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  • Polymer and Materials Science  (8)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 943-965 
    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 intrinsic properties of a yarn are brought about by its physical structure. This structure in its turn is controlled by the process conditions applied. A quantitative description is given of the effect of temperature, time, and tension during annealing on the structure of poly(ethylene terephthalate) yarns. Annealing of a yarn at elevated temperature leads to improvement of packing of the molecules within the crystals. Consequently, the crystalline density is not a constant but is largely dependent on the conditions under which crystallization has taken place. The growth of the PET crystals is not an isotropic process; the strongest growth is observed in the direction of the dipole interactions. The effects of tension and annealing time are also discussed. A prolonged annealing time causes an increase in crystallinity, while time and tension influence the growth of the crystals to some extent. However, for the experimental conditions used in this investigation, temperature is by far the most important factor. Generally speaking, PET fibers annealed at low temperature show low crystallinity built up of many small crystals. Yarn annealed at a high temperature, on the other hand, is composed of fewer big crystals together with large adjacent amorphous regions and relatively high overall crystallinity. Finally, the effect of this observed structural morphology on the dyeing behavior of PET yarns is discussed in a qualitative way. Two main effects controlling the dye uptake of PET yarn are proposed, viz., the total amount of amorphous regions and the accessibility of these regions.
    Additional Material: 22 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2229-2243 
    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: As-spun fibers of poly(ethylene terephthalate), PET, made at winding speeds ranging from 2000 to 6000 m/min exhibit quite different physical structures. Yarns wound at relatively low speeds are amorphous, whereas those spun at high speeds contain well-developed crystals of closely packed molecules. In this study the structures have been characterized by means of various techniques such as differential scanning calorimetry, x-ray diffraction, density, and pulse propagation measurements. Based on the results obtained, an arrangement of the molecules in the various yarns is proposed. It is shown that these arrangements can account for the extreme wide variety in contraction behavior found experimentally. Finally, the results obtained are compared with those of other investigations into orientation-induced crystallization.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 595-616 
    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: From an industrial point of view, it is effective to have a relation between process conditions and resulting product properties. In practice there are many possible process conditions, whereas properties are generally interrelated in a complex way. Thus, there is a strong need for a physical understanding of the product properties in terms of process settings. This comprehension should also allow one to predict possible consequences for the properties when new process conditions become available. To obtain that physical understanding for the development of production processes of PET yarns, use has been made of a simple two-phase model of crystalline and amorphous regions. As process parameters the spinning speed and the drawing temperature were chosen. As the drawing temperatures are only known as machine-setting values, they are simply referred to as “low” and “high.” As mechanical properties the shrinkage, modulus, tenacity, and dynamic mechanical behavior are discussed.
    Additional Material: 24 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 713-732 
    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 yarns were wound at speeds varying from 700 to 5500 mpm. The effect of the winding speed on both α- and γ-type crystals in these undrawn yarns was studied. Also the effects of dry heat, tension, and heating in saturated steam were included in this investigation, since they provide useful information for drawing and heat-setting processes. The emphasis was put on the characterization of the crystalline part of the yarns. By applying recently developed techniques, relative amounts of the two crystalline components, as well as their orientation factors, could be determined. Concerning the undrawn, conditioned yarns, it was found that the amount of γ type increases with the winding speed. The γ crystals are much better oriented than the α crystals, and the crystal dimensions of the γ structure largely depend on the winding speed in contrast to those of the α crystals. Indications were found that γ crystals are mainly generated from orientation-induced nuclei at speeds higher than 2500 mpm and that α crystals grow slowly at relatively low temperatures after moisture pickup during conditioning. Drawing at high ratios causes a transition from γ to α, while the thermal stability of the γ crystals appears to be slightly below that of the α crystals, resulting in γ crystal to α crystal transitions at extremely high temperatures or under usual autoclaving conditions.
    Additional Material: 22 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 3069-3093 
    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 quantitative model for fitting infrared spectra of polyethyleneterephthalate samples over the region from 1100 to 720 cm-1 has been evaluated. The absorbance was described as the sum of a linear base line and a set of symmetrical bell-shaped Pearson VII curves. Using this model, experimental transmission spectra of yarns, measured with the electric vector parallel and perpendicular to the fiber axis, were fitted. It was found that each of the trans bands near 972 and 845 cm-1 consists of two components, a narrow and a broad one. These two components represent the crystalline and amorphous phases respectively. The band due to the out of plane benzene ring C—H deformation vibration at about 875 cm-1 appeared also to be composed of two contributions. In this case, the narrow component was found to be due to molecules having interactions with direct neighbors. So this narrow component not only contains the molecules in the crystalline phase but also those forming part of bundles which are too small to be detected by x-ray diffraction. For a detailed insight into the molecular arrangement of the amorphous regions, the infrared detection of trans-guache transitions, fold content, detection of bundlelike structures, and molecular stress on tie molecules turned out to be of great practical importance. The structural details, which can be revealed by the infrared technique, cannot be obtained by other means. The potential of the method is illustrated with some practical examples.
    Additional Material: 17 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 121-134 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Types of nylon 6 yarn which contain large γ crystals cannot be described by a model comprising three Pearson VII curves, as we formerly proposed. Hence, a new extended computer program has been developed containing five Pearson VII lines. Two lines are related to the α phase, two to γ-phase crystals, and the fifth describes the amorphous contribution. Some physical relations between parameters could be derived and were incorporated into the computer program. This program provides extremely good fits to all equatorial diffractometer scans which can be obtained from nylon 6 yarns, including those containing large γ crystals. The parameter accuracy is quite satisfactory for diffractometer traces with well-resolved peaks from both α and γ crystals. However, if the traces are poorly resolved or the samples do not contain a sufficient amount of the γ modification, resulting in a lack of detailed information, the parameter accuracy can be rather poor. For those cases special versions of the computer program were developed which contain further empirical interrelations between parameters. With these programs crystal sizes and molecular distances within the crystals of both the α and β modifications can be determined. The method has also been applied to radial scans at various small azimuthal angles with respect to the equator. In that way the relative amounts of the α and γ crystals as well as their orientation factors could be determined. Various aspects of this investigation are illustrated by some examples.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 921-940 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A wide-angle x-ray method has been developed by which quantitative structural information can be obtained on nylon-6 yarns. To this end, experimental equatorial diffractometer scans measured in transmission were fitted to a mathematical model describing the profiles as the envelopes of three bell-shaped functions. Four different models were investigated using, respectively, Gauss, Lorentz (Cauchy), Logistic, and Pearson-VII functions. The last model, which can be regarded as a generalized Lorentz function, gave the best fit. On the basis of a statistical analysis of the results of well-separated x-ray peaks, two parameters could be fixed. Another reduction of the number of parameters was achieved by interrelating the peak areas of the two outer reflections. These reductions widened the applicability of a computer program based on the aforementioned model to highly overlapping x-ray peaks. So the whole variety of x-ray scans, which can be obtained from nylon-6 yarns made under widely varying process conditions, can be well described. The fitting procedures provide unique solutions and hence objectively determined parameters.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 941-954 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A mathematical model developed in an earlier paper describes the experimental x-ray profiles of equatorial nylon-6 reflections in terms of Pearson VII functions. The present paper deals with the physical aspects and interpretations of the interrelations of the parameters obtained and the relation between these parameters and the results of other types of measurements. It was found that the growth of the crystallites perpendicular to the chain axis is not isotropic, the strongest growth being in the direction of the hydrogen bonds. Growth and perfection of the crystallites are found to be highly correlated. Large crystals are related to short distances between the planes containing the hydrogen bonds and so to densely packed, i.e., perfect unit cells. This correlation forms the basis for the observed similarity between our quantification technique and the method of the crystal perfection index introduced by Statton. Curve resolution, however, makes the method better applicable for poorly crystallized samples. Comparison of the results with those of small-angle x-ray scattering gave a high degree of consistency with respect to the determined crystal size. In the literature mention is made of a relation between the dimensions and the melting point of the crystals; this relation is confirmed by comparing the appropriate x-ray parameters with DTA results of methoxymethylated nylon 6-yarns.Information about the γ-phase can be obtained from equatorial and meridional reflections. The expected relationship between the relevant peak areas was established. This reported evidence shows the physical validity of the parameters obtained using the Pearson VII model for the analytical description of x-ray reflections of nylon-6 yarns.
    Additional Material: 11 Ill.
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