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Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid
We describe the voltammetric behavior of an anion-exchange membrane, hexamethyl-p-terphenyl poly(benzimidazolium) (HMT-PMBI). The anion-exchange properties of HMT-PMBI chemically modified electrodes were investigated using K(4)Fe(CN)(6) and K(2)IrCl(6) as redox probes. The permselectivity properties...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013716/ https://www.ncbi.nlm.nih.gov/pubmed/31941118 http://dx.doi.org/10.3390/s20020443 |
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author | Rees, Matthew Wright, Andrew G. Holdcroft, Steven Bertoncello, Paolo |
author_facet | Rees, Matthew Wright, Andrew G. Holdcroft, Steven Bertoncello, Paolo |
author_sort | Rees, Matthew |
collection | PubMed |
description | We describe the voltammetric behavior of an anion-exchange membrane, hexamethyl-p-terphenyl poly(benzimidazolium) (HMT-PMBI). The anion-exchange properties of HMT-PMBI chemically modified electrodes were investigated using K(4)Fe(CN)(6) and K(2)IrCl(6) as redox probes. The permselectivity properties of HMT-PMBI chemically modified electrodes were ascertained using tris(2-2’)bipyridyl-ruthenium(II) chloride Ru(bpy)(3)(2+). Cyclic voltammetry and chronoamperometry were utilized to extract parameters such as the concentration of the redox mediators inside the films and the apparent diffusion coefficients. We found the concentration of K(4)Fe(CN)(6) and K(2)IrCl(6) redox species within HMT-PMBI-coated films to be on the order of 0.04–0.1 mol·dm(−3), and values of D(app) ca. 10(−10)–10(−9) cm(2)·s(−1). To evaluate the possibility of using such a polymer coating in electroanalysis, HMT-PMBI-modified electrodes were utilized for the voltammetric detection of uric acid in artificial urine, Surine(®) and ascorbic acid in Vitamin C samples. The results showed that HMT-PMBI-coated electrodes can detect uric acid in Surine(®) with a limit of detection (LoD) of 7.7 µM, sensitivity of 0.14 µA·µM(−1)·cm(−2), and linear range between 5 μM and 200 μM, whereas for Vitamin C tablets, the LoD is 41.4 µM, the sensitivity is 0.08 µA·µM(−1)·cm(−2), and the linear range is between 25 μM and 450 μM. |
format | Online Article Text |
id | pubmed-7013716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70137162020-03-09 Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid Rees, Matthew Wright, Andrew G. Holdcroft, Steven Bertoncello, Paolo Sensors (Basel) Article We describe the voltammetric behavior of an anion-exchange membrane, hexamethyl-p-terphenyl poly(benzimidazolium) (HMT-PMBI). The anion-exchange properties of HMT-PMBI chemically modified electrodes were investigated using K(4)Fe(CN)(6) and K(2)IrCl(6) as redox probes. The permselectivity properties of HMT-PMBI chemically modified electrodes were ascertained using tris(2-2’)bipyridyl-ruthenium(II) chloride Ru(bpy)(3)(2+). Cyclic voltammetry and chronoamperometry were utilized to extract parameters such as the concentration of the redox mediators inside the films and the apparent diffusion coefficients. We found the concentration of K(4)Fe(CN)(6) and K(2)IrCl(6) redox species within HMT-PMBI-coated films to be on the order of 0.04–0.1 mol·dm(−3), and values of D(app) ca. 10(−10)–10(−9) cm(2)·s(−1). To evaluate the possibility of using such a polymer coating in electroanalysis, HMT-PMBI-modified electrodes were utilized for the voltammetric detection of uric acid in artificial urine, Surine(®) and ascorbic acid in Vitamin C samples. The results showed that HMT-PMBI-coated electrodes can detect uric acid in Surine(®) with a limit of detection (LoD) of 7.7 µM, sensitivity of 0.14 µA·µM(−1)·cm(−2), and linear range between 5 μM and 200 μM, whereas for Vitamin C tablets, the LoD is 41.4 µM, the sensitivity is 0.08 µA·µM(−1)·cm(−2), and the linear range is between 25 μM and 450 μM. MDPI 2020-01-13 /pmc/articles/PMC7013716/ /pubmed/31941118 http://dx.doi.org/10.3390/s20020443 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rees, Matthew Wright, Andrew G. Holdcroft, Steven Bertoncello, Paolo Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title | Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title_full | Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title_fullStr | Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title_full_unstemmed | Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title_short | Voltammetry at Hexamethyl-P-Terphenyl Poly(Benzimidazolium) (HMT-PMBI)-Coated Glassy Carbon Electrodes: Charge Transport Properties and Detection of Uric and Ascorbic Acid |
title_sort | voltammetry at hexamethyl-p-terphenyl poly(benzimidazolium) (hmt-pmbi)-coated glassy carbon electrodes: charge transport properties and detection of uric and ascorbic acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013716/ https://www.ncbi.nlm.nih.gov/pubmed/31941118 http://dx.doi.org/10.3390/s20020443 |
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