TL;DR: In this article, an apparatus and method in which one or more taggants that are intrinsically located or extrinsically placed in an article or product are detected by X-ray fluorescence analysis to identify or verify the article of its point of manufacture.
Abstract: An apparatus and method in which one or more taggants that are intrinsically located or extrinsically placed in an article or product (11). The taggants are detected by X-ray fluorescence analysis (20, 21) to identify or verify the article of its point of manufacture. The taggants are manufactured as part of the article or the taggant is placed into a coating, label, or otherwise embedded within the article for the purpose of later verifying the presence or absence of these elements by X-ray fluorescence, thus determining the unique elemental composition of the taggant within the article.
TL;DR: In this paper, a series of branched fluorescent sensing compounds with thiophene units in the arms and triphenylamine centers for the detection of nitrated model compounds for 2,4,6-trinitrotoluene (TNT) and the plastic explosives taggant 2,3,dimethyl-2,3-dinitrobutane (DMNB) were investigated.
Abstract: We have investigated a series of branched fluorescent sensing compounds with thiophene units in the arms and triphenylamine centers for the detection of nitrated model compounds for 2,4,6-trinitrotoluene (TNT) and the plastic explosives taggant 2,3-dimethyl-2,3-dinitrobutane (DMNB). Stern−Volmer measurements in solution show that the fluorescence is more efficiently quenched by nitroaromatic compounds when compared to a non-nitrated quencher, benzophenone. Simple modification of the structure of the sensing compound was found to result in significant changes to the sensitivity and selectivity toward the nitrated analytes. A key result from time-resolved fluorescent measurements showed that the chromophore−analyte interaction was primarily a collisional process. This process is in contrast to conjugated polymers where static quenching dominates, a difference that could offer a potentially more powerful detection mechanism.
TL;DR: This is the first peer reviewed report of a SPME-IMS system that is shown to extract volatile constituent chemicals and detection taggants in explosives from a headspace for subsequent detection in a simple, rapid, sensitive, and inexpensive manner.
Abstract: Ion mobility spectrometry (IMS) is a rugged, inexpensive, sensitive, field portable technique for the detection of organic compounds. It is widely employed in ports of entry and by the military as a particle detector for explosives and drugs of abuse. Solid phase microextraction (SPME) is an effective extraction technique that has been successfully employed in the field for the pre-concentration of a variety of compounds. Many organic high explosives do not have a high enough vapor pressure for effective vapor sampling. However, these explosives and their commercial explosive mixtures have characteristic volatile components detectable in their headspace. In addition, taggants are added to explosives to aid in detection through headspace sampling. SPME can easily extract these compounds from the headspace for IMS vapor detection. An interface that couples SPME to IMS was constructed and evaluated for the detection of the following detection taggants: 2-nitrotoluene (2-NT), 4-nitrotoluene (4-NT), and 2,3-dimethyl-2,3-dinitrobutane (DMNB). The interface was also evaluated for the following common explosives: smokeless powder (nitrocellulose, NC), 2,4-dinitrotoluene (2,4-DNT), 2,6-dinitrotoluene (2,6-DNT), 2,4,6-trinitrotoluene (2,4,6-TNT), hexahydro-1,3,5-trinitro-s-triazine (RDX), and pentaerythritol tetranitrate (PETN). This is the first peer reviewed report of a SPME-IMS system that is shown to extract volatile constituent chemicals and detection taggants in explosives from a headspace for subsequent detection in a simple, rapid, sensitive, and inexpensive manner.
TL;DR: In this article, a method of tagging and detecting objects is disclosed which comprises the steps of applying a volatile taggant to the object; and subsequently detecting the presence of the taggants by the absorption, transmittance, reflectance, photon emission or fluorescence of the tagged object.
Abstract: A method of tagging and detecting objects is disclosed which comprises the steps of: (a) applying a volatile taggant to the object; and (b) subsequently detecting the presence of the taggant by the absorption, transmittance, reflectance, photon emission or fluorescence of the taggant and therefore a proximity of the tagged object. The present invention therefore provides optical sensing means which do not require physical separation of differing compounds for discrimination thereof.
TL;DR: In this article, the authors used a handheld ion mobility spectrometer to detect two taggants (EGDN and DMNB) with a reduced mobility of 1.45 cm2 V−1 s−1 with detection limits estimated to be about 10 ppbv.