The stability of TNT, RDX and PETN in simulated post-explosion soils:Implications of sample preparation for analysis

Explosives residues in soils may be a useful source of evidence following the detonation of an improvised explosive device (IED), such as a vehicle-borne IED. Soil samples collected from the vicinity of an explosion scene will often be stored for some time prior to analysis, yet explosives residues in soil samples are susceptible to rapid degradation or transformation. Although some research has assessed the use of different storage temperatures with a view to reducing explosives' degradation over time, further research examining the degradation of explosives in soil when stored under a variety of storage conditions is crucial to determine the optimal sample collection and storage procedures for soil containing explosives residues. In this work, three different soils were spiked with solutions of TNT, RDX and PETN and stored either at room temperature, refrigerated or frozen. Samples were extracted over 6 weeks, with additional samples gamma-irradiated or nitrogen purged prior to storage. Experimental results indicate that TNT underwent very rapid degradation at room temperature, attributed to microbial action, whereas PETN and RDX proved to be more stable. Gamma irradiation and nitrogen purging proved of some benefit for mitigating TNT degradation, with lower storage temperatures ultimately proving the most effective method of mitigating degradation

Chlorate-based homemade explosives: A review

Abstract Chlorates and perchlorates, inorganic salts known for their potent oxidizing properties, find utility in various products such as pyrotechnics, matches, and disinfectants. Their chemical properties also make them suitable for homemade explosives, resulting in their extensive use by criminals. Hence, the forensic analysis of these compounds is vital for investigating crimes involving their utilization. A wide array of analytical techniques is available for detecting and quantifying these substances, offering forensic investigators an extensive toolkit to effectively analyze and identify chlorates and perchlorates in various samples. Recent research highlights the potential for leveraging the information obtained from analyzing these materials, including for intelligence purposes. The future of forensic analysis in this domain lies in extracting additional information, such as source attribution, through methods like chemometrics, thereby enhancing forensic intelligence capabilities. This article is categorized under: Forensic Chemistry and Trace Evidence > Explosive Analysis Forensic Chemistry and Trace Evidence > Trace Evidence Forensic Chemistry and Trace Evidence > Emerging Technologies and Method

Preliminary Investigations into the Source Attribution of Party Sparklers Using Trace Elemental Analysis and Chemometrics

In Australia, party sparklers are commonly used to initiate or prepare inorganic based homemade explosives (HMEs) as they are the most easily accessible and inexpensive pyrotechnic available on the market. As sparkler residue would be encountered in cases involving these types of devices, the characterisation and source determination of the residue would be beneficial within a forensic investigation. The aim of this study is to demonstrate the potential of using trace elemental profiling coupled with chemometric and other statistical techniques to link a variety of different sparklers to their origin. Inductively coupled plasma – mass spectrometry (ICP-MS) was used to determine the concentration of 50 elements in 48 pre-blast sparkler samples from eight sparkler brands/classes available in Australia. Extracting ground-up sparkler residue in 10% nitric acid for 24 hours was found to give the most reliable quantification. The collected data were analysed using Principal Component Analysis (PCA) to visualise the distribution of the sample data and explore whether the sparkler samples could be classified into their respective brands. ANOVA based feature selection was used to remove elements that did not significantly contribute to the separation between classes. This resulted in the development of a 7-elemental profile, consisting of V, Co, Ni, Sr, Sn, Sb, W, which could be used to correctly classify the samples into eight distinct groups. Linear Discriminant Analysis (LDA) was subsequently used to construct a discriminant model using four out of six samples from each class. The model successfully classified 100% of the samples to their correct sparkler brand. The model also correctly matched 100% of the remaining samples to the correct class. This demonstrates the potential of using trace elemental analysis and chemometrics to correctly identify and discriminate between party sparklers. </p

Reactions of Organic Peroxides with Alcohols in Atmospheric Pressure Chemical Ionization—the Pitfalls of Quantifying Triacetone Triperoxide (TATP)

Over the last several decades, mass spectrometry has become one of the principle methods for compound identification and quantification. While for analytical purposes, fragments which are not fully characterized in terms of origin and intensity as a function of experimental conditions have been used, understanding the nature of those species is very important. Herein we discuss such issues relative to triacetone triperoxide (TATP) and its frequently observed fragment at m/z 89. This “fragment” has been identified as the gas-phase reaction product of TATP with one or two methanol molecules/ions. Additionally, the origin and conditions of other fragments at m/z 91, 75, and 74 associated with TATP will be addressed. Similar analytical issues associated with other multi-peroxide organic compounds [hexamethylene triperoxide diamine (HMTD), methyl ethyl ketone peroxides (MEKP)] will also be discussed. Solution storage conditions for TATP, HMTD, and tetramethylene diperoxide diamine dialdehyde have been determined. [Figure not available: see fulltext.]