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  • 1995-1999  (4)
  • Polymer and Materials Science  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 55-67 
    ISSN: 0887-624X
    Keywords: VPi ; ADMVN ; AIBN ; syndiotacticity-rich HMW PVA ; PVA microfibrillar fiber ; Pn ; saponification ; PVPi ; conversion ; initiation rate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl pivalate (VPi) was polymerized in bulk by ultraviolet-ray initiation at low temperatures using 2,2′-azobis(2,4-dimethylvaleronitrile) (ADMVN) and 2,2'-azobis(isobutyronitrile) (AIBN) as photoinitiators. High molecular weight (HMW) poly(vinyl pivalate) (PVPi), having a number-average degree of polymerization (Pn) of 13,000-28,000, was obtained at conversions below 30% and converted by saponification to a syndiotacticity-rich HMW poly(vinyl alcohol) (PVA) microfibrillar fiber with Pn of 7300-18,300, syndiotactic diad (S-diad) and triad contents of ∼ 64% and ∼ 39%, respectively, and crystal melting temperature (Tm) of ∼ 249°C. ADMVN gave higher Pn than AIBN. On the other hand, conversion was smaller with the former than with the latter, and it was found that the initiation rate of ADMVN was lower than that of AIBN. Pn of PVA was constant while Pn of the precursor PVPi increased with increasing conversion. The syndiotacticity, Tm and thermal stability of PVA obtained from PVPi were much superior to those of PVA derived from poly(vinyl acetate) prepared under the same polymerization conditions. Polymerization of VPi at lower temperatures gave PVA with higher syndiotacticity. © 1997 John Wiley & Sons, Inc.
    Additional Material: 15 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 62 (1996), S. 473-480 
    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 kinetics of polycondensation and copolycondensation reactions were investigated using bis(4-hydroxybutyl) terephthalate (BHBT) and bis (2-hydroxyethyl) terephthalate (BHET) as monomers. BHBT was prepared by ester interchange reaction of dimethyl terephthalate and 1,4-butanediol. BHBT and BHET were polymerized at 270°C in the presence of titanium tetrabutoxide (TBT) as a catalyst. Applying second-order kinetics for polycondensation, the rate constants of polycondensation of BHBT and BHET, k11 and k22, were calculated as 3.872 min-1 and 2.238 min-1, respectively. BHBT and BHET were also copolymerized at 270°C using TBT. The rate constants of crossreactions in the copolycondensation of BHBT and BHET, k12 and k21, were obtained by using the results obtained from a proton nuclear magnetic resonance (1H-NMR) spectroscopy and a high-performance liquid chromatography (HPLC). It was found that the rate constants during the copolycondensation of BHBT and BHET at 270°C decreased in the order k21 〉 k11〉 k22 〉 k12 and the monomer reactivity ratio of BHBT was four or five times larger than that of BHET. In calculating the crossreactions, the method by the 1H-NMR spectroscopy gave more accurate results than that by the HPLC. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1637-1645 
    ISSN: 0887-6266
    Keywords: ester interchange reaction ; Monte Carlo method ; copolymerization ; degree of randomness ; miscible polyester blend ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of reaction variables on the degree of randomness in copolymers formed by ester interchange reaction in miscible polyester melt blends were systematically investigated using a Monte Carlo method. Three reaction variables such as the molecular weight difference between two component polymers, the blend ratio, and the reaction ratio of end attack to bond flip, were particularly considered on the cubic lattice model. Ester interchange reactions were assumed to take place during reptational chain motions. It was found that the copolymerization was dependent upon the molecular weight difference and reaction ratio: As the molecular weight difference becomes smaller and when both end attack and bond flip reactions are involved simultaneously, the copolymerization is accelerated. However, the blend ratio does not affect the copolymerization process. This result is discussed in relation to the polymer chain conformation for the ester interchange reaction. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1637-1645, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 2175-2183 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conformational change of α-keratose in the polyelectrolyte complex (PEC) formation with chitosan was investigated by means of differential scanning calorimetry and infrared spectroscopy. The change of the secondary structure of α-keratose in the reaction mixture was estimated quantitatively with circular dichroic spectra by the curve fitting method. The α-helix structure of 30% and above of α-keratose was found to be destructed and transformed into random structures at a mixing ratio of maximum PEC formation.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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