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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 10584-10586 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1293-1303 
    ISSN: 0887-6266
    Keywords: extended-chain crystals ; low molecular weight linear polyethylene ; revision of Flory's theory of fusion ; interfacial free energy ; bulk-isothermal crystallization ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: To analyze extended-chain crystalline systems composed of linear polyethylene, Flory's conventional theory of fusion is reconsidered by introducing a new concept of crystallinity. When this new treatment is applied to a melting case of a low molecular weight polyethylene fraction (Mn = 5600) isothermally bulk crystallized, a certain result that very large lamellar thickness was caused by a very small increase in crystallization temperature can satisfactorily be explained by a significant change in interfacial free energy of the crystallite end. Further, it shows 14-17 kJ/mol as a nonequilibrium value range of interfacial free energy for highly crystalline polyethylene fractions of low molecular weight Mn ≦ 5600 by using the previous data presented by other workers. A similar result is also obtained on the Mn = 5600 fraction by analyzing from a standpoint of equilibrium crystallinity. In either case, the estimated range of interfacial free energy is consistent with the conventional range. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1293-1303, 1998
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2775-2782 
    ISSN: 0887-624X
    Keywords: surface crystallinity ; gel melting ; crystallite size ; size distribution ; EP copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A characterization for crystalline junction polymer gels has been extended by introducing a new parameter which implies a measure of the number of the polymer molecules passing through the crystallizing junctions. The parameter has been considered in a theoretical gel melting relation derived by Takahashi, Nakamura, and Kagawa and a crystallite size distribution has also been considered. The equation obtained was examined on ethylene-propylene copolymer gels by using the previous data of melting temperatures determined from DSC, crystallite sizes from x-ray and DSC measurements, and reaction probabilities from 13C-NMR measurements. Consequently, the parameter was found to be helpful as one additional measure. Also, it was confirmed that the average crystallite sizes estimated in several different ways were all in good agreement with the conventional data. © 1996 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 653-659 
    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 properties of poly(vinyl alcohol) (PVA) hydrogels containing saccharose were examined. The effect of the addition of saccharose to atactic PVA (α-PVA) gels on their melting temperatures was larger than that for syndiotacticity-rich PVA (s-PVA) gels and the melting temperature was above 100°C for α-PVA gels with saccharose contents of 60 wt %. However, the fusion enthalpy (ΔH) of the α-PVA gels was at most 100 kJ/mol. The release of solvent (water/saccharose) from gels in air decreased with an increase in the saccharose content and the equilibrium was achieved after standing for 20 days for the α-PVA and s-PVA gels with saccharose contents above 40 and 20 wt %, respectively. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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