS) simultaneous detection and estimation in aqueous media. PGE surface was modified by 1-hexylpyridinium hexafluorophosphate (HPHP) using cyclic voltammetry (CV). The modified surface was characterized by scanning electron microscope (SEM) and energy dispersive X-ray microanalysis (EDX). The modified electrode showed an excellent electro-analytical activity towards simultaneously HQ, CC and RS, at pH 6.8 in aqueous media. The scan rate effect was diffusion controlled and the concentration effect was linear with current. The limit of detection (LOD) for HQ, CC and RS was found to be 6.38 μmol L¹, 4.56 μmol L¹ and 19.6 μmol L¹, respectively. The sensitivity for HQ, CC and RS was found to be 448.49 μAmM -1 cm -2 , 627.35 μAmM -1 cm -2 and 146.10 μAmM −1 cm −2 , respectively, in a ternary mixture of dihydroxybenzene isomers (DHBIs). The cost of using PGE was lower than that of the conventional electrodes. isomers, ionic liquid, pencil graphite electrode and differential pulse voltammetry.","PeriodicalId":20334,"journal":{"name":"Portugaliae Electrochimica Acta","volume":"1 1","pages":""},"PeriodicalIF":1.1000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Low Cost Electrochemical Sensor for Simultaneous Detection and Estimation of Dihydroxybenzene Isomers\",\"authors\":\"N. T. Tonu, M. A. Yousuf\",\"doi\":\"10.4152/pea.2022400105\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An ionic liquid (IL) based pencil graphite electrode (PGE) sensor was electrochemically fabricated for hydroquinone (HQ), catechol (CC) and resorcinol (RS) simultaneous detection and estimation in aqueous media. PGE surface was modified by 1-hexylpyridinium hexafluorophosphate (HPHP) using cyclic voltammetry (CV). The modified surface was characterized by scanning electron microscope (SEM) and energy dispersive X-ray microanalysis (EDX). The modified electrode showed an excellent electro-analytical activity towards simultaneously HQ, CC and RS, at pH 6.8 in aqueous media. The scan rate effect was diffusion controlled and the concentration effect was linear with current. The limit of detection (LOD) for HQ, CC and RS was found to be 6.38 μmol L¹, 4.56 μmol L¹ and 19.6 μmol L¹, respectively. The sensitivity for HQ, CC and RS was found to be 448.49 μAmM -1 cm -2 , 627.35 μAmM -1 cm -2 and 146.10 μAmM −1 cm −2 , respectively, in a ternary mixture of dihydroxybenzene isomers (DHBIs). The cost of using PGE was lower than that of the conventional electrodes. isomers, ionic liquid, pencil graphite electrode and differential pulse voltammetry.\",\"PeriodicalId\":20334,\"journal\":{\"name\":\"Portugaliae Electrochimica Acta\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Portugaliae Electrochimica Acta\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4152/pea.2022400105\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Portugaliae Electrochimica Acta","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4152/pea.2022400105","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 2
摘要
采用电化学方法制备了离子液体铅笔石墨电极(PGE)传感器,用于水中对苯二酚(HQ)、儿茶酚(CC)和间苯二酚(RS)的同时检测和估计。采用循环伏安法(CV)对PGE表面进行了六氟磷酸1-己基吡啶(HPHP)修饰。用扫描电镜(SEM)和能谱x射线微分析(EDX)对改性后的表面进行了表征。在pH为6.8的水溶液中,改性电极同时对HQ、CC和RS具有良好的电分析活性。扫描速率效应受扩散控制,浓度效应与电流呈线性关系。检测限(LOD)分别为6.38 μmol L¹、4.56 μmol L¹和19.6 μmol L¹。在二羟基苯异构体(DHBIs)的三元混合物中,HQ、CC和RS的灵敏度分别为448.49 μAmM -1 cm -2、627.35 μAmM -1 cm -2和146.10 μAmM -1 cm -2。使用PGE的成本低于传统电极。异构体,离子液体,铅笔石墨电极和差分脉冲伏安法。
Low Cost Electrochemical Sensor for Simultaneous Detection and Estimation of Dihydroxybenzene Isomers
An ionic liquid (IL) based pencil graphite electrode (PGE) sensor was electrochemically fabricated for hydroquinone (HQ), catechol (CC) and resorcinol (RS) simultaneous detection and estimation in aqueous media. PGE surface was modified by 1-hexylpyridinium hexafluorophosphate (HPHP) using cyclic voltammetry (CV). The modified surface was characterized by scanning electron microscope (SEM) and energy dispersive X-ray microanalysis (EDX). The modified electrode showed an excellent electro-analytical activity towards simultaneously HQ, CC and RS, at pH 6.8 in aqueous media. The scan rate effect was diffusion controlled and the concentration effect was linear with current. The limit of detection (LOD) for HQ, CC and RS was found to be 6.38 μmol L¹, 4.56 μmol L¹ and 19.6 μmol L¹, respectively. The sensitivity for HQ, CC and RS was found to be 448.49 μAmM -1 cm -2 , 627.35 μAmM -1 cm -2 and 146.10 μAmM −1 cm −2 , respectively, in a ternary mixture of dihydroxybenzene isomers (DHBIs). The cost of using PGE was lower than that of the conventional electrodes. isomers, ionic liquid, pencil graphite electrode and differential pulse voltammetry.
期刊介绍:
Portugaliae Electrochimica Acta is a bi-monthly Journal published by the Portuguese Electrochemical Society since 1983. Portugaliae Electrochimica Acta publishes original papers, brief communications, reviews and letters concerned with every aspect of theory and practice of electrochemistry, as well as articles in which topics on history, science policy, education, etc. in the electrochemical field (teaching or research) may be discussed.