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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 21 (1956), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 26 (1970), S. 1923-1927 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    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 6 (1962), S. 585-599 
    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: Tensile stress-induced crazing in polystyrene, poly(methyl methacrylate), and polycarbonate has been carefully examined by optical and electron microscopy. Examination of the surface of crazed specimens and the cross sections of individual crazes leads to the conclusion that the crazes are not void cracks, but are filled with a craze matter. The craze matter is readily distinguishable from the surrounding resin and is seen to exist in continuity with it. Further experiments confirm the existence of the craze matter and tend to indicate its structural and mechanical properties. These experiments include: microscopic examination of the walls of fractured crazes, micro x-ray diffraction of craze matter, studies of the strength of crazed specimens under static loads and under increasing tensions, studies of the effect of heat and solvent on crazed specimens, and observations on the ability of crazes to form special networks. The results indicate that the craze matter may be formed by localized resin deformation leading to a load bearing oriented structure. A hypothesis of the mechanism of craze formation is proposed in light of the new and varied information reported in the paper. Study of the kinetics of craze growth suggests the division of the mechanism into three parts: initiation, propagation, and termination. The initiation step describes the concentration of strain energy and the precursory molecular arrangements in the immediate vicinity of inhomogeneities. These are the changes which occur during the time lapse between stress application and first appearance of crazes. The propagation step comprises the sudden and relatively rapid localized resin deformation which creates the craze matter. The shapes of the growing crazes and their diminishing growth rates are attributable to known resin properties. The termination step represents the apparent cessation of craze growth with continued long times of stress application. At this stage in the existence of crazes the proposed hypothesis must blend into the theories of time delayed rupture. It is concluded that stress crazing is basically a molecular slippage rather than a molecular cleavage phenomenon. Considerations, therefore, are to be directed more towards intermolecular forces than intramolecular forces.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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: Long-term weathering studies of the subject transparent thermoplastic polymer revealed that sheets extruded from pristine resine gradually became hazy. Electron microscopy of fracture surfaces showed that minute voids were created during outdoor exposure. By the application of the Mie light scattering theory, it was possible to calculate that the average void size was 4 × 103 Å and that the concentration of voids numbered about 106/mm3. Yet the total void volume of the poorest sample, which had a haze value of 26%, was less than 0.05%. The average void size decreased over a three-year period, but the concentration increased with exposure. A mechanism of void formation was formulated based on photo-induced moleculàr degradation. Chemical evidence suggests that molecular degradation occurs by complete unzippering of a molecule, resulting in the formation of carbon dioxide and 2,2,4-trimethylpentene-3-al. The aldehyde is believed to plasticize the polymer in the vicinity of a growing void and the carbon dioxide acts as a blowing agent, therby generating a void. Simultaneously, free radicals formed during molecular decomposition initiate further degradation of neighboring molecules. The propensity of this resin to haze can be effectively overcome by suitable cleanup and stabilization procedures.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 2719-2719 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 917-922 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High molecular weight, linear polyethers were prepared by polymerizing a series of ring-substituted phenyl glycidyl ethers by using the ferric chloride-propylene oxide and dibutylzinc-water catalyst systems. The α-naphthyl, β-naphthyl, p-phenylphenyl, the o-, m-, and p-methyl, and the o- and p-chlorophenyl polymers resemble the parent polymer in that they are readily crystallizable polyethers which have melting points above 170°C. The other substituted poly(phenyl glycidyl ethers), including the o- and p-isopropyl, p-tert-butyl, p-octyl, and 2,4,6-trichloro derivatives show much less tendency to crystallize and are lower melting. The x-ray and electron diffraction data established that poly(o-chlorophenyl glycidyl ether) crystallizes in an orthorhombic unit cell; data obtained in a parallel study of unsubstituted poly(phenyl glycidyl ether) did not allow assignment of a specific structure.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 4 (1966), S. 531-536 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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