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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 2 (1969), S. 497-502 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 14 (1981), S. 909-915 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 14 (1981), S. 915-920 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
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    Unknown
    Oxford : Periodicals Archive Online (PAO)
    Medium aevum. 33 (1964) 195 
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  • 5
    ISSN: 1573-4846
    Keywords: hydroxypolybenzoxazoles ; sulfopolybenzobisthiazoles ; organic-inorganic composites ; heat-resistant ceramers and interfacial bonding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Hybrid organic-inorganic composites were prepared by precipitating silica into hydroxypolybenzoxazole (HPBO) and sulfopolybenzobisthiazole (SPBT) polymers, with interfacial bonding between the phases improved by use of isocyanatopropyltriethoxy silane and N, N-diethylaminopropyltrimethoxy silane, respectively. The materials were transparent, and scanning electron micrographs indicated a uniform distribution of silica particles of domain sizes less than 1 μm. Values of the tensile modulus and tensile strength of the HPBO-silica composites were found to increase with the silica content. Values of the modulus of the SPBT-silica composites also increased in this manner, but the improvements in tensile strength were nearly independent of the amount of silica. The composites exhibited thermal decomposition temperatures of approximately 400–500°C, and the thermal stability was significantly increased for both HPBO and SPBT materials with increase in silica content. The water absorption amount for both types of composites decreased significantly compared to that of the pure polymers, suggesting excellent weatherability.
    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 B: Polymer Physics 34 (1996), S. 1881-1891 
    ISSN: 0887-6266
    Keywords: crosslinking ; poly(p-phenylene benzobis thiazole) ; PBZT ; methyl pendant PBZT ; 13C solid state NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to influence the compressive strength of the rigid rod polymeric fibers, methyl pendent poly(p-phenylene benzobisthiazole) fibers have been heat treated in the 400 to 550°C temperature range in air and in nitrogen for varying times to achieve intermolecular crosslinking. These fibers have been examined using Fourier transform infrared (FTIR) spectroscopy, 13C solid-state nuclear magnetic resonance (NMR) swelling behavior, and scanning electron microscopy. 13C NMR has also been carried out on solutions of as-spun fibers. Fibers heat-treated at 400°C, both in nitrogen and in air, up to heat-treatment times of 60 min are insoluble in 99% chlorosulfonic acid, however no direct evidence of crosslinking has been obtained for these fibers using spectroscopic techniques, suggesting that in these fibers the degree of crosslinking must be very low. Evidence that methyl groups are precursors to certain crosslinks was first seen via a weak methylene resonance in 13C solid-state NMR, corresponding to about 2% of the original methyl intensity, in a sample heat-treated at 450°C in air. Fibers heat-treated in nitrogen at 550°C for 10 minutes do not exhibit any swelling in chlorosulfonic acid, are brittle, have lost most methyl groups; however, some CH2 groups form. In this fiber, the carbon intensity for the CH2 group in the 13C solid-state NMR is 18% of the intensity for the CH3 group in the as-spun fiber. The fibers heat-treated at 400 and 450°C show a fibrillar morphology, while the fibrillar morphology is not observed in the fibers heat-treated at 550°C in nitrogen for 10 min. Based on this work, it is our judgment that if heat treatment of this material is to improve compressive strength, the heat treatment protocol of time and temperature will probably be critical and the highest temperatures of exposure will probably lie in the 450 to 550°C range. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 401-410 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel phenylated quinoxaline tetraamines have been prepared and polymerized with 1,4,5,8-naphthalenetetracarboxylic acid in polyphosphoric acid solution. The resulting BBB-type polymers with pendant phenyl groups along the polymer backbone are soluble in m-cresol. The polymers, with inherent viscosities ranging from 0.3 to 0.6 dl/g in sulfuric acid, exhibited thermal stabilities near 500°C under nitrogen and near 400°C in air.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1925-1931 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyphenylquinoxalines has been synthesized by the reaction of p,p′-oxydibenzil with aromatic tetraamines containing varying numbers of fused rings. It was found that the glass transition temperatures of the resultant polymers increased as the the number of adjacent fused rings in the polymers was increased. This provided the basis for achieving glass transition temperatures for the polymers in excess of 400°C, substantially higher than the state-of-the art polyphenylquinoxalines. All of the polymers displayed both the good thermal stability and the solubility in m-cresol characteristic of the polyphenylquinoxaline family of polymers.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyphenylquinoxalines containing 2,2′-bis(phenylethynyl)diphenylene moieties along the polymer backbone have been synthesized. As anticipated, these polymers were found to undergo a novel curing reaction consisting of an intramolecular cycloaddition (IMC) of pendant groups to a dibenzoanthracene backbone structure. The IMC reduces chain mobility, and the fused ring structure increases the glass transition temperature of the polymer. The potential of this approach to curing high-temperature polymers was demonstrated in the processing of one such polymer having an initial Tg of 215°C. Curing at 245°C with no evolution of volatiles produced a Tg of 365°C. This very significant increase in potential use temperature via a volatiles-free IMC cure provides promise for a tough phenyiquinoxaline resin system which can be used to fabricate reinforced composites that have use temperatures far exceeding processing temperatures.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 265-272 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In previous studies on poly{(7-oxo-7, 10H-benz[de]imidazo[4′,5′:5,6]-benzimidazo-[2,1-a]isoquinoline-3,4:10,11-tetrayl)-10-carbonyl} it was observed that the polymer exhibits very unusual film-forming properties. The ladder polymer forms supermolecular aggregates in solution which translates to a high degree of interchain packing in the bulk. New ladder imidazoisoquinoline polymers have been prepared in an effort to relate the variance of molecular structure to the aggregation behavior of this class of polymers. The polymers were prepared from the solution polycondensation of 1,4,5,8-naphthalene tetracarboxylic acid or dianhydride with 1,2,5,6-tetraaminonaphthalene, 2,3,7,8-tetraaminophenazine and 2,3,7,8-tetraaminodibenzofuran. It was found that the extent of interchain packing in the bulk is dependent to a large degree on the molecular geometry of the polymer backbone.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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