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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1069-1071 
    ISSN: 0887-6266
    Keywords: ESR ; hydrogels ; morphology ; water ; PHEMA ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1040-0397
    Keywords: Carbon paste electrodes ; Sensors ; Flow detectors ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A review is presented dealing with the use of carbon paste as an electrode maaterial for electrochemical sensors (311 references). It covers mainly publications which appeared during the period 1990-1993; numerous applications demonstrate the widespread applicability of carbon paste in the field of electrochemical analysis, such as voltammetry, amperometry, and potentiometry, but also as an electrode for electrochemical detectors in flow systems.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 46 (1995), S. 233-240 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of comb-like ionenes with aliphatic side chains of different length and organic main chain spacer groups of different size have been synthesized by the step-growth polymerization of long aliphatic chain-substituted diamines with α,ω-dibromoalkanes. Highly ordered films of layered structure have been obtained by solution casting. The long side chains crystallize with an interdigitating hexagonal packing perpendicular to the film plane. The perfection of the side chain packing is related to the size of the spacer group in the main chain as well as to the valence of the counterions, but also depends on the thermal history of the samples. It is in all cases comparable to the quality of aliphatic chain packing in LB multilayers of surfactants. The comb-like ionenes exhibit liquid-crystalline textures above their side chain melting transition.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2805-2809 
    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
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1307-1318 
    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 bisphenol A-polyamine hardener based epoxy adhesive (EP) was modified by polyblending with Kraft lignin (L). EP-L polyblends with an L content up to 40% by weight were cured at room temperature or above their glass transition temperature (Tg). Previous data have shown that the thermal and viscoelastic properties, as well as adhesive performance of the EP-L polyblends, are influenced by the curing temperature and by the L content in thermally cured polyblends. A reasonable explanation for the different behavior of EP-L polyblends as function of the curing temperature and their L content could be the enhanced degree of bonding between L and the EP network taking place at elevated temperature. This bonding was specifically considered to take place between L and possible unreacted amine groups of the hardener. Characterization of the EP-L polyblends was performed to search for evidence of irreversible chemical bonding between L and the EP network in thermally cured EP-L polyblends. FTIR studies, L extractibility from the crosslinked, polyblends, and quantitative data concerning the reactivity of L toward the polyamine hardener are discussed.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 2869-2877 
    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: Various methods of thermogravimetric analysis were compared in case of polystyrene degradation. The reaction order, the activation energy and the preexponential factor were evaluated from common TG curves experimentally obtained. In most cases a 5-mg sample of polystyrene with 110,000 molecular weight was decomposed at heating rate of 10°C/min. The reaction was found under this experimental condition to be of first order with activation energy of 61.0 kcal/mole, though there were slight differences depending on the analytical methods used.
    Additional Material: 10 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1759-1776 
    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: Proper substrate preparation is an indispensible step for achieving strong adhesive joints. One consequence of such surface treatment is the enhancement of degree of mechanical interlocking between polymers and substrates, which, according to the literature, seems to increase the strength of the joint. A novel method based on photolithography is developed to texture aluminum oxide surface by controlling the pit size and its spatial distribution. Surface profile, surface physical chemical properties of this sample, and the lap shear strength of epoxy adhesive joints are compared with those of the phosphoric acid anodized (PAA) sample. It is shown that the lap shear strength of the textured sample is superior to that of the PAA sample. Surface profile data and mathematical analysis suggest that the inferiority of the PAA sample is probably due to the trapped air in the large pit in the surface resisting the penetration of adhesives. It also concludes that the high surface area provided by the multitude small pits in PAA sample is far from being fully utilized. This study opens up a new avenue to rationally improve the strength of adhesive joint by controlling the surface profile, the surface chemical properties, and the pressure during bond formation.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1537-1550 
    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 bisphenol A based epoxy adhesive (EP) was modified by polyblending with Kraft Lignin (L). A systematic investigation of the thermally cured EP-L polyblends with up to 40% by weight L was undertaken. Adhesive shear tests, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and solid-state CP-MAS NMR spectroscopy were performed to establish the effect of L on the mechanical properties of the polyblends and on the morphology of these crosslinked structures. The possibility of an enhanced degree of bonding between L and the EP network is discussed. This bonding can arise from a chemical reaction between L and some unreacted amine groups present in the hardener.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 2181-2186 
    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: Permeation behavior of pure CO2, O2, and N2 and separation characteristics of CO2-air mixtures were examined using hollow fiber modules of asymmetric cellulose triacetate membrane at 30°C. The ideal separation factor for CO2 relative to N2 ranged from 21 to 24. Permeation behavior for pure CO2 was interpreted in terms of the total immobilization model, i.e., a limiting case of the dual-mode mobility model for glassy polymer, where the diffusion coefficient for Henry's law mode is not assumed to be constant and depends on gas pressure via a modified free-volume model. Based on pure gas permeabilities to CO2, O2, and N2, simulation for the separation of CO2-air mixtures was made using a counter-current plug flow model, and the result fitted the corresponding experimental data fairly well. Membrane plasticization induced by CO2 had negligible effect on permeation to mixture of CO2 and air in the range of CO2 composition up to 50% and upstream total pressure up to 1.5 MPa.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 1577-1591 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A set of isothermally melt-crystallized polyethylene samples was examined using small-angle x-ray scattering (SAXS). Time and temperature of crystallization were the variable parameters used to create the set of samples. Following background subtraction, desmearing, and application of the Lorentz factor to the raw SAXS data it is possible to see many orders of reflection. This suggests that much higher degrees of order are present in isothermally melt-crystallized samples than had previously been thought possible. A combination of SAXS and DSC data indicates that there is no evidence for isothermal thickening in these samples. This study, coupled with data obtained from PE single crystals, produced information concerning the extrapolation of single-crystal data to fit bulk systems. In addition, the equilibrium melting point T0m determined is somewhat lower than previously claimed. This study also suggests that the surface energy of the mature crystals is always lower than that of the nucleated state and/or the nucleation factor Kσen increases with decreasing supercooling.
    Additional Material: 11 Ill.
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