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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 401-411 
    ISSN: 0887-624X
    Keywords: novolac resin ; poly(ethylene oxide) ; interpolymer complexes ; crosslinkable ; polymer morphology ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crosslinkable interpolymer complexes of novolac resin and poly(ethylene oxide) (PEO) were prepared by mutual mixing ethanol solutions of novolac and PEO. Fourier transform infrared (FTIR) studies revealed that the driving force for the formation of novolac/PEO complex is hydrogen bonding interaction between the hydroxyl groups of novolac and the ether oxygens of PEO. The morphology and thermal properties of the complexes before and after curing were investigated by optical microscopy and differential scanning calorimetry (DSC). It was found that the uncured novolac/PEO complexes had a single composition-dependent glass transition temperature (Tg). The curing with 15 wt % hexamine (HMTA) (relative to novolac content) resulted in disappearing of Tg behaviour for both the neat novolac and the novolac-rich complexes, owing to less mobility of the novolac chain segments. The melting temperature (Tm) and crystallization rate of the HMTA-cured novolac/PEO complexes decreased with increasing novolac content, and no Tm was observed for the cured complexes with PEO content less than 50%. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 401-411, 1998
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 315-322 
    ISSN: 0959-8103
    Keywords: poly(N-vinyl-2-pyrrolidone) ; novolac resin ; interpolymer complexes ; polymer blends ; crosslinking ; 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 formation of complexes between poly(N-vinyl-2-pyrrolidone) (PVP) and novolac resin in various solvents was studied. Interpolymer complexes were formed in methanol, ethanol, 2-butanone, cyclohexanone and N,N-dimethylformamide (DMF). However, only polymer blends were obtained in N-methyl-2-pyrrolidone. The nature of the solvent has a profound influence on the degree of interpolymer association. The formation of 1/1 and 2/1 ([novolac]/[PVP]) interpolymer complexes in DMF solution was shown by measurements of reduced viscosity, conductivity and clear point. Differential scanning calorimetry revealed the single-phase nature of both the blends and the complexes of uncured novolac/PVP. The complexes had higher glass transition temperatures than those of the blends with the same composition, and the strength of the interactions between the components in the complex is much higher than that in the blend. The driving force in the formation of the interpolymer complexes between novolac and PVP is the hydrogen-bonding interaction between the hydroxyl of the novolac and the proton-accepting groups of PVP. Both the blends and the complexes were cured with 15 wt% hexamethylenetetramine relative to novolac content. The cured novolac/PVP blends were only partially miscible, but significant amounts of complex still existed in the cured complexes. Fourier transfer infrared spectroscopy revealed that the interaction between the components was rather strong for both the uncured and cured blends.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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