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  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Tetramethyl bisphenol-A polyarylate (TMPAR) was miscible with poly(styrene-coacryloni trile) 's(SANs) containing 4, 7, 10, and 13wt% of acrylonitrile(AN) repeating unit. As the content of tetrabromo bisphenol-A polyarylate(TBPAR) repeating unit in the random copolymer of TMPAR and TBPAR was increased, the miscibility window in the blends with SANs was narrowed. The intramolecular repulsion between styrene and AN repeating units in SAN was suggested to be the main driving force for the miscibility of SANs with the random copolymers of TMPAR and TBPAR.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 30 (1993), S. 461-467 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Poly(styrene-co-vinyl phenol) (STVPh)/poly(ɛ-caprolactone)(PCL) blends showed enhanced miscibility over polystyrene/PCL blend, and showed single glass transition temperature when the contents of vinyl phenol (VPh) in copolymer were higher than 10 wt % (maximum content of VPh in STVPh used in this study was 20 wt%). STVPh 4, STVPh 7, STVPh 10 (4, 7, 10 were VPh wt%)/PCL blends showed cloud points on heating for miscible blend system, and this phase separation was reversible on cooling. From melting point depression of PCL, interaction parameter, B. for miscible STVPh 12/PCL blend system was evaluated.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 37 (1996), S. 361-367 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The polyamides with aromatic rings in the main chain were synthesized by the solution polymerization of 4,4′-diphenylmethane diisocyanate and aliphatic dicarboxylic acid in the presence of catalyst. The thermal properties and the miscibility behaviours with polyamide-6,6 of these aromatic polyamides were studied. The aromatic polyamides synthesized with one kind of dicarboxylic acid had typical thermal properties of crystalline polymers, whereas those synthesized with the mixtures of dicarboxylic acids were not easily crystallized. The observed miscibility behaviours showed some differences from those predicted by binary interaction model.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 35 (2000), S. 1579-1583 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Segmented thermoplastic polyurethanes (TPUs), which consist of an amorphous soft segment from 1,3-butanediol and hexamethylene diisocyanate (HDI) and a crystalline hard segment from 4,4′-bis-(6-hydroxy hexoxy)biphenyl and tolylene 2,4-diisocyanate were synthesized. Their thermal and mechanical properties, shape memory effect, utilizing amorphous soft segment domain as reversible phase and crystalline hard segment domain as frozen phase, were examined. The reversibility observed on repeated deformation was improved as the magnitude of deformation was reduced and the hard segment content was increased, or by crosslinking with excess HDI.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 194 (1992), S. 91-101 
    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: In der vorliegenden Arbeit wurden die strukturellen, thermischen, rheologischen und molekularen Eigenschaften von Polyethylen ultraniedriger Dichte (PE-ULD) untersucht. Da PE-ULD hauptsächlich als Modifikator von anderen Polyolefinen verwendet wird, wurde das rheologische Verhalten besonders ausführlich untersucht.
    Notes: Ultra low density polyethylene (PE-ULD), the newest and most recently commercialized member of polyethylene family, has been characterized in terms of structure, thermal and rheological properties, and molecular parameters. Since the prime use of PE-ULD is polyolefin modifier, emphasis is put on the melt rheology of the samples to provide data base for blending with other resins.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 192 (1991), S. 133-144 
    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 Phasen- und Mischbarkeitsverhalten der binären und ternären Polymermischungen von Polyarylat (PAR), Phenoxid und Poly(butylenterephthalat) (PBT) wurde untersucht. Die Mischungen wurden durch Ausfällen aus gemeinsamen Lösungen hergestellt, und die Mischbarkeit wurde durch DSC-Messungen und Transparenz der Schmelze beurteilt. Im Falle der binären Blends zeigten PAR/PBT und Phenoxid/PBT Mischbarkeit, während sich PAR/Phenoxid nicht mischen ließ. Die Mischbarkeitstendenz der unmischbaren PAR/Phenoxid-Mischungen konnte jedoch durch Zugabe von PBT erhöht werden; eine ausreichende Menge PBT machte die ternären Mischungen mischbar, so daß diese eine einzige Tg in der DSC-Kurve zeigten. Im ternären Phasendiagramm war das Maximum der Mischbarkeitsgrenze in Richtung auf die Phenoxidseite hin verschoben, was auf die bessere Mischbarkeit von PAR/PBT im Vergleich zu Phenoxid/PBT zurückgeführt wird.
    Notes: The phase and miscibility behavior of binary and ternary blends containing polyarylate (PAR), polyhydroxyether of bisphenol AIUPAC: poly[oxy(2-hydroxytrimethylene)oxy-1,4-phenylene-isopropylidene-1,4-phenylene]. (Phenoxy), and poly(butylene terephthalate) (PBT) were studied. The blends were prepared by solution-precipitation method and miscibility was examined by DSC and melt transparency. In binary blends, PAR/PBT and Phenoxy/PBT blends show miscibility, while PAR/Phenoxy appeared to be immiscible. However, the miscibility of incompatible PAR/Phenoxy blend was enhanced by addition of PBT. The addition of sufficient amount of PBT caused the ternary blend to have a single glass transition temperature. The shape of miscibility boundary of ternary blend was skewed to the apex of Phenoxy, which was attributed to the better miscibility of PAR/PBT than that of Phenoxy/PBT.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 21-28 
    ISSN: 0887-6266
    Keywords: polyarylate ; polystyrene ; block copolymer ; compatibility ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The compatibilizing effect of polyarylate-polystyrene (PAR-PS) block copolymer prepared from macroazo initiator was examined in polyarylate/polystyrene blends from the view-points of morphology, density, and thermal, mechanical, and rheological properties. PARPS block copolymer enhanced the mutual dissolution of the homopolymers. Reduced dispersed-domain size and increased density showed the efficiency of the block copolymer as a compatibilizing agent. Results from mechanical and rheological properties could also be explained by the compatibilizing effect of PAR-PS block copolymer in the blends. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 15 (1994), S. 265-270 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 36 (1995), S. 239-245 
    ISSN: 0959-8103
    Keywords: poly(esterurethane) ; copolyamide segments ; thermal and mechanical properties ; 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: Thermoplastic polyurethane elastomers (TPUs) from diol-terminated poly(ethylene adipate) (PEA), 1,4-butanediol (BD) and 4,4′-diphenylmethane-diisocyanate (MDI) were modified by copolymerizing with diamine-terminated nylon-6/6,6 copolyamide (CPA) oligomers. The effects of content and molecular weight of CPA segments on the thermal and mechanical properties of TPU were studied. PEA segments showed enhanced crystallization when some of the hard segments were replaced by CPA segments, showing weaker CPA-PEA interaction. The crystallinity of the hard segments was reduced, probably due to some interaction and phase mixing between hard and CPA segments. The modulus of TPU also decreased, more markedly with CPA segments of higher molecular weight.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1805-1818 
    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: Rheological properties of two polyesters; poly(ethylene terephthalate) (PET) and bisphenol A-50/50 isophthalic/terephthalic acid based polyarylate (PAR), and their 85/15, 50/50, and 30/70 (PET/PAR) blends were investigated using a RDS rheometer, 290-310°C. Measurements included complex viscosity and modulus. Activation energy for flow and relaxation spectrum were subsequently calculated. Results indicated that PET/PAR blends are rheologically incompatible, i.e., zero-shear viscosities of the blends showed a negative deviation from the averages of the two homopolymers with a sharp minimum at 85/15 composition. The relaxation spectrum for 85/15 blend also showed a relaxation plateau, a characteristic of rigid particle suspension. The morphology of the polymer blends was examined from cryogenically fractured and etched surface using a scanning electron microscopy (SEM). Morphological observation indicated that PAR-rich phases, order of 0.1μm, were finely dispersed in PET phase for 85/15 blend, whereas the dispersion of PET phase in PAR-rich phase was in spherical form, order of 0.5μm in diameter, for the 50/50 blend.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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