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  • Articles: DFG German National Licenses  (14)
  • 1985-1989  (14)
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  • Articles: DFG German National Licenses  (14)
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Years
Year
  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 140 (1986), S. 127-134 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die chemischen Reaktionen im Hydrolysat von epoxy-funktionalisierten Silanen wurden mit Hilfe der Fourier-Transform-IR-Spektroskopie untersucht. Hierbei wurde festgestellt, daß die durch Hydrolyse entstandenen Silanolgruppen beim Erhitzen sowohl den Epoxyring öffnen als auch selbst kondensieren. Die Kinetik dieser Reaktionen wurde untersucht und die relativen Reaktionsgeschwindigkeiten berechnet.
    Notes: Chemical reactions in the epoxy-functional silane hydrolyzate bulk have been studied by Fourier transform infrared spectroscopy (FT-IR). It was found that the silanol group opened the epoxy ring upon heating, concurrently with the silanol condensation. The kinetics of these reactions were studied, and the relative reaction rates were obtained.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 142 (1986), S. 17-27 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Reaktion zwischen Polyvinylpyridinen und Epoxyverbindungen wurde sowohl in homogenen Lösungen als auch im festen Zustand mit Hilfe der Fourier-Transform-Infrarotspektroskopie und anderer Techniken untersucht. Es wurde beobachtet, daß die Pyridinseitengruppe mit den Epoxygruppen unter Bildung von Netzwerken, die Pyridon- und cyclische Amidstrukturen enthalten, reagiert. Diese Reaktion wurde ebenso in der Grenzflächenregion zwischen Polyvinylpyridin und Überzügen aus γ-Glycidoxypropyltrimethoxysilanhydrolysat auf Poly(ethylenterephthalat)-Fasern beobachtet.
    Notes: Chemical reactions of poly(vinyl pyridine)s and epoxy compounds were studied both in homogeneous solution and in solid state by Fourier transform infrared spectroscopy and other techniques. The pyridine side group was found to react with the epoxy group, forming networks which contain pyridone and cyclic amide structures. This reaction was observed also in the interfacial region of poly(vinyl pyridine) and γ-glycidoxypropyltrimethoxysilane hydrolyzate coatings on poly(ethylene terephthalate) fiber substrates.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 7 (1986), S. 231-238 
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: FT-IR spectroscopy was used to collect spectra of γ-aminopropyltriethoxy silane (γ-APS) coupling agent deposited on KBr plates, modeling the silane interphase of composites, to study the effects of heating the γ-APS film under various environmental conditions. This coupling agent is used in fiber-reinforced epoxy composites. An aminebicarbonate salt forms when the sample is dried in a moist carbon dioxide environment giving rise to a series of bands from 2800 to 2000 centimeter-1 (cm-1) and bands at 1637 cm-1, 1330 cm-1, 696 cm-1, and 663 cm-1. The primary amine group is split into two bands at 1572 cm-1 and 1486 cm-1 in the NH3+ form. Heating removes the aminebicarbonate salt at temperatures above 95°C and condenses the γ-APS polymer to a polysilsesquioxane film. The aminebicarbonate salt partially reforms if the γ-APS film is stored in a moist CO2 environment. At temperatures above 120°C the primary amine of γ-APS is oxidized in air to imine groups. In the process of evolving the CO2 the polymer is further condensed and the amine groups can be converted to imines if the temperatures exceeds 120°C. Both processes reduce the reactivity of the coupling agent with the epoxy resin. The structure of the silane interphase must be controlled during the processing of the composite to yield materials with maximum properties.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 9 (1988), S. 151-157 
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Differential scanning calorimetry, Fourier transform infrared, and solid-state carbon 13 nuclear magnetic resonance were used to study the silane coupling agent/epoxy resin interface. Penetration of epoxy into the hydrolyzed silane has been shown. The addition of a solvent can further increase the penetration of epoxy into the hydrolyzed silane by decreasing the viscosity of the epoxy. Bulk models of the gradient in the silane coupling agent/epoxy interface have shown that the concentration of silane and the degree of hydrolysis of the silane can determine the rigidity or mobility of the interphase region. When the silane is hydrolyzed, the possible formation of entanglements may increase the rigidity of the system and decrease the degree of phase separation through the formation of an interpenetrating network.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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