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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 673-679 
    ISSN: 0887-6266
    Keywords: scanning force microscopy ; hectorite ; polystyrene ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Many important layered silicate-polymer nanocomposite materials may be synthesized using an in-situ polymerization process. Using this technique, organic monomers are intercalated into the interlayer regions of the hosts, where subsequent polymerization may then occur. In this paper, we report on the in-situ polymerization of styrene in Cu(II)-exchanged hectorite thin films. Scanning force microscopy (SFM) images of the polymer surface reveal that the surface polystyrene is generally aggregated into groups of elongated strands. SFM imaging of the interclay regions, in conjunction with X-ray diffraction (XRD) and electron spin resonance (ESR) data, indicates that approximately 20-30% of these regions contain polystyrene, with minimal reduction in the majority of Cu2+ sites observed. XRD data shows little or no intercalation of the monomer into the true intergallery regions. Instead, the polymer likely forms in intercrystallite or planar defect regions. In addition, two distinct phases of polymeric material are found within these defect regions, a highly polymerized polystyrene in addition to a polystyrene form exhibiting greater material stiffness. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 673-679, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2243-2271 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A continuum rheological theory, endowed with generalized structural significance, has recently been developed. Based on nonequilibrium thermodynamics, it relates stress σ, strain rate \documentclass{article}\pagestyle{empty}\begin{document}$\dot \varepsilon$\end{document} and temperature in terms of material evolution through a series of structural states. The theory has previously had success in dealing with crystalline metals and surface physics, and here it is applied to crosslinked rubbery polymers in the nominally amorphous condition. Structure is believed to be related to interchain associations, chain entanglements, chain ends, and other defects in the hypothetical ideal network which by itself would lead to neo-Hookean predictions in uniaxial deformation, σnH ∝ λ2  -  λ-1, where λ is the stretch ratio. Predictions are made for σ(λ) in both tension and compression and shown to be more compatible with data than either σnH(λ) or the Mooney - Rivlin expression σMR(λ). Only two parameters are required, moduli Go (reflecting initial structure) and Gs (the steady-state condition), and rate effects are incorporated through Go(\documentclass{article}\pagestyle{empty}\begin{document}$\dot \varepsilon$\end{document}) and Gs(\documentclass{article}\pagestyle{empty}\begin{document}$\dot \varepsilon$\end{document}). The phenomena of yielding and stress softening in cyclic tensile loading are also predicted, suggesting advantages to this approach relative to conventional viscoelastic continuum models.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2119-2147 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of chain structure and processing variables on the microstructure and linear viscoelastic behavior of a series of copolyether-ester block polymers are described. In addition, the random copolyester analogs of the hard block are examined. The ester segments are composed of two isomers, poly(tetramethylene terephthalate) (PTMT) and poly(tetramethylene isophthalate) (PTMI), which possess significantly different crystallization kinetics. The ratio of PTMT to PTMI in the series has been systematically varied to alter the crystallizability without changing the chemical composition. The results of differential scanning calorimetry, wide-angle x-ray diffraction, and dynamic mechanical characterization are presented. Copolymerization of a second ester shortens the average sequence length of the first ester, resulting in melting-point depression for crystals of the first polyester and substantial lowering of the dynamic mechanical storage modulus above the glass transition of the intercrystalline phase. The melting-point depression may be predicted by using Flory's model for random copolymers, but the calculated heats of fusion are significantly lower than those obtained from diluent melting-point depression.
    Additional Material: 20 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-2: Polymer Physics 9 (1971), S. 209-243 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The shear creep and creep recovery behavior of narrow molecular weight distribution polystyrene samples of low molecular weight, 1.1 × 103, 3.4 × 103, and 1.57 × 104 are reported as a function of temperature, near and above the glass temperature. Time-temperature equivalence for the total creep compliance is found to be nonapplicable, and in fact the steady-state recoverable compliance, Je, is a strong function of temperature. The time-scale shift factors for the recoverable compliance are analyzed in the light of free volume theory. Viscosity data are presented for samples with molecular weights between 1.1 × 103 and 6.0 × 105. The temperature dependence of the characteristic time constant ηJe can be explained in terms of free volume concepts whereas that of viscosity η cannot. Effects of residual molecular weight heterogeneity are demonstrated.
    Additional Material: 18 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-2: Polymer Physics 4 (1966), S. 1029-1029 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1617-1626 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The swelling curves of 6μ films of low conversion homopolymers and copolymers of acrylamide (AM) and N-isopropylacrylamide (NIPAM) were obtained in water by an optical microscope technique. Poly(AM) swelled appreciably faster than poly(NIPAM) but there was no apparent correlation between overall swelling rate and copolymer composition. A 57/43 (mole %) AM-NIPAM copolymer swelled fastest. Sequence distribution calculations indicated that its backbone structure tended toward comonomer alternation, which might reduce the extent of hydrogen bonding in the film. The amount of water sorbed during swelling, as approximated from increasing film thickness, was proportional to the square root of time and agreed well with previous work in the literature. Homopolymer films from runs of ca. 50% conversion consistently swelled slower than their low conversion counterparts, probably due to branching and increased entanglements. Heating also promoted slower film swelling due to a tightening of the film structure and/or a low degree of imidization. Monomer reactivity ratios and Alfrey-Price Q and e values for NIPAM were calculated. Cloud points of 5% aqueous solutions of the copolymers were measured and found to decrease with increasing NIPAM content.
    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 Part A-2: Polymer Physics 4 (1966), S. 385-400 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Replicas of fracture surfaces of fractions of linear polyethylene, which were crystallized at elevated temperatures for extended time periods, were examined by electron microscopy. Striated. lamella-type crystallites were observed for all molecular weights over the range 3.2 × 103-5.7 × 105. In agreement with Anderson's previous report, for molecular weights of 12,000 or less, the crystallite thicknesses were comparable to the extended chain length. As the molecular weight increased above this level, however, the crystallite sizes increased only slightly and hence at high molecular weights were very much smaller than the extended chain length. From the measured melting temperatures, crystallite interfacial free energies were calculated from the theory for the melting of finite size crystals comprised of chains of finite length. The crystallite interfacial free energy was found to increase with molecular weight. Based on these results, a crystallization process is outlined which allows for the formation of either extended chain crystallites, or crystallites whose size is much smaller than the extended chain length without any change in nucleation mechanism or arbitrary adjustment in growth mechanism with molecular weight.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 3065-3077 
    ISSN: 0887-6266
    Keywords: polyurethanes ; AFM ; atomic force microscopy ; phase separation ; crosslinking ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of polyurea urethanes was isothermally synthesized from toluene diisocyanate (TDI), water, and trifunctional poly(propylene oxide) in the temperature range of 50-150°C. Morphologies of the samples vary significantly as a function of reaction temperature. In this system, phase separation competes with polymerization and crosslinking. Both transmission electron microscopy and atomic force microscopy have shown a network type of structure for the 50°C samples, while the 150°C samples appear to be homogeneous. Infrared analysis shows that samples prepared at 150°C possess a morphology that is less strongly hydrogen bonded and has a broader distribution of hydrogen-bonded states compared to those prepared at lower temperatures. From this combination of techniques, it can be inferred that phase separation occurs faster than crosslinking at low temperatures; consequently, a phase-separated morphology forms. In contrast, crosslinking occurs faster than phase separation at higher reaction temperatures. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 3065-3077, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 241-263 
    ISSN: 0887-6266
    Keywords: isotactic polypropylene ; propylene/ethylene copolymers ; injection molding ; SCORIM ; mechanical properties ; impact testing ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The aim of the research reported in these two articles was to explore the relationship between processing conditions and the physical properties of different grades of isotactic polypropylene injection moldings and propylene/ethylene copolymers. This first article describes the methods and processing conditions used for molding, together with mechanical test results. Both conventional and shear-controlled orientation injection molding (SCORIM) have been employed for the production of moldings. SCORIM is based on the application of specific macroscopic shears to a solidifying melt, which in turn, facilitates enhanced molecular alignment. SCORIM results in more pronounced molecular orientation than conventional injection molding, which is consistent with the substantial increase in Young's modulus of moldings produced by SCORIM. By controlling the processing parameters it is possible to control and enhance the stiffness without loss of tensile strength. An increase of up to four times in impact strength has been achieved with SCORIM as well as a substantial increase in Young's modulus. The conventional injection moldings containing pronounced molecular orientation exhibited impact resistance well below that for the SCORIM moldings. The mechanical tests carried out at 80°C showed that the high-temperature mechanical properties of all the materials, converted into moldings using SCORIM, exhibited substantial enhancement when compared with moldings of the same material converted by conventional injection molding. © 1997 John Wiley & Sons, Inc.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 415-430 
    ISSN: 0887-6266
    Keywords: aliphatic polyketone ; ethylene-carbon monoxide copolymer ; PK ; isotactic polypropylene ; injection moulding ; molecular alignment ; morphology ; SCORIM ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This article relates to an investigation of injection moulding a new commercial polymer, an aliphatic polyketone (PK). A terpolymer and a 30% glass-filled grade were used as study materials together with an isotactic polypropylene that was used as a basis for comparison. Both conventional injection moulding and shear-controlled orientation injection moulding (SCORIM) were employed in processing. Tensile testing was carried out at 80°C as well as at room temperature. Polarized light microscopy and wide-angle x-ray diffraction were used in the characterization of the mouldings. An increase of up to 30% in Young's modulus and 35% in ultimate tensile strength, and a 70-90% increase in strain at peak were gained for the terpolymer (PK) at room temperature, as a result of SCORIM processing. A substantial improvement at 80°C was also recorded for unfilled SCORIM PK mouldings, and is attributed to the pronounced molecular alignment that was induced in SCORIM mouldings, as shown by Debye patterns. It is notable that the SCORIM mouldings of PK exhibit a greater tensile strength at 80°C than the SCORIM mouldings of isotactic polypropylene at 23°C. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 415-430, 1997
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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