Abstract

A novel analysis of explosives via the coupling of an airline passenger personnel portal with a high-flow (HF), high-resolution (HR) ion mobility spectrometry (IMS) was shown for the first time. The HF–HR–IMS utilized a novel ion aperture grid design with a 63Ni ionization source while operating at ambient pressure in the positive ion mode at 200 °C. The HF–HR–IMS response characteristics of 2,4,6-trinitrotoluene (TNT), 4,6-dinitro- o-cresol (4,6DNOC), and cyclo-1,3,5-trimethylene-2,4,6-trinitramine (RDX) were investigated. Modifications made to the HF–HR–IMS exhaust and ionization source created an 800% increase in the total ion current (TIC), from 0.85 to 6.8 nA. This translated into a 65% ion response increase for TNT when compared with a traditional IMS. A mixture of TNT and (4,6DNOC) was used to successfully demonstrate the resolving power of the species with similar reduced mobility constants ( K o), 1.54 and 1.59, respectively. The reactant ion (H 2O) n H +, peak was also used to measure the resolving power of the spectrometer while varying the internal diameter of three different aperture openings from 1.00 to 3.54cm. This provided a resolving power range of 50–60, double that typically achievable by commercial IMS instruments. Most important, these changes made in this new instrumental design can be implemented to all existing and future IMS's to greatly enhance the achievable IMS resolving power.

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