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The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile

Authorized Users Only
2010
Authors
Marinović, Vedrana M.
Marinović, Sanja
Jovanović, M.
Jovanovic, J.
Štrbac, Svetlana
Article (Published version)
Metadata
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Abstract
The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated by cyclic voltammetry on a platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT. The obtained cyclic voltammograms showed three distinct reduction peaks in the potential range of -0.45 to -0.8 V (vs. an Ag/AgCl (3M KCl) reference electrode), which refer to the multi-step process of TNT reduction. The calibration curves of the dependence of the first peak current on the TNT concentration were linear in the ranges 4.4-638.4 mu M and 0.11-4.40 mu M for two different scan rates, 200 my s(-1) and 20 mV s(-1), respectively. The detection limit was 0.11 mu M. Acetonitrile chemisorption on Pt surface took place and caused thus modified platinum electrode to exhibit an electrochemically stabile behaviour. Hence, a very high reproducibility over a prolonged time and voltammetric cycling was provided for using a Pt wire that is easy to handle as a suitable ...material for TNT sensing. Additionally, it was confirmed by testing the acetonitrile modified Pt wire for TNT detection in river water.

Keywords:
Trinitrotoluene / Electrochemical reduction / Platinum / Acetonitrile
Source:
Journal of Electroanalytical Chemistry, 2010, 648, 1, 1-7
Publisher:
  • Elsevier
Funding / projects:
  • Modifikacija metalnih i nemetalnih materijala elektroprovodnim polimerima za primenu u novim tehnologijama (RS-142044)
  • Mezoporozni i nanomaterijali u katalitičkim i sorpcionim procesima (RS-166001)

DOI: 10.1016/j.jelechem.2010.07.008

ISSN: 1572-6657

WoS: 000282399400001

Scopus: 2-s2.0-77956411619
[ Google Scholar ]
19
18
URI
http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5619
Collections
  • Radovi istraživača / Researchers’ publications (TMF)
Institution/Community
Tehnološko-metalurški fakultet
TY  - JOUR
AU  - Marinović, Vedrana M.
AU  - Marinović, Sanja
AU  - Jovanović, M.
AU  - Jovanovic, J.
AU  - Štrbac, Svetlana
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5619
AB  - The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated by cyclic voltammetry on a platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT. The obtained cyclic voltammograms showed three distinct reduction peaks in the potential range of -0.45 to -0.8 V (vs. an Ag/AgCl (3M KCl) reference electrode), which refer to the multi-step process of TNT reduction. The calibration curves of the dependence of the first peak current on the TNT concentration were linear in the ranges 4.4-638.4 mu M and 0.11-4.40 mu M for two different scan rates, 200 my s(-1) and 20 mV s(-1), respectively. The detection limit was 0.11 mu M. Acetonitrile chemisorption on Pt surface took place and caused thus modified platinum electrode to exhibit an electrochemically stabile behaviour. Hence, a very high reproducibility over a prolonged time and voltammetric cycling was provided for using a Pt wire that is easy to handle as a suitable material for TNT sensing. Additionally, it was confirmed by testing the acetonitrile modified Pt wire for TNT detection in river water.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile
EP  - 7
IS  - 1
SP  - 1
VL  - 648
DO  - 10.1016/j.jelechem.2010.07.008
ER  - 
@article{
author = "Marinović, Vedrana M. and Marinović, Sanja and Jovanović, M. and Jovanovic, J. and Štrbac, Svetlana",
year = "2010",
abstract = "The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated by cyclic voltammetry on a platinum electrode in aqueous sodium chloride solutions with acetonitrile containing different concentrations of TNT. The obtained cyclic voltammograms showed three distinct reduction peaks in the potential range of -0.45 to -0.8 V (vs. an Ag/AgCl (3M KCl) reference electrode), which refer to the multi-step process of TNT reduction. The calibration curves of the dependence of the first peak current on the TNT concentration were linear in the ranges 4.4-638.4 mu M and 0.11-4.40 mu M for two different scan rates, 200 my s(-1) and 20 mV s(-1), respectively. The detection limit was 0.11 mu M. Acetonitrile chemisorption on Pt surface took place and caused thus modified platinum electrode to exhibit an electrochemically stabile behaviour. Hence, a very high reproducibility over a prolonged time and voltammetric cycling was provided for using a Pt wire that is easy to handle as a suitable material for TNT sensing. Additionally, it was confirmed by testing the acetonitrile modified Pt wire for TNT detection in river water.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile",
pages = "7-1",
number = "1",
volume = "648",
doi = "10.1016/j.jelechem.2010.07.008"
}
Marinović, V. M., Marinović, S., Jovanović, M., Jovanovic, J.,& Štrbac, S.. (2010). The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile. in Journal of Electroanalytical Chemistry
Elsevier., 648(1), 1-7.
https://doi.org/10.1016/j.jelechem.2010.07.008
Marinović VM, Marinović S, Jovanović M, Jovanovic J, Štrbac S. The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile. in Journal of Electroanalytical Chemistry. 2010;648(1):1-7.
doi:10.1016/j.jelechem.2010.07.008 .
Marinović, Vedrana M., Marinović, Sanja, Jovanović, M., Jovanovic, J., Štrbac, Svetlana, "The electrochemical reduction of trinitrotoluene on a platinum wire modified by chemisorbed acetonitrile" in Journal of Electroanalytical Chemistry, 648, no. 1 (2010):1-7,
https://doi.org/10.1016/j.jelechem.2010.07.008 . .

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