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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 32 (1997), S. 3571-3575 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The synthesis of the title matrix-mediated nanocomposite was performed in both poly(4-vinylpyridine) homopolymer and vinylstyrene-4-vinylpyridine copolymers. NH2–NH2 was used as the reducing agent to prepare the polymer-supported metallic particles which were later converted into fine oxide powders by oxidation. The structure and morphology of the products were studied by Fourier transform infrared spectroscopy, wide angle X-ray diffraction, transmission electron microscopy as well as electron spectroscopy for chemical analysis and magnetic measurements. The wide angle X-ray diffraction patterns contained reflections that could be assigned to Fe3O4 particles while no reflections were observed that correspond to ultrafine iron powders. The magnetization behaviour of the nanocomposite was determined by the degree of loading of Fe in the polymer matrix.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 37 (1996), S. 377-383 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary A new type of coordination polyurethane was prepared by incorporating the transition metal ions into the pyridine containing thermoplastic polyurethane films. Then the metal ions dispersed in the polyurethane matrix were reduced by controlling the exposure of the metal sites to NaBH4 under mild condition. The reduction of the polyurethane metal complex films resulted in the production of amorphous ultrafine metal powders. The size of these powders was controlled by the content of the metal ions and the polarity of the polymer matrix. A polar polymer backbone and lower metal ion concentration favored to achieve a smaller particle. It was also found that the polymer chains prohibited the excessive aggregation of the metal atoms and have protective effect on the final metal powders.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Ion conducting polyurethane electrolyte with redox active ferrocene groups which are fixed to the polymer backbone by covalent bonds was prepared. It has been found that the resulting polyurethane electrolyte has high conductivity even at lower temperature. And the temperature dependence of conductivity follows well the Arrhenius equation. Solid state electrochemical property was measured by cyclic voltammetric method with microdisk electrodes at different temperature. The results indicated that the polyurethane electrolyte has good redox stability, as well as reiteration, and show electrochemical activity in the solid state.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1539-1546 
    ISSN: 0887-6266
    Keywords: nucleophilic substitution ; polyurethane metal complexes (PUC) ; coordination interaction ; phase separation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: N-Picolyl polyurethanes (PUPY) were synthesized by nucleophilic substitution. The blends of these polyurethanes with various of transition metal chlorides [cobalt(II), nickel(II), and copper(II)] were studied by spectroscopic and thermal analysis. Ultraviolet-visible and infrared spectroscopic evidence indicates that a tetrahedral cobalt(II) complex with two pendent picolyl groups in the first-shell coordination sphere of Co2+ is formed in a series of blends with different molar ratio (from 10/1 to 2/1) of picolyl groups to cobalt(II) ions. According to the result of Small-Angle X-ray Scattering (SAXS), Differential Scanning Calorimetry (DSC), and Dynamic Mechanical Thermal Analysis (DMTA), coordination interaction between ligands in hard segments and metal ions provides a driving force for phase separation. The coordination strength of pyridine with Ni2+ is stronger than Co2+ and Cu2+. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1539-1546, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 651-668 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two series of polyurethane zwitterionomers based on 4,4′-methylene-di(phenyl isocyanate) (MDI), N-methyl diethanolamine (MDEA)Systematic IUPAC name: 2,2′-(methylimino)diethanol., and either 1350 molecular weight hydroxyl terminated polybutadiene or 1000 molecular weight poly(tetramethylene oxide)Systematic IUPAC name: poly(oxytetramethylene). were synthesized. Zwitterionization was accomplished by quaternizing the tertiary amine of MDEA with 1,3-pro-panesultone. In Both series, IR analysis suggests that the sulfonate ion SO3- associates with the counter ion on the chain extender and the acidic hydrogen of the urethane linkage. Ammonium sulfonation shifts the soft segment Tg of polyether-based material to lower temperatures suggesting that ionization improves microphase separation. The soft segment Tg of the polybutadiene system is unaffected by ionization. IR dichroism measurements show that with increasing ammonium sulfonation both the hard and soft segments in the polyether-polyurethane zwitterionomers orient to a greater extent with deformation. In contrast, in the poly-butadiene-based zwitterionomers the orientability of the hard segment decreased with ionization while the soft segment showed significant chain alignment. Coupling the dichroism measurements to stress-strain results suggests that the hard segment domains of the polyether-polyurethane system possess more of an interconnected structure, while the polybutadiene-poly-urethane system contains hard segment domains which are largely isolated. The formation of different morphologies in the two systems of zwitterionomers may be due to the different interdomain surface tensions.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 1027-1036 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Polyether polyurethanes based on 4,4′-diphenylmethane diisocyanate (MDI), N-methyl diethanolamine (MDEA), and polytetraniethylene oxide (PTMO) were synthesized with varying levels of hard segment content. The tertiary amine of MDEA was sulfonated with γ-propane sultone thereby converting the polyether polyurethane to a polymeric zwitterion. The effect of the chemical composition and the degree of ammonium sulfonation on the extent of phase segregation, and physical properties were studied by differential scanning calorimetry (DSC), dynamic mechanical analysis and tensile testing. It was found that the MDEA chain extender inhibits microphase separation of the polymer in the solid state. As the degree of ammonium sulfonation increases in the zwitterionomers, an improvement of phase separation and domain structure was observed. In addition the tensile properties change dramatically with increasing sulfonate content going from properties characteristic of soft, weak gum rubbers to those of hard, strong thermoplastic elastomers.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 799-806 
    ISSN: 0887-6266
    Keywords: ionomer ; polyether ; synthesis ; characterization ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this study, a series of polyether-ester ionomers was prepared by neutralizing the carboxylic acid groups in 1 : 1 copolymers of benzenetracarboxylic dianhydride (BTDA) and poly(tetramethylene oxide) or poly(ethylene oxide) glycol. The base polymers were in a liquid state while the ionomers were in solid state and a separate ionic phase was formed. The local structure and the morphology of the ionomers were investigated by dynamic mechanical analysis, Fourier transform infrared spectroscopy, and small-angle x-ray scattering as well as extended x-ray absorption fine structure. Clearly, the geometric structure of the ionic sites varied with the nature of the metal ions and the morphology of the ionomers was determined by the microstructure of the ion aggregates. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 799-806, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 745-751 
    ISSN: 0887-6266
    Keywords: polyurethane ionomer ; ionic conductivity ; single ion transport ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of lithium and sodium salts of sulfonated polyethylene oxide (PEO) polyurethane ionomers in different levels of ionization were prepared. It has been found that this material is a new type of ionic conductive polymer, characterized by a single-ion transport mechanism and good mechanical properties. The ionization level significantly influences the ionic conductivity of the samples. When the mole ratio of the metal ion and ether oxygen atom is about 0.05, the ionomers exhibit maximum cationic conductivity. An optimal cationic conductivity of 1.0 × 10-5 S/cm is obtained at about 70°C without any addition of organic plasticizer. The conductivity increases apparently when propylene carbonate and low MW PEO are added to the polyurethane ionomer. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 581-588 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyurethanes based on methylene bis(p-phenyl isocyanate), bis(hydroxymethyl) propanoic acid, and poly (tetramethylene oxide) were synthesized, and their morphology and physical properties investigated. The acid polyurethanes exhibited very poor phase separation and mechanical properties, but upon neutralization with alkali metals phase separation improved dramatically and the materials resembled tough elastomers. The choice of cation played a much less important role than hard segment content in determining morphology and properties. Small-angle x-ray scattering patterns of these ionic polyrethanes exhibit two peaks, one characteristic of scattering between the hard and soft domains and the other reflecting scattering from aggregates of ionic groups residing within the hard domains. While ionic aggregation is the primary driving force for phase separation in these materials, their morphology more closely resembles that for nonionic polyurethanes than that for conventional ionomers, because the ionic groups exist in blocks composed primarily of rigid diisocyanate residues.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 365-374 
    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: Two series of segmented polyurethanes based on 3/2/1 and 2/1/1 molar ratios of methylene diphenyldiisocyanate (MDI), N,N-bis (2-hydroxyethyl) isonicotinamide (BIN), and poly(tetramethylene oxide) (PTMO, MW = 1000) were synthesized and blended with different metal acetates. The thermal behavior and mechanical properties of the pyridinecontaining polyurethane precursors and their blends were characterized by DSC, DMTA, and tensile testing. The results suggest that coordination between pyridine groups in the hard segments and the metal ions in the acetates improves hard-domain cohesion and phase separation and, subsequently, has an effect on mechanical properties. The varying ability of the pyridine group to coordinate with different cations results in different extents of phase separation. The interaction of pyridine with Ni or Cu (II) is much stronger than with Zn. It is shown that coordination interactions can be a driving force for phase separation and hard-domain aggregation in multiblock copolymer systems. Two different morphologies are proposed for polyurethanes of differing stoichiometry to explain the differences in the results from DMTA and tensile testing. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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