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Turn‐off Fluorescent Sensing of Energetic Materials using Protonic Acid doped Polyaniline: A Spectrochemical Mechanistic Approach
The trace detection of energetic materials (EMs) is a challenge due to the very low vapor pressure possessed by these compounds. Polyaniline (PAni) possesses variable oxidation and reduction states, which makes it strike different from other conducting polymers in understanding the mechanism of fluo...
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Published in: | Zeitschrift für anorganische und allgemeine Chemie (1950) 2021-02, Vol.647 (4), p.331-340 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The trace detection of energetic materials (EMs) is a challenge due to the very low vapor pressure possessed by these compounds. Polyaniline (PAni) possesses variable oxidation and reduction states, which makes it strike different from other conducting polymers in understanding the mechanism of fluorophore‐analyte interaction leads to the designing of selectivity and sensitivity of analytes; also, fluorophore as a sensing device. The present work is aimed at trace detection of some very prominent EMs; nitroarenes viz., 1,3,5‐trinitroperhydro‐1,3,5‐triazine (RDX), trinitrotoluene (TNT); nitramines viz., hexanitrohexaazaisowurtzitane (CL‐20) and nitro ester viz., pentaerithroltetraniterate (PETN) employing para‐toluenesulfonic acid as a dopant for PAni nanofibers (P‐PAni). The P‐PAni helps overcome the dual difficulties of PAni, i.e., solubility and removal of π stacking when dimethylformamide (DMF) is used as a solvent. P‐PAni showed good quenching response and selectivity towards EMs, with the LOD being the best for CL‐20 (0.717 μM·L–1). The sensing studies further collaborated with the Cyclic Voltammetry, FTIR and Raman Spectroscopy studies gave a detailed understanding of the bipolaron‐polaron transition mechanism accompanying the electron transfer process in the fluorescence quenching study. |
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ISSN: | 0044-2313 1521-3749 |
DOI: | 10.1002/zaac.202000321 |