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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1461-1472 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal analysis has been carried out on drawn nylon 6 filaments annealed at various temperatures between 150 and 210°C and then methoxymethylated to various degrees. It is shown that the melting point inherent to the morphology of drawn nylon 6 can be obtained from samples in which the reorganization of defect crystallites in the course of thermal analysis is prevented by a proper degree of methoxymethylation of amorphous regions. The melting point thus obtained is in linear relation with the reciprocal crystallite size in the direction of fiber axis which has been obtained from small-angle x-ray data and crystallinity. The extrapolation and the slope of this linear relation give the equilibrium melting point of nylon 6 as 245°C and an end-surface free energy of 42 erg/cm2. The results seem to provide strong support for the presence of chain-fold surfaces in the drawn and annealed polymers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 53-62 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ethylene - propylene and ethylene - butene-1 copolymers with up to 1.7 side groups per 100 carbons have been crystallized at 227°C. and under 4100-4900 atm. pressure. The resulting crystalline polymers are at least partially of extended-chain crystal morphology. Comparison with the same polymers crystallized at atmospheric pressure, which gives folded-chain crystal morphology, revealed: (1) a density higher by 0.008-0.019 g./cm.3 depending on copolymer content; (2) a similar decrease of crystallinity with side group concentration; (3) a similar decrease of the beginning of melting from 125°C. for homopolymer to 65°C. for 1.7 side groups per 100 carbons; (4) a higher (138 ± 0.8°C.) experimental maximum melting point which, in contrast, is independent of copolymer content and seems to vary only with the fraction of low molecular weight material; (5) a decreasing amount of high-melting crystals with increasing copolymer content (72-8%) and an increasing amount of low-melting crystals (27-53%) with increasing copolymer content. In addition, superheating, which reached 5.5°C. for 50°C./min. heating rates, was detected. It was concluded that high-pressure crystallization leads, at least for part of the crystals, to solid solution formation, while atmospheric pressure crystallization does not. Which mode of crystallization is achieved seems kinetically determined. Experimental techniques were dilatometry, DTA, and calorimetry.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 3707-3720 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of linear polyethylene crystallized under pressures up to 5300 atm. has been investigated. Electron micrographs of fracture surfaces obtained from these samples show that the majority of the polymer, at the highest pressures, crystallizes in the form of extended chain lamellae which can be as thick as 3 μ. Electron diffraction patterns show that the molecules are normal to the lamellae. At lower pressures part of the polymer crystallizes in the form of folded chain lamellae, the proportion increasing with decreasing pressure. Well defined kink bands can be observed in the thicker extended chain lamellae. It is suggested that either molecular weight fractionation or an end-to-end alignment of the molecules and subsequent folding takes place during the growth of the extended chain lamellae.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 3697-3706 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene of the linear, low-pressure type has been crystallized under pressure (up to 5400 atm.) from the melt. Crystallization conditions of constant supercooling and constant cooling rates were employed. The resulting solid was analyzed at atmospheric pressure. In contrast to solution crystallization under pressure above 2000 atm., extended chain lamellae of increasing thickness become dominant. These show a maximum melting point of 140°C. and in this research, densities of up to 0.994 g./cm.3. Combining these data on large crystals with the experimental maximum melting temperatures and thickness data on low and atmospheric pressure crystallized lamellae yields a surface free energy of 91 ergs/cm.2 for folded chain lamellae crystallized at low pressure.
    Additional Material: 2 Ill.
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  • 5
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal breakdown of the crystalline lattice of polyethylene grown by quenching from solution (dendrites) and by cooling slowly from solution (single crystals) and melt has been investigated as a function of heating rate. The dendrites showed strong reorganization at temperatures only little above the crystallization temperatures. Heating rates as fast as 20°C./min. could not avoid this reorganization. Heating rates between 10 and 20°C./min. were necessary to have a constant melting point for single crystals grown from solution. The measured melting points were proportional to the thickness and perhaps the density of the samples as determined by interference microscopy and by the density gradient column method. Surface free energy values calculated from the lowering of the melting points range from 81-96 ergs./cm.2. Literature values on specific heats and specific volumes of bulk samples allowed a discussion of the premelting behaviour of semicrystalline polyethylene. It is found that the defects frozen-in below the glass transition temperature “grow” above 250°K. depending upon the overall crystallinity. This destroys the additivity of the specific heat as well as the specific volume. Correlation with NMR and dynamic mechanical loss measurements are attempted. The difference between melting and dissolution temperature in toluene (0.5-8.0 mg. polyethylene/g. toluene) for slowly cooled bulk as well as solution crystals was found to be 26°C., placing the maximum dissolution temperature of polyethylene crystals in toluene at 111°C.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 513-516 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 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 7 (1969), S. 115-120 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 8 (1970), S. 41-45 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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