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  • 1
    Publication Date: 1975-11-01
    Print ISSN: 1073-5623
    Electronic ISSN: 1543-1940
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Springer
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1077-1093 
    ISSN: 0887-6266
    Keywords: nucleation ; crystallization kinetics ; polypropylene ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A nucleation rate function is proposed for use in analyzing the overall crystallization kinetics of polymers. This function allows for the possibility that the nucleation rate varies substantially during the crystallization. This feature is particularly useful in analyzing nonisothermal crystallization, but it can be used to analyze isothermal crystallization as well. The nucleation rate function was used in the derivation of a modified transformation kinetics equation of the Avrami type. The modified Avrami equation was found to be suitable for kinetics analysis for the data obtained from nonisothermal crystallization at rapid cooling rates. Kinetics parameters used to describe nonisothermal crystallization under rapid cooling rates are presented and discussed. These include crystallization induction time, plateau (crystallization) temperature, crystallization half-time, crystallization rate constant, Avrami index, and newly defined quantities called nucleation index, geometric index, and nucleation rate constant. The procedure used to obtain the nucleation rate constant and nucleation index for the nucleation rate function is described and illustrated by application to the analysis of the crystallization kinetics of polypropylene. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1077-1093, 1997
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 681-692 
    ISSN: 0887-6266
    Keywords: high-density polyethylene ; nonisothermal crystallization kinetics ; plateau temperature ; regime transition ; crystallinity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The quiescent nonisothermal bulk crystallization kinetics of two high-density polyethylene resins were investigated by a modified light-depolarizing microscopy (LDM) technique. The technique allows studies at average cooling rates up to 2500°C/min. The polymer was found to crystallize at a pseudo-isothermal temperature even at these very high cooling rates. The overall bulk crystallization rate increased rapidly as the cooling rate and supercooling increased. Crystallization kinetics was analyzed by Avrami analysis. Avrami exponents near 3 suggested spherical growth geometry and instantaneous nucleation at predetermined sites. Observation of spherulites by optical microscopy together with a number density of spherulites that changed little with increase in cooling rate or supercooling supported this model of crystallization behavior. Analysis of the half-time of crystallization based on the Lauritzen and Hoffman secondary nucleation theory indicated that the regime II-III transition was found to occur at a degree of supercooling of approximately 22°C. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 681-692, 1998
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2011-2032 
    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 series of polypropylene (PP)/nylon 6 (N6) blends of composition 75/25, 50/50, and 25/75 have been prepared in a screw extruder combined with a Koch static mixer. The phase morphology was observed with a scanning electron microscope. The influence of heating in the reservoir of a rheometer followed by subsequent extrusion through a capillary on the phase morphology was investigated. Phase size growth as a function of time was observed under quiescent and mild deformation rate conditions. The discrete phase size was observed to decrease with increasing extrusion rate through dies. The shear viscosity and principal normal stress difference of the blends were measured as a function of composition. The crystalline orientation of both polypropylene and nylon 6 in blend melt spun fibers was characterized by wide angle X-ray diffraction and interpreted in terms of Hermans-Stein orientation factors. The orientation increases with drawdown ratio. The orientation factors for the polypropylene phase vary with spinline stress in a manner independent of composition and identical to that for pure polypropylene. Extracting melt spun blend fibers with formic acid has produced small-diameter polypropylene minifilaments with diameters of the order of microns.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1671-1682 
    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 mathematical model of the melt spinning process that includes crystallization has been used to compute the velocity, diameter, temperature, and birefringence as a function of distance from the spinneret. An improved inversion procedure is described and is shown to give better results for the computed apparent elongational viscosity and heat-transfer coefficient data. The computed profiles have been compared directly to the experimental profiles determined earlier and reported in Part I of this paper. The results show that the model describes the major features of the melt spinning process. The reasons for the observed differences between experimental profiles and those computed from the model are discussed.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 20 (1976), S. 1823-1847 
    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 variation of crystalline morphology and mechanical properties of polyethylene fibers was studied as they were sequentially melt spun, drawn, twisted, heat set, and untwisted. Twisting of as-melt spun fibers was also investigated. The morphology was characterized using wideangle x-ray diffraction, small-angle x-ray diffraction, and scanning electron microscopy techniques. Drawing results in high crystalline orientation, fibrillation, and large increases in modulus and tensile strength. Effects due to variation of spinning conditions were noted. Twisting either as-spun or drawn fibers decreased the axial orientation, modulus, tensile strength, and usually also the elongation to break. The changes in these properties increased with twist angle. Twisting also caused transformation of a small fraction of the sample to the monoclinic form of polyethylene. Heat setting caused healing of voids generated during drawing and increased the perfection and periodicity of the stacking of lamellar crystals along the fiber axis. Heat setting also caused the monoclinic polyethylene to transform back to the orthorhombic form, and it increased the modulus and tensile strength. Untwisting returned the orientation in the fiber to essentially that which it would have if it had not been twisted, but untwisting also resulted in the formation of kink bands.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 3553-3567 
    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 comparative study of the stress induced crystallization of natural (Hevea, Guayule) and synthetic high cis-1,4-polyisoprenes at room temperature is presented. Hevea and Guayule are both found using WAXS to crystallize into the unit cell of Morss and Bunn previously described for Hevea. DSC studies of polyisoprenes held at -25°C indicate that Hevea and Guayule crystallize more rapidly than synthetics. Studies of relative birefringence and stress decay following uniaxial extension confirm this. Under conditions of comparison at the same stress, raw Hevea crystallizes more rapidly than extracted Hevea, Guayule, and the other polyisoprenes.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 3679-3695 
    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: An experimental study of the kinematics of inflation of poly(ethylene terephthalate) (PET) parisons in a Corpoplast stretch blow molding process is reported. LVDT displacement transducers have been placed at various positions along the length and at the top of a specially designed and built mold. A six-channel LVDT demodular circuit was built and attached to a minicomputer. Studies were conducted at 90 and 100°C at various pressures. Kinematic models were developed for the parison inflation, and stress fields along the deforming surface of the parison were computed using membrane theory.
    Additional Material: 19 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 1541-1556 
    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: An investigation was carried out of the high speed melt spinning of three polypropylene resins with melt flow indices of 12, 35, and 300. On-line measurements were made of diameter, birefringence, and temperature as a function of distance from the spinneret for a range of spinning conditions for each polymer. A plateau (decrease of cooling rate) in the temperature profile was associated with the occurrence of crystallization in the spinline. The position of this plateau correlated with a rapid rise in the birefringence profile and a rapid decrease in the rate of drawdown in the diameter profile. The temperature and birefringence profiles were used to determine the temperature and position on the spinline at which the onset of crystallization occurred. It was found that the position and temperature of crystallization onset varied considerably with changes in take-up velocity, extrusion temperature, and resin melt index (weight average molecular weight). The crystallization onset occurred nearer the spinneret and at higher temperatures with (1) an increase of take-up velocity, (2) a decrease of extrusion temperature, or (3) a decrease of resin melt flow index. An analysis was carried out to estimate the rate of stress development with distance along the spinline; the results were also used to estimate the stress at the onset of crystallization for each spinning condition. It was concluded that the observed behavior could be attributed to the role of spinline stress in producing molecular orientation and consequent increase of crystallization rate.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 447-463 
    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: On-line experimental measurements of filament diameter, temperature, and birefringence as a function of distance from the spinneret were carried out during melt spinning of two nylon 6 resins of differing molecular weight. Filament tension was also measured. A rapid diameter attenuation or “necking” was observed in the spinline for both resins at take-up velocities above 6000 m/min. Evidence of crystallization in the spinline was also observed at these high spinning speeds. An analytical technique was used to extract apparent elongational viscosity for each resin and heat transfer coefficient for the melt spinning process from the experimental results.
    Additional Material: 13 Ill.
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