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  • 1
    ISSN: 0935-9648
    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
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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: Ein Styrol/Maleinsäureanhydrid-Copolymeres (ST-co-MA), hergestellt aus Styrol und Maleinsäureanhydrid in Dimethylsulfoxid mit Azoisobutyronitril als Initiator, wurde durch eine Kondensationsreaktion auf Poly(vinylalkohol) (PVA) gepfropft. Die Strukturen der Produkte wurden mittels IR-Spektroskopie untersucht. Die Abhängigkeit der Pfropfterpolymerzusammensetzung, -viskosität und -ausbeute von der Konzentration der Reaktanden sowie die mechanischen Eigenschen von aus den Pfropfprodukten hergestellten Membranen wurden ermittelt. Bei der Untersuchung der Permeationseigenschaften zeigte sich, daß die Membranen bei allen Zusammensetzungen von Alkohol/Wasser-Gemischen bevorzugt für Wasser durchlässig sind. Mit steigendem PVA-Anteil in den Membranen und wachsendem Ethanolanteil der Alkohol/Wasser-Mischung nimmt die Durchlässigkeit ab und die Selektivität zu. Weiterhin wird der Einfluß der Größe der permeierenden Moleküle auf die Durchlässigkeit und Trenneigenschaften diskutiert.
    Notes: Graft copolymerization of styrene-maleic anhydride copolymer (ST-co-MA) onto poly(vinyl alcohol) (PVA) was carried out by a condensation-coupling reaction through esterification. The ST-co-MA copolymer was obtained by the copolymerization of MA and ST in dimethyl sulfoxide (DMSO), using azoisobutyronitrile as initiator. The structure of the reaction products was confirmed by infrared analysis. The dependence of composition, viscosity and yield of the graft terpolymers on the concentration of the reactants are presented in detail. Mechanical properties of membranes with different compositions were measured over a wide range of composition. It was found that water was permeated through the membranes preferentially in all ranges of feed compositions. The permeation decreased and the selectivity increased with increasing ethanol concentration in the feed and with increasing PVA content in the membrane. The effect of the molecular size of the permeating species on both permeation and separation is also discussed.
    Additional Material: 12 Ill.
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  • 3
    ISSN: 0887-6266
    Keywords: FT-IR ; step-scan interferometry ; 2D-IR ; polyethylene ; rheo-optical characterization ; time-resolved vibrational spectroscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical analysis coupled with polarized step-scan FTIR transmission and two-dimensional correlation analysis (2D FTIR) has been used to monitor the submolecular orientational responses of the components of a semicrystalline 50 : 50 blend of low-density polyethylene (LDPE) and perdeuterated high-density polyethylene (d*-HDPE) to a small amplitude uniaxial 23.47 Hz sinusoidal mechanical strain. Perdeuteration of the HDPE component allowed the distinction of its response from that of the LDPE in the blend samples. The experiments were carried out at room temperature. Analysis of the data indicates that the crystalline parts of the two components reorient at different rates, with the functional groups of the high-density portion reorienting faster, in general, than those of the LDPE in response to the mechanical strain. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 799-803 
    ISSN: 0142-2421
    Keywords: Nylon-6,6 ; static SIMS ; ToF-SIMS ; polymer surface analysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The characteristic static SIMS spectra of the cyclic monomer of Nylon-6,6 have been obtained from the isolated and purified material. The spectra are sufficiently different from those obtained from bulk Nylon-6,6 polymer. Intense fragment ions corresponding to (M+H)+ and (M-H)- are observed in the positive and negative ion spectra, respectively. Results from both quadrupole and ToF-SIMS measurements are presented. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 4 (1983), S. 243-248 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1085-1096 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The tacticity of poly(methyl methacrylate) (PMMA) samples made by emulsion polymerization (EP) has been determined by NMR spectroscopy at higher resolution than any previous study. When photoinitiation is employed at room temperature, the polymer obtained is highly syndiotactic and more stereoregular than that obtained in homogeneous radical polymerization under the same conditions. The percentage of racemic dyads and the length of racemic sequences vary significantly with the degree of conversion and the temperature, but not with variation of the hydrophobic or the hydrophilic part of the detergent molecules. A magnetic field of 5 kG or less accelerates the polymerization reaction and increases the polymer molecular weight when dibenzyl ketone is employed as oil-soluble photoinitiator, and has an indirect influence on the polymer tacticity. From measurements of the temperature dependence of the polymer steric composition, the difference of activation enthalphy and entropy of the meso and racemic additions have been calculated. The values do not follow the correlations from precedent literature for radical polymerization in solution if the reaction is considered a first-order Markov process. The persistence ratio p depends on the detergent and the temperature of the EP; in some cases its difference from unity exceeds the experimental error. These results are interpreted as a conformational effect of the locus of the polymerization in the first stage of the EP (when micelles are present) that favors the racemic addition more than is expected in a homologous solvent such as an alkane, e.g., at the same temperature.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 47 (1996), S. 511-519 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We have investigated the morphology of a heavily disordered conducting polymer, polypyrrole doped with large polymeric anions. An extensive microscopy study (scanning electron microscopy, atomic force microscopy and transmission electron microscopy) together with previously obtained information on the samples' electronic properties conveys to us the following image: the observed globules of diameters between 10 and 100 nm originate from the polymeric dopants forming coils with the doping centers concentrated on the coil surfaces and the polypyrrole surrounding the whole. In this way polypyrrole-rich “sheets” run through the whole sample and guarantee the electrical continuity which prevails even in samples with polypyrrole volume fractions as low as several per cent. For the first time, the building block of the “fractal” cauliflower structure, observed also in many other electrochemically prepared conducting polymers, could be identified.
    Additional Material: 13 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 623-643 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A theoretical analysis has been made of the graft polymerization process in terms of the quantitative interrelationship between the initiation rate Ri, the kp/kt1/ ratio of the monomer, the equilibrium solubility M of the monomer in the polymer, the polymer film thickness L, and the diffusivity D of the monomer in the polymer. It is shown how the values of these parameters in any grafting system interact to lead to diffusion-controlled graft polymerization. Whether graft polymerization is diffusion-free or diffusion-controlled depends on the values of Kp, d, kp/kp1/2, and L as gathered in the parameter A = [(Kp/kt1/2)Ri, D,/1/2] L/2. When the values of the various terms are such that A is less than 0.1 (i.e., D is large while Ri, kp, and L are small), the reaction is diffusion-free. When A is greater than 3 (i.e., D is small while Ri, kp, and L are large), the reaction is diffusion-controlled. The derived equations showing the relationship between kinetic and diffusional parameters are theoretically applicable to all grafting systems, i.e., for all monomer-polymer combinations under all conditions of reaction temperature, radiation intensity and polymer film thickness. The theoretical analysis has been verified for the rate and degree of polymerization for the radiation-induced graft polymerization of styrene to polyethylene.
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 40 (1996), S. 251-259 
    ISSN: 0959-8103
    Keywords: birefringence ; injection molding ; photoelasticity ; digital image ; 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 birefringence of injection molded parts was measured using a digital photoelasticity system, which combines a digital image analysis technique and the half-fringe photoelasticity (HFP) method The effects of processing conditions, including melt temperature, mold temperature, filling time and packing pressure, on the birefringence development in the molded parts were investigated. It was found that temperature and pressure are the two dominant factors that determine the birefringence development in the parts during the molding process. Frozen-in birefringence of the molded parts decreases with increasing melt temperature, mold temperature and injection speed. Birefringence of the parts also increases with increased packing pressure, especially around the gate area. Numerical simulations using the Leonov viscoelastic fluid model predict similar dependence of birefringence of parts on processing conditions. Simulated results are also consistent with measured values.
    Additional Material: 13 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2237-2245 
    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: A novel method to prepare polymer metallized films was found by using polymer metal chelate films treated with wetted metal plates (or metal powders). The polymer metal chelate films were prepared by metal salts mixed with the polymers containing a functional group, such as poly(vinyl alcohol) (PVA), polyamide, polyacrylamide (PAAm), and polyurethane (PU). This novel method is called the retroplating-out method. Polymer metallized films exhibited low surface resistivity around 10-1 Ω/cm2 by using this novel method. The surfaces of these films were shown to be metallized by means of X-ray analysis. The conduction mechanism was verified reasonably well by using scanning electron microscope (SEM) and UV-visible absorption data.
    Additional Material: 4 Ill.
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