Abstract

Although the eminent threat of a terrorist group detonating an improvised nuclear device (IND) in an urban environment is low, it is crucial that countries develop modern nuclear forensic capabilities to expedite response in a post-detonation scenario. In particular, new instruments need to be created to shorten dissolution time, expedite chemical separation, and improve forensic analysis of the nuclear melt glass that is created during the detonation of the device. To expedite this process, an instrument was designed to thermally couple a gas chromatograph (GC) to a time-of-flight inductively coupled plasma time-of-flight mass spectrometer (ICPTOFMS) In order to couple these two instruments, another instrument was designed to provide an isothermal atmosphere between the GC and TOFICPMS to expedite rapid gas separations processes. By using gas separations instead of the current wet chemistry processes, the required separation and analysis time of the melt glass significantly decreases. The new instrument would also provide a more detailed analysis of the elemental and isotopic composition of the melt glass. By completing these tasks simultaneously, this significantly decreases the required time to conduct these separations and improves the elemental and isotopic analysis.

Highlights

  • According to the analysis addressed by Garrison et al and Hanson et al [8], the temperature of the column drastically changes the results of the chromatography

  • The results indicated that at the maximum operating temperature of the quartz column (300 ̊C) the temperature varied 2.3% of a degree (±1 ̊C)

  • The NH4∙Ho[hfac]4 and NH4∙Er[hfac]4 were injected via syringe into the gas chromatograph (GC) system, with concentrations of ~4 mg/mL dissolved in ethyl ether, respectively

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Summary

Introduction

In the event that an improvised nuclear device is detonated the debris that is generated contains valuable elemental and isotropic data to help identify the age and processing location of the nuclear material. To obtain this information wet chemistry analysis techniques are used; these methods for investigating post-detonation debris and materials are tedious and prolonged. The samples eluted from the GC will be transported to the mass spectrometer (MS) for analysis through a column encased in a temperature controlled coupling unit Using this combination of instrument, separations of post-event debris can be performed while simultaneously acquiring elemental and isotopic signatures in the same experiment. Initial experiments have shown that this apparatus can improve separation times from the standard ~7 hr. to < 1 hr

Theory
Building New Instrument
Results
Conclusion
Disclosure
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