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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 262 (1984), S. 22-45 
    ISSN: 1435-1536
    Keywords: Isotactic polystyrene ; gels ; structure ; morphology ; conformation ; X-ray diffraction ; electron microscopy ; DSC ; FTIR ; crystallization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The thermoreversible gelation phenomena exhibited by isotactic polystyrene (i-PS) was examined in depth, utilising a variety of experimental techniques. The primary aims were identification, relationship, description and visualisation of the morphologies corresponding to the two types of crystallization as diagnosed by the different crystal structures revealed by X-ray diffraction. While centred on electron microscopy the investigation used X-ray and electron diffraction, differential scanning calorimetry and Fourier transform infra-red spectroscopy in combination. A satisfactory correlation between all these techniques was established, including the important reassurance that the characteristics of the gel state are preserved on drying, a feature necessitated by most structure methods. Thei-PS gel system as a whole displays particularly clearly the distinction between gel forming and chain folded lamellar crystallization and the coexistence, morphological relationship and competition between the two crystallizable species. In addition, and most significantly, the gel crystals possess a crystal structure involving extended chains, close to an all-trans conformation, which are quite different to those obtained from conventionally crystallizedi-PS (31 helix). This former extended conformation in itself has become the starting point for new geometric and stereochemical considerations and in addition offers a convenient diffraction based fingerprint to delineate between the two modes of crystallization. Thus the conversion of the gel crystal structure to the conventional 31 helix structure on heating could be monitored. Further, that in the processes of heat annealing, remnants of these gel fibres initiate the development and dictate the orientation of a shish-kebab type platelet growth with the 31 helix crystal structure. This conversion process has been followed by electron microscopy and supplemented infra-red spectroscopy, low angle X-ray diffraction and differential scanning calorimetry. The different roles of fibres and platelets on stretching have been identified. Conditions for the existence of the gel crystals in their different variants are specified with relevance to ongoing arguments and discussions in the subject. Further, it was established that passing through the gel phase significantly enhanced the crystallization in the conventional crystal form making the normally slowly crystallizingi-PS into a fast crystallizable polyolefin.
    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. 2401-2412 
    ISSN: 0887-6266
    Keywords: nylon 2 4 ; chain folding ; lamellar crystals ; structure and morphology ; crystallization ; electron microscopy ; Brill transformation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain-folded lamellar crystals of nylon 2 4 have been prepared from dilute solution by addition of poor solvent. Two crystal structures are observed at room temperature: a monoclinic form I, precipitated at elevated temperature, and a less-defined, orthorhombic form II, precipitated at room temperature. The unit cell parameters for both forms are similar to those reported for its isomer, nylon 3. Nylon 2 4 form II is a liquid-crystal-like or disordered phase, consisting of hydrogen-bonded sheets in poor register in the hydrogen bond direction. Form I crystals have two characteristic interchain spacings of 0.41 nm and 0.39 nm at room temperature and on heating, exhibit a structural transformation and a Brill temperature (250°C) characteristic of many other even-even nylons. Nylon 2 4 is a member of the nylon 2 Y and nylon 2N 2(N+1) families, and the form I crystals show behavior commensurate with both. We propose they contain a proportion of intersheet hydrogen bonds at room temperature, similar to that for the nylon 2 Y family, and the short dimethylene alkane segments mean that the structure consists of hydrogen-bonded a-sheets, with an amide unit in each fold, similar to that of nylon 4 6. The fold geometry and sheet structure is compared with chain-folded apβ-sheet polypeptides and nylon 3. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2401-2412, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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