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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1273-1283 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The two endotherms found during DSC analysis of annealed or drawn poly(ethylene terephthalate), PET, are discussed in greater. detail. Earlier workers proposed that the endotherms were the result of separate morphologies, i.e., extended-chain and folded-chain crystals, but more recently Roberts and others have presented data on the effect of DSC heating rate on annealed PET endotherm areas which indicate that the higher temperature endotherm is the result of recrystallization in the DSC. The present work explains the reasons for recrystallization, and presents data showing that samples cooled at various rates from the melt also exhibit recrystallization in the DSC, in much the same manner as samples annealed for different lengths of time. Further, by prolonged annealing before analysis, part of the recrystallization exotherm can be observed in the DSC scan. Drawn nylon 66 also exhibits recrystallization in the DSC, in a manner similar to annealed or slowly crystallized PET. The amount of material that recrystallizes is determined by the time and supercooling available between first melting and the ultimate recrystallization temperature, i.e., a temperature at which there is too little time and temperature driving force for further recrystallization to occur. Infrared absorption data show an increase in “regular” fold content during prolonged annealing of PET, while dynamic mechanical data show a marked decrease in a dispersion that is likely associated with the looser fold crystal morphologies. Annealed PET does superheat in the DSC, leaving unanswered the question as to whether any partially extended material is present along with the regular-fold material. For cold-drawn PET, the infrared data indicate disappearance of regular folds and the dynamic mechanical data indicate disappearance of the looser folds. Cold-drawn PET also superheats. These data indicate a likelihood of at least partially extended morphologies in cold-drawn PET; these observations do not apply to PET drawn at high temperatures or to polyethylene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 417-436 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A technique for estimating Mc, the molecular weight between crosslinks, of amine-cured epoxy resins is described. The technique is based upon the stoichiometry of the curing reaction and the amount of primary amino and epoxy groups remaining in the polymer at a given time. The Mc values so calculated are shown to be consistent with Mc results obtained from separate measurements of swelling and the polymer-solvent interaction parameter χ1 for the range of polymer concentration in which both measurements could be obtained. A means of estimating the relative reaction rates of the primary and secondary amino groups with the epoxy groups is given. Under proper curing conditions the amine-epoxy reaction goes very nearly to completion. The presence or absence of an exotherm has no noticeable effect on the course of the reaction between bisphenol A-epichlorohydrin (Epon 828) and methylene dianiline.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 437-445 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical properties of a series of epoxy polymers of known network structure have been investigated. It was shown that the distance between crosslinks could be predicted from either the shift in the glass transition temperature Tg or by use of the dynamic modulus above Tg. The front factor in the equation of state for rubber elasticity was near unity for stoichiometric equivalence of epoxy and amine and increased slowly with excess of either component.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1779-1791 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphological character of uniaxially oriented poly(ethylene terephthalate) (PET) films was investigated as a function of draw ratio. Dynamic mechanical, infrared, and crystallite-size measurements were made on the samples. In addition, selective degradation experiments and molecular weight determinations were employed. The dynamic mechanical measurements indicated a sharp decrease in irregular folds for draw ratios of 3.0 and higher, which also coincided with the essentially complete disappearence of regular folds (from the 988 cm-1 band in the infrared spectra) in unannealed samples. Infrared studies of drawn samples annealed under different conditions gave evidence in support of a structure in which the chains are stretched out. Apparent crystallite-size measurements showed a sudden increase in length of the crystals in the direction of the draw beyond a draw ratio of 3.0. Molecular weight measurements showed a large increase in average chain length in the residue after selective degradation of amorphous material and folds; undrawn and slightly drawn samples gave a much lower Mn. Based on these observations, it is postulated that for higher draw ratios and present drawing conditions, the crystals are of the straight chain type, somewhat similar to the fringed-micelle crystal concept.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1793-1801 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain folding in unoriented poly(ethylene terephthalate) (PET) films has been investigated as a function of annealing time and temperature. To meet this objective dynamic mechanical, infrared, and molecular weight measurements were used, together with selective chemical degradation to remove chain folds and amorphous regions. The β dispersion in the dynamic mechanical spectrum of PET is here tentatively associated with motions of methylene and/or carboxyl groups in irregular chain folds; the β dispersion is not found in quenched amorphous polymer, in polymer where amorphous regions and chain folds have been removed, or in highly annealed PET where the irregular folds have regularized. Upon mild crystallization and annealing (30 min at 110°C) of initially amorphous film a large β dispersion appears and then diminishes upon further annealing at 220°C. As the β dispersion diminishes, the infrared regular fold band increases more than the crystallinity band, indicating regularization of folds. The molecular weight of the degraded residue corresponds approximately to typical fold-period dimensions (∼130 Å), and increases on annealing as expected from lamellar thickening. The degradation process has, by fold removal, reduced the chains in the crystals to a very short, uniform length.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1321-1322 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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