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Analysis of Explosives by GC‐UV
Authors:Jan Andrasko Ph.D.  Ludmila Lagesson‐Andrasko Ph.D.  Johan Dahlén Ph.D.  Bengt‐Harald Jonsson Ph.D.
Affiliation:1. GC‐UV Center, Kobergsgr?nd 2, Link?ping, SE‐587 31 Sweden;2. Additional information and reprint requests:;3. Jan Andrasko, Ph.D.;4. GC‐UV Center;5. Kobergsgr?nd 2;6. Link?ping SE‐587 31;7. Sweden;8. E‐mail:;9. Department of Physics, Chemistry and Biology (IFM), University of Link?ping, Link?ping, SE‐581 83 Sweden
Abstract:A mixture of explosives was analyzed by gas chromatography (GC) linked to ultraviolet (UV) spectrophotometry that enabled detection in the range of 178–330 nm. The gas‐phase UV spectra of 2,4,6‐trinitrotoluene (TNT), 2,4‐dinitrotoluene (DNT), ethylene glycol dinitrate (EGDN), glycerine trinitrate (NG, nitroglycerine), triacetone triperoxide (TATP), and pentaerythritol tetranitrate (PETN) were successfully recorded. The most interesting aspect of the current application is that it enabled simultaneous detection of both the target analyte and its decomposition products. At suitable elevated temperatures of the transfer line between the GC instrument and the UV detector, a partial decomposition was accomplished. Detection was made in real time and resulted in overlaid spectra of the mother compound and its decomposition product. Hence, the presented approach added another level to the qualitative identification of the explosives in comparison with traditional methods that relies only on the detection of the target analyte. As expected, the decomposition product of EGDN, NG, and PETN was NO, while TATP degraded to acetone. DNT and TNT did not exhibit any decomposition at the temperatures used.
Keywords:forensic science  ultraviolet detection  gas chromatography–  ultraviolet spectrophotometry  ultraviolet spectra  explosive analysis  triacetone triperoxide  nitrate esters
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