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  • Polymer and Materials Science  (4)
  • Astrophysics
  • electric utility
  • 1995-1999  (4)
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1075-1079 
    ISSN: 1022-1352
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polymer nanoparticles were prepared from monomers such as styrene (St), butyl methacrylate (BMA), butyl acrylate (BA), methyl methacrylate (MMA), and methyl acrylate (MA) using a modified microemulsion polymerization process. With this process high polymer: surfactant weight ratios (7 : 1 or greater), relatively concentrated (10-30 wt.-%) latexes and small (10-20 nm) particle diameters were attained. Nucleation mechanisms were investigated through observations of the particle size change during the polymerization.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1927-1938 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A descriptive model was developed, using viscometry and light scattering, that explains the anomalous rheological behavior of solutions of amphiphilic acrylic copolymers upon the addition of water. The rheological behavior can be explained by considering the relative magnitudes of three interactions: the intra-and intermolecular electrostatic interactions between the ionizable acid groups in the copolymer, the intramolecular hydrophobic in-teractions, and the intermolecular hydrophobic interactions. The initial addition of water enhances the ionization of the acid groups, causing the electrostatic interactions between the acid groups to dominate the other two interactions. This leads to expansion of the polymer molecules and, consequently, to a relatively constant viscosity during dilution with water. Upon attaining the maximum ionization of the acid groups on the chain, the intra-molecular hydrophobic interactions dominate the electrostatic repulsion, and the chains start to contract. Further addition of water leads to aggregation of the polymer chains into large polymolecular domains, resulting in a sharp decrease in the viscosity. Intermolecular hydrophobic interactions dominate the rheological behavior in this stage of water dilution. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1609-1618 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Oligomers derived from terephthalic acid and 1,6-hexanediol or 1,10-decanediol have been chemically modified through end-grafting with succinic anhydride or trimellitic anhydride followed by glycidyl neodecanoate. The grafted oligomers are paste-like semisolids or viscous liquids at room temperature. As the grafted oligomers are heated, their viscosity goes down to a minimum, then up to a maximum, and then down again. Combined DSC, crossed polarizing microscopy, and wide-angle x-ray diffraction indicate that the grafted oligomers form crystalline domains dispersed in amorphous phase. The grafted oligomers are soluble in common organic solvents, such as toluene, at lower concentrations (〈14-51 wt %) and form stable dispersions at higher concentrations. High solid coatings formulated with mel-amine or isocyanate resins gave glossy films with excellent combined hardness and impact resistance. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1237-1251 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: 13C-nuclear magnetic resonance (NMR) spectroscopy was employed to study the linkages in three commercial fully methylocated melamine-formaldehyde (HMMM) resins and their partially self-condensed resins by acid catalysis, in order to probe the structures linking melamine units. Distortionless enhancement by polarization transfer (DEPT) experiments show that the partially self-condensed resins contain both methylene ether and methylene linkages between melamine units. The extent of these linkages were estimated by quantitative 13C-NMR spectroscopy using inverse gated decoupling techniques. The results show that the ratios of methylene ether and methylene linkages to the triazine moiety vary from resin to resin. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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