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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1775-1782 
    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: To prepare self-emulsificable urethane acrylate resin, PEG-modified urethane acrylates (PMUA), containing polyoxyethylene chains as a terminal hydrophilic group and urethane acrylate anionomers (UAA) incorporated dimethylolpropionic acid (DMPA) as a pendant hydrophilic one were synthesized. For PMUA emulsions, the reaction molar ratio of PEG to 2-hydroxyethyl methacrylate (2-HEMA) significantly influenced the viscosity and droplet size of the emulsion and tensile strength of cured films. These emulsions were stable to pH change and the addition of electrolyte, but coagulated around 60°C. In the case of UAA, emulsions, however, were very stable to elevated temperatures and coagulated in adding even a little bit of electrolyte. For soap-free emulsions of the mixture of PMUA and UAA, emulsion stabilities of these mixtures against temperature, pH change, the addition of electrolyte, and the rate of shear and freeze-thaw increased synergetically. Additionally, the tensile strength of cured films was also improved. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 2429-2436 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to prepare the soap-free emulsion of urethane acrylates, poly(ethylene glycol)-modified urethane acrylates (PMUA), containing poly(oxyethylene) chains as terminal groups, were synthesized by reaction of poly(ethylene glycol) (PEG) with residual isocyanate groups. The size of the droplets of PMUA emulsions decreases as the molar ratio of PEG to 2-hydroxyethyl methacrylate (2-HEMA) increases. The interfacial activity of PMUA was confirmed by the measurement of the adsorption isotherm at the water/benzene interface. The chain length of poly(oxyethylene) and the type of polyol (PTMG, PPG) affects significantly the size of the droplets and the stability of the PMUA emulsions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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