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  • 1
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Modification of fluorine-containing polymers has recently received much attention due to new chemistries allowing for refunctionalization of these materials, especially their surfaces. In this article results are discussed which demonstrate various interesting modifications (including incorporations of —OH and oxygen comprised functionality) to expanded poly(tetrafluoroethylene) (ePTFE) surfaces. This is effected through the use of low damage, radio frequency glow discharge (RFGD) processes. The low damage conditions, which preserve the original pore structure/morphology of these RFGD treated materials, are supported by Scanning Electron Microscopy (SEM) while the resulting atomic and molecular effects are investigated through other surface analytical methodology. All materials reported in this investigation have been subjected to intensive structural analyses utilizing Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), and wettability profiles obtained through contact angle measurements using a large series of liquids having varying surface tensions and surface reactive functionality. Through this multitechnique analysis of both expanded PTFE and poly(vinylidene fluoride) (PVDF) treated surfaces, a model is supported which illustrates surfaces possessing both high and low energy regions comprising both oxygen and fluorine functionality in close molecular proximity.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 719-727 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The scope of polyformal formation from nitro- and fluorodiols has been explored further with a series of α, ω-diols. Polymers with M̄ns of 2000-4000 were generally obtained but M̄ns approaching 10,000 are possible in some cases. Effects of monomer structure and reaction parameters on polymer molecular weight are described. The polymers were characterized by GPC, 1H-NMR, and DSC analysis.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recent work in our laboratories has fully characterized the surface region of a segmented poly(ether-urethane) (PEU) extending from the air/polymer interfacial region through bulk depths in the micron range. This characterization utilized energy and angle dependent Electron Spectroscopy for Chemical Analysis (ESCA), Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR), and Comprehensive Wettability Profiling (contact angle using a homologous series of liquids) as defined by Zisman. In this study this same multi-analytical-technique approach is used to elucidate changes in these PEU surfaces induced through an H2O Radio Frequency Glow Discharge (RFGD) plasma. This investigation reports both qualitative and quantitative changes due to the modification treatments as well as the permanency of the changes effected on these surfaces through the plasma treatment. From our analyses, the amount of surface residing polyurethane (hard segment) is observed to increase due to a proposed plasma etching mechanism. Further, the addition of oxygen containing functionality is detected at the modified surfaces unique with respect to the unmodified PEU. These surface modifications which show large increases in wettability, are finally observed to be semi-permanent over a time period of 6 months.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and optical resolution of α-phenyl β-amino-ethylpropionate led to the preparation of optically active α-phenyl β-propiolactones (PhPL) of different optical purities. The enantiomeric excess of PhPL was determined using 200 MHz 1H-NMR spectroscopy, after complexation with tris[3-(trifluoromethyl hydroxymethylene)-d-camphorato]europium III. It was then polymerized, in bulk and in solution, using a potassium acetate/crown ether complex as initiator. The optically active poly(PhPL)s thus obtained are insoluble in most organic solvents, whereas atactic poly(PhPL)s are soluble in CCl4, CHCl3, and dichloroethane. Several differences are observed between the physical properties of optically active and atactic poly(PhPL)s. However, atactic poly(PhPL)s are semi-crystalline polymers, similar to poly(α-disubstituted β-propiolactone)s, but in contrast with poly(α-methyl β-propiolactone). Melting (Tf) and glass transition temperatures, as well as enthalpy of fusion (ΔH), vary with the optical purity of the polymers. For example, atactic poly(PhPL) exhibits a Tf = 94°C and ΔH = 9 J/g as compared to Tf = 119°C and ΔH = 37 J/g for a poly(PhPL) having an enatiomeric excess of 50%.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 129-134 
    ISSN: 0887-624X
    Keywords: ionomers ; telechelic polymers ; quaternary ammonium sulfonate ; thermal stability ; degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal stability of telechelic polystyrenes bearing quaternary ammonium iodide or ammonium sulfonate end groups is presented. It appears that the ammonium iodide functions are stable below 200°C. Above that temperature, the polystyrene irreversibly looses its functional end groups. The weight loss then observed leads to the conclusion that a Hofmann-type degradation mechanism is likely to take place. In contrast, the ammonium sulfonate-terminated polystyrene begins to degrade at 180°C and leads to a polymer which is no longer end-capped with sulfonic acid or sulfonate groups. This behavior is of importance, especially for the study of multiblock ionic copolymers which are prepared by blending two telechelic polymers, one of them bearing sulfonic acid end groups and the other one tertiary amine functional groups. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2417-2426 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of 1,3-di(5-[2,2,1]-bicyclohexyl-2,3-dicarboxylic anhydride)-1,1,3,3-tetramethyldisiloxane, 1, as a curing agent in the presence of typical epoxy resins with Lewis bases as catalysts produces thermosets with HDTs of 320°C. The solubility of 1 in the epoxy resin allows for the preparation of a one-component formulation. A latent catalyst was developed which employs amine complexes of cobalt bis(2,4-pentanedionate). These formulations exhibit long term storage at ambient conditions, yet cure rapidly at 180-200°C.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 85-97 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Normally brittle polystyrene (PS) can be toughened effectively by the inclusion of a few weight percent of low molecular weight polybutadiene (PB). The PB, which can be made to phase separate into submicron sized, randomly dispersed pools, locally plasticizes the glassy phase in the vicinity of a growing craze; the resulting reduction in craze flow stress and increased craze velocity lead to significant enhancement of toughness when strain rates are below approximately 10-1 s-1. Craze velocities were measured in PS containing 1 to 5 wt % of a low molecular weight PB (2300 g/mol). The results were compared to a version of the interface convolution mechanism for craze growth that has been modified to account for the localized plasticization effect of the low molecular weight diluent. Addition of 5 wt % PB led to craze velocities that are three orders of magnitude larger than observed for pure PS. The model deviated significantly from the experimental data at the higher and of the PB concentration range studied here, but it did exhibit the general form of the observed dependence of craze velocity on PB content. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 815-822 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Two alternative nonhalogen routes for the synthesis of phenylsilanes have been explored. In the first method, 2,3-dimethylbutadiene is reacted with divinyltetramethyldisiloxane via a Diels-Alder reaction. The product can then be aromatized. In the second method, cyclohexadiene undergoes hydrosilylation and the resultant product can be aromatized using palladium on carbon with nitrobenzene as an electron accepter. Phenylsilicones can be prepared in a single step in which a silicone hydride fluid and cyclohexadiene are refluxed in the presence of Pt/C (platinum on carbon) and nitrobenzene. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 53 (1994), S. 1251-1259 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The crazing behavior of blends of polystyrene (PS) and a low molecular weight polybutadiene (PB) was examined as part of a continuing study of toughening mechanisms in thermoplastic polymers. These PS/PB blends attain high levels of toughness from the stress-activated plasticizing action of the polybutadiene (PB), a mechanism that is active only in the region of a growing craze. The plasticization is therefore localized and leads to enhanced toughness without loss in stiffness. The net result of this plasticization is a reduction in craze flow stress accompanied by an increase in craze velocity, which, in turn, allows the specimen to reach substantial strains-to-fracture in uniaxial deformation under an imposed strain rate. The ability of the PB to plasticize a growing craze is expected to be a function of the mobility of the PB. To investigate the role of diluent mobility, tensile tests and craze velocity measurements were conducted at -20°C and compared with previously published results collected at 23°C. Although the blends displayed high levels of toughness at 23°C, the blends tested at -20°C showed brittle behavior. Craze velocities measured at -20°C were 2 orders of magnitude lower than the results at 23°C. Addition of 3 wt % PB at -20°C led to craze velocities only as large as those found in pure PS at 23°C. Comparison of the craze velocities with an asymptotic theoretical model describing the dependence of the craze velocity on the PB content showed good agreement with the results at -20°C and only fair agreement with the room-temperature results. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 1503-1505 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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