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  • 1
    ISSN: 1349-9432
    Keywords: spatial light modulator ; liquid crystal ; amorphous silicon ; phase modulation ; liquid crystal display ; diffraction efficiency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract An optically addressed parallel-aligned nematic-liquid-crystal spatial light modulator (PAL-SLM) has been studied as a dynamic phase-only light modulation device. The phase modulation characteristics of the PAL-SLM using a liquid crystal display (LCD) as an addressing mask were investigated by analyzing diffraction efficiencies resulting from binary gratings projected from the LCD. A more than 2π phase-only modulation depth was achieved. The highest first-order diffraction efficiency of approximately 38% was also obtained; this is close to the theoretical limit. The experimental results of diffraction efficiencies depending on the phase modulation depth are in good agreement with the simulation for the system operation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1349-9432
    Keywords: spatial light modulator ; liquid crystal display ; phase-only modulator ; diffraction efficiency ; oblique incident ; phase modulation ; amorphous silicon ; liquid crystal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract To realize a high efficiency electrically addressable phase-only modulator, we have coupled a liquid crystal display (LCD) to an optically addressed parallel-aligned nematic liquid crystal spatial light modulator (PAL-SLM) with a set of lenses. Phase modulation exceeding 3ϖ at 532 nm wavelength was obtained. We obtained linear transfer characteristics for phase modulation at various desired phase levels after calibration and adjustment of the transfer characteristics of the PAL-SLM and the LCD. Diffraction efficiency of 40% for binary phase grating and of 90% for 8-level blazed phase grating, which were very close to the simulation values, were observed. The power loss of the readout light was caused when passed through a half mirror, therefore, we examined a setup using an oblique readout light at the modulator. Very high diffraction efficiency was obtained from the setup by optimizing the polarization direction and optical path for this light, and the orientation of liquid crystals. Since the modulator can perform at better than 90% diffraction efficiency and at nearly 100% reflectivity, various high efficiency systems utilizing such modulators are expected.
    Type of Medium: Electronic Resource
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  • 3
    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: Copolymers of aliphatic aldehydes containing a trimethylsilyl group were prepared at -78°C in toluene using diethylaluminum diphenylamide as an initiator. The copolymer depolymerized into monomeric aldehydes on exposure to soft X-rays. When the copolymer was used as a soft X-ray resist, almost complete development was accomplished by exposure alone. No development step was required. The soft X-ray sensitivity of poly(3-trimethylsilylpropanal-co-propanal) was 50 mJ/cm2 at the film thickness of 1.0 μm. A composite resist system consisting of a novolac resin and an aldehyde copolymer containing trimethylsilyl groups has also been developed and used as an alkaline-developable positive electron-beam and soft X-ray resist.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 1029-1032 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Polyolefinic thermoplastic elastomer (TPE) is a two-phase material in which cured EPDM (ethylene-propylene-diene rubber) particles are densely dispersed in a PP (polypropylene) matrix. It can be melt-processed at high temperatures and behaves like a vulcanized rubber at ambient temperature. The question is on its strain recovery, i.e., why the TPE can shrink back from the highly deformed states, even though the matrix consists of the ductile polymer. We constructed a two-dimensional model with four rubber inclusions in ductile matrix and carried out the elastic-plastic analysis on the deformation mechanism of the two-phase system by FEM (finite element method). FEM analysis revealed that, even at the highly deformed states at which almost the whole matrix has been yielded by the stress concentration, the ligament matrix between rubber inclusions in the stretching direction is locally preserved within an elastic limit and it acts as an “in-situ formed adhesive” for interconnecting rubber particles. It will provide a key mechanism of the strain recovery in the two-phase system.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 33 (1993), S. 175-182 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: The change in morphology and interface quantities have been analyzed for an immiscible polymer blend during reactive processing. A model polymer/polymer combination, hydroxy-terminated poly(ε-caprolactone)/liquid rubber with α, ω-carboxy groups, was employed. The blend was subjected to light scattering measurements, ellipsometry, and gel permeation chromatography (GPC). Size reduction of the dispersed phase during processing was followed by a systematic decrease in the correlation distance ζ and an increase in the specific interfacial area Ssp, both by the Debye-Bueche plot of light scattering profiles. Also observed was the time variation of the volume fraction of interface Vλ estimated as a product of the Ssp and the interfacial thickness by ellipsometry. The changes in ζ, Ssp, and Vλ with processing were accelerated when a coupling agent,γ-aminopropyltriethoxysilane (APS), was added. The amount of block copolymer formed in-situ in the APS-loaded system was estimated by GPC with RI and UV detectors. For the size reduction kinetics in both APS-loaded and -unloaded systems, Rittinger's law was found to be applicable.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1863-1869 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: A ternary alloy of polyamide-6 (PA), poly(phenyleneether) (PPE), and rubber has a three-phase structure, in which PPE particles with rubber inclusions are dispersed in a PA matrix. This is an excellent thermoplastic with high impact strength and high heat resistance. To understand the morphology-properties relationship, we undertook a two-dimensional finite element method (FEM) analysis on the deformation mechanism of the ternary alloy. A three-phase model was constructed so that five hybrid particles of PPE-shell and rubber-core were embedded in the PA matrix. When the model was deformed at room temperature, the rubber domain induced yielding of the PPE-shell and the PA-matrix and at large strains the yielded zone expanded to pervade the whole space. This suggests that the toughening mechanism is essentially the same as in the binary alloy of PA and rubber (rubber-toughened PA). At higher temperatures (e.g., at 100°C) the stress concentration occurred not only in the PA matrix but also in the PPE-shell. It implies that the PPE-shell is highly responsible for bulk deformation, even though it is part of the dispersed phase. At high temperatures, the rigidity of PPE affects the alloy bulk rigidity so that the ternary system exhibits high heat resistance.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: The dispersions of both reactive and nonreactive polymer-polymer blend systems achieved in three different mixers are compared. The dispersions are prepared using an industrial scale twin-screw extruder, a laboratory internal mixer, and a miniature cup and rotor mixer. The morphology development in the three mixers is remarkably similar: The dispersed phase is stretched into sheets and ribbons; these sheets and ribbons then break into cylinders, which subsequently break into droplets via Rayleigh-type instabilities. Drop size distributions can be accurately predicted if we know the size of cylinders formed in the high shear fields of the mixer. There is a significant effect of quenching time on blend morphology - i.e, to properly evaluate mixing, blends must be quenched extremely quickly (well within a minute). Otherwise, we need to consider the morphology development during the quenching time, which may not be relevant to the mixing. There is a uniform shear stress in the miniature mixer, unlike the other mixers, which have varying stress levels. It is shown that a high stress level followed by a lower stress level is required in polymer blending to achieve efficient mixing. In the high stress level, the dispersed phase is stretched into extended shapes, which undergo instabilities and break up upon entering the low stress level. In the miniature mixer, the dispersed phase sees only one stress level, and thus very extended shapes persist at the end of mixing. The final dispersions in the twinscrew extruder and internal mixer at matched maximum shear rates are almost identical. For similar shear rates in the miniature mixer, the final dispersion of reactive blends is comparable to the other mixers. However, the miniature mixer does a poor job in dispersing high viscosity uncompatibilized blends, and the mixing conditions must be altered to obtain efficient mixing.
    Additional Material: 14 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 29 (1991), S. 1541-1546 
    ISSN: 0887-6266
    Keywords: blends, miscible, local order in ; light scattering, depolarized, by miscible blends of dissimilar polymers ; ordering and specific interaction in miscible blends of dissimilar polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Depolarized light scattering measurements on single-phase mixtures of dissimilar polymers, poly(methyl methacrylate) (PMMA)/poly (acrylonitrile-co-styrene) (SAN, AN content = 15 wt %) and PMMA/poly (vinylidene fluoride) (PVDF) were carried out. The effective mean-square optical anisotropy γ2 of the mixtures was found to be much higher than that estimated by the simple additivity of γ2 of component polymers. From the deviation, the order parameter (1 + J12) was estimated to be in a range of 2-13, depending on the blend composition. This suggests local ordering in the single-phase mixtures, i.e., nematic alignment of the locally stretched dissimilar chains. In contrast, the deviation was slight in the polymer/solvent systems, SAN/MMA (monomer) and PVDF/butanone. The degree of ordering decreased with increasing temperature. T. The Specific interaction evidenced by FTIR spectroscopy exhibited a similar temperature dependence. Thus, local ordering seems to be induced by specific interactions and chain connectivity. The temperature dependence of J12 was successfully described by the Landau-de Gennes theory; J-112 ∞ (T + T0)/ T, T0 being the isotropic-nematic transition temperature, as in the case of liquid crystals.
    Additional Material: 9 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 26 (1988), S. 807-816 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Blending brittle polymer particles in a ductile polymer matrix is a new way to obtain toughened plastics. Although the nylon-6/poly(acrylonitrile-co-styrene) (SAN) system is a ductile/brittle combination, the blend does not result in a toughened plastic. We have investigated the effect of adding a small amount of a third component, poly(styrene-co-maleic anhydride) (SMA), to the nylon/SAN system. SMA significantly improves the tensile and impact strength of the blend. Morphological observations indicate a finer dispersion of the SAN particles when SMA is present in the blend. The improved dispersion is attributed to the formation of nylon-SMA graft copolymer, and infrared analysis supports this supposition. That is, a “compatibilizer” seems to be produced during melt mixing of the ternary system. The role that the compatibilizer plays in improving the stress transfer in the two-phase system and its potential to induce a brittle-ductile transition of the glassy SAN particles are considered to explain the toughening mechanism.
    Additional Material: 7 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 26 (1988), S. 1761-1768 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Orientation relaxation of dissimilar chains in the molten miscible blends, poly(methyl methacrylate)/poly(vinylidene fluoride) and poly(methyl methacrylate)/poly(vinylidene fluoride-co-trifluoroethylene), were investigated by measuring (1) the change of infrared dichroic ratio with time after the uniaxial stretching of film specimens, (2) the shear stress relaxation spectrum, and (3) birefringence relaxation in shear. The dissimilar polymers showed an identical time variation of the normalized Hermans orientation function. The blend showed a relaxation spectrum with a single characteristic relaxation time τc, depending on the blend composition. The birefringence relaxed monotonically, remaining positive. These results suggest that the dissimilar polymers do not relax independently but cooperatively. This behavior may be induced by a constraint due to the specific interactions between the dissimilar polymers, e.g., weak hydrogen bonding. For the cooperative chain relaxation, a third power relationship was found; τc/τe vprop; (M/Me),3 where τe and Me are the relaxation time and molecular weight of entanglement strand, respectively, and M is the number average molecular weight in the blend.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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