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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1235-1237 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 479-496 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chromatographic techniques are described which can be used to isolate and identify the linear and the cyclic oligomers of poly(ethylene terephthalate). Extraction of the oligomers from high molecular weight polymer produces at least eight different cyclic species, some of which are isolated and identified.The cyclic dimer, the cyclic trimer, and the cyclic tetramer of poly(ethylene terephthalate) have also been prepared by acid chloride esterification and transesterification. Similar materials can be isolated from the ethylene glycol distillate obtained from the polymer melt. The mechanism of cyclic oligomer formation has been studied by determining the rate of formation of the cyclic oligomers during polymerization and during melt extrusion of polyesters which did not initially contain cyclic oligomers. The rate of formation depends upon the concentration of hydroxyl groups; hence, the cyclic oligomers are formed by transesterification from the chain ends or cyclodepolymerization. Therefore oligomers are inevitably produced during polymerization.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 2637-2640 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Further evidence is presented to show that the chromophore of polyacrylonitrile is formed by polymerization of the nitrile groups, rather than by dehydrogenation of the polymer backbone. The polyimine structure formed is resistant to hydrolysis; hence, the nitrogen content of hydrolyzed polymer increases with increased chromophore formation.
    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 9 (1971), S. 1807-1822 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of gel formation and color formation in poly(hexamethylene adipamide), nylon 66, is found to be dependent upon the rate of removal of the volatile products of degradation. If a sample of nylon is heated above its melting point in a sealed tube, the material will remain soluble for extended periods of time as the intrinsic viscosity first passes through a maximum, then a minimum, followed by the abrupt formation of insoluble material. The color remains reasonably white. On the other hand, if the volatile material is permitted to escape, rapid gelation and color formation will occur, even in the complete absence of oxygen. Intermediate rates of gelation and color formation can be obtained by control of the rate of volatile material distillation. The decrease in molecular weight evidenced in the sealed tubes is probably due to hydrolysis and ammonolysis of the amide groups which occur simultaneously with the formation of multifunctional crosslinking agents. The volatile material contains an intense absorption in the 290 mμ region. Analysis of the volatile material shows that it contains inter alia, water, carbon dioxide, ammonia, cyclic monomer, hexylamine, hexamethyl-eneimine, hexamethylenediamine, cyclopentanone, 2-cyclopentylcyclopentanone, 2-cyclopentylidinecyclopentanone, and 1,2,3,5,6,7-hexahydrodicyclopenta[b,e]pyridine, which has an intense absorption at 287 mμ, ε = 8.87 × 104l./mole-cm, (methanol).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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