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Thermally activated shape memory polymers (SMPs) have attracted great interest in recent years for application in adaptive shape-changing (morphing) aero structures. However, these components require materials with transition temperatures well above the glass transition temperatures of most widely available SMPs while also maintaining processability and property tailorability. In the present study, a series of novel polyaspartimide-urea based polymers are synthesized and characterized. The glass transition temperature and shape memory properties are varied using a diisocyanate resin creating a urea crosslinking moiety between the polyaspartimide chains. Overall, a family of high temperature SMPs was synthesized and characterized showing high thermal stability (>300 °C), toughness, strong shape memory effects, and tailorable properties.

Current optical polymeric materials for advanced fiber laser development are susceptible to degradation due to the heat generated in high power usage. A suitable replacement light stripping material was explored to overcome this problem by examining optical and physical properties such as transmission/absorption, refractive index, thermal conductivity, and thermal stability. The synthesis and characterization of two new polyurea/silica ORMOSILs (ORganically MOdified SILicates) suitable for high temperature (up to 300 °C) optical applications are reported herein. A one-pot, room temperature synthesis is based upon commercially available bis-isocyanates and an amino-silane. These materials exhibit the combined traits of both glass and polymer by displaying optical clarity over a wide range of wavelengths stretching from the edge of the UV (250 nm) to well into the NIR (2,000 nm), refractive indices in the visible spectrum (n = 1.50–1.63), thermal conductivities of 0.26 ± 0.09 W/mK (ORMOSIL-A) and 0.27 ± 0.07 W/mK (ORMOSIL-B), and thermal stabilities up to 300 °C. The hybrid materials were found to be easily processed into films but thick casts (>2 mm) were subject to increased rates of cracking and longer curing times. Although this is typical of sol–gel chemistries, the organic constituents of ORMOSILs reduce this effect as compared to purely inorganic sol–gels. The effect of thermal aging on the materials’ properties will also be presented as well as a comparison of these materials and the current state of the art light stripping material.

High molecular weight sulfonated poly(arylenethioethersulfone) homopolymer containing hexafluoroisopropylidene moiety (6F-SPTES-100) was synthesized from the monomers 3, 3′-disulfonated-4, 4′-difluorodiphenylsulfone and 4, 4′-(hexafluoroisopropylidene) diphenylthiol, using 4-fluorobenzophenone as the end-capping agent in polar aprotic solvents at temperatures up to 180 °C to provide the desired polymeric composition for utilization as proton exchange membrane (PEM) in fuel cells applications. Tough, ductile freestanding membranes were fabricated from N, N-dimethylacetamide (DMAc) by solvent-casting. The end-capped 6F-SPTES-100 polymer was fully characterized and the membrane was found to have proton conductivity as high as 180 mS/cm which was measured at 85 °C and 65% relative humidity. The proton conductivity of 6F-SPTES-100 was approximately two and half times higher than that of Nafion-117 under comparable conditions. The swelling and solubility characteristics of the 6F-SPTES-100 polymer in water are directly related to the high degree of sulfonation of the polymer backbone.

Fluorinated sulfo-pendants poly(arylenethioethersulfone) copolymer, which contained 50 mol% sulfonate content per repeat unit (6F-SPTES-50), were synthesized by a nucleophilic polycondensation from 4,4-(hexafluoroisopropylidene)-diphenylthiol, 3,3′-disulfonate-4,4′-difluorodiphenylsulfone and 4,4′-difluorodiphenylsulfone. The 6F-SPTES-50 copolymer possessed high molecular weight, exhibited good film formability and thermal stability, and maintained adequate mechanical strength after immersion in water for 24 h. The proton conductivities of the 6F-SPTES-50 copolymer membrane increased with temperatures, reaching values above 120 mS/cm at 85 °C and 85% relative humidity. Preliminary MEA test shows acceptable performance, which indicated that these materials are promising proton exchange membranes (PEMs) for fuel cells operated at medium temperatures.

A series of novel shape memory polymers, synthesized from 4-4-bismaleimidodiphenyl-methane, an extended chain aliphatic diamine, and a bis-isocyanate, have been created and characterized with the aim of providing a family of robust high temperature shape memory polymers with tailorable transition temperatures for use in reconfigurable aerospace structures. In the present study, three of the polymers are chosen for more detailed study of their thermomechanical properties. These materials are compared to commercial resins Veriflex® and Veriflex-E® which are styrene- and epoxy-based proprietary formulations, respectively. The thermal and mechanical properties are determined utilizing thermogravimetric analysis and dynamic mechanical analysis. The temperatures at which 2% weight loss is observed in dry air ranges from 272 to 305 °C for the synthesized polymers, and occurs at 242 and 317 °C for the commercial Veriflex® and Veriflex-E® respectively. The glass transition temperatures, as measured by the peak in the tan(δ) curve, for the synthesized polymers range from 110 to 144 °C which is a higher than the Veriflex® and Veriflex-E® achieve at 84.3 and 100 °C respectively. With operation temperatures of subsonic structural aircraft components often reaching 121 °C (250 °F), the transition temperatures of the bismaleimide-based shape memory polymers are clearly desirable to ensure that shape memory polymers used in aircraft structures will not be prematurely triggered by the existing heat loads. In addition, the shape memory performance of the bismaleimide-based shape memory polymers compares well with the Veriflex® and Veriflex-E® resins.Copyright © 2011 by ASME

The advantages of thermoelectric energy conversion technologies are briefly summarized. Recent material advances are discussed, with the focus on one-dimensional (1-D) self-assembled molecular materials as building blocks for new thermoelectric materials. The preparation, doping, and thermal characterization of phthalocyanine based materials are presented. The thermal conductivity of the doped material is lower than the undoped material even though the electrical conductivity of the doped material is orders of magnitude higher than the undoped material. This is counter intuitive against the backdrop of the Wiedemann-Franz treatment of thermal conductivity in electrical conductors from which one would expect thermal and electrical conductivity to both increase with introduction of additional charge carriers. These unusual results can be understood as a competition between the generation of an increased number of charge carriers and enhanced phonon scattering resulting from the introduction of chemical dopants. The thermal conductivity of the undoped phthalocyanines has been found to be small and only modestly temperature dependent in the 50-300 C range, but it is larger than a previous, indirect measurement.

The advantages of thermoelectric energy conversion technologies are briefly summarized. Recent material advances are discussed, with the focus on one-dimensional (1-D) self-assembled molecular materials as building blocks for new thermoelectric materials. The preparation, doping, and thermal characterization of phthalocyanine based materials are presented. The thermal conductivity of the doped material is orders of magnitude higher than the undoped material. This is counter intuitive against the backdrop of the Wiedemann-Franz treatment of thermal conductivity in electrical conductors from which one would expect thermal and electrical conductivity to both increase with introduction of additional charge carriers. These unusual results can be understood as a competition between the generation of an increased number of charge carriers and enhanced phonon scattering resulting from the introduction of chemical dopants.