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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2609-2616 
    ISSN: 0887-6266
    Keywords: blends ; organosilicon polymers ; polystyrene ; poly(2,6-dimethyl-1,4-phenylene oxide) ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Blends of organosilicon polymers with polystyrene, PS, and poly(2,6-dimethyl-1,4-phenylene oxide), PPE, were investigated by transmission electron microscopy and differencial scanning calorimetry. Blends with poly(tetramethylsilphenylenesiloxane), PTMPS, showed a morphology characterized by globular domains dispersed in the organic matrix. An apparent homogeneous system was observed when poly(dimethylsilphenylene), PDSP, was mixed with PPE. A crystalline phase was found in samples with a higher PDSP content. The morphology of PS/PDSP blends with low PDSP content showed a dendritic phase dispersed in the PS-rich matrix. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2609-2616, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 1257-1271 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Shear influences on the phase separation behaviour of four different blends of ethylene glycol/propylene glycol oligomers, exhibiting upper critical solution temperatures, were investigated. Cloud point curves at rest (turbidity measurements) are reported for all systems, spinodal conditions (light scattering) and tie-lines (analysis of the coexisting phases) are given for some examples. Phase diagrams under shear were obtained from rheological data. They demonstrate that the demixing temperatures of systems where both glycols bear OH end-groups are lowered up to ca. 1°C by shear rates of 1000s-1; the critical composition, generalized to the non-equilibrium conditions of flow, is markedly shifted. These observations are explained in terms of the generalized Gibbs energy (containing the mechanical energy the system stores during flow) as a consequence of the strongly interacting end-groups of the glycols. This interpretation is backed by the fact that the shear effects disappear when the glycols are methylated.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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