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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 33 (1987), S. 161-163 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 1 (1987), S. 57-59 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 2 (1988), S. 142-145 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 2 (1988), S. 197-199 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 981-988 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studied here are miscible binary cosolvents for polystyrene, for which polystyrene is insoluble in either of the individual solvents. Polymer-solvent interactions in solutions of atactic polystyrene in acetone/diethyl ether and in methylcyclopentane (MCP)/acetone binary cosolvents have been investigated using nuclear magnetic resonance (NMR) spectroscopy. Polystyrene 13C chemical shifts were measured as a function of miscible binary solvent compositions and temperature. The NMR data were used to calculate “association constants” as a measure of specific interactions of the solvent components with all sites on the polymer. In mixtures of acetone and diethyl ether, 13C-NMR indicates a weak interaction between the polystyrene phenyl ring and the diethylether solvent component. In the polystyrene/MCP/acetone system, present NMR data reveal no preferential interactions. Additional NMR measurements were performed on polystyrene in mixtures of CCl4/acetone. From these results, it is concluded that although preferential polymer-solvent interactions are present in some cosolvent systems, they are not a prerequisite for such behavior.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 2587-2603 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solid-state coextrusion has been used to prepare uniaxially drawn films from isotropic poly(ethylene 2,6-naphthalate) (PEN) of a minimum degree of crystallinity (ca. 5%) both below and above its glass transition temperature Tg. The onset of cold crystallization (Tc) of the drawn films has been studied as a function of the extrusion temperature (ET) and the draw ratio (EDR). It has been shown that Tc decreases markedly on draw, as much as 95°C, and, at constant draw ratio Tc goes through a minimum in the Tg region. For undrawn PEN, annealing below 153°C has no significant effect on Tc. To evaluate the crystallization rate constant (k) and the activation energy (Ea) of the drawn specimens, a nonisothermal DSC procedure has been used. With increasing EDR, k increases markedly and Ea goes down over threefold compared with the undrawn polymer. At high ET, strain-induced crystallization has also been shown to play an important role in lowering Ea for cold crystallization. Thermal shrinkage above Tm indicates a high elastic recovery, underlining the efficiency of deformation, ca. 93%, achieved by solid-state coextrusion.
    Additional Material: 16 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 83-90 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal-nematic phase transition of a copolyester consisting of 20 mol% poly(ethylene terephthalate) and 80 mol% p-hydroxybenzoic acid (PHB) was characterized by depression of the crystal-nematic transition by the addition of a liquid crystal diluent. This copolyester contains blocks of crystalline PHB. Its transition behavior was compared with thatrandom copolyester with diluent of the same composition. From the extrapolated transition temperature depression data, the heat of transition per mole of p-oxybenzoate was calculated as about 1.3 kcal/mol, with an entropy of about 2 cal/deg mol. This assumes that only the p-oxybenzoate unit crystallized from the nematic state. The validity of the Flory-Huggins model for this transition point depression was confirmed graphically by comparison with two different thermotropic-liquid crystal polyesters. These results may represent the first reported crystal-nematic temperatures and heats generated by the dilution method for liquid crystal copolyesters of this type.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2459-2472 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polycarbonate is known to crystallize thermally, but only slowly and to a limited (25%) extent. The melting points reported exhibit a wide variation. We have found that the melting temperature of polycarbonate may be drastically increased by employing a sequence of vapor-induced crystallization and annealing treatments. The crystals formed by the treatment with organic vapor act as a nucleation or precursor state for further crystallization into larger, more perfect lamellae. An initial peak melting temperature of 195°C has been annealed up to 239°C, and then to 295°C by a double-heat treatment. This sample is 60% crystalline, based on heat-of-fusion calculations. An equilibrium melting point of 335°C has been obtained for PC from an extrapolation of reciprocal lamellar thickness.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 795-805 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(aryl-ether-ether-ketone) (PEEK) films and rods have been solid-state extruded at 154 and 310°C, respectively. The crystal orientation functions, melting behavior, density, and tensile properties of the drawn PEEK films (EDR ≤ 3.7) and rods (EDR ≤ 5.5) have been measured. As extrusion draw ratio (EDR) was increased, the c-axis orientation function, melting temperature, and tensile modulus and strength increased. Moduli up to 6.5 GPa and the strengths up to 600 MPa, 3 and 6 times the values of undrawn films, respectively, were obtained for the drawn films. The thermal expansivities along (α‖) and perpendicular (α⊥) to the draw direction of PEEK rods were measured from -40 to +10°C. As EDR was increased, α⊥ increased, but α‖ decreased. At EDRs of 3.8 and 5.5, α‖ even exhibited negative values (about -5 × 10-6°C-1), probably due to reversible contraction of elongated tie-molecules.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 741-753 
    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: Three low density polyethylenes, one long branched (A) and two linear (B and C), have been solid-state-extruded at several constant temperatures from ambient to 80°C and to draw ratios ≤ 8. The initial densities and melt indices of A, B, and C are 0.920, 0.920, and 0.935 g/cm3, and 1.9, 0.8, and 1.2, respectively. Melt-crystallized cylindrical billets were extruded through conical dies in an Instron Capillary Rheometer. The linear polymers were found to draw by extrusion more readily than the branched; all three strain-harden. Density, birefringence, tensile, and thermal properties have been evaluated as functions of extrusion temperature and draw ratio. Despite a measured loss via die swell, substantial orientation takes place during solid-state extrusion as evidenced by increases in transparency, birefringence, and tensile modulus (up to 4.5 times that of the original isotropic polymer). Depending on the polymer and the draw temperature, density does go through a minimum or shows a monotonic increase with draw by extrusion. A minimum in modulus is also observed at low draw and at all draw temperatures for all three polymers. The highest tensile moduli achieved are 0.73, 0.46, and 1.5 GPa for A, B, and C, respectively, at their highest draw ratio. The melting point for polymer B decreases with extrusion draw ratio, whereas it remains constant after a small initial drop, for the two others. For all three low density polyethylenes, birefringence increases rapidly with extrusion draw and then levels off at high draw. The birefringence limit is similar for A and B, i.e., 0.046 ± 0.004, but higher for C, i.e., 0.068 ± 0.009. This work extends beyond others in that it studies the effect of short as well as long branches in solid-state extrusion by comparing the linear and long branched LDPE polymers and LDPE with prior evaluations of HDPE.
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