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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 3365-3368 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Inversion recovery cross polarization (IRCP) NMR was used to study the solid state morphologies of plasticized and neat poly(vinyl butyral-co-vinyl alcohol) (PVB), of polyether polyurethane elastomers (PU), and of low density polyethylene (LDPE). IRCP decay data for these polymers were best fit to a biexponential two-component model modulated by T1ϱH relaxation. These results clearly display the two-phase nature of these polymers, as well as the potential applicability of the IRCP technique.
    Type of Medium: Electronic Resource
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  • 3
    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: A correlation has been established between the dynamic storage modulus (E') and the mean cross polarization time constants 〈TCH〉 for a set of five morphologically diverse polymers, including one at two temperatures and one at two plasticizer concentrations. The correlation is only possible when the TCH values for all of the motional environments within the polymers are considered. An inversion recovery cross polarization (IRCP) NMR technique is used to obtain motional and morphological information from the main chain carbons of each polymer. After comparing simplified correlation functions for the two parameters, an experimental relationship between them is established that suggests that TCH and E' are both modulated by a similar distribution of molecular motions.
    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 46 (1992), S. 295-301 
    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: Samples of plasticized poly(vinyl butyral-co-vinyl alcohol) (PVB) are found to exhibit multiple thermal transitions as observed by dynamic mechanical analysis (DMA) and differential scanning calorimetry (DSC). Arrhenius plots using DSC and DMA data suggest that two of the transitions are glass-type ones. Variable temperature solid-state 13C-NMR experiments show a temperature-dependent line-broadening pattern for all PVB backbone carbons with maximum broadening at 55°C or at about 50°C above the second-order-type transitions α1 and α2 as measured by DSC. Using Arrhenius plots, the NMR transition is found to best correlate with α1, which is consistent with glass transition behavior. The solid-state NMR spectra also show that vinyl alcohol tacticity remains unresolved up to a temperature of about 95°C, beyond which line narrowing begins to occur. High-temperature thermal transitions are also observed by DSC and DMA, which suggest that the onset of motion involving vinyl alcohol sequences may be responsible for these transitions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1999-2003 
    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 sedimentation behavior of alumina powder has been studied in the presence of poly-vinylpyrrolidone (PVP) and poly(vinylpyrrolidone-co-vinyl acetate) (PVP/VA) in both thermodynamically “good” and “poor” solvents for the PVP homopolymer. PVP/VA provides higher sediment densities than does its PVP homopolymer counterpart. Solutionstate 13C-T1 spin-lattice relaxation measurements were made on analogous mixtures both with and without alumina powder. The NMR results suggest that the PVP/VA copolymer is anchored to the alumina powder surface by means of VA moieties, whereas the PVP moieties extend into the continuous phase of the slurry medium. Thus, the higher settling densities that are observed in the presence of PVP/VA can be attributed to a steric stabilization mechanism. © 1993 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 677-681 
    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: A relationship between dynamic storage modulus (E′) and the mean cross-polarization time constants 〈TCH〉 for 16 polymer data sets has been established by using a standard linear solid model. This model is used in an attempt to equate the process of cross-polarization with mechanical rigidity by virtue of the implicit dependence of each phenomenon on molecular motion. The apparent validity of the relationship between these parameters indicates that cross-polarization in polymers can be a function of molecular motion in addition to microscopic spin dynamics. The limitations as well as practical applications of this relationship are discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
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  • 7
    Publication Date: 1992-06-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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