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  • morphology  (4)
  • Polystyrene  (2)
  • crystallization  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 267 (1989), S. 494-499 
    ISSN: 1435-1536
    Keywords: Polystyrene ; (M w≳106) ; intrinsic viscosity ; adsorption-entanglementlayers ; toluene ; decaline
    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 Adsorption-entanglement layers have been shown to interfere with the measurement of intrinsic viscosity of high-molecular weight (M w≳106) atactic polystyrene solutions. Values of the intrinsic viscosity, corrected for the pressure of any such layers are reported. The Mark-Houwink relationship is thus shown to fail at high molecular weights.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 271 (1993), S. 328-342 
    ISSN: 1435-1536
    Keywords: Polyethylene ; crystallization ; morphology ; single crystal ; spherulite ; axialite
    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 Three-dimensional shape of polyethylene single crystals grown from the melt has been studied. Two distinct types of lateral habit have been obtained: lenticular shape (type A) and truncated lozenge (type B) in the range of regime I and II. Electron microscopy has revealed chair-like shape of type B crystal and reconfirmed the planar shape of type A crystal. In the type B crystal, spiral growth has occurred frequently in the {110} sectors and the sense of the handedness of spiral terraces has been maintained. It has been, suggested that the frequens occurrence of spiral growth is responsible for a morphological change (axialite-spherulite) accompanying the regime I–II transition. The origin of the chair-like crystals has been discussed and, a possible mechanism has been suggested for the formation of spiral terraces; the mechanism is based on a distortion caused by the three-dimensional shape of chair-like crystals. It has been found that the chair-like crystals are curved in the opposite way to S-shaped lamellae observed by Bassett and Hodge in banded spherulites. In fact, the present work has led to the recognition of further classes of crystal with curving cross-sections and of distinctions between them. In final analysis, a unifying thread has been identified between lateral habits, growth kinetics and three-dimensional shape of lamellae, in turn, leading to some rationalization of multilayer developments including twisting in banded spherulites, the latter based on existing suggestions in the literature.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 271 (1993), S. 469-479 
    ISSN: 1435-1536
    Keywords: Polystyrene ; polyvinylalcohol ; latices ; ellipsoidal particles
    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 A method is described for the preparation of monodisperse ellipsoidal particles of polystyrene in the colloidal size range. Monodisperse polystyrene particles were dispersed in a solution of polyvinyl alcohol. This dispersion was then allowed to form, by evaporation, a thin film of polyvinyl alcohol containing spherical polystyrene particles. Strips of this film were clamped into a metal frame, heated rapidly in an oil bath to 200°C and stretched to a predetermined extent in order to convert the spherical particles into ellipsoids; the film was then cooled. A wide range of axial ratios for a variety of initial particle sizes was obtained by this method.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 261 (1983), S. 721-735 
    ISSN: 1435-1536
    Keywords: Polyethylene ; shish-kebabs ; overgrowth-spacing ; morphology
    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 platelet component of shish-kebabs crystallizes after the core, during cooling or storage below the formation temperature of the core. Three basic platelet morphologies were previously identified which were mutually interconvertible, a process we have termed “hairdressing”. In this paper we show that these three categories are special cases of a continuous range of overgrowth spacings. Crystallization at high temperatures gives widely spaced overgrowths and, as the crystallization temperature is reduced, so the overgrowth spacing decreases gradually. In the extreme case (only obtainable by quenching) the overgrowths become so close as to overlap and appear continuous. We also report a variety of further effects which were caused by exposing the shish-kebabs, while in solvent, to temperatures above their initial formation temperature. A new theoretical approach is described which considers the depletion of material available to form new overgrowths during crystallization. Two versions of this theory are presented (one a computer simulation and one analytic); interpreting our results on the basis of this theory we show that shish-kebabs crystallize at high temperatures even when quenched (90°C and above except in a few exceptional circumstances) and we are able to explain all the features of shish-kebab crystallization that we have observed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1877-1894 
    ISSN: 0887-6266
    Keywords: liquid crystals ; crystallization metastable phases ; rates of phase transformation ; morphology ; competition between phases ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of the monotropic liquid crystal forming polyether, poly-n-nonyl-4 4′-biphenyl-2-chloroethane, was investigated using DSC calorimetry and polarizing optical microscopy. The principal theme was the nature of crystallization from the nematic liquid crystalline state, which in the monotropic system could be directly compared with the more familiar crystallization from the isotropic melt using one and the same compound. Novel, polarizing optical structures were observed that combine features of both the usual LCPs (fine “grains”) and those of the conventional crystallizeable polymers (spherulites) with differing degrees of prominence of each according to crystallization conditions. The considerations of such structural observations, combined with the calorimetric results and the newly gained information on the kinetics of the crystallization process, reveal an acceleration of the overall crystallization rate at the stage where liquid crystal formation sets in as assessed by calorimetry but not as registered with the polarizing microscope, leading to wider issues regarding the conception of “amorphous crystalline ratio” and its extension to the liquid crystal state. Beyond polymers, the new findings lead to the more general considerations on metastable phases, specifically to their emergence and competition with the phases of ultimate stability. In this respect the present study on a monotropic LCP provides an illustrative example of a more general treatment presented previously. © 1995 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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