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  • 1
    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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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 1331-1341 
    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: Silica is a common component in silicone elastomer formulation. Silica is known to have surface hydroxyl groups and the reactions and interactions of these surface groups with various materials have been studied extensively in the past. It is believed that the iron octoate used to combat oxidative embrittlement in silicone elastomer formulations may also react with the surface of silica, specifically fumed silica. Dynamic mechanical spectroscopy (DMS), Fourier Transform Infrared Spectroscopy (FT-IR), Electron Scanning for Chemical Analysis (ESCA), and Gel Permeation Chromatogrphy (GPC) were used to study the influence of untreated fumed silica and silica treated with dimethylsiloxane species on the iron octoate reaction. The rate of reaction was studied as a function of loading of silica. From analyzing rates of backbone scission and salt consumption, it is found that the iron octoate reacts preferentially with the surface of untreated fumed silica. Conversely, iron octoate appears to have no preferential reaction with the surface of the treated fumed silica.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 893-897 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 2295-2298 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1751-1760 
    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: The effect of potential catalysts on the curing reaction of a new type of phenolic resins obtained from benzoxazine precursors is studied. These novel resins solve the shortcomings of traditional phenolics because they cure by a ring-opening mechanism that avoids the release of volatiles. Isothermal and nonisothermal differential scanning calorimetry (DSC) data is used to determine the influence of the catalysts on the curing kinetics. Fourier transform infrared (FTIR) spectroscopy is also applied. The benzoxazine chosen for this study is a purified benzoxazine monomer based on bisphenol-A, formaldehyde, and aniline. The as-synthesized benzoxazine precursor is also studied to determine the influence of the dimers and higher oligomers in the curing mechanism. The presence of these structures seems to catalyze the curing reactions. The activation energy and overall reaction order of the as-synthesized precursor are determined. Among the catalysts tested, adipic acid shows the most promising results. For all the cases studied the curing reaction is autocatalyzed up to a diffusion-controlled stage. © 1995 John Wiley & Sons, Inc.
    Additional Material: 18 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 28 (1990), S. 1121-1135 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The surface of graphitized carbon fibers is oxidatively treated by nitric acid. Fourier transform infrared attenuated total reflection spectroscopy has been utilized to monitor the influence of the surface species on the curing of an epoxy system. A curve-fitting program is used to deconvolve the overlapped infrared bands. The integrated intensities of the ester, anhydride, epoxy, and carboxylic acid, plotted against the curing time, clearly show the dependence of the crosslinking process on the concentration of the surface species. The surface groups themselves act as a catalyst: there exists an optimal concentration below which an activation of the curing process occurs. Above that concentration, a retardation of the curing process has been detected.
    Additional Material: 12 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 27 (1989), S. 1611-1627 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 4,4′-Diethynyldiphenylmethane thermally polymerizes by a free radical mechanism to a highly crosslinked structure of interest as a high temperature composite matrix resin. The polymerization reaction was characterized by differential scanning calorimetry, Fourier-transform infrared (FTIR) spectroscopy, 1H and 13C nuclear magnetic resonance (NMR) spectroscopy, and microdi-electrometry. The predominant reaction mechanism appears to be linear polymerization through the acetylene end groups, which follows first-order kinetics. However, during the early stages of reaction a second, more rapid polymerization mechanism is evident; it is postulated that this is the formation of a cyclic trimer, which is kinetically favored but sterically prohibited as the crosslinked network grows. Formation of a liquid crystalline trimer is hyppthesized; such intermediate formation is supported by intensity increases in the aromatic region of the NMR spectra, by FTIR difference spectroscopy comparisons with model compounds, and by enhancement of conductivity as observed by microdielectrometry.
    Additional Material: 11 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. 1095-1106 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A potential ceramic precursor, a phenylpropylsilsesquioxane co-oligomer from Petrarch Systems (Petpps), was studied under conditions where fiber spinning is performed. The reaction kinetics of residual silanols of Petpps are studied using Fourier transform infrared spectroscopy in the temperature range 100-150°C. The activation energy and the reaction order of the silanol condensation reaction in the molten Petpps are determined. A combination of gel permeation chromatography, liquid chromatography, and nuclear magnetic resonance spectroscopy is used to study the possibility of copolymerization between the phenyl and propyl silane moieties.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 489-495 
    ISSN: 0887-6266
    Keywords: infrared spectra of Nylon-6 chain conformation ; Nylon-6 chain conformation, FT-IR separation of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Specific infrared absorptions for each form of Nylon-6 have been indentified. Quenched films were prepared by melt casting and converted in turn to the α-crystalline and γ-crystalline structures. The films were examined using Fourier transform infrared spectroscopy (FTIR) with the attenuated total reflection configuration and by X-ray diffractometry. The FTIR spectrum of the pure mesomorphous component of the quenched film was calculated by subtracting away the contribution of α-crystalline peaks present due to incomplete quenching. A curve-fitting procedure was applied to the pure mesomorphous and gamma crystalline spectra. Several peaks in the mesomorphous spectrum are observed to develop a shoulder upon conversion to the γ-crystalline form. This is due to the extra gauche character imparted to the C—N bond between the methylene unit and the amide group. These and other band assignments were confirmed by analysis of model compounds.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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