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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 84 (1962), S. 1383-1391 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 82 (1960), S. 46-53 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of fracture 8 (1972), S. 465-468 
    ISSN: 1573-2673
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 60 (1962), S. S31 
    ISSN: 0022-3832
    Keywords: 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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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 505-511 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Crystalline polymers are heterogeneous materials consisting of two distinct phases. They may therefore be treated as molecular versions of engineering composite materials. This paper summarizes the physical model which, when used in conjunction with composite theory, yields a complete calculational format for stiffness, expansion strain, and yield strength. The important input parameters to the calculation are the mechanical properties of the individual constituent phases (crystalline and amorphous), the crystallite aspect ratios, the volume fraction crystallinity, allowable failure strains for a continuous crystal system, and a measure of stress concentrations and strength reduction caused by the discontinuous nature of the actual crystalline reinforcing phase. An expression for the strength reduction factor is developed and details of the stiffness and yield strength calculations are presented for high density polyethylene (HDPE). Comparison with experiment for HDPE yields excellent agreement well within the necessary design accuracy. Agreement with experiment in the case of low density polyethylene (LDPE) is not as good, but within expectations considering the degree of theory refinement and the poorer morphological data base for LDPE.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 1000-1009 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Among the increased structural demands now being made on both unfilled and reinforced plastics is that of dimensional stability under various performance environments. Crystalline polymers are heterogeneous materials consisting of two distinct phases and, as such, can be treated as molecular versions of engineering composites. This paper first outlines the general physical model whereby a crystalline polymer is considered to be a multi-ply laminate of unidirectionally reinforced plies. The calculational format is then detailed for the prediction of the stiffness and thermal expansion coefficient of an isotropic sheet of crystalline polymer and a sample calculation is given for quenched high density polyethylene. A data base is presented for the stiffness and thermal expansion coefficient of low and high density polyethylene having quenched, slowcooled, and annealed thermal histories. Comparison between experimental and predicted results yields good agreement in all cases to better than 25 percent. Implications and limitations of the predictive technique are discussed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 15 (1975), S. 129-129 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 496-504 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 strength of randomly oriented short fiber composites has been modeled by a quasi-isotropic laminate. Lamination theory and a failure criterion will be used to approximate the stress-strain response of a composite as it is loaded to failure. Experimental data are presented and compared with the maximum-strain failure criterion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3935-3950 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rupture properties of sulfur and zinc oxide vulcanizates of a carboxylic rubber have been experimentally determined. When the logarithm of the strength at break is plotted against the logarithm of the strain at break, failure envelopes are obtained for the two vulcanizates which diverge at long times or high temperatures. As a consequence of this experimental fact it is apparent that, while there exists a failure envelope which uniquely describes a given viscoelastic system, there is no general shape of the failure envelope representative of all the rupture properties of an elastomer through all degrees of vulcanization. It is shown that the molecular fracture theory of Bueche and Halpin provides a quantitative basis for the analysis of the strength properties of elastomers through a wide range of vulcanizate quality, provided the specific character of the network structure is taken into account. It is suggested that the so-called “unique” strength properties of metal oxide vulcanizates are in reality a natural reflection of a sparse network crosslinkage concentration.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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