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  • Articles  (3,463)
  • Chemistry  (3,463)
  • 1965-1969  (3,463)
  • Physics  (3,463)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 1 (1967), S. 35-56 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 1 (1967), S. 173-275 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 67 Ill.
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  • 3
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 17 Ill.
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  • 4
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heterogeneous olefin polymerization catalysts generally consist of a transition metal compound from groups IVB or VB in combination with an organometallic compound from groups I, II, and III of the periodic table of the elements, but in some instances may contain a third component possessing at least one strongly complexing ligand atom. The composition of a coordination catalyst of this type determines both the rate of polymerization of the α-olefin and the stereoregularity of the polymer produced. In order to predict activity and stereospecificity of catalysts for the polymerization of α-olefins, data from the polymerization of propylene using catalysts of the following types were correlated: (1) titanium(III) chloride catalysts in which the organometallic component was varied, (2) coordination catalysts containinig a ligand third component in which the ligand was varied, and (3) coordination catalysts in which the transition metal component was varied.The electronegativity of an orgariometallic compound is known to be important in determining its reactivity with ethers, hydrogen, and other reagents. Both the ionic size and the electronegativity of the central atom appear to be important in determining the utility of both the organometallic and the transition metal compounds as components for coordination catalysts. In general, organometallic and transition metal compounds having small central atoms with similar electronegativities favor the formation of stereospecific catalysts.The present correlation has made it possible to predict the activity and stereospecificity of coordination catalysts for olefin polymerization.
    Additional Material: 11 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 1 (1967), S. 119-172 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 23 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 2 (1967), S. 71-113 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 6 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 31-38 
    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 swelling and dissolution of heat-set nylon 6 fiber in aqueous sulfuric acid were examined. Steam-set fiber having good dyeability swells with much more difficulty than the dry-heat-set and unset fibers. Similar phenomena are seen in the examination of density of nylon 6 fiber subjected to heat setting, and it is found that the resistance to swelling depends on the crystalline region rather than on the amorphous region.
    Additional Material: 7 Ill.
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  • 8
    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 infrared spectrum of deuterated ε-caprolactam was examined. It was confirmed spectroscopically that the hydrogen of the N—H group in ε-caprolactam is exchanged for deuterium after repeated exchange reactions. The deuterated ε-caprolactam was polymerized, and the infrared spectrum of the polymer (called as N—D polymer) is compared with that of the normal nylon 6 polymer (called N—H polymer) which was steam-set in D2O vapor at 135°C. Characteristic absorption bands of N—D polymer are observed at 967, 896, 888, 876, and 719 cm.-1. The water accessibility of both N—H and N—D polymer was estimated from the spectra of both samples subjected to the repeated steam setting in D2O and H2O alternately at 130°C. The results show that at the initial stage of the repeated steam setting, H2O and D2O molecules may penetrate into the ordered regions in the polymers and partially break down intermolecular hydrogen bonds; such phenomenon may be followed by an exchange reaction and recrystallization. Subsequent stages of steam setting, however, no longer bring about such an effect.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 91-115 
    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 degree of penetration, the diffusion constant, and the uptake of dyestuffs of different molecular sizes were measured in undrawn and drawn nylon 6 filament, heat-set under various conditions in order to determine the pore structure in the amorphous regions. Unset and dry-heat-set nylon 6 can be penetrated only with difficulty by the dyestuffs having molecular lengths above about 30 and 25 A., respectively. The apparent diffusion coefficients and molecular weight of dyestuffs are approximately hyperbolic. The relations are considerably different, depending on the degree of drawing and conditions of the heat setting. Further, the relations among molecular size, amount of absorbed dyestuffs, and fraction of amorphous region capable of being penetrated by dyestuff are discussed with reference to the lateral-order distribution of nylon 6, as evaluated from the accessibility to D2O vapor.
    Additional Material: 14 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3795-3818 
    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 low plasticizer concentrations on the glass transition temperature of poly(methyl methacrylate) (PMMA) has been studied experimentally for diethyl phthalate (DEP) and methyl methacrylate (MMA) as plasticizers. Volume dilatometry, differential thermal analysis, and a torsional pendulum were used to determine glass transition temperatures. The monomer-plasticized PMMA samples were prepared by polymerizing MMA to a limiting conversion which was found to depend primarily on temperature. At temperatures slightly above the glass transition temperature of a MMA-PMMA system, a polymerization reaction occurred at a rate rapid enough to complicate the interpretation of the dilatometric and differential thermal analysis methods for determining the glass transition temperature. However, the torsional pendulum method could be used since it did not require measurements to be made at temperatures where polymerization could occur. The differential thermal analysis results showed that the temperature at which the polymerization reaction was first detectable was related to the glass transition temperature of the MMA-PMMA solution. The measured glass transition temperatures were compared with the predictions of the theories of Fox, Kelley, and Bueche, and Dimarioz and Gibbs on the effect of plasticizer concentration on the depression of the glass transition temperature.
    Additional Material: 13 Ill.
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