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  • Polymer and Materials Science  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1287-1299 
    ISSN: 0887-624X
    Keywords: ester interchange ; triglyceride oil ; poly(ethylene terephthalate) ; copolymer ; castor oil ; vernonia oil ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Naturally functionalized triglyceride oils are renewable resources which contain reactive chemical groups, hydroxyl in the case of castor oil, and epoxide in the case of vernonia oil. In this article, the reaction of these groups, and the ester linkages between the glycerol and acid residue portions of the oil molecule with poly(ethylene terephthalate) (PET) is investigated through a variety of means. Multiple reactions are possible in the triglyceride-PET system, some of which form a copolymer that increases miscibility, and if allowed to continue, forms a completely random copolymer mixture. Among the numerous reactions possible, PET-ester exchange with the hydroxyl or epoxide functionality of the triglyceride oils is found to be the most significant, and the effects of these and other reactions are observed and structural implications discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 953-968 
    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: Semi-interpenetrating networks have been synthesized from vernonia oil-sebacic acid polyester network and poly(ethylene terephthalate) (PET). Bond interchange reactions during mixing of the two materials led to the formation of a miscible copolymer mixture, in which the vernonia oil was then cross-linked with sebacic acid. The materials were phase-separated, exhibiting two glass transitions, when the network was synthesized at 160°C, below the crystallization temperature of PET: however, a single stable glass transition (Tg) results after the material is heated to above the melting temperature of PET and cooled. When the vernonia polyester network was completely formed at 250°C, above the crystallization temperature of PET, noncrystalline, single-Tg material was created. The two-phase semi-IPNs were much tougher than were their constituent materials, with the 50% semi-IPN over 15 times tougher than the PET from which it was made and over 50 times tougher than the neat vernonia oil elastomer, with tensile energy to break of 1780 kJ/m3. The single-Tg material was nearly 2.5 times as tough as the two-phase material, with energy to break of 4400 kJ/m3. The microstructure of the two-phase 50% semi-IPN was investigated by transmission electron microscopy, which showed regularly shaped spherulites of 10-20 μm in diameter, as compared to irregularly shaped spherulites observed in a similar 50/50 castor oil urethane/PET semi-IPN, in which the network formed simultaneously with PET crystallization. Scanning electron microscopy of the semi-IPN fracture surfaces showed microscopic fibrils several hundred nanometers in diameter in both the two-phase and single-Tg materials, although only the two-phase semi-IPN had a macroscopically rough surface. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 1035-1050 
    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 crystallization of poly(ethylene terephthalate) (PET) in blends with naturally functionalized triglyceride oils and their networks has been investigated. Crystallization kinetics of PET in the presence of small amounts of castor oil is improved, both in cooling from the melt state, and in heating from the glassy state. In conjunction with the nucleating agent sodium benzoate, either chemically bonded to castor oil or as a simple mixture, even greater enhancements of crystallization are observed. The PET crystallinity in semi-IPNs and blends of low to intermediate castor oil-HMDI polyurethane content are higher than that of neat PET (on a per gram of PET basis). Crystallinity in compositions with a high triglyceride oil network content is greatly affected by the presence of the network, with large melting point depressions, and loss in overall crystallinity. In cases where the triglyceride oil network is completely formed in a miscible melt with PET, the PET is unable to crystallize on cooling, resulting in amorphous semi-IPNs. Plasticization due to the oil, nucleation from added agents, bond interchange reactions between the oil and the PET, overall chemical composition, and the presence of a triglyceride oil network are found to have a controlling influence over the type and extent of PET crystallinity in the compositions. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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