Terahertz (THz) wavelengths have attracted recent interest in multiple disciplines within engineering and science. Situated between the infrared and the microwave region of the electromagnetic spectrum, THz energy can propagate through non-polar materials such as clothing or packaging layers. Moreover, many chemical compounds, including explosives and many drugs, reveal strong absorption signatures in the THz range. For these reasons, THz wavelengths have great potential for non-destructive evaluation and explosive detection. Three-dimensional (3-D) reflection imaging with considerable depth resolution is also possible using pulsed THz systems. While THz imaging (especially 3-D) systems typically operate in transmission mode, reflection offers the most practical configuration for standoff detection, especially for objects with high water content (like human tissue) which are opaque at THz frequencies. In this research, reflection-based THz synthetic-aperture (SA) imaging is investigated as a potential imaging solution. THz SA imaging results presented in this dissertation are unique in that a 2-D planar synthetic array was used to generate a 3-D image without relying on a narrow time-window for depth isolation [1]. Novel THz chemical detection techniques are developed and combined with broadband THz SA capabilities to provide concurrent 3-D spectral imaging. All algorithms are tested with various objects and pressed pellets using a pulsed THz time-domain system in the Northwest Electromagnetics and Acoustics Research Laboratory (NEAR-Lab).

Non-destructive methods of material interrogation are used to locate hidden explosives and thwart terrorism attempts. In one such method materials are bombarded with neutrons which react with the nuclei of the atoms within causing a de-excitation process emitting a gamma-ray. The spectrum displayed by the collection of these gamma-rays gives valuable information regarding the material’s elemental make-up. It has been hypothesized that gamma-rays from neutron-induced gamma-ray reactions on light elements with atomic numbers less than 20, including most of the gamma-rays of interest in explosives detection, are Doppler-broadened. This thesis focuses on the gamma ray spectra from the 4438 keV gamma ray in the 12C (n, n’γ) reaction wherein Doppler broadening was investigated. A graphite sample was exposed to 14 MeV neutrons and the 12C gamma ray spectra collected using an HPGe detector positioned at four different angles with respect to the neutron beam; near 00, 450, 900 and 1350. No other experimental parameter was changed. The resultant gamma ray spectra indicated Doppler broadening had occurred.

Studies of biomolecular interactions are of interest for several reasons. Beside basic research, the knowledge gained from such studies is also very valuable in for example drug target identification. Medical care is another area where biomolecules may be used as biomarkers to aid physicians in making correct diagnosis. In addition, the highly specific interactions between antibodies and almost any substance opens up the possibilities to design systems for detection of trace amounts of both biological and non-biological substances within environmental restoration, law enforcement, correctional care, customs service and national security. A biochip, which contains a biologically active material, offers a means of monitoring the molecular interactions in the above applications in a sensitive and specific manner. The biochip is a key component of a biosensor, which also includes components for transforming the interaction events into a human-readable signal. This thesis describes the use of poly(ethylene glycol) (PEG) in biochip design. Two different approaches are presented, the first based on ethylene glycol (EG)-containing alkyl thiol self-assembled monolayers (SAMs) on flat gold and the second on photo-induced graft copolymerisation of PEG-containing methacrylate monomers onto various substrates. The former is a two dimensional system where EG-terminated thiols are mixed with similar thiols presenting tail groups that mimic the explosive substance 2,4,6-trinitrotoluene (TNT). In an immunoassay, the detection limit for TNT was determined to fall in the range 1-10 µg/L. In the second approach, a branched three dimensional biosensor matrix (hydrogel) is proposed. The carboxymethylated (CM) dextran matrix, which is commonly used within the biosensing community, is not always ideal for studies of biointeractions, due to the non-specific binding frequently encountered in work with complex biological solutions and various proteins. To employ PEG, which displays a low non-specific binding of such species, is therefore an interesting option worth investigating. The use of a branched graft polymerised PEG matrix in biosensor applications is novel as compared to previous reports which have focused on linear PEG chains. The latter approach provides, at maximum, one functional group, per surface anchoring point, for immobilisation of sensor elements. Thus, it has the inherited disadvantage that it limits the number of available immobilisation sites. The present PEG matrix contains a large number of functional groups, for immobilisation of sensor elements, per grafting site and offers the potential of improved response upon binding to the analyte as demonstrated in a series of successful sensor experiments. Furthermore, the nature of the process enables easy preparation of matrix patterns and gradients. In a PEG matrix gradient, protein permeability is studied and the capabilities of immobilising proteins are demonstrated. By combining the patterning technique with different monomers in a two-step process, an inert platform, lacking chemical attachment sites, is provided with arrays of spots (with immobilisation capabilities), which are conveniently addressed via microdispensing and used for biosensor purposes. The EG-terminated thiols present another means of generating such inert platforms, a route which is also investigated. To further explore the sensor quality of these spots, the concepts of patterning and gradient formation are combined and studied. / Det är intressant att studera biomolekylära interaktioner av många anledningar. För att kunna bedriva framgångsrik läkemedelsutveckling är det oerhört viktigt att känna till hur olika molekyler samverkar i människokroppen. Inom sjukvården kan biomolekyler användas som biomarkörer, då närvaro av dem eller förändringar av deras koncentrationer är kopplade till sjukdomstillstånd, och därmed hjälper läkaren att ställa rätt diagnos. Dessutom kan de mycket specifika interaktionerna mellan antikroppar och (i princip) valfri substans användas för detektion av spårämnen vid miljösaneringsarbete, gränskontroller, polisarbete, fängelser och arbete med nationell säkerhet. Den här avhandlingen beskriver hur polymeren polyetylenglykol (PEG) kan användas vid design av biochip. Ett biochip är en liten anordning, som kan användas för att detektera specifika molekyler med hjälp av en biologisk interaktion. Traditionellt har PEG använts inom biomaterialsektorn, men återfinns även i hygienartiklar som tvål och tandkräm. Ett annat användningsområde är konservering av bärgade träskepp och i en del litiumjonbatterier ingår PEG som en komponent. Dessutom pågår utveckling av PEG-innehållande skyddsvästar. I det här arbetet används PEG framför allt på grund av sin förmåga att minimera ospecifik inbindning av proteiner, som utgör en stor del av gruppen biomolekyler, till ytor på biochip. Två olika typer av ytbeläggningar, som innehåller den här polymeren, har använts. Den första typen ger mycket tunna (~0.000003 mm), tvådimensionella filmer medan den andra ger en något tjockare (~0.00005 mm), tredimensionell struktur (matris). De tvådimensionella filmerna har använts för att utveckla en sprängämnesdetektor med mycket hög känslighet (detektionsgräns mellan 1-10 ppb). En viktig beståndsdel i detta system är antikroppar riktade mot sprängämnet trinitrotoluen (TNT). Den tredimensionella matrisen är mer generell och kan användas för att studera många olika molekylära interaktioner. Tillverkningsmetoden av matrisen är baserad på belysning med ultraviolett ljus och är därmed lämpad för att skapa mönstrade ytor. Genom att blockera delar av ljusflödet begränsas tillväxten av matrisen till de belysta delarna. På så sätt har bland annat så kallade mikro-arrayer, bestående av mikrometerstora (tusendels millimeter) strukturer i ett regelbundet mönster, tillverkats. Tekniken tillåter även tillverkning av gradienter, där matrisens tjocklek varierar längs med provet, genom att belysa olika delar av provytan olika länge. Genom att undersöka dessa gradienter har information om matrisens genomsläpplighet för proteiner kunnat extraheras. Gradientkonceptet har även kombinerats med mikro-arraytillverkningen och gett möjlighet att studera interaktioner mellan flera olika modellproteiner och deras motsvarande antikroppar i olika tjocka matriser på en och samma yta. Det finns ett stort antal sätt att utnyttja interaktionerna mellan olika molekyler på ett biochip. Ett tilltalande tillvägagångssätt är exempelvis att i en mikro-array binda in olika molekyler som kan fånga kliniskt intressanta biomolekyler, i syfte att skapa en hälsoprofil. Ett sådant biochip skulle ge möjlighet att parallellt detektera eller bestämma koncentrationen av ett stort antal biomolekyler i till exempel en droppe blod. På så sätt kan en diagnos snabbt ställas, kanske till och med utan att patienten behöver uppsöka sjukvården. Den utvecklade PEG-matrisen har god potential att fungera i en sådan applikation.

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An investigation is presented of the behavior of time-reversal focusing in soils. Initial numerical models demonstrate time-reversal focusing to be effective in elastic media, including when a large number of scattering objects were present in the medium. When scattering objects are present, time-reversal focusing demonstrates superior focusing ability when compared to other excitation methods such as uniform excitation or time-delay focusing. Multiple experimental investigations of experimental time-reversal focusing performed in sand evaluate time-reversal focusing effectiveness when multiple near-surface scattering objects are present in the medium. Experimental results demonstrate that time-reversal focusing is effective in the experimental context as well as the numerical models. Further experiments examine time-reversal focusing in more extreme cases where the entire ballistic wave is blocked, and the only energy reaching the focus point is reflected from scattering objects in the medium. A comparison to other focusing methods demonstrates that under these conditions, most focusing attempts with traditional methods will fail completely while time-reversal focusing does not. Additional configurations of time-reversal focusing examine its effectiveness when scattering is caused by an asymmetrical surface layers. The impact of an asymmetrical or non-uniform excitation array is also examined for time-reversal focusing in the presence of scattering objects. An investigation of the effects of scattering object geometry on focusing resolution in time-reversal focusing is also presented. Scattering object field density is found to have a strong, but diminishing effect on focusing resolution as the scattering object field density increased. Loss of surface wave energy available for focusing due to mode-conversion is found to be correlated with the density of the scattering object field. The impact of the weak non-linear nature of the soil on time-reversal focusing is examined through a study of time-reversal focusing behavior for a variety of amplitudes that generate different levels of non-linearity in the soil. This study of nonlinearity is coupled with a study of the impact of noise on time-reversal focusing. It appears that both non-linearity and noise have an impact on time-reversal focusing effectiveness. Further, the loss from these mechanisms seems to be interrelated. Noise seems to enhance non-linear loss in the soil.

Afin de pallier aux problèmes dus aux limites de détection des capteurs et des détecteurs usuels, un système de préconcentration est indispensable. Ce microcomposant permet d’accumuler le ou les vapeur(s) à détecter à l’aide d’un adsorbant et permet de les libérer sous l’effet d’une montée brutale de la température vers un détecteur. Une amplification de la concentration et donc du signal est ainsi obtenue.Cette thèse poursuit le développement d’un préconcentrateur pour la détection de vapeurs toxiques et d’explosifs. Ce préconcentrateur sera constitué d’un microcomposant en silicium rempli d’un adsorbant et muni d’une résistance de chauffage sur sa face inférieure. Des capillaires métalliques permettent d’assurer la circulation du gaz dans le dispositif. Différents types de préconcentrateurs ont été développés avec différents adsorbants afin satisfaire les conditions pour des applications concernant les composés organiques volatils (COV) et les explosifs. L’optimisation des phases d’adsorption et de désorption est cruciale pour le procédé.Le couplage entre un micro-chromatographe et un préconcentrateur a été réalisé et a montré l’apport de ce microcomposant pour la chromatographie. L’analyse d’un mélange de COV a pu être réalisée avec des concentrations initiales de l’ordre de 40 ppb alors que la limite de détection de l’appareillage était de quelques ppm. Un facteur d’enrichissement de 800 a été atteint.L’avantage de l’utilisation du silicium poreux a également été mis en évidence pour l’adsorption de gaz avec des faibles pressions de vapeur saturante. Cette propriété est intéressante pour la préconcentration de vapeur d’explosifs. / In order to overcome problems due to the conventional sensors detection limits, a preconcentration system is required. Accumulation of vapor(s) for detection is possible with an adsorbent and allows releasing them toward a detector, under the effect of a sudden rise of the temperature. Amplification of the concentration and the signal are obtained.This thesis continues the development of a preconcentrator for the detection of toxic gas and explosives. This preconcentrator is made of a silicon microcomponent filled with an adsorbent and a heater at its back. Two metal capillary allow ensuring the gas flow into the device. Various designs of preconcentrators were developed with different adsorbents to satisfy the requirements for volatile organic compounds (VOCs) and explosives applications.The optimization of adsorption and desorption phases is very important for the process.The coupling between a micro-chromatograph and a preconcentrator was conducted and showed the contribution of the microcomponent to the chromatography. Analysis of a VOCs mixture was achieved with initial concentrations in the order of 40 ppb, whereas the detection limit was of a few ppm. An enrichment factor of 800 was achieved.The advantage of using porous silicon was also demonstrated for the gas adsorption with low saturation vapor pressure. This result is interesting for explosive vapor préconcentration.

Laser Induced Breakdown Spectroscopy (LIBS) is showing great potential as an atomic analytical technique. With its ability to rapidly analyze all forms of matter, with little-to-no sample preparation, LIBS has many advantages over conventional atomic emission spectroscopy techniques. With the maturation of the technologies that make LIBS possible, there has been a growing movement to implement LIBS in portable analyzers for field applications. In particular, LIBS has long been considered the front-runner in the drive for stand-off detection of trace deposits of explosives. Thus there is a need for a better understanding of the relevant processes that are responsible for the LIBS signature and their relationships to the different system parameters that are helping to improve LIBS as a sensing technology. This study explores the use of LIBS as a method to detect random trace amounts of specific organic materials deposited on organic or non-metallic surfaces. This requirement forces the limitation of single-shot signal analysis. This study is both experimental and theoretical, with a sizeable component addressing data analysis using principal components analysis to reduce the dimensionality of the data, and quadratic discriminant analysis to classify the data. In addition, the alternative approach of ‘target factor analysis’ was employed to improve detection of organic residues on organic substrates. Finally, a new method of characterizing the laser-induced plasma of organics, which should lead to improved data collection and analysis, is introduced. The comparison between modeled and experimental measurements of plasma temperatures and electronic density is discussed in order to improve the present models of low-temperature laser induced plasmas.

This thesis presents a robust method for estimating the relaxations of a metallic object from its electromagnetic induction (EMI) response. The EMI response of a metallic object can be accurately modeled by a sum of real decaying exponentials. However, it is diffcult to obtain the model parameters from measurements when the number of exponentials in the sum is unknown or the terms are strongly correlated. Traditionally, the time constants and residues are estimated by nonlinear iterative search that often leads to unsatisfactory results. In this thesis, a constrained linear method of estimating the parameters is formulated by enumerating the relaxation parameter space and imposing a nonnegative constraint on the parameters. The resulting algorithm does not depend on a good initial guess to converge to a solution. Using tests on synthetic data and laboratory measurement of known targets the proposed method is shown to provide accurate and stable estimates of the model parameters.

Nuclear quadropole spectroscopy is a modern analytical method for detecting specific solid state materials, e.g. explosives, drugs etc. It uses phenomenon of atomic nucleus called nuclear quadrupole moment. NQR method is very similar to common nuclear magnetic resonance (NMR) that is why major principles are explained using NMR. The thesis deals with basic principle of NQR, its usage for explosives detection and also detection of other chemical compounds and many other useful applications. The thesis deals with specific circuit design, techniques for sufficient sensitivity, impedance matching and circuit isolation. Practical part consists of simulations as well as designs of a few impedance transformers, pi-networks, and coils. Also experimental probe was created. In the last part, NQR workplace was assembled and a few chemical compounds were detected. These were KClO3, NaClO3 and NaNO2 . Finally minimum detectable amount of potassium chlorate as the strongest signal of these was determined.

Indiana University-Purdue University Indianapolis (IUPUI) / Canines are regularly utilized by law enforcement agencies to detect explosives. However, the mechanism by which canines respond to explosive vapors is not well understood, leading to difficulties in canine training and testing. It is known that the amount of vapor generated from explosive compounds is dependent upon several factors including sample amount, vapor pressure, and the degree of confinement. Underlying these factors is the basic process of evaporation of an unconfined explosive, which is rucial to understanding how explosive vapors behave in other, more confined, systems. In Stage One of this study, evaporation rates were determined for several explosive liquids using an analytical balance. These rates were compared to one another as well as to theoretical models for the evaporation of liquids. In general and as expected, mass decreased linearly with time and evaporation rates decreased logarithmically as boiling point increased. Several examples of solvent “pinning” on a metal surface were also observed. While an empirical model for the evaporation of unconfined explosive liquids was developed, a comprehensive model for the escape of explosive vapors from sealed containers (i.e., a suitcase, knapsack, or IED container itself) is needed. The second part of Stage One of this study was to determine that the flow rate of explosive vapors escaping from relatively large orifices does not conform to Fick’s Law of Diffusion. Fick’s model states that the flow rate is linearly dependent upon the cross sectional area of the orifice and the material’s diffusion coefficient. Instead, the flow rate was found to be linearly dependent upon the diameter of the orifice due to the tendency of the flow to diffuse outwards from its circular edge. A clear relationship between flow rate and diffusion coefficient was seen, however. Additional uncertainty arises concerning the complexity of the odor generated from explosive compounds. Because explosive vapors are often complex (they consist of multiple chemical compounds), confusion exists regarding the cause of canine alert; that is the “odor compound” that allows for canine detection of various explosives. Although 2, 4- dinitrotoluene (DNT) has been explored as a potential odor compound, the possibility of a nitrated explosive inherently producing nitrated gas upon decomposition has not. Stage Two of this study focused on evaluating nitrate as a potential cause of canine alerts. An LC/MS method for the detection of nitrate ions in Composition C-4 and flake trinitrotoluene (TNT) was developed and tested. Instrumental analysis was not successful in detecting nitrate ions in any of the explosives tested. The lack of nitrate was confirmed using a diphenylamine color test for nitrates, thus eliminating nitrate as an odor compound and cause of canine alert to nitroaromatic compounds. 2, 4-DNT has been introduced as a potential odor compound of TNT, however, the mechanisms behind its vapor emission have not been thoroughly explored. More specifically, due to the “sticky” nature of the 2, 4-DNT isomer, the effects of surface adhesion to container walls are of concern. In particular, whether the amount of material lost to surface adhesion is significant enough to effect canine detection of TNT. A second focus of Stage Two explored this concern. A GC/MS method for the detection and separation of TNT and DNT isomers in liquid extracts was developed and the amount of 2, 4-DNT residues adhering to container walls was quantified. These values, compared to the amount 2,4-DNT expected to saturate each container (determined by the Ideal Gas Law), showed a significant preference of 2,4-DNT in the solid phase as opposed to in the gas phase. The amount of residue adhering to the walls of a gallon can differed from expected values by nearly 70%. The amount of material extracted from a quart can exceeded expected values by 137%. The apparent sticky nature of 2, 4-DNT resulted in a significant loss of material needed to fully saturate a container and thus canine detection success may be affected. In the final stage of this study, theories regarding odor compounds and odor availability of nitromethane, TNT, and Composition C-4 were tested using certified explosives-detecting canines. These trials included thirty-three canine-handler teams from eight government agencies. The odor availability of nitromethane was tested by placing varying volumes of nitromethane in containers with differing degrees of confinement and studying the effects on canine detection success. The odor availability trial showed no significant effect of sample amount or degree of confinement on canine detection so long as the sample volume was sufficient to saturate its container. In this study that volume was determined to be < 1 mL. Detection of 2, 4-DNT, TNT-NESST (Non-Hazardous Explosives for Security Training and Testing), and flake TNT were also studied using certified canines. The purpose of this was to identify the odorant responsible for canine alert to the explosive TNT. These trials showed a significant response to 2, 4-DNT compared to TNT and its training aid; this suggests that 2, 4-DNT is the primary cause of canine alerts to TNT. Additionally, Composition C-4 and RDX-NESTT were tested along with potential odor compounds that included the manufacturing solvent, cyclohexanone, the energetic “taggant” 2, 3-dimethyl-2.3-dinitrobutane (DMNB), the plasticizer dioctyladipate (DOA) and its degradation product 2-ethyl-1-hexanol. While some response to DMNB and cyclohexanone was seen, the most significant response was to the actual Composition C-4. This suggests that the cause of canine alert to Composition C-4 is the explosive mixture as a whole and not a single chemical component of the mixture