Determination of triacetone triperoxide using ultraviolet femtosecond multiphoton ionization time-of-flight mass spectrometry

被引:16
|
作者
Ezoe, Ryota [1 ]
Imasaka, Tomoko [2 ]
Imasaka, Totaro [1 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Appl Chem, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[2] Kyushu Univ, Grad Sch Design, Chem Lab, Minami Ku, Fukuoka 8158540, Japan
[3] Kyushu Univ, Div Optoelect & Photon, Ctr Future Chem, Nishi Ku, Fukuoka 8190395, Japan
基金
日本学术振兴会;
关键词
Multiphoton ionization; Mass spectrometry; Molecular ion; Triacetone triperoxide; Explosive; ALDOL CONDENSATION; BASIS-SETS; ELECTRON; PULSE; LASER;
D O I
10.1016/j.aca.2014.10.045
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Triacetone triperoxide (TATP), an explosive compound, was measured using gas chromatography combined with multiphoton ionization time-of-flight mass spectrometry (GC/MPI-TOFMS). By decreasing the pulse width of a femtosecond laser from 80 to 35 fs, a molecular ion was drastically enhanced and was measured as one of the major ions in the mass spectrum. The detection limits obtained using the molecular (M center dot+) and fragment (C2H3O+) ions were similar or slightly superior to those obtained using conventional mass spectrometry based on electron and chemical ionization. In order to improve the reliability, an isotope of TATP, i.e., TATP-d18, was synthesized and used as an internal standard in the trace analysis of TATP in a sample of human blood. TATP could be identified in a two-dimensional display, even though numerous interfering compounds were present in the sample. Acetone, which is frequently used as a solvent in sampling TATP, produced a chemical species with a retention time nearly identical to that of TATP and provided a C2H3O+ fragment ion that was employed for measuring a chromatogram of TATP in conventional MS. This compound, the structure of which was assigned as phorone, was clearly differentiated from TATP based on a molecular ion observable in MPI-TOFMS. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:508 / 513
页数:6
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