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    Electrochemical detection of explosive compounds in an ionic liquid in mixed environments: Influence of oxygen, moisture, and other nitroaromatics on the sensing response

    74427.pdf (1.164Mb)
    Access Status
    Open access
    Authors
    Lee, Junqiao
    Silvester, Debbie
    Date
    2019
    Type
    Journal Article
    
    Metadata
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    Citation
    Lee, J. and Silvester, D. 2019. Electrochemical detection of explosive compounds in an ionic liquid in mixed environments: Influence of oxygen, moisture, and other nitroaromatics on the sensing response. Australian Journal of Chemistry. 72 (2): pp. 122-129.
    Source Title
    Australian Journal of Chemistry
    DOI
    10.1071/CH18396
    ISSN
    0004-9425
    School
    Nanochemistry Research Institute
    Funding and Sponsorship
    http://purl.org/au-research/grants/arc/FT170100315
    URI
    http://hdl.handle.net/20.500.11937/74142
    Collection
    • Curtin Research Publications
    Abstract

    From a security point of view, detecting and quantifying explosives in mixed environments is required to identify potentially concealed explosives. Electrochemistry offers a viable method to detect nitroaromatic explosive compounds owing to the presence of easily reducible nitro groups that give rise to a current signal. However, their reduction potentials can overlap with interfering species, making it difficult to distinguish particular compounds. We have therefore examined the effect of oxygen, moisture, and other nitroaromatic species on the cyclic voltammetry and square wave voltammetry of nitroaromatic compounds of a range of mixed environments, focussing on 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (DNT) as model analytes, and using the hydrophobic room-temperature ionic liquid (RTIL) [P14,6,6,6][NTf2] as the solvent. Oxygen (0-20 % vol.) minimally affected the current of the first reduction peak of TNT in [P14,6,6,6][NTf2], but significantly affects the current for DNT. The impact of water (0 to 86 % relative humidity), however, was much more dramatic-even in the hydrophobic RTIL, water significantly affected the currents of the analyte peaks for TNT and DNT, and gave rise to additional reduction features, further contributing to the current. Additionally, the voltammetry of other related di- and tri-nitro compounds (2,6-dinitrotoluene, 1,3-dinitrobenzene, 2,4,6-trinitrotoluene, 1,3,5-trinitrobenzene, and musk xylene) was also studied to understand how different substituents on the aromatic ring may affect the reduction potentials. A 50: 50 mixture of TNT and DNT revealed that both analytes could be separately identified and quantified using square wave voltammetry. Overall, this information is useful in determining the effect of other species on the current signals of electrochemical explosive sensors, and reveals that it may be necessary to dry the aprotic RTIL electrolyte when used in humid environments.

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