Fast detection of triacetone triperoxide (TATP) from headspace using planar solid-phase microextraction (PSPME) coupled to an IMS detector

被引:32
|
作者
Fan, Wen [1 ,2 ]
Young, Mimy [1 ,2 ]
Canino, Jon [3 ,4 ]
Smith, James [3 ,4 ]
Oxley, Jimmie [3 ,4 ]
Almirall, Jose R. [1 ,2 ]
机构
[1] Florida Int Univ, Dept Chem & Biochem, Miami, FL 33199 USA
[2] Florida Int Univ, Int Forens Res Inst, Miami, FL 33199 USA
[3] Univ Rhode Isl, Dept Chem, Kingston, RI 02881 USA
[4] Univ Rhode Isl, DHS Ctr Excellence Explos Detect, Kingston, RI 02881 USA
关键词
Ion mobility spectrometer (IMS); Planar solid-phase microextraction (PSPME); Solid-phase microextraction (SPME); Triacetone triperoxide (TATP); ION MOBILITY SPECTROMETRY; PEROXIDE-BASED EXPLOSIVES; ELECTROSPRAY-IONIZATION; GAS-CHROMATOGRAPHY; VAPOR;
D O I
10.1007/s00216-012-5878-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Triacetone triperoxide (TATP) is a high explosive synthesized from easily available reactants making it accessible for illicit uses. In this study, fast detection of TATP is achieved using a novel planar solid-phase microextraction (PSPME) as a preconcentration and sampling device for headspace analysis offering improved sensitivity and reduced sampling time over the conventional fiber-based solid-phase microextraction (SPME) when followed by ion mobility spectrometer (IMS) detection. Quantitation and comparison of the retention capabilities of PSPME as compared to the commercially available SPME were determined using TATP standards and analyzed using gas chromatography-mass spectrometry for SPME analysis and a commercial IMS with no instrumental modification for PSPME. similar to Static and dynamic headspace extractions were used and compared for PSPME extractions, in which low milligram quantities of TATP were detected within 30 s of static mode sampling and less than 5 s in the dynamic mode sampling for PSPME-IMS.
引用
收藏
页码:401 / 408
页数:8
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