88 research outputs found

    TEPIC - A New High Temperature Structural Foam

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    The formulation, processing characteristics, microstructure and mechanical properties of a new structural foam, suitable for use at service temperatures up to 200 C, are reported. In each of these respects, the foam is compared to an existing material, called APO-BMI that is currently in use. When these two foams are directly compared, the new foam, called TEPIC, is found to be superior in its mechanical performance. TEPIC is formulated from a non-carcinogenic isocyanate, a di-functional epoxide, and glass microballoons. The authors' approach was to combine chemistries known to form thermally stable products. The principal polymerization products are an oxizolidinone produced by the reaction of the isocyanate with the epoxide and isocyanurate rings formed by the trimerization of the isocyanate. Processing has been examined and large-scale production is discussed in detail. Compared to APO-BMI processing, TEPIC processing is facile and economical. The structure of the foam resembles a traditional rigid polyurethane foam rather than that of the APO-BMI. That is, the foam is comprised of a continuous resin phase rather than weakly bonded glass microballoons. At a density of 0.42 g/cm{sup 3} or greater, maximum pore size in TEPIC was less than 2 mm, as required for the application

    Imaging indicator for ESD safety testing.

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    This report describes the development of a new detection method for electrostatic discharge (ESD) testing of explosives, using a single-lens reflex (SLR) digital camera and a 200-mm macro lens. This method has demonstrated several distinct advantages to other current ESD detection methods, including the creation of a permanent record, an enlarged image for real-time viewing as well as extended periods of review, and ability to combine with most other Go/No-Go sensors. This report includes details of the method, including camera settings and position, and results with wellcharacterized explosives PETN and RDX, and two ESD-sensitive aluminum powders

    Synthesis, characterization and reactivity of some permethyltantalocene alkylidenes and unusually stable metallaoxetanes

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    Several tantalaoxetanes have been prepared and the X-ray crystal structure of O-exo-Cp_2*Ta(OCHPhCH_2)CH_3 is reported (Cp* = η^5-C_5Me_5). The kinetic products of the reactions of Cp_2*Ta(=CH_2)CH_3 with paraformaldehyde or benzaldehyde are O-endo-Cp_2*Ta(CH_2CH_20)CH_3 and O-endo-Cp_2*Ta(CH_2CHPhO)CH_3, respectively. These tantalaoxetanes undergo an acid and base-catalyzed isomerization to O-exo-Cp_2*Ta(OCH_2CH_2)CH_3 and O-exo-CP_2*Ta(OCHPhCH_2)CH_3 followed by thermal decomposition to Cp_2*Ta(=O)CH_3 and the appropriate olefin. Cp_2*Ta(=CH_2)H deoxygenates epoxides to form Cp_2*Ta(=O)CH_3 and olefin. No intermediates are observed in this deoxygenation under conditions where the appropriate tantalaoxetanes are stable and would have been spectroscopically observed. Stereolabeled epoxides were deoxygenated to probe the mechanism for the possible intermediacy of a 1,4-biradical. Retention of stereochemistry of the resulting olefin was observed and is indicative of a concerted mechanism. These results and their implications for the mechanism of olefin epoxidation are discussed. Treatment of Cp*_2 TaCI_2 with a variety of substituted benzyl potassium reagents affords an equilibrium mixture of CP*_2 Ta(=CHC_6H_5)H, 1, and Cp*_2 Ta(o-CH_2C_6H_4)H, 2, which interconvert presumably via the unstable 16 electron intermediate [Cp*_2Ta(CH_2C_6H_5)]. Several derivatives substituted at the phenyl ring have been prepared to explore the effect of both sterics and electronics on the a-hydrogen migration equilibrium. Trapping of the benzyl intermediate by methylenetrialkylphosphoranes results in methylene transfer to give Cp*_2 Ta(=CH_2)CH_2C_6H_5. The substituted benzyl derivatives have provided a system to determine the influence of phenyl sUbstituents on migratory aptitude of the benzyl group
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