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  • Articles  (155)
  • Polymer and Materials Science  (155)
  • 2020-2023
  • 2010-2014
  • 1965-1969  (155)
  • 1935-1939
  • 1968  (155)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1183-1202 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crosslinked samples of polyethylene were prepared by electron irradiation of both high- and low-density polymers in the crystalline state. A further crosslinked sample was obtained by curing a high-density polyethylene by reaction with dicumyl peroxide at 180°C. The stress-strain-birefringenece relations were obtained on specimens cut from these samples at temperatures between 130 and 250°C. All samples showed a substantial decrease in stress-optical coefficient with increasing degree of crosslinking and with increasing temperature. The stress-optical properties at each temperature were extrapolated to zero degree of crosslinking to give quantities characteristic of the Gaussian network. Comparison of these properties with the theory of networks of rotational isomeric chains with both independent and interdependent rotation allows estimates to be obtained for (1) the trans-gauche energy differences in rotation around skeletal bonds and (2) the difference in principal optical polarizabilities for the CH2 group in the elastomeric state. This latter quantity is shown to be more nearly given by Denbigh's than by Bunn and Daubeny's bond polarizability values.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 181-183 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 1193-1197 
    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: Methyl methacrylate-styrene-acrylonitrile copolymers, alone and with polybutadiene modification, were examined for changes in impact strength and yellowness after thermal and light aging. The copolymer displayed no change in strength or clarity, while the butadiene-modified material showed increase in yellowness and loss in impact resistance. It is apparent that these changes are primarily due to the decomposition of the butadiene phase in the impact material, and this conclusion might be applied to diene-containing blends in general.
    Additional Material: 4 Ill.
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  • 4
    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: Mercerized cellulose in the form of 7/2 yarn was reactivated with 17.5% sodium hydroxide and then heated at 100°C. with 5 moles of trityl chloride, in pyridine, per anhydroglucose unit. The time of reaction was varied, giving ether derivatives of the cellulose containing 0.31-0.79 triphenylmethyl groups (DS) per anhydroglucose unit. Controls consisted of (1) the untreated cellulose yarn and (2) a portion subjected to all the reaction conditions except the reactant. The density of the product decreased hyperbolically with increasing substitution. The mixed x-ray pattern of the untreated control cellulose (35% cellulose I, 43% cellulose II) was largely converted by the activation treatment (10% cellulose I, 53% cellulose II). As reaction proceeded the crystal structure largely disappeared. The assumption is that substitution was confined almost exclusively to the primary hydroxyl position. The behavior of tensile stiffness, elastic recovery, and work recovery was explored at temperatures from about 25 to 225°C. Considerable improvement, which generally increased with increasing substitution, was observed in both elastic and work recovery at all temperatures studied.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 447-453 
    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: Disubstituted monoisocyanates were synthesized and their reactivities studied by the spectroscopic method.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 2 (1968), S. 165-171 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A quantitative method for determining residual ethylene oxide in plastic and rubber catheters using gas-liquid chromatography has been developed. Tests on ethylene oxide stabilized catheters indicated that the amount of ethylene oxide in the catheters decreased as a function of aeration time up to 48 hr. After this period, a steady concentration of ethylene oxide in the catheters appeared to have been reached up to one week's testing.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 269-273 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 1-4 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 773-778 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 2001-2012 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Emulsion polymerization of methacrolein produces a polyacetal which can be converted through the action of sodium hydroxide to an alternating copolymer of methallyl alcohol and sodium methacrylate. Support for the alternating structure was gained primarily through a study of the polylactone formed through subsequent acidification of the sodium salt. Thus, the poly(methallyl alcohol-sodium methacrylate) copolymer was acidified under selected conditions to give a soluble polylactone containing 14.2 mole-% of residual acid and hydroxyl groups. This number agrees quite closely with the value of 13.5 mole-% which one would predict from the random cyclization of a true alternating copolymer. Cyclization of a random copolymer of poly(methallyl alcohol-sodium methacrylate) in a random fashion would have resulted in a value of about 36.8 mole-%. The results also support both the 1,2 vinyl polymerization of methacrolein and a nonrandom attack of the polymethacrolein by base. In a completely separate set of experiments, the value of r1 and r2 for the copolymerization of styrene (M1) and methacrolein (M2) were determined to be 0.22 ± 0.02 and 0.88 ± 0.02, respectively.
    Additional Material: 6 Ill.
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