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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. 625-631 
    ISSN: 0887-624X
    Keywords: copolymers ; furfuryl acrylate ; hydroxyethyl methacrylate ; biomaterials ; glass transition temperature ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of furfuryl acrylate (F) and 2-hydroxyethyl methacrylate (H) were prepared by free radical polymerization in DMF solution at 50°C, using 2,2′-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were calculated according to the general copolymerization equation using the Fineman-Ross and Kelen-Tüdös linearization methods, as well as the Tidwell and Mortimer nonlinear least-squares treatment. The reactivity ratios obtained were rF = 0.93 and rH = 1.42. The microstructure of copolymer chains is described on the basis of first-order Markov statistics, and the copolymer glass transition temperatures were determined calorimetrically. The variation of Tg with the copolymer composition is discussed according to modern methods, considering the sequence distribution of monomeric units along the copolymer chains. Also the Tg of the corresponding homopolymers was determined giving the values Tg(F) = 321 K and Tg(H) = 358 K, whereas the Tg of the corresponding alternating diad has an average value of TgFH = 326 K. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2759-2766 
    ISSN: 0887-624X
    Keywords: fotopolymerization ; free radical polymerization ; furfuryl acrylate ; furfuryl methacrylate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect and the participation of the furfuryl ring, in particular the hydrogen at position C-5 in the free radical polymerization are analyzed following the polymerization of furfuryl acrylate (FA) and furfuryl methacrylate (FM) initiated by AIBN under photochemical activation. The results obtained indicate that the polymerization of FA deviates from the classical free radical kinetic scheme, giving rise to crosslinked polymers even at a degree of conversion lower than 7%. This behavior is well explained taking into consideration the participation of the furfuryl ring which acts as a degradative transfer agent. This was demonstrated by the kinetic analysis of the free radical polymerization of MMA initiated by the thermal decomposition of AIBN in the presence of different concentrations of furfuryl acetate. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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