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  • Polymer and Materials Science  (200)
  • unknown  (36)
  • 1955-1959  (236)
  • 1
    Publication Date: 2004-12-03
    Keywords: unknown
    Type: NACA 1957 FLIGHT PROPULSION CONF. 1957; P 1-12
    Format: text
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 368-370 
    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: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 371-371 
    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
    Type of Medium: Electronic Resource
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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: Measurements of the density of a large number of experimental isotactic polypropylenes have shown that the specific volume is linearly related to per cent crystallinity as determined from x-ray data. The density is also linearly related to the absorbance of certain absorption bands in the infrared spectrum of isotactic polypropylene. The infrared data allow a determination of the density of the amorphous polymer which is in good agreement with literature values and with a value determined from the x-ray data by extrapolation to zero crystallinity. It is found that there is a rough, approximately linear correlation between crystallinity (by density) of unextracted polypropylene and the per cent insoluble residue remaining after extraction with boiling n-heptane or after successive extraction with other solvents and heptane. In all instances, the amount of residue exceeds the crystalline content. The crystallinity-insolubility relationship is influenced by molecular weight (as judged by intrinsic viscosity). An increase in crystallinity at constant [η] corresponds to an increase in insolubility; at constant crystallinity, a larger [η] corresponds to greater insolubility. In terms of density, the unextracted polymer may not be regarded as simply a mixture of two well-defined components, since the density of insoluble residue increases with the density of the whole polymer.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 17 (1955), S. 159-177 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of nylon 6 (—NH (CH2)5CO—)p has been determined by interpretation of the x-ray diffraction patterns given by drawn, rolled fibers. The determination was part of a program to investigate the relation between structure and physical properties, in particular melting point. Nylon 6 melts 50°C. lower than its isomer nylon 66 (—NH (CH2)6NH·CO (CH2)4CO—)p; it had been suggested that this was due to deficient hydrogen-bond formation in nylon 6 crystallites. The unit cell contains eight chemical units (—NH (CH2)5CO—) and is monoclinic with a = 9.56 A., b = 17.24 A., c = 8.01 A., and β = 671/2°. Calculated density = 1.23. Observed density for a drawn monofilament = 1.16. The structure consists of planar chains of CH2 groups and amide groups tilted 7° from the (001) plane. Alternate chains in this plane are oppositely directed, an arrangement which allows all hydrogen bonds to be made perfectly. The hydrogen-bonded sheets of atoms are packed in an “up-and-down” staggered configuration along the c-axis. Distances between atoms in neighboring molecules are all normal van der Waals contact distances. It appears, from a general survey of polyamide melting points published elsewhere, that the determining factor is the number of CH2 groups between the amide “anchor points” - polymers with odd numbers of CH2 groups melt lower than those with even numbers. The present work shows that the odd number of CH2 groups in this polymer does not lead to deficient hydrogenbond formation, and that the lower melting point of nylon 6 as compared with nylon 66 must be ascribed to some other cause, possibly connected with the propagation of vibrations along odd-numbered chain segments.
    Additional Material: 10 Ill.
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  • 6
    ISSN: 0022-3832
    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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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies are presented on the preparation of graft copolymers by the gamma-ray irradiation of various polymer-monomer combinations. The following graft copolymers have been prepared and evaluated for specific applications: (1) vinylcarbazole grafted to polyethylene to produce a higher temperature dielectric material; (2) styrene grafted to polyethylene and sulfonated to produce a cation exchange membrane of high mechanical strength, low resistivity, and high permeaselectivity; (3) surface grafting of styrene to polytetrafluoroethylene for modification of adhesive properties; (4) acrylonitrile grafted to polydimethylsiloxane to increase solvent resistance of the latter.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 15 (1955), S. 51-67 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Infrared absorption spectra were used to study the structural changes resulting from oxidation in a number of unvulcanized, purified polymers under a variety of experimental conditions. The results showed that as oxidation progressed, the structural changes which were detected were qualitatively the same for all of the polymers under all of these experimental conditions. Correlation of volumetric measurements with spectral data indicated that considerably more oxygen was absorbed by the polymer samples before structural changes could be detected than the minimum amount required for the initial detection of the hydroxyl and carbonyl structures. From the interpretation of information from the absorption spectrum, it is believed that the structural evidence is in substantial agreement with current theories on autoxidation. Although the initial hydroperoxide formation is not observed in the spectrum, it is quite probable that this reaction takes place with almost immediate decomposition which results in a net hydroperoxide concentration so low as to make infrared methods insensitive for its detection. Correlation of physical properties with structural studies indicate that little change in these properties take place until the hydroxyl and carbonyl structures become evident in the infrared spectrum.
    Additional Material: 17 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 17 (1955), S. 133-135 
    ISSN: 0022-3832
    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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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 39 (1959), S. 419-426 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Exposure of mixtures of natural rubber latex and methyl methacrylate to γ-radiation from a Co-60 source results in polymerization of the methyl methacrylate to give a mixture of the homopolymer and grafted polymer. The ratio of grafted polymer to homopolymer and the molecular weight of the homopolymer are both considerably higher than in similar systems where polymerization was initiated by a redox catalyst. The ability of the irradiated to form continuous films on drying is much greater than that of corresponding redox-polymerized systems. This difference is attributed primarily to the location of the polymerized methyl methacrylate throughout the individual latex particles, the polymerized methacrylate being more uniformly distributed in the case of the irradiated latex. Use of polymerization retarders which are soluble in methyl methacrylate swollen rubber supplies evidence that an increased proportion of the polymerized methacrylate is located in the surface regions of the latex particles. Conversely, a more uniform distribution of the polymer is obtained by the use of water-soluble retarders. The probable significance of these results in relation to emulsion copolymer systems is pointed out.
    Additional Material: 2 Ill.
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