4.7 Article

Development of a gold nanoparticles-based colorimetric sensor for the indirect determination of ammonium dinitramide and tetryl

Journal

TALANTA
Volume 226, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2021.122187

Keywords

Ammonium dinitramide detection; Tetryl detection; Nitrite sensor; Propellants; Explosives; Gold nanoparticles

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A sensitive and practical sensing method based on nanoparticle technology was developed for the accurate detection of Ammonium dinitramide (ADN) in the presence of other explosives, demonstrating high detection sensitivity and reliability. Additionally, the method showed promise for application in the detection of other explosive materials and was statistically validated against reference methods.
Ammonium dinitramide (ADN) is a strong, environmentally friendly oxidizer used in composite solid rocket propellants. As there is no reliable colorimetric sensor for ADN assay applicable to in-field screening, we developed a sensitive and practical sensing method to determine it in the presence of other explosives and possible interferents, based on the detection of nitrite formed from ADN degradation under UV light in a slightly alkaline (i.e. of lower alkalinity than needed to hydrolyze nitramines) solution by a nanoparticle-based colorimetric sensor. The ADN-derived nitrite formed a colored product via a Griess reaction using gold nanoparticles modified with 4-aminothiophenol (4-ATP-AuNPs) along with a coupling reagent N-(1-naphthyl)ethylene diamine (NED) for forming an azo dye. The method used for ADN detection could also be applied to tetryl samples at a different wavelength. The limit of detection (LOD) was 0.012 mg L-1 for ADN and 0.615 mg L-1 for tetryl. Interference effects of energetic materials like trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) and pentaerythritol tetranitrate (PETN) to ADN determination could be overcome. In addition, common soil ions did not adversely affect the nanosensor performance. The developed method was statistically validated against reference voltammetric, UV, and HPLC methods using t- and F- tests.

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