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Enhanced electrospray ionization mass spectrometric detection of hexamethylene triperoxide diamine (HMTD) after oxidation to tetramethylene diperoxide diamine dialdehyde (TMDDD)
被引:8
作者:
Krawczyk, Tomasz
[1
]
机构:
[1] Silesian Tech Univ, Fac Chem, Dept Chem Organ Technol & Petrochem, PL-44100 Gliwice, Poland
关键词:
LIQUID-CHROMATOGRAPHY;
TRACE ANALYSIS;
SENSITIVE DETERMINATION;
MOBILITY SPECTROMETRY;
PEROXIDE EXPLOSIVES;
DESORPTION;
D O I:
10.1002/rcm.7385
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
RATIONALE: Hexamethylene triperoxide diamine (HMTD) is one of the peroxide-based explosives that are difficult to detect using standard analytical methodologies. METHODS: It was analyzed by electrospray ionization mass spectrometry (ESI-MS) on a UPLC-TOF instrument. Alkali metal salts were used to promote the formation of ions. RESULTS: In the full scan positive ion mode a 3ng (13 pmol) limit of detection was achieved if [HMTD+Me](+) ions (Me=Li, Na, K) were detected. It was found that HMTD easily undergoes oxidation to tetramethylene diperoxide diamine dialdehyde (TMDDD) in the source as well as in the samples. TMDDD can be detected as [TMDDD+Me](+) ions, but better ionization efficiency leads to the detection limit of TMDDD at the 2pg (0.01 pmol) level. In butyl acetate the yield of oxidation of HMTD to TMDDD reaches 25% within 20min at 120 degrees C, which offers a simple way of improving the detection limit of HMTD by two orders of magnitude. CONCLUSIONS: A simple procedure of detection of HMTD that matches the most sensitive methods available was developed. It uses standard equipment available in many laboratories. It was shown that the frequently reported [HMTD-H](+) cation observed by various authors was in fact a misinterpretation of the results, and should be attributed to [TMDDD+H](+). Copyright (C) 2015 John Wiley & Sons, Ltd.
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页码:2257 / 2262
页数:6
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