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Published on: June 14, 2018
Detection of Triacetone Triperoxide by High Kinetic Energy Ion Mobility Spectrometry
Christoph Schaefer1, Martin Lippmann1, Michiel Beukers2,3
1Institute of Electrical Engineering and Measurement Technology, Department of Sensors and Measurement Technology, Leibniz University Hannover, Appelstr. 9A, Hannover 30167, Germany.
High Kinetic Energy Ion Mobility Spectrometry (HiKE-IMS) offers sensitive trace gas analysis with reduced cross-sensitivities. This study demonstrates its use for detecting triacetone triperoxide (TATP) by analyzing its unique ion mobility fingerprint.
Area of Science:
- Analytical Chemistry
- Spectrometry
- Trace Gas Analysis
Background:
- High Kinetic Energy Ion Mobility Spectrometry (HiKE-IMS) is a low-effort technique for detecting gaseous molecules in complex environments.
- Operating at reduced pressures (10-60 mbar) minimizes ion-neutral collisions, reducing cross-sensitivities and eliminating the need for prior separation.
- HiKE-IMS allows operation over a wide range of electric field strengths (E/N up to 120 Td), enabling separation based on low-field mobility and field-dependent mobility.
Purpose of the Study:
- To employ HiKE-IMS for the detection of triacetone triperoxide (TATP).
- To explore TATP ionization pathways and field-dependent ion mobilities.
- To establish a database of TATP ion mobilities as a function of E/N for reliable detection.
Main Methods:
- Utilized High Kinetic Energy Ion Mobility Spectrometry (HiKE-IMS) for TATP analysis.
- Investigated TATP ionization using different primary reactant ions (H3O+ and NH4+).
- Measured ion mobilities across a range of reduced electric field strengths (E/N).
Main Results:
- Proton transfer ionization with H3O+ resulted in TATP fragmentation.
- Using NH4+ as the reactant ion produced a TATP·NH4+ adduct, which fragmented at high E/N.
- A unique fingerprint of TATP was generated, comprising various ion species and their field-dependent mobilities.
Conclusions:
- HiKE-IMS provides a versatile platform for trace gas analysis, including sensitive TATP detection.
- The field-dependent fragmentation of the TATP·NH4+ adduct offers additional data for reliable identification.
- Operating HiKE-IMS at variable E/N can significantly reduce false positive rates in TATP detection.
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