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  • Physics  (71)
  • Wiley-Blackwell  (71)
  • American Chemical Society
  • American Institute of Physics (AIP)
  • 2000-2004
  • 1995-1999  (71)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2465-2481 
    ISSN: 0887-6266
    Keywords: tensile drawing ; morphology ; polybutylene ; terephthalate ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The concept of the drawing of a molecular network has been employed to derive a total network draw ratio from the combination of the two deformations occurring in the production of poly(butylene terephthalate), PBT, fibers by the consecutive processes of melt spinning and cold drawing. The mechanical properties of PBT can then be more readily explained in terms of increases in this total network draw ratio. However, the preorientation and crystallization that occurs in the melt-spinning process can occur at different strain rates and temperatures, depending on the wind up speed employed, on the extensional viscosity of the polymer, and on the variation of the extensional viscosity with temperature. Therefore, for polymers such as poly(butylene terephthalate), which can exist in two crystalline forms, the morphology of the final drawn fiber might be expected to depend on the first melt-spinning stage of the process as well as on the total network draw ratio. In this work, density, birefringence, mechanical measurements, and WAXD measurements, which have been made on the melt-spun fibers and on the drawn fibers, are described. Small differences in some of the drawn yarn mechanical properties at the same overall network draw ratio are related to the crystallinity and in particular to differences in the proportion of the α and β phases present in the drawn yarn. These in turn are related to differences in the temperature and stress during melt spinning and drawing. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2465-2481, 1997
    Additional Material: 18 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1501-1514 
    ISSN: 0887-6266
    Keywords: multicomponent ; latex ; interpenetrating polymer networks ; IPN ; core/shell ; damping ; loss area ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The integrals of the linear loss shear modulus vs. temperature (loss area, LA) and linear tan δ vs. temperature (tan δ area, TA) were characterized for various core/shell latex particles with synthetic rubber, poly(butadiene-stat-styrene) [P (Bd/S), 90/10], and interpenetrating polymer networks (IPN) as the cores. The IPN cores were composed of P(Bd/S) (Tg ≃ - 70°C) and an acrylate based copolymer (Tg around 10°C) for potential impact and damping improvement in thermoplastics. Poly(styrene-stat-acrylonitrile) (SAN, 72/28) was the shell polymer for all these polymers. Under the same loading, for both toughening and damping controls, among the IPN core/shell, blend of separate core/shell, and multilayered core/shell polymers, the IPN core/shell polymers were the best dampers. However, the other core/shell polymers also showed higher LA values than P(Bd/S)/SAN core/shell polymer. A comparison of LA values via a group contribution analysis method was made, the effect of particle morphology and phase continuity on damping being studied. Inverted core/shell latex particles (glassy polymer SAN was synthesized first) showed much higher LA and TA values than normal core/shell ones (rubbery polymer was synthesized first). Models for maximum LA and TA behavior are proposed. The damping property was essentially controlled by the phase miscibility and morphology of the core/shell latex particles. The LA values for each peak in these multiphase materials provided some indication of the several fractional phase volumes. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1501-1514, 1997
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1679-1694 
    ISSN: 0887-6266
    Keywords: crystallization kinetics ; thermotropic liquid crystalline polymers ; polyimide ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We have studied the nonisothermal and isothermal crystallization kinetics of an aromatic thermotropic liquid crystalline polyimide synthesized from 1,2,4,5-benzenetetracarboxylic dianhydride (PMDA) and 1,3-bis[4-(4′-aminophenoxy) cumyl] benzene (BACB) by means of differential scanning calorimetry (DSC). Polarized light microscopy (PLM) and wide-angle X-ray diffraction (WAXD) results confirm that this polyimide exhibits a smectic texture. Nonisothermal crystallization showed two strong and one weak exothermic peaks during cooling. The phase transition from isotropic melt to liquid crystalline state is extremely fast which completes in several seconds. The mesophase transition has a small Avrami parameter, n, of approximate 1. The isothermal crystallization of 253-258°C has been examined. The average value n is about 2.6 and the temperature-dependent rate constant k changes about two orders of magnitude in the crystallization temperature range of 6°C. The slope of ln k versus 1/(TcΔT) is calculated to be -2.4 × 105, which suggests nucleation control, via primary and/or secondary nucleation for the crystallization process. During the annealing process, a new phase (slow transition) is induced, which grows gradually with annealing time. At lower annealing temperatures (220-230°C), the slow transition process seems not to be influenced by the crystals formed during cooling process and its Avrami parameter n is ca. 0.3-0.4. However, the slow transition was hindered by the crystals formed during cooling process when annealed at higher temperature (230-240°C). © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1679-1694, 1998
    Additional Material: 15 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2103-2109 
    ISSN: 0887-6266
    Keywords: ethylene-vinyl alcohol copolymers ; multiple-pulse proton NMR ; spin diffusion ; comonomer content ; crystallinity ; long spacing ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Capitalizing on the superior sensitivity of proton NMR, relatively rapid estimates of three parameters, namely, comonomer content, crystallinity, and long spacing, are determined for three ethylene/vinyl alcohol copolymers using solid-state proton NMR measurements. Multiple-pulse techniques are utilized (a) in conjunction with magic angle spinning for measuring comonomer content, (b) in conjunction with a T1xz relaxation measurement for determining crystallinity, and (c) in conjunction with a T1xz-based spin diffusion measurement for determining the long spacing. These three parameters, extracted from data collected in a total spectrometer time of about 20 min, are compared with similar parameters obtained using more conventional DSC, SAXS (including synchrotron), and solution-state NMR measurements. Agreement is found to be good. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2103-2109, 1998
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1009-1012 
    ISSN: 0887-6266
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No abstract.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2825-2833 
    ISSN: 0887-6266
    Keywords: holographic gratings ; morphology ; functionality ; liquid-gel demixing ; network ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of transmission gratings with varying Bragg spacings formed using polymer-dispersed liquid crystals were examined using high-resolution scanning electron microscopy and image analysis techniques. The effect on the morphology of small changes in the overall functionality of the prepolymer syrup was observed. An increase in the amount of monofunctional compound resulted in small, nearly spherical domains (〈100 nm in diameter) confined in well-defined lamellae for samples with a 0.49 μm Bragg spacing. A decrease in concentration (an effective increase in monomer functionality) at this Bragg spacing resulted in larger domains (100-200 nm) with much greater distribution of sizes and shapes. The local volume fractions of discrete liquid crystalline (LC) domains was considerably larger in the latter case. An increase in the Bragg spacing to 1.35 μm also resulted in well-defined lamellae of LC domains, although much more coalescence into irregularly shaped individual domains was observed. Surprisingly, the local volume fraction of LC increased in the larger Bragg spacing samples. The morphology results are discussed qualitatively in terms of liquid-gel demixing where the inherent crosslink density and elasticity of the polymeric host must be considered in phase separation processes on the nanoscale. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2825-2833, 1997
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2887-2894 
    ISSN: 0887-6266
    Keywords: light-activated polymers ; cure kinetics ; photocure ; photopolymerization ; nucleation ; growth ; Avrami equation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The purpose of this article is to develop a mathematical model that describes photocure and photopolymerization kinetics. This model is neither wholly phenomenological nor mechanistic, but contains elements of both. We draw an analogy between the classical Avrami approach for first-order phase transformations and the kinetic phenomena that occur during photocuring, and take into account cure inhibition due to a decrease in mobility of the constituents. The result is an explicit algebraic two-parameter expression for the extent of cure versus time. More importantly, the two parameters have physical significance, and to some extent can be predicted a priori. The model is compared to three sets of unrelated data, and excellent agreement is obtained, except for part of the data at the onset of the reactions. Physical insight obtained by comparing our theory with experiments supports the existence of preferred sites for initiating the reaction, and indicates that irradiation is the rate-limiting step in the overall cure process in the limit of small irradiation intensities. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2887-2894, 1998
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 749-761 
    ISSN: 0887-6266
    Keywords: polycarbonate ; polyglutanimide ; polymer blends ; copolymer ; compatibilization ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Imide units copolymerized with MMA units have been selected in order to improve compatibility between PC and acrylics through specific interaction or internal repulsion. Good dispersion of acrylic inside a PC matrix has been observed upon melt mixing, which can be partially explained by the good rheological agreement between these two polymers. Transmission electron microscopy has shown that the system remains phase separated from 5 to 95 wt % of PC. Phase diagrams for three different imide concentrations have been drawn. Results obtained by DSC (conventional and with enthalpy relaxation) are similar to those obtained by optical cloud point detection. The phase diagrams show the raise of the PC/PMMA demixtion curve (LCST type) when percentage of imide increases in the acrylic phase. Theoretical calculations on binary interaction energy density show a slight improvement of the interaction between acrylic and PC when imide percentage increases. Cloud point measurements on 50/50 PC/acrylic blends varying the imide concentration show that the improvement of compatibility deduced from the raise of the demixtion curve (LCST type) is more related to a kinetic effect (the high Tg of imidized samples is reducing macromolecule mobility) than specific interactions. The calculated favorable interactions are probably too weak to be detected with cloud point measurements. The microstructures obtained after crystallization of the PC phase under solvent vapors in phase separated PC/acrylics blends can also be explained by Tg effects. Moreover, solvent vapor exposure could be a powerful tool to determine the real thermodynamic behavior of the blends at room temperature. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 749-761, 1997
    Additional Material: 19 Ill.
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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. 1449-1461 
    ISSN: 0887-6266
    Keywords: adhesion ; oxide coating ; fragmentation test ; molecular orientation ; substrate temperature ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fragmentation tests in the uniaxial mode were performed on poly(ethylene terephthalate) (PET) films coated with a 100 nm thin silicon oxide layer. The coating's fragmentation process was analyzed in light of the mechanical behavior of the polymer substrate. It was shown that, upon unloading samples strained to less than 4% nominal strain, strain recovery leads to the closure of coating cracks. The usual fragmentation diagram, which shows the crack density (CD) versus applied strain, was used to identify the various energy dissipation mechanisms controlling the fragmentation process. An alternative presentation of CD versus true stress provided accurate measurements of both fragmentation and saturation onsets. The interfacial strength was modeled from the CD at saturation according to the Kelly-Tyson approach, including a Weibull distribution of the coating strength. The prediction was compared to the substrate shear stress at saturation. Effects of substrate yield, temperature, and molecular orientation are discussed. It was shown that the coating deposition by evaporation on the PET substrate did not induce structural changes at the polymer interface, whereas heat treatments increased the polymer crystallinity in the interfacial zone, resulting in higher interfacial strength. © 1997 John Wiley & Sons, Inc. J. Polym Sci B: Polym Phys 35: 1449-1461, 1997
    Additional Material: 13 Ill.
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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. 1621-1631 
    ISSN: 0887-6266
    Keywords: pulsed photothermal radiometry ; thermal diffusivity ; polymer films ; chain orientation ; thermal anisotropy ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We have developed a pulsed photothermal radiometry technique for determining the thermal diffusivity parallel to the surface of a polymer film that involves flashing a line-shaped laser beam on the surface of the sample at right angle to its length, and monitoring the temperature change with time at a distance from the line source using an infrared detector. Combining this with our previous laser-flash radiometry method for thermal diffusivity measurement perpendicular to the film surface, we can now measure the thermal diffusivity of a polymer film along all directions. These two techniques have been used to study uniaxially and biaxially oriented poly(ethylene terephalate) and uniaxially drawn ultrahigh molecular weight polyethylene films. For uniaxially oriented poly(ethylene terephalate), the thermal diffusivity along the draw direction is substantially higher than that in the transverse direction, which in turn, is slightly higher than that in the thickness direction. For a polyethylene film with a draw ratio of 200, the axial thermal diffusivity is extremely high, being about five times that of stainless steel. The anisotropy of the thermal diffusivity of this film exceeds 90. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1621-1631, 1997
    Additional Material: 12 Ill.
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