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  • Polymer and Materials Science  (235)
  • 1980-1984  (235)
  • 1970-1974
  • 1960-1964
  • 1940-1944
  • 1981  (235)
Collection
Publisher
Years
  • 1980-1984  (235)
  • 1970-1974
  • 1960-1964
  • 1940-1944
Year
  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3467-3473 
    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: Binary blends of poly(vinyl chloride) and a poly(ether urethane) containing 20 and 40 weight percent, respectively, of poly(vinyl chloride) have been prepared by solution blending from tetrahydrofuran and their degree of mixing investigated using dynamic mechanical analysis. In the polyurethane, transitions were found at -19°C and -119°C. The former was attributed to the glass transition and the latter to a Schatzki type of motion of the polyether sequences. This latter transition occurred at a temperature which is higher than the literature value for the low temperature transition in poly(tetrahydrofuran), which is equivalent to the polyether sequence in the polyurethane. This discrepancy is attributed to the influence of neighboring hard segments present because of incomplete segmental phase separation of the polyurethane. For the blends only one very broad transition was observed, indicating that there was substantial mixing of these two polymers. Three ternary blends were prepared, also by solution blending, containing poly(vinyl chloride), Hytrel, and the polyurethane in the ratios 1:1:1, 1:2:1, and 2:1:1, respectively. In the first two blends there was clear evidence of phase separation. It was only in the 2:1:1 blend that an apparently significantly compatible material resulted.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3487-3491 
    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: A solution blend of poly(vinyl chloride) and a segmented poly(ether ester) and blends containing these two polymers plus poly(methyl acrylate) were investigated by dynamic mechanical analysis and electron microscopy. The binary blend, which contained 75% by weight of the poly(ether ester), showed only one loss peak, but also evidence of some phase separation. It is believed that the polyether sequences of the poly(ether ester) are extensively mixed with poly(vinyl chloride). Poly(methyl acrylate) was added to spread the damping range and produce a material of potential use as an acoustic damper. It is evident from both electron microscopy and dynamic mechanical analysis that poly(methyl acrylate) is substantially incompatible in the other polymers.
    Additional Material: 4 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3669-3688 
    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 radiation crosslinking of poly(vinyl chloride), PVC, with trimethylolpropane trimethacrylate, TMPTMA, has been examined. The polyfunctional TMPTMA undergoes rapid polymerization incorporating the PVC into a three-dimensional network. The kinetics and mechanism of these crosslinking reactions were studied with particular reference to dose dependence and thermal treatment. The gel was rapidly formed with a TMPTMA polymerization rate greater than that of the PVC grafting reaction. Only 30-40% of the available bonds were used in the initial polymerization. The remaining 60-70% of the double bonds predominantly react in the final stages of crosslinking (80-100% gelation). The macroscopic properties (e.g., solubility, glass transition temperatures, mechanical characteristics, etc.) of the PVC-TMPTMA blend are discussed in terms of the molecular crosslinking mechanism. The effect of thermal treatment, during and after irradiation, on the reaction rates and mechanism is examined.
    Additional Material: 16 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 15 (1981), S. 111-113 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Additional Material: 3 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3035-3037 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2175-2184 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work a study is made of the degradation on ozonation of unfractionated polystyrene (PS) in CCl4 solution. It was found that the ozone attack of PS molecules is accompanied by hydrogen abstraction from tertiary CH bonds and by the formation of ozonides due to the reaction of ozone with the aromatic rings. A scheme of PS degradation in solution is suggested; several kinetic parameters are evaluated.
    Additional Material: 5 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2799-2816 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of some wholly aromatic polyamides based on unsubstituted and chloro- and nitro-substituted diamines by low temperature solution polymerization is described. Poly(1,3-phenylene isophthalamide) and poly(chloro-2,4-phenylene isophthalamide) were selected for further investigation. To study the two polyamides on a systematic basis their model diamides were synthesized. These materials were characterized with respect to chemical structure and purity by elemental analysis, infrared (IR), and nuclear magnetic resonance (NMR) spectroscopic techniques. The usefulness of the model compounds in the interpretation of the polymer spectra is also demonstrated.
    Additional Material: 2 Ill.
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  • 18
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Fibres of boron-silicate-glass are destructed at the surface by ion bombardment from plasma of a radio-frequency glow discharge. The alkaline elements are sputtered away, but partly readsorbed as hydroxides. The strength of fibres decreases strongly on shorttime of plasma exposition. In a plasma of ammonia N-containing groups are formed on the surface of fibres.
    Notes: Borsilicatglasfasern werden durch den Beschuß mit Ionen aus dem Plasma einer Hochfrequenz-Glimmentladung oberflächlich umstrukturiert. Die Alkalielemente werden bevorzugt herausgesputtert und z. T. in Hydroxidform wieder abgelagert. Die Fasern verlieren auch nach nur kurzer Plasmabehandlungszeit stark an Eigenfestigkeit. Bei Behandlung im NH3-Plasma bilden sich an der Faseroberfläche N-haltige funktionelle Gruppen.
    Additional Material: 4 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1155-1166 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyesters containing conjugated diacetylenic groups in the polymer backbone were synthesized by interfacial condensation of 3,5-hexadiyne-1,6-diol and diacid chlorides of succinic, glutaric, adipic, azealic, sebacic, terephthalic, and isophthalic acids. The polyesters were characterized by their infrared and ultraviolet absorption spectra, elemental analysis, and viscosity measurements. Powder x-ray patterns indicated high degress of crystallinity. The polyesters were found to be highly photoreactive. The relative photoreactivities of the polyester films were determined by the adhesion method. Only small differences in the reactivity have been observed despite structural changes in the R group in the polymer backbone. Differential thermal analysis behavior of all polymers in the temperature range ambient to 300°C and isothermal behavior of HGI at two different temperatures have been studied.
    Additional Material: 7 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 677-688 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Resonance Raman and optical spectroscopy have been used to study foils having a metallic appearance which were produced by the hammering or rolling of single crystals of toluene sulfonate diacetylene polymer. The spectroscopic properties of the bulk material in the foils were found to be almost indistinguishable from those of underformed crystals. In contrast, the blue-green surface skin of the foils appeared to consist of intact polymer chains without significant crystalline order.
    Additional Material: 7 Ill.
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