Feasibility of use of medical dual energy scanner for forensic detection and characterization of explosives, a phantom study.

OBJECTIVE: Detection of explosives is a challenge due to the use of improvised and concealed bombs. Post-bomb strike bodies are handled by emergency and forensic teams. We aimed to determine whether medical dual-energy computed tomography (DECT) algorithm and prediction model can readily detect and distinguish a range of explosives on the human body during disaster victim identification (DVI) processes of bombings. MATERIALS AND METHODS: A medical DECT of 8 explosives (Semtex, Pastex, Hexamethylene triperoxide diamine, Acetone peroxide, Nitrocellulose, Pentrite, Ammonium Nitrate, and classified explosive) was conducted ex-vivo and on an anthropomorphic phantom. Hounsfield unit (HU), electron density (ED), effective atomic number (Zeff), and dual energy index (DEI),were compared by Wilcoxon signed rank test. Intra-class (ICC) and Pearson correlation coefficients (r) were computed. Explosives classification was performed through a prediction model with test-retest samples. RESULTS: Except for DEI (p = 0.036), means of HU, ED, and Zeff were not statistically different (p > 0.05) between explosives ex-vivo and on the phantom (r > 0.80). Intra- and inter-reader ICC were good to excellent: 0.806 to 0.997 and 0.890, respectively. Except for the phantom DEI, all measurements from each individual explosive differed significantly. HU, ED, Zeff, and DEI differed depending on the type of explosive. Our decision tree provided Zeff and ED for explosives classification with high accuracy (83.7%) and excellent reliability (100%). CONCLUSION: Our medical DECT algorithm and prediction model can readily detect and distinguish our range of explosives on the human body. This would avoid possible endangering of DVI staff.

Visible-Light Actinometry and Intermittent Illumination as Convenient Tools to Study Ru(bpy)3Cl2 Mediated Photoredox Transformations.

Photoredox catalysis provides many green opportunities for radical-mediated synthetic transformations. However, the determination of the underlying mechanisms has been challenging due to lack of quantitative methods that can be easily implemented in synthetic labs, where this research tends to be centered. We report here on the development, characterization and calibration of a novel actinometer based on the photocatalyst tris(2,2'-bipyridyl)ruthenium(II) chloride (Ru(bpy)3Cl2). By using the same molecule as the photocatalyst and the actinometer, we eliminate problems associated with matching sample spectral distribution, lamp-sample spectral overlap and other problems intrinsic to doing quantitative photochemistry in a laboratory that has little expertise in this area. In order to validate our actinometer system in determining the quantum yield of a Ru(bpy)3Cl2 photosensitized reaction, we test the Ru(bpy)3Cl2 catalyzed oxidation of benzhydrol to benzophenone as a model chain reaction. We also revive the rotating sector method by updating the technique for modern LED technologies and demonstrate how intermittent illumination on the timescale of milliseconds to seconds can help probe a chain reaction, using the benzhydrol to benzophenone oxidation to validate the technique. We envision these methods to have great implications in the field of photoredox catalysis, providing researchers with valuable research tools.

Self-assembled dipole nanolasers.

Visible light excitation of silver nanoparticles in the presence of polymerizable monomers and selected dyes triggers the self-assembly of nanolasers in a synthetically simple process. The new nanolasers incorporate a thin, fully organic gain medium that allows the tuning of the core absorption to a selected dye, or of the dye to a preselected core material. This versatile synthesis of surface plasmon lasers, or "spasers", has unique simplicity and enables spatial and temporal control of the nanolaser fabrication process.

Rapid one-pot propargylamine synthesis by plasmon mediated catalysis with gold nanoparticles on ZnO under ambient conditions.

Surface plasmon excitation of gold nanoparticles on ZnO in the presence of an aldehyde, an amine and phenylacetylene led to rapid and selective formation of propargylamines with good yields (50-95%) at room temperature. Plasmon mediated catalysis is the best available route for this ternary coupling.

Ultraclean derivatized monodisperse gold nanoparticles through laser drop ablation customization of polymorph gold nanostructures.

We report a novel nanosecond laser ablation synthesis for spherical gold nanoparticles as small as 4 nm in only 5 s (532 nm, 0.66 J/cm(2)), where the desired protecting agent can be selected in a protocol that avoids repeated sample irradiation and undesired exposure of the capping agent during ablation. This method takes advantage of the recently developed synthesis of clean unprotected polymorph and polydisperse gold nanostructures using H(2)O(2) as a reducing agent. The laser drop technique provides a unique tool for delivering controlled laser doses to small drops that undergo assisted fall into a solution or suspension of the desired capping agent, yielding monodisperse custom-derivatized composite materials using a simple technique.

High-temperature organic reactions at room temperature using plasmon excitation: decomposition of dicumyl peroxide.

Photoexcitation of gold nanoparticles in their plasmon transition around 530 nm provides the means to carry high-energy reactions at room temperature. In the case of dicumyl peroxide (with activation energy of 34.3 kcal/mol) the reaction occurs in less than 1 min under 532 nm laser excitation. The results suggest that the peroxide is exposed to temperatures of ~500 °C for submicrosecond times, and provides a guide as to which type of organic reactions may benefit from plasmon-mediated energy delivery.