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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1601-1618 
    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 effects of a number of chemically nonreacting organic on shrinkage and stress-strain properties of preoriented semicrystalline poly(ethylene terephthalate) filaments have been studied. The changes in shrinkage and mechanical properties are found to be highly dependent on time and temperature, as well as on tension applied on the yarn during the treatment. The changes brought about by the solvents at lower temperatures (i.e., below 100°C) are either comparable with or more than those produced by thermal treatments in air or silicone oil above 200°C. The possibility of using slovent treatment for setting polyester for dimensional stability at low temperature as an alternative to the normal dry-heat-setting method has been discussed.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 223-230 
    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: Poly(ethylene terephthalate) filament yarn has been annealed in nitrogen atmosphere, in silicone oil, or in nonreacting organic solvents. Morphological changes resulting from the annealing processes have been followed by Raman spectroscopy. Crystallinity, as evidenced by the width of the 1730 cm-1 carbonyl stretching vibration, is shown to affect the macroscopic properties of these filaments. Furthermore, these spectroscopic results, together with shrinkage measured, suggest that the shrinkage and the crystallization processes in the polymer fiber proceed at different rates in different fluid media.
    Additional Material: 2 Ill.
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  • 3
    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: Nylon 6, nylon 66, and polyester [poly(ethylene terephthalate)] filament yarns were heat set at different temperatures in oil under a variety of experimental conditions. The effect of time of heat setting, tension on the yarn during heat setting, as well as the effect of the initial tenacity and extension on subsequent changes in the mechanical properties of the heat-set yarns have been studied. The breaking strength, elongation at break, and work of rupture have been found to be different for samples heat set while slack and at constant length. The breaking strength remains more or less constant over a wide range of heat setting temperatures up to 240°C in the case of nylon 66 and polyester, and up to 200°C in the case of nylon 6, contrary to the observations of Dumbleton et al. When treated in the slack condition, the breaking extension increases by about 1-2.5 times the control value, while heat setting at constant length produces a decrease in the case of nylon 66 and a marginal increase in the case of nylon 6 and polyester. The initial modulus decreases irrespective of the conditions under which the filaments are heat set. From measurements of the shrinkage and the residual shrinkage in boiling water it appears that dimensional stability can be achieved by heat setting even at constant length. Heat setting produces significant improvement in the crease recovery and resiliency of the fibers. Heat setting has also been found to significantly increase the overall crystallinity of the fibers as determined by critical dissolution time and parallel and perpendicular refractive indices. The overall orientation of the polymer chains, as determined from sonic velocity measurements, decreases on heat setting in the slack condition. Heat setting at constant length produces a marginal improvement in the overall orientation only in the case of nylon 66 yarns. Shrinkage occurs instantaneously. Crystallinity, on the other hand, improves with increasing time of heat setting.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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