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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 435-441 
    ISSN: 0887-624X
    Keywords: macro-azoinitiator ; polyarylate ; polystyrene ; block copolymer ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A macro-azoinitiator containing polyarylate segment and azo group was prepared by the solution polycondensation of azobiscyanopentanoyl chloride and hydroxy-terminated polyarylates having viscosity-average molecular weights of 6200, 8100, and 12 400. These macro-azoinitiators were used in the radical polymerization of styrene to synthesize polyarylate-polystyrene block copolymers. Thermal properties measured by the differential scanning calorimetry indicated the phase separated morphology of the block copolymers except at low molecular weight of the block constituents. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 2
    ISSN: 0935-9648
    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
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 217 (1994), S. 9-17 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Phasenverhalten und der bistabile elektro-optische Effekt von Mischungen eines flüssigkristallinen Polymeren mit Farbstoff-Seitengruppen (LCP) und eines niedermolekularen Flüssigkristallgemisches (LC) wurden untersucht. Das smektische Farbstoff-LCP ist mit dem nematischen LC in einem weiten Konzentrations- und Temperaturbereich mischbar. Die Mischungen lassen sich in einem elektrischen Wechselfeld bei niedrigen und hohen Frequenzen reversibel vom trüben in den transparenten Zustand schalten. Beide Zustände sind auch bei ausgeschaltetem Wechselfeld stabil.
    Notes: Phase behaviour and bistable effect of dye side chain liquid crystalline polymer (dye LCP)/low molecular weight liquid crystal (LC) mixtures have been investigated. The smectic dye LCP was observed to be miscible with the nematic LC over wide ranges of concentration and temperature. The electro-optical effects of the dye LCP/LC mixtures could be classified into the turbid and the transparent states upon a respective application of electric fields at low and high frequencies. Both transparent and turbid states of the mixture could be maintained stable, despite an electric field having been turned off.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 29-35 
    ISSN: 0887-6266
    Keywords: FTIR ; ion-dipole interaction ; ionomer ; poly(ethylone oxide) ; styrene-sodium methacrylate copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fourier-transform infrared (FTIR) spectroscopy was used to examine specific interactions contributing to the partial miscibility in blends of styrene-sodium methacrylate copolymer (S-NaMA) and poly(ethylene oxide) (PEO). From the shifts of carboxylatelon and ether group stretching bands, an important specific interaction was found involving ion-dipole bonding between the ionic group in styrene ionomer and the ether group in PEO. The asymmetric stretching vibration frequency of the carboxylate ion group increases as the fractional amount of PEO in the blend is increased, while the symmetric stretching frequency is decreased. The transition value of the fraction of PEO, above which both vibration frequencies of the carboxylate ion mentioned above remained almost unchanged, increases as the concentration of ionic groups in ionomer is increased. The ether group stretching band shifts to higher frequencies as the PEO content in the ionomer/PEO blend is increased. From the differential scanning calorimetry (DSC) and FTIR studies, we find that the iondipole interaction is the important mechanism that determines the miscibility of S-NaMA/PEO blends. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 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. 69-83 
    ISSN: 0887-6266
    Keywords: epoxy resin ; poly(ether sulfone) ; physical aging ; DSC ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The physical aging process of 4,4′-diaminodiphenylsulfone (DDS) cured diglycidyl ether bisphenol-A (DGEBA) blended with poly(ether sulfone) (PES) was studied by differential scanning calorimetry (DSC) at four aging temperatures between Tg-50°C and Tg-10°C. At aging temperatures between Tg-50 and Tg-30°C, the experimental results of epoxy resin blended with 20 wt% of PES showed two enthalpy relaxation processes. One relaxation process was due to the physical aging of PES, the other relaxation process was due to the physical aging of epoxy resin. The distribution of enthalpy relaxation process due to physical aging of epoxy resin in the blend was broader and the characteristic relaxation time shorter than those of pure epoxy resin at the above aging temperatures (between Tg-50 and Tg-30°C). At an aging temperature between Tg-30 and Tg-10°C, only one enthalpy relaxation process was found for the epoxy resin blended with PES, the relaxation process was similar to that of pure epoxy resin. The enthalpy relaxation process due to the physical aging of PES in the epoxy matrix was similar to that of pure PES at aging temperatures between Tg-50 and Tg-10°C. © 1997 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 198 (1997), S. 2373-2386 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Enthalpy relaxation due to physical aging of hydroxyl-terminated poly(ether sulfone)s (PES) with various molecular weights was studied by DSC at three aging temperatures between Tg - 45°C and Tg - 10°C. The experimental results revealed that both the average enthalpy relaxation time 〈τ〉 and limiting enthalpy relaxation ΔH∞ decrease slightly with increasing molecular weight for PESs aged at the same temperature intervals Tg - Ta (where Ta 〈 Tg). This behavior is not quite consistent with the enthalpy relaxation process of polystyrene. Agrawal reported that the relaxation spectra for polystyrenes with different molecular weights could be superimposed when Tg - Ta was the same. The experimental results of the present work suggest that the motion of segments is affected by intermolecular hydrogen bonding through the —OH groups of the PES chain ends.
    Additional Material: 8 Ill.
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  • 7
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Model supports consisting of a thin layer of SiO2 on a silicon single crystal have been used to study ZrO2/SiO2/Si model systems made by the same wet chemical preparation methods as used in the preparation of technical catalysts. The results obtained with the models are in good agreement with those on ZrO2 catalysts on porous silica supports.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 215-221 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dependence of the molecular dimension of polypeptides in helicogenic solvents on molecular weight was calculated by using the Zimm-Bragg-Nagai theory in collaboration with the broken-rod model, in which the excluded volume effect was taken into account by setting the equivalent chain to be a nonintersecting chain. Our calculated results for PBLG in helicogenic solvents were compared with experiment with good agreement. The flexibility of the helices of PCBL and PELG as broken rods corresponded to that of PBLG without excluded volume effect (i.e., the broken rod of a self-intersecting chain) in a comparison of their experimental data with our calculated results for PBLG of self-intersecting and nonintersecting chains. Over a wide range of molecular weights M our theory explains the dependence of the length per monomeric residue h on M, even for short chains in which h 〉 1.5 Å.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1119-1124 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For calculating the ratio of the intrinsic viscosities of branched and linear polymers of the same molecular weight, [η]B/[η]L, a new theory taking into account the excluded volume effect is presented. By using the modified Flory equation, the excluded volume effect of branched polymers is predicted with the aid of the first-order perturbation theory. The linear expansion factor αs is converted to the hydrodynamic expansion factor αη by using the Kurata-Yamakawa theory. Our calculated results, i.e., [η]B/[η]L and 〈s2〉B/〈s2〉L, agree well with experiment for various type branched polymers, i.e., randomly branched and comb-shaped polymers of poly(vinyl acetate).
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 54 (1982), S. 193-202 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Development of crystallizers. The control of the crystallization kinetics and the spatial variation of the crystal mass are of decisive importance for the operation of industrial crystallizers. The influence of micro- and macro-attrition is demonstrated with particular reference to collisions with impeller blades and to breakage of crystals between impeller and draft tube. Spatial variations of supersaturation and crystal mass within the crystallizer have been shown to influence crystal size distribution. These variations are described by physical and mathematical models. Crystal size distributions measured in both pilot and industrial crystallizers show that simulation with the proposed models is very reliable. A model approach provides valuable support for the development of industrial crystallizers and also for the development of control using microprocessors.
    Additional Material: 10 Ill.
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