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  • Polymer and Materials Science  (310)
  • Physics  (62)
  • 1980-1984  (235)
  • 1960-1964  (75)
  • 1981  (235)
  • 1960  (75)
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  • 1980-1984  (235)
  • 1960-1964  (75)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Deterioration of plastic films under soil burial conditionsIssued as N.R.C.C. # 18807. (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 509-519 
    Details
    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 deterioration of polyolefin, poly(ethylene terephthalate), and polyamide films under soil burial conditions extending up to 32 months has been investigated. Based on changes in their elongation at break, the films can be ranked in order of increasing sensitivity to degradation: Polyester ≃ polypropylene 〈 low-density polyethylene ≃ high-density polyethylene 〈 nylon 6.6. The degraded nylon 6.6 and polyethylene films were characterized by infrared and luminescence spectroscopy and scanning electron microscopy, as well as by wet analysis for hydroperoxides. From a comparison with the well-known oxidative sensitivity of nylon 6.6 in oxygenated water at slightly elevated temperatures, the rapid deterioration of nylon 6.6 film during soil burial was also concluded to be an oxidative process. The somewhat smaller, but significant, embrittlement of the polyethylenes studied could not be simply explained by thermal oxidation (with only trace oxidation products detectable) or microbiological attack (deterioration being unaffected by surface activation to enhance wettability).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260211
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  • 2
    Electronic Resource
    Electronic Resource
    Aromatic polyamides. II. Thermal degradation of some aromatic polyamides and their model diamides (1981)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2817-2834 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation behavior of poly(1,3-phenylene isophthalamide) and poly(chloro-2,4-phenylene isophthalamide) was investigated with the aid of some appropriate model compounds. The pyrolysis products of these materials were identified by gas chromatography (GC), gas chromatography/Fourier transform infrared spectroscopy (GC/FT-IR), and gas chromatography/mass spectrometry (GC/MS). The residual chars were characterized by IR spectroscopy. Thermogravimetric analysis (TGA) was applied to study the effect of end-group concentration on the degradation characteristics of the two polyamides. Kinetic parameters that describe the thermal degradation of the polyamides were also evaluated by TGA. The results of this investigation suggest that the thermal decomposition of these aromatic polyamides involves homolytic as well as hydrolytic cleavages of the amide units.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1981.170191115
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  • 3
    Electronic Resource
    Electronic Resource
    Spectroscopic studies of solutions, suspensions, and precipitates of poly(1,6-di-p-toluene sulfonyloxy-2,4-hexadiyne) (1981)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 321-334 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Optical-absorption, fluorescence, and Raman spectra for solutions, suspensions, and precipitates of poly(1,6-di-p-toluene sulfonoxy-2,4-hexadiyne) in and from nitrobenzene, acetone, and chloroform are presented. These are interpreted in terms of the occurrence of two forms of the polymer chain; a quasicrystalline form with properties close to those of single crystal polymer and a chain-extended form occurring in solution and colloidal particles, with an absorption energy of about 2.5 eV (20,000 cm-1). No evidence is found for the presence of very short polymer chains in partially polymerized monomer at low conversion. The relationship of these results to those for deformed single crystals is briefly discussed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1981.180190212
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  • 4
    Electronic Resource
    Electronic Resource
    Reticulated versus crenelated surfaces on macroporous polystyrene-divinylbenzene membranes (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 591-602 
    Details
    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: Reticulated polystyrene-divinylbenzene (PSt-DVB) copolymer membranes or thin sheets were prepared using two different methods. The first method employed a nonsolvating diluent which dissolves the monomer but precipitates the polymer. This resulted in skinned membranes with the skin being nonporous, being either crenelated or smooth. The second method used paraffin wax as the inert phase. The wax was precipitated by cooling, followed by polymerization of the styrene. The wax was then solvent extracted. This resulted in a reticulated structure both on the surface and in the interior of the membrane. The resulting products from the two methods were compared using scanning electron microscopy. The objective of this study was to prepare a skinless, macroporous, crosslinked polystyrene, as polymer I for the preparation of novel interpenetrating polymer network (IPN) materials.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260218
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  • 5
    Electronic Resource
    Electronic Resource
    Assessment of the adhesive bond properties of allyl 2-cyanoacrylate (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1941-1949 
    Details
    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 adhesive bond of allyl 2-cyanoacrylate between steel substrates has been analyzed and compared to that of ethyl 2-cyanoacrylate. Mechanical strength as well as thermomechanical, calorimetric, thermogravimetric, and dynamic mechanical response was observed. It was demonstrated that the allyl 2-cyanoacrylate bonds exhibit improved temperature resistance owing to the formation of heat-induced crosslinks in the adhesive layer, resulting in much improved lap-shear strengths. Scanning electron microscopy of the fracture surfaces showed that plastic deformation occurred in the allyl 2-cyanoacrylate adhesive after thermal aging, while interfacial and brittle failure dominated all other cases.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260618
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  • 6
    Electronic Resource
    Electronic Resource
    Polymers from vinyl fluorideThis paper was presented at the Symposium on New Products and Applications for Fluorine-Containing Materials before the Division of Industrial and Engineering Chemistry at the 136th National Meeting of the American Chemical Society, Atlantic City, September, 1959. Contribution No. 546 from the Central Research Department, E. I. du Pont de Nemours and Company, Inc., Wilmington, Delaware. (1960)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 55-61 
    Details
    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 free-radical polymerization of vinyl fluoride has been studied with the use of organic peroxide and azo initiators over the temperature range of 60-150°C. and at pressures of 75-1000 atm. Molecular weights of the polymers by osmotic pressure or radiotracer techniques were found to vary over the range of 45,000 to 180,000 depending on polymerization conditions employed. Stabilized high molecular weight polyvinyl fluoride may be compression-molded into tough, high-impact strength bars, or the unstabilized material may be cast into films from solvents such as dimethylformamide. The films, which may be cold drawn, are tough, brilliantly clear, and have tensile strengths near 8000 lb./in.2 They are also extremely resistant to weathering, maintaining clarity and cold drawability even after ten years' exposure in Florida.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1960.070041008
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  • 7
    Electronic Resource
    Electronic Resource
    Isocyanate modified polyimidesNCL Communication No. 2704. (1981)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 99 (1981), S. 117-123 
    Details
    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: Vier verschiedene, mit 3,3′-Sulfonyl-bis(phenylisocyanat) modifizierte Polyimide wurden synthetisiert und die elektrischen Eigenschaften der Polymer-Filme wurden gemessen.
    Notes: The synthesis of four different polyimides modified by 3,3′-sulfonyl-bis(phenyl isocyanate) was achieved and the electrical properties of polymer films were measured.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1981.050990110
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  • 8
    Electronic Resource
    Electronic Resource
    Thermal and pulse NMR analysis of water in poly(2-hydroxyethyl methacrylate) (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3719-3728 
    Details
    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: Hydrophilic three-dimensional methacrylate polymer networks (hydrogels) were prepared from 2-hydroxyethyl methacrylate (HEMA) monomer and tetraethylene glycol dimethacrylate (TEGDMA) as crosslinker. The nature and states of water in these hydrogels were studied by differential thermal analysis and pulse NMR relaxation spectroscopy. The thermal studies showed no endotherm peak for ice melting in the lower water content (bound water region); there are two endotherms peaks for higher water content hydrogels near 0°C. The amounts of bound water, intermediate water, and bulklike (free) water in the hydrogels were determined from a quantitative analysis of the endotherms of the water melting transitions. The water structure ordering in the hydrogels were discussed in terms of the fusion entropy and enthalpy obtained from the endotherm. Nuclear magnetic relaxation spectroscopy was also used to understand the mobilities of the water protons in the hydrogels and the interaction of water molecules with the gel networks. The measured spin-lattice relaxation time (T1) values for water protons in the hydrogels are greatly reduced compared to that of liquid water. The measured values of spin-spin relaxation times (T2) of water protons in the hydrogels are approximately 10 times less than that of T1 and are almost constant in the region of bound water content. Beyond the bound water content region in the hydrogels, the T2 values rapidly increase as the water content increases.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070261118
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  • 9
    Electronic Resource
    Electronic Resource
    Compatibility in a blend of poly(2,3-dichloro-1-propyl acrylate) and poly(glycidyl methacrylate-co-ethyl acrylate) (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2001-2013 
    Details
    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 compatibility of mixtures of poly(2,3-dichloro-1-propyl acrylate) and poly(glycidyl methacrylate-co-ethyl acrylate) has been investigated by measurement of the following properties: density, light transmission, glass transition temperature, vapor absorption, and NMR relaxation times. To varying degrees, all results provided evidence supporting the contention that these mixtures are compatible.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260623
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  • 10
    Electronic Resource
    Electronic Resource
    Interpenetrating polymer networks based on ionically crosslinked polymers: Reacidification and annealing as morphological variables (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 141-147 
    Details
    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 carboxylic elastomer based on butadiene, styrene, and methacrylic acid was polymerized and neutralized to form an ionomeric network I. Sequential IPNs were formed by synthesizing in situ polystyrene crosslinked with divinylbenzene as network II. Annealing studies were carried out, with and without reacidification, to ascertain the role played by ionic crosslinks in influencing morphology and mechanical behavior. Finally, the product is reneutralized, resulting in are arranged, relaxed structure. Ionic crosslinks in polymer I provide an in situ decrosslinking mechanism which permits molecular rearrangements to be induced. By annealing the material, a more cocontinuous phase morphology with concomitant modulus increases is attained. This investigation suggests an alternative method of inducing dual phase continuity in multipolymer combinations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260112
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