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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 555 (Sept. 2007), p. 459-465 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Molded polyurethane foams for car seats are based on petrochemical polyols ofmolecular weight 4000-6000 and copolymer polyols containing micron size polymeric particles.Copolymer polyols (CPP) typically constitute 30% of the mixture with the base polyol. They helpcell opening, increase load bearing and tear strength of the foams, but they are relatively expensive.Hyperbranched polyols of petrochemical origin were used in molded foams.[1] They are solid inthe pure form and due to high crosslinking density could be incorporated at low concentration inconjunction with copolymer polyols. Instead, we have made hyperbranched polyols which could bea total replacement for CPP in molded foams. Six hyperbranched polyols with primary andsecondary hydroxyl groups and different hydroxyl numbers were prepared from soybean oil andtested in flexible foams. Novel polyols were liquid even at very high molecular weights and couldcompletely replace copolymer polyols. Functionality of these polyols increased linearly withmolecular weight to very high values, resulting eventually in their high crosslinking power. Theeffects of the type of hydroxyl groups (primary vs. secondary), hydroxyl number (from 85 to 135mg KOH/g), and concentration (7.5-30%) in the mixture with the base polyol on foam propertieswere analyzed. It was found that hyperbranched polyols could replace copolymer polyolscompletely but their effect on cell morphology and mechanical properties varied with the type ofpolyol and concentration
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 267 (1989), S. 1077-1086 
    ISSN: 1435-1536
    Keywords: Dielectricproperties ; polyurethane ; elastomers ; phaseseparation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Three series of segmented polyurethanes based on MDI, variable chain extender, and polypropylene oxide of MW=1000, 2000, and 3000 were synthesized and their dielectric behavior examined. Dielectric relaxations in the segmented polyurethanes were investigated between −150°C and +150°C in the 100 Hz to 10 kHz range. In general, three transitions, designated asα, β, and γ were observed, and ascribed in accordance with calorimetric relaxations to glass transitions of the hard and soft segments, and Shatzki-type motions, respectively. The effect of structure variables such as soft segment size, type of chain extender (ethylene glycol, butane diol, and hexane diol) and soft segment concentration, as well as the effect of interaction of the phases on dielectric properties was discussed. It was found that a certain degree of phase mixing exists in all series, detected by the variation of theT g of the soft segment with soft segment concentration, contrary to DSC results, which was ascribed to thermal treatment prior to the dielectric measurements. It appears that interfacial polarization becomes important only above theα transition temperature.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 977-986 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating copolymers of α-methylstyrene (α-MeSt) and maleic anhydride (MAn) were prepared by free-radical-initiated polymerization in bulk, benzene, or butanone as solvents. By applying the generalized model described by Shirota and co-workers, the reactivity ratios k1c/k12 and k2c/k21 were calculated from the change of copolymerization rate with monomer feed at constant total monomer concentration. From the equation Rp = Rp(f) + Rp(CT) were calculated Rp(f) and Rp(CT), and it was found that in benzene the reaction proceeds predominantly by the addition of CT-complex monomers, while in butanone, cross propagation of free monomers predominates. Termination occurs predominantly by homotermination of α-MeSt macro free radicals, kt22, although the cross termination kt21 is also operative.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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