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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3543-3550 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerization of para-phenylenediamine sulfate (PPD-S), hydrazine sulfate (Hy-S), and terephthalic acid (TA) in SO3 yielded solutions of poly[p-(disulfonatophenylene)terephthalamide]-co-poly(p-phenylene-1,3,4-oxadiazole) (SPT-co-POx). Reaction of PPD-S, TA, and 4,4′-sulfonyldibenzoic acid (SDBA) in SO3 gave sulfonated copolyamide (SPT-co-SPSDB) solutions. Solutions of both SPT-co-POx (mole % ratios of 70:30 to 90:10) and SPT-co-SPSDB (75:25 to 90:10) were anisotropic, illustrating liquid crystalline behavior for polymeric structures containing significant amounts of noncoaxial backbone components.
    Additional Material: 3 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 751-765 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High-strength/high-modulus polyethylene (PE) fibers have been obtained from linear polymers by melt-spinning the polyethylene followed by hot-drawing the spun filaments. Fibers with different tensile properties were made by changing the extrusion, solidification, and drawing conditions and by use of different types of polyethylene. Potential correlations of fiber strength with morphological parameters such as crystallite dimensions, and crystalline and amorphous orientation were examined. The integrated meridional small-angle x-ray scattering intensity is the only morphological parameter which was found to correlate well with the strength of fibers prepared under different conditions and from different polymer types. Implications with respect to the molecular mechanism of PE fiber drawing are also discussed.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 707-712 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Samples of poly(vinyl trifluoroacetate) with differing stereosequences have been prepared. The NMR signals at 56.4 Mc./sec. corresponding to the three types of triadstereosequences of the trifluoroacetate groups (isotactic, heterotactic, and syndiotactic) can be resolved. The results for specific polymers are discussed.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 283-296 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ordered heterocycle copolymers of high thermal stability were prepared from aromatic dianhydrides reacted with aromatic diamines containing preformed benzoxazole or benzothiazole units. These ordered benzoxazole-imide and benzothiazole-imide copolymers were prepared in the form of their soluble precursor polyamic-acids, which, after fabrication to desired shapes, were converted to the thermally stable polymer. In general, these polymers are more resistant to air oxidation at elevated temperatures than are simple aromatic polyimides, and their thermoöxidative stability is equal to or greater than that reported for benzoxazole or benzothiazole homopolymers. Unlike the o-hydroxyamide precursors to simple polybenzoxazoles, the amic acid precursors to benzoxazole-imide ordered copolymers do not require temperatures above 300°C to complete ring closure nor inert atmospheres to prevent polymer degradation during ring formation. Excellent self-supporting films and film coatings for metals were prepared. Selected compositions were readily spun to excellent fiber.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1377-1389 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fibers of benzoxazole-imide ordered copolymers were prepared by cyclodehydrating the amide-phenol units of precursor polyamide-o-hydroxyimide fibers at 375°C in nitrogen. The precursor polyamide-o-hydroxyimides were obtained by the reaction of 3,3′-dihydroxybenzidine with diacid chlorides containing preformed imide rings. The benzoxazole-imide fibers are very thermally stable, especially with respect to retention of tensile properties after heat aging in air. For example, the benzoxazole-imide fibers after heating aging in air for 35 days retained 75% or more of their original tenacities and 50% or more of their original elongations to break. The original fibers did not have high tenacities, probably because of the rather extreme thermal treatment required to cyclodehydrate the amide-phenol units of the precursor fiber. The ultraviolet light stability of one benzoxazole-imide fiber was outstanding for a fiber of the polyheterocycle type: there was no loss in strength or elongation after 140 hr of exposure in a Fade-Ometer. Fibers of ordered amide-imide polymers based on the same imide-containing diacid chlorides used for the benzoxazole-imide polymers were also prepared. They were substantially less thermally stable than their benzoxazole-imide fiber counterparts, as expected.
    Additional Material: 6 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 2429-2439 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new class of linear, thermostable polymers is reported. The compositions are ordered heterocycle copolymers in which two different heterocycles alternate regularly along the polymer chain. Examples of combinations studied are: oxadiazole-benzimidazole, oxadiazole-pyromellitimide, and thiazole-pyromellitimide. The heterocycle copolymers, or alternatively, the corresponding precursor polymers, were prepared by condensing preformed di-or tetrafunctional blocks which contain one type of heterocycle with a second di- or tetrafunctional monomer under such conditions that no rearrangement of bonds occurred. The polymers are characterized in general by neither melting nor decomposing below 500°C. when heated in an inert atmosphere at a rate of about 10°C./min. Some of the copolymers are readily soluble in organic solvents; many, however, are soluble only in solvents such as concentrated sulfuric acid. In the case of the more intractable polymers, soluble precursor polymers can usually be prepared. In such precursor polymers only one of the heterocycles is preformed; the second heterocycle is formed by post-treatment after the polymer has been fabricated into an end product. All of the polymers yielded self-supporting films, some having very high strength; films of several of the polymers were hot-drawable. Drawn film of an ordered oxadiazoleimide copolymer was shown to be well oriented and moderately crystalline.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 3027-3037 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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