DART-MS analysis of inorganic explosives using high temperature thermal desorptionOfficial contribution of the National Institute of Standards and Technology; not subject to copyright in the United States.Electronic supplementary information (ESI) available: Additional figures, MS spectra, and data as noted in the text can be found in the online version. See DOI: 10.1039/c7ay00867h

• Main Authors: Forbes, Thomas P, Sisco, Edward, Staymates, Matthew, Gillen, Greg
• Format: Journal Article
• Language: English
• Published: 31.08.2017
• ISSN: 1759-9660; 1759-9679
• DOI: 10.1039/c7ay00867h

An ambient mass spectrometry (MS) platform coupling resistive Joule heating thermal desorption (JHTD) and direct analysis in real time (DART) was implemented for the analysis of inorganic nitrite, nitrate, chlorate, and perchlorate salts. The resistive heating component generated discrete and rapid heating ramps and elevated temperatures, up to approximately 400 °C s −1 and 750 °C, by passing a few amperes of DC current through a nichrome wire. JHTD enhanced the utility and capabilities of traditional DART-MS for the trace detection of previously difficult to detect inorganic compounds. A partial factorial design of experiments (DOE) was implemented for the systematic evaluation of five system parameters. A base set of conditions for JHTD-DART-MS was derived from this evaluation, demonstrating sensitive detection of a range of inorganic oxidizer salts, down to single nanogram levels. DOE also identified JHTD filament current and in-source collision induced dissociation (CID) energy as inducing the greatest effect on system response. Tuning of JHTD current provided a method for controlling the relative degrees of thermal desorption and thermal decomposition. Furthermore, in-source CID provided manipulation of adduct and cluster fragmentation, optimizing the detection of molecular anion species. Finally, the differential thermal desorption nature of the JHTD-DART platform demonstrated efficient desorption and detection of organic and inorganic explosive mixtures, with each desorbing at its respective optimal temperature. Coupling resistive heating thermal desorption and direct analysis in real time demonstrated trace mass spectrometric detection of inorganic oxidizer explosives.