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Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)

The explosive triacetone triperoxide (TATP), which can be prepared from commercially readily available reagents following an easy synthetic procedure, is one of the most common components of improvised explosive devices (IEDs). Molecularly-imprinted polymer (MIP) electrochemical sensors have proved...

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Autores principales: Mamo, Samuel Kassahun, Gonzalez-Rodriguez, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299062/
https://www.ncbi.nlm.nih.gov/pubmed/25490589
http://dx.doi.org/10.3390/s141223269
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author Mamo, Samuel Kassahun
Gonzalez-Rodriguez, Jose
author_facet Mamo, Samuel Kassahun
Gonzalez-Rodriguez, Jose
author_sort Mamo, Samuel Kassahun
collection PubMed
description The explosive triacetone triperoxide (TATP), which can be prepared from commercially readily available reagents following an easy synthetic procedure, is one of the most common components of improvised explosive devices (IEDs). Molecularly-imprinted polymer (MIP) electrochemical sensors have proved useful for the determination of different compounds in different matrices with the required sensitivity and selectivity. In this work, a highly sensitive and selective molecularly imprinted polymer with electrochemical capabilities for the determination of TATP has been developed. The molecular imprinting has been performed via electropolymerisation onto a glassy carbon electrode surface by cyclic voltammetry from a solution of pyrrole functional monomer, TATP template and LiClO(4). Differential Pulse Voltammetry of TATP, with LiClO(4) as supporting electrolyte, was performed in a potential range of −2.0 V to +1.0 V (vs. Ag/AgCl). Three-factor two-level factorial design was used to optimise the monomer concentration at 0.1 mol·L(−1), template concentration at 100 mmol·L(−1) and the number of cyclic voltammetry scan cycles to 10. The molecularly imprinted polymer-modified glassy carbon electrode demonstrated good performance at low concentrations for a linear range of 82–44,300 μg·L(−1) and a correlation coefficient of r(2) = 0.996. The limits of detection (LoD) and quantification (LoQ) achieved were 26.9 μg·L(−1) and 81.6 μg·L(−1), respectively. The sensor demonstrated very good repeatability with precision values (n = 6, expressed as %RSD) of 1.098% and 0.55% for 1108 and 2216 μg·L(−1), respectively. It also proved selective for TATP in the presence of other explosive substances such as PETN, RDX, HMX, and TNT.
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spelling pubmed-42990622015-01-26 Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP) Mamo, Samuel Kassahun Gonzalez-Rodriguez, Jose Sensors (Basel) Article The explosive triacetone triperoxide (TATP), which can be prepared from commercially readily available reagents following an easy synthetic procedure, is one of the most common components of improvised explosive devices (IEDs). Molecularly-imprinted polymer (MIP) electrochemical sensors have proved useful for the determination of different compounds in different matrices with the required sensitivity and selectivity. In this work, a highly sensitive and selective molecularly imprinted polymer with electrochemical capabilities for the determination of TATP has been developed. The molecular imprinting has been performed via electropolymerisation onto a glassy carbon electrode surface by cyclic voltammetry from a solution of pyrrole functional monomer, TATP template and LiClO(4). Differential Pulse Voltammetry of TATP, with LiClO(4) as supporting electrolyte, was performed in a potential range of −2.0 V to +1.0 V (vs. Ag/AgCl). Three-factor two-level factorial design was used to optimise the monomer concentration at 0.1 mol·L(−1), template concentration at 100 mmol·L(−1) and the number of cyclic voltammetry scan cycles to 10. The molecularly imprinted polymer-modified glassy carbon electrode demonstrated good performance at low concentrations for a linear range of 82–44,300 μg·L(−1) and a correlation coefficient of r(2) = 0.996. The limits of detection (LoD) and quantification (LoQ) achieved were 26.9 μg·L(−1) and 81.6 μg·L(−1), respectively. The sensor demonstrated very good repeatability with precision values (n = 6, expressed as %RSD) of 1.098% and 0.55% for 1108 and 2216 μg·L(−1), respectively. It also proved selective for TATP in the presence of other explosive substances such as PETN, RDX, HMX, and TNT. MDPI 2014-12-05 /pmc/articles/PMC4299062/ /pubmed/25490589 http://dx.doi.org/10.3390/s141223269 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mamo, Samuel Kassahun
Gonzalez-Rodriguez, Jose
Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title_full Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title_fullStr Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title_full_unstemmed Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title_short Development of a Molecularly Imprinted Polymer-Based Sensor for the Electrochemical Determination of Triacetone Triperoxide (TATP)
title_sort development of a molecularly imprinted polymer-based sensor for the electrochemical determination of triacetone triperoxide (tatp)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299062/
https://www.ncbi.nlm.nih.gov/pubmed/25490589
http://dx.doi.org/10.3390/s141223269
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