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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 256 (1978), S. 718-719 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 258 (1980), S. 1335-1342 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary Structural and thermodynamic characteristics of liquid-crystalline solutions of four cellulose derivatives in a range of solvents were studied. Basic observations were made on these systems using polarized light microscopy, small angle light scattering, dilute solution and concentrated solution viscosities. The polymers studied include hydroxypropyl cellulose (HPC), cellulose acetate butyrate (CAB), ethyl cellulose (EC), and cellulose triacetate (CT). The formation of the liquid crystalline phase was shown to strongly depend on polymer concentration, solvent type and temperature. The critical volume fraction of polymer required to form the liquid crystal phase varied significantly as the solvent changed. The critical volume fraction decreased with increasing solvent acidity and polymer intrinsic viscosity in a given solvent. The breadth of the two phase region seems to decrease with increasing acidity. The liquid crystalline phase was in most cases determined to be cholesteric. In all cases positively birefringent cellulose derivatives form negative spherulitic domains. In one case, the negativity birefringent system (cellulose triacetate) formed positively birefringent spherulitic liquid crystalline domains. This is interpreted to mean the structure organizes itself by a tangential alignment of polymer chains within the domain. SALS measurements appear to detect domains and in some cases cholesteristic pitch.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1528
    Keywords: Thermotropic liquid crystal ; cellulose derivative ; shear viscosity ; principal normal stress difference ; dynamic viscosity ; storage modulus ; extrudate swell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Samples of cellulose acetate butyrate (CAB) hydroxypropyl cellulose (HPC) and ethyl cellulose (EC) are contrasted with commercial (atactic) polystyrene (PS) and isotactic polypropylene (PP) in studies of (i) differential scanning calorimetry, (ii) quiescent polarized light microscopy (iii) optical retardation variation following an imposed stress field. It is concluced that HPC and EC are thermotropic liquid crystals, while CAB behaves in a manner similar to a vitrifying isotropic melt such as PS. Studies of the shear viscosity and dynamic viscosity indicate HPC and EC exhibit yield values while CAB shows a zero shear viscosity and Vinogradov-Malkin reduced viscosity curve identical to PS. The normal stress and extrudate swell behavior of CAB are also similar to PS. The HPC and EC exhibit substantially reduced extrudate swell. Measurement of the principal normal stress difference behavior of the HPC melt is troubled by the existence of yield values.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2035-2043 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polystyrenes having both modified and unmodified endgroup structures were synthesized. These polystyrenes were then subjected to dynamic mechanical testing below their glass transition temperature. The modified structures were shown to influence the β transition of polystyrene. While the mechanism of this secondary transition has been speculated but never unequivocally substantiated in the past, the evidence presented here strongly support the idea that the β transition of polystyrene arises from chain-end motions.
    Additional Material: 5 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 18 (1974), S. 2355-2365 
    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: This paper reports a new phenomenological observation regarding the stress crazing of glassy polystyrene. It was found that the applied stress to initiate a craze, often called the critical crazing stress, is independent of molecular weight. Further, the gross structure of the craze does depend on molecular weight, and other phenomenological aspects previously reported have been reaffirmed. These observations are interpreted in the light of knowledge from the literature and provide a better understanding of the crazing process.
    Additional Material: 6 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 23 (1979), S. 2315-2326 
    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 present investigation deals with amorphous polystyrene crazing behavior at both the molecular and macroscopic levels. The nature of the amorphous state is considered from the perspective of statistical fluctuation theory, especially when a mechanical force field is acting on the polymer. Past crazing studies have rather fully described the phenomenological behavior. However, these studies did not generate a fundamental molecular explanation of crazing. We now suggest a molecular approach based on the density and density distribution of physical entanglements between polymer chains as a function of molecular weight. This approach permits the molecular entanglement concept and the phenomenological parameters such as stresses and temperatures associated with crazing to be related through the use of fluctuation theory. Two fundamental results are obtained and specifically demonstrated for polystyrene. First, an accurate theoretical prediction of the volume associated with microvoid formation is explicitly determined. Second, the dependence of the number of crazes on molecular weight is also shown.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1913-1926 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation of the reflective component of small-angle x-ray scattering patterns of polystyrene crazes is performed. It is shown that the strong streak parallel to the tensile axis consists predominantly of reflected radiation, while the remaining pattern is composed entirely of diffracted radiation. X-ray reflection off unparallel regions of crazes is discussed and the nature of the reflection is also considered in terms of collimation quality. An analysis methodology based on craze tip angular distribution is proposed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 506-509 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 essentially triblock poly(m-phenylene isophthalamide-b-ethylene oxide) with sequence PEO-(MPD-I)-PEO or (MPD-I)-PEO-(MPD-I) and their admixtures with (PEO)n were studied as solution cast films. Experimental techniques included transmission optical microscopy, transmission electron microscopy, electron diffraction, and X-ray diffraction. Characterization of these systems showed that structure could develop in two ways. The first way was the development of a typical polycrystalline structure of the (MPD-I) segment by the action of such agents as formic acid. In a second manner, however, a non-typical development was manifested by the appearance of crosses In the polarized opticial microscope. These samples showed only an amorphous halo when subjected to wide angle X-ray diffraction measuremfents. Their small angle pattern suggested scattering by dispersed particles. Other experiments indicated the crosses would form only under an unusually restrictive set of conditions, principally that the PEO present must be above a certain molecular weight and concentration and, furthermore, that the solvent must contain a salt such as LiCl. These observations led us to speculate that optical activity of the films showing crosses could occur either by chain orientation near the interface of a spherical particulate second phase or from stress induced bond polarization resulting from the film formation process.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 81-89 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 method to obtain the tenacity and Young's modulus of nonwoven webs without direct measurement of web thickness is proposed. This has been tested with several series of samples with different basis weight. It was found that these properties were nearly Independent of the sample gage length, and both tenacity and modulus generally decreased with increase in the die temperature, the air pressure at the die, or the die to collector distance [DCD]. The web stiffness as measured by bending rigidity followed similar trends. The elongation Lo break also decreased as die temperature and air pressure at The die increased, but it increased with increasing DCD. The average filament diameter in the web decreased with increasing die temperature or air pressure at the die. The single filament strength was measured and compared with strength properties of web and of high-speed melt spun filament prepared from the same resins. The strength of single filaments in the web lie in between those of the web and high-speed spun filaments. The mechanical properties of melt blown web were interpreted in terms of the changes in Fiber diameter, the level of interfilament bonding, the molecular orientation developed in the filament, the diameter uniformity along the individual filaments in the web, and the presence of voids in the filament.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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