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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1979-1984 
    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: Thermotropic behavior of hydroxyethyl celloulose acetate (HECA) was studied by polarizing microscopy, DSC, and X-ray diffraction. It was found that HECA was an anisotropic liquid between the temperature from 130 to 185°C on heating, and when the temperature was over 185°C, it became isotropic. In cooling, however, mesophase began to form at about 165°C. The transformation temperature decreased with decreasing molecular weight and the temperature region of transformation decreased with decreasing the distribution of the molecular weight for HECA. The kinetic ability of tranformation appeared the maximum with molecular weight. The HECA liquid crystal is cholesteric and the distance between layers of ordered molecular chains was enlarged when HECA was transformed from liquid crystalline glass to the liquid crystalline state. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 1479-1486 
    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: In this paper, the blends of the carbon dioxide copolymer, poly(propylene carbonate) (PPC), with nitrile rubber (NBR) were studied by DSC, DMA, TEM and TG. PPC can enhance the mechanical properties of NBR, while oil resistance and tensile set at break of NBR/PPC systems were as good as that of NBR. The coagent of triallylisocyanurate or maleic anhydride with carbon black can much improve the curing efficiency of dicumyl peroxide in NBR/PPC systems. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 654-664 
    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: An experimental and theoretical study of reaction injection molding (RIM) of polyurea was conducted in this work. A lab-scale RIM machine was used to carry out the polyurea bulk polymerizations. A “free-table” viscometer was designed to measure the fast rheological changes and liquid-solid transition. A mathematical model was proposed to simulate the fast reaction and rheological changes in the polyurea RIM process. The parameters of this model were determined based on the solution polymerization data from FTIR and Haake rheometer measurements. Combined with an appropriate heat transfer equation, this model predicts fairly well the adiabatic temperature and viscosity rises of bulk polyurea reactions in RIM.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 125-132 
    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: Ethyl-cyanoethyl cellulose (E-CE)C/poly (acrylic acid) (PAA) composites were prepared by polymerizing acrylic acid (AA) in (E-CE) C/AA cholesteric liquid crystalline solutions. The morphology and structure and the compatibility of composites prepared in different conditions were studied by small-angle light scattering (SALS), differential scanning calorimetry (DSC), X-ray spectrometry, polarizing microscopy, and electron microscopy. Ho-mogeneous composites with the cholesteric structure could be obtained by photopolymerization. During the photopolymerization, however, the morphology of the liquid crystalline domains became crylindric and the axial direction of the cylindric domain was at an angle of about 45° to the layers of the ordered molecular chains. The polymerization initiated by azobisisobutyronitrile (AIBN) resulted in the phase separation. The morphology of the liquid crystalline domains was maintained although the cholesteric structure of the composite was partly destroyed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 1371-1379 
    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 series of polyurethane adhesives - polyethyleneadipateurethane (PEAU), polybuthyleneadipateurethane (PBAU), and polyhexyleneadipateurethane (PHAU) - with the same MW and hard/soft segment ratio, based on the three polyesters polyethyleneadipate (PEA), polybuthyleneadipate (PBA), polyhexyleneadipate (PHA), with 4,4′-diphnylmethane diisocyanate (MDI), and butendiol were synthesized by solution polymerization. The crystallinity of these polyesters and polyurethanes (PUs) and the compatibility of blends of PUs with PVC were studied by means of wide-angle x-ray diffraction (WAXD), differential scanning calorimetry (DSC), dynamic thermomechanical analysis (DMA), testing of solubility, and phase contrast microscopy. The results indicated that PBAU/PVC and PHAU/PVC were compatible systems, but PEAU/PVC was incompatible. The adhesive strengths of the three adhesives were quite different from one another, in the order of PBAU ≥ PHAU ≫ PEAU. The influences of crystallinity and compatibility on adhesion were discussed, and the Diffusion Theory for PU-PVC systems was recommended. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 533-540 
    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: Ethyl-cyanoethyl cellulose [(E-CE)C]/cross-linked polystyrene (PS) composites were prepared via polymerization of styrene in (E-CE)C/styrene solution with glycol diacrylate as a cross-linking reagent. The polymerization of the solution, morphology, and miscibility of (E-CE)C/PS composites were studied with polarizing microscopy, small-angle light scattering (SALS), differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). It was found that the mixing state of the (E-CE)C/PS system and the thermal stability of composites were modified by cross-linking of PS. In the intensively cross-linked composite prepared from the anisotropic solution, there existed cylindrical domains in which (E-CE)C spherulites were dispersed in PS. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 55 (1995), S. 981-987 
    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: Two technical methods were developed for transcrystalline growth in order to create perfect transcrystalline growth for both thermoplastics and liquid crystalline polymers. A principle was suggested for oriented crystallization that the nucleation is created with high density along a one-dimensional or on a two-dimensional unit, while the nucleation in the matrix is suppressed. The steric hindrance was a key factor to create the transcrystalline growth in isothermal crystallization. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 493-498 
    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: The ethyl-cyanoethyl cellulose [(E-CE)C]/poly(acrylic acid) [PAA] composites were prepared via in situ photopolymerization of the (E-CE)C/acrylic acid (AA) solutions, in which the morphology and structure of (E-CE)C was retained as the same as that in the solution. The strength and the modulus of the composites depended on their morphology and structure. The strength of the composites with a completely amorphous state or with a completely cholesteric order did not significantly change with increasing (E-CE)C content, although the strength of the composites with completely cholesteric order is much higher than with the completely amorphous state. However, when the (E-CE)C content changed from 33.8% to 42.5%, in which the composites had both cholesteric order and amorphous phases, the strength of the composites greatly increased with increasing (E-CE)C. The elastic modulus of the composites with completely isotropic structure decreases with increasing (E-CE)C content but abruptly increases with increasing the fraction of cholesteric phase in the composites. The (E-CE)C with cholesteric order had a significant enhancing effect on the strength of the composites. The stress-strain curves indicated that the composites with completely amorphous or completely cholesteric order were breakable, while they were tough in the case when they had both cholesteric and amorphous phases. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 684-692 
    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 free radical copolymerization model is proposed for simulating the reaction rates and conversions of styrene monomer and unsaturated polyester resins during curing. This model is based on film theory in which the rate constants reflect both reaction and diffusion resistances. Differential scanning calorimetry in combination with Fourier transform infrared spectroscopy is used to measure the overall and individual reactivities of reacting species. Model parameters are determined from experimental data. The applicability of this model is demonstrated in a cure simulation.
    Additional Material: 6 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 1237-1245 
    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: Infrared absorbance measurements as a function of temperature down to 13°K have been made on poly(ethylene terephthalate) and polystyrene. Transition temperatures are assigned to the temperatures where there are abrupt changes in the absorbance or integrated band intensities. Bands of known structural origin arising from either crystal-line or amorphous phases are studied to probe the structure basis and environment effect for each transition. Transitions are found around 50, 120, 180, and 220°K for PET and around 50° and 235°K for polystyrene.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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