Narrow Results

The objective of the present study was to better understand the photophysics of explosives and chemical warfare simulants in order to develop better performing analytical tools. Photoionization mass spectra were taken using three optical schemes. The first was resonance-enhanced multiphoton ionization (REMPI) using few-ns duration 248 or 266 nm laser pulses. The second scheme was non-resonant multiphoton ionization (MPI) using 100 fs duration laser pulses at wavelengths between 325 and 795. The third approach was single photon ionization (SPI) using few-ns duration 118 nm laser pulses. For all the molecules investigated, mass spectra resulting exposure to ns-duration 248 or 266 nm laser pulses consisted of only low molecular weight fragments. Using fs-duration laser pulses produced more complicated, potentially analyzable, fragmentation patterns, usually with some parent peak. Single photon ionization gave the best results, with mass spectra consisting of almost only parent peak, except for the case of TATP.

The objective of this paper is to show that explosives may potentially be detected by passive standoff FTIR radiometry. It is demonstrated that many explosives exhibit a signature (fingerprint) in the longwave infrared (LWIR) region (i.e., 8 – 14 μm). Simulations using the radiative transfer model, MODTRAN4, clearly suggest that such materials can be identified when a thermal contrast exists between the material and its environment. The explosives considered in this study include octogen (HMX), trinitrotoluene (TNT), cyclonite (RDX), and the plastic explosives, C-4 and Detasheet-C. In addition, passive FTIR measurements of HMX have been performed in the field at standoff distances up to 60 m. The development of a passive standoff detection capability based on FTIR radiometry may be a potentially useful addition to the arsenal of measurement techniques that currently exist for the detection and identification of explosive threats.

The objective of the present study was to better understand the photophysics of explosives and chemical warfare simulants in order to develop better performing analytical tools. Photoionization mass spectra were taken using three optical schemes. The first was resonance-enhanced multiphoton ionization (REMPI) using few-ns duration 248 or 266 nm laser pulses. The second scheme was nonresonant multiphoton ionization (MPI) using 100 fs duration laser pulses at wavelengths between 325 and 795. The third approach was single photon ionization (SPI) using few-ns duration 118 nm laser pulses. For all the molecules investigated, mass spectra resulting exposure to ns-duration 248 or 266 nm laser pulses consisted of only low molecular weight fragments. Using fs-duration laser pulses produced more complicated, potentially analyzable, fragmentation patterns, usually with some parent peak. Single photon ionization gave the best results, with mass spectra consisting of almost only parent peak, except for the case of TATP.

The objective of this paper is to show that explosives may potentially be detected by passive standoff FTIR radiometry. It is demonstrated that many explosives exhibit a signature (fingerprint) in the longwave infrared (LWIR) region (i.e., 8 – 14 μm). Simulations using the radiative transfer model, MODTRAN4, clearly suggest that such materials can be identified when a thermal contrast exists between the material and its environment. The explosives considered in this study include octogen (HMX), trinitrotoluene (TNT), cyclonite (RDX), and the plastic explosives, C-4 and Detasheet-C. In addition, passive FTIR measurements of HMX have been performed in the field at standoff distances up to 60 m. The development of a passive standoff detection capability based on FTIR radiometry may be a potentially useful addition to the arsenal of measurement techniques that currently exist for the detection and identification of explosive threats.