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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.

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 sulfonated poly(sulfonium cation) polymers, sulfonated poly(arylenethioethersulfone)s (SPTES)s possess up to two sulfonate groups per repeat unit, and can be easily converted into corresponding acid form of the SPTES polymer to form a tough, ductile, free-standing, pinhole-free membranes with excellent mechanical properties. The SPTES polymers exhibit good water affinity and excellent proton conductivity due to the high water uptake. Proton conductivities between 100 and 300 mS/cm (at 65 °C, 85% relative humidity) were observed for the SPTES polymers with 50 mol% (SPTES-50) to 100 mol% (SPTES-100) of sulfonated monomer. The evaluation by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and thermomechanical analysis (TMA) showed that the SPTES polymers have excellent thermal stability, mechanical properties, and dimensional stability, making them excellent candidates for the next generation of proton exchange membranes (PEMs) in fuel cell applications.

A carboxylated polysulfone (C‐PSF) was reacted with 3‐(glycidoxypropyl)trimethoxysilane (GPS) in a sol–gel reaction to form hybrid networks. Specifically, GPS was grafted to the C‐PSF chains at their epoxy ends by ring‐opening reactions and then the methoxy silane groups at their other ends were crosslinked through the usual hydrolysis and condensation reactions. These C‐PSF/GPS cross‐linked binary networks are of interest in their own right, but this type of network was also used in the incorporation of polybenzimidazole (PBI) rigid‐rod polymer to form a C‐PSF/PBI/GPS ternary composite. In this case, the network structures obtained by carrying out the same reaction in the presence of PBI chains successfully suppressed their undesirable segregation within the composite. The transparencies of the preparative solutions and the dried films indicated that the dispersion of PBI was maintained in these environments, presumably at the nano‐ or molecular level. The ternary composites were characterized u...

Molecular composites were prepared from sulfonated modifications of polysulfone and polyphenylsulfone by incorporating relatively stiff polybenzimidazole (PBI) chains into them. The composites were characterized by Fourier-transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), thermal mechanical analysis (TMA), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The FT-IR results demonstrated strong specific interactions between the sulfonated polymers and the PBI, which was presumed to be the reason for the enhanced miscibility observed. Miscibility was also indicated in the DSC and TMA results, by the presence of a single glass transition temperature (which was composition dependent), although there did appear to be a small degree of phase separation. TGA results showed improvements in the thermal stability of the polymer matrix because of the incorporation of PBI. Results from SEM were also consistent with considerable miscibility. Microcellular foams processed from these molecular composites had partial open-cell cell structures, with average cell sizes ranging from 0.2 to 5 μm, in unusual bimodal cell-size distributions.

Differential scanning calorimetry has been used to investigate the structural relaxation in a bulk metallic glass designated Vit 4. Results indicate that Vit 4 has a broad glass transition region with a glass transition temperature of approximately 621 K and an activation enthalpy of 834 kJ/mol. Despite the broad transition region, Wunderlich’s model suggests that structural relaxation in Vit 4 involves the cooperative motion of a single bead. The relaxation behavior was well described by the Tool–Narayanaswamy equation, with x and β values not significantly different from other glass formers. The dynamic and thermodynamic fragility of Vit 4 is compared with other glasses.

As an alternative method for processing polyaniline (PANI) from its conducting (protonated) state, vacuum casting of PANI from a methanesulfonic acid (MSA) solution provided films with electrical conductivity values of about 130–150 S/cm. In addition, we similarly prepared blended films of PANI · MSA and poly(p-phenylene benzobisthiazole) (PBZT). This process eliminated the need for a subsequent protonation step and had the additional advantage that the conjugated PBZT may provide alternative conducting pathways. Conductivity values of the composite films ranged from 100 pS/cm to 124 S/cm, and the films displayed critical concentration behavior with a PANI threshold concentration of 2.75% and a critical exponent of 4. Transmission electron micrographs displayed phase-separated regions with PANI forming a continuous network at high concentrations. Thermogravimetric analysis results demonstrated the thermal and thermooxidative stability advantage of the blends due to the PBZT component. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2539–2548, 2001

At the turn of the 20th century, Mendel's laws were found to be applicable to human blood groups. Within two decades, blood group genetics were applied to problems of parentage. Expansion of immunohematology into leukocyte antigen identification produced the single most informative, expressed polymorphism. About the same time, analysis of a great number of soluble protein polymorphisms followed advances in electric separation methods, enzymology, and immunochemistry. As new, independent loci were discovered, the power to exclude the falsely accused increased, and it became possible to apply Bayesian principles to determined probabilities of biologic relationships. The revolution in nucleic acid technology has dramatically improved analysis and statistical inferences. By the turn of the 21st century, laboratories should be able to determine biologic parentage with virtual certainty.

Immunogenetic study of alleged first-degree relatives was undertaken among 258 prospective United States immigrants from Haiti. Methods involved serotyping red cells for ABO, Rh, and MN antigens and typing leukocytes for HLA, A, B, and C locus antigens. Kinship was definitely excluded in a relatively low 4.2% of cases involving putative parents and children. Among cases involving alleged siblings, estimates of fraud appeared slightly higher, but the method is suspect because even in true sibships, there may be an absence of obligatory gene markers. Data suggests that some cases involved half-siblings rather than fraud. Of demonstrated exclusions of parent or child, HLA detected the lack of kinship in 87.4% versus 16.9% by red cell typing. However, there were cases in which exclusions were found by red cell methods alone; furthermore, red cell plus HLA typing allows for a calculation of probability of kinship that is analogous to calculations in paternity studies. Together, the red cell and leukocyte systems offer a prior probability of exclusion of parent-child relationships in 91.3%.