4.8 Article

Mass Spectrometry Detection and Imaging of Inorganic and Organic Explosive Device Signatures Using Desorption Electro-Flow Focusing Ionization

Journal

ANALYTICAL CHEMISTRY
Volume 86, Issue 15, Pages 7788-7797

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac501718j

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Funding

  1. Department of Defense Science, Mathematics, and Research for Transformation Fellowship
  2. The U.S. Department of Homeland Security Science and Technology Directorate [IAA HSHQDC-12-X-00024]
  3. National Institute of Standards and Technology

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We demonstrate the coupling of desorption electro-flow focusing ionization (DEFFI) with in-source collision induced dissociation (CID)) for the mass spectrometric (MS) detection and imaging of explosive device components, including both inorganic and organic explosives and energetic materials. We utilize in-source CID to enhance ion collisions with atmospheric gas, thereby reducing adducts and minimizing organic contaminants. Optimization of the MS signal response as a function of in-source CID potential demonstrated contrasting trends for the detection of inorganic and organic explosive device components. DEFFI-MS and in-source CID enabled isotopic and molecular speciation of inorganic components, providing further physicochemical information. The developed system facilitated the direct detection and chemical mapping of trace analytes collected with Nomex swabs and spatially resolved distributions within artificial fingerprints from forensic lift tape. The results presented here provide the forensic and security sectors a powerful tool for the detection, chemical imaging, and inorganic speciation of explosives device signatures.

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