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  • 1995-1999  (3)
  • 1955-1959
  • 1925-1929
  • Polymer and Materials Science  (3)
  • morphology  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1733-1740 
    ISSN: 0887-6266
    Keywords: polyesters ; pigment dispersion ; acid-base interaction ; dispersion rheology ; adsorption ; chain configuration ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rheological properties have been measured for solutions of polyesters containing quantities of inorganic and organic pigments. Complex behavior patterns were simplified by computing the effective volume fraction of dispersed solids, taking in account the thickness of polymer layers adsorbed on pigment surfaces. The dimension of interphases created by the adsorbed polymers was rationalized by applying principles of specific interaction between polymers and pigment surfaces. The parameters of specific interaction were obtained from inverse gas chromatographic data. Pigment sedimentation data were used to identify a range of specific interactions best suited to stabilize dispersions of the solids. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    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 35 (1997), S. 2457-2464 
    ISSN: 0887-6266
    Keywords: polyamide 6 ; aluminum borate whiskers ; poly(ε-caprolactam) ; crystallinity ; composites ; interphase ; morphology ; wide-angle X-ray scattering ; differential scanning calorimetry ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of aluminum borate whiskers upon the morphology of polyamide 6 was studied by wide-angle X-ray scattering and by differential scanning calorimetry. The whiskers did not promote the formation of either the hexagonal γ or the monoclinic β crystalline phase. A new experimental procedure has been devised for the production of very thin polymer layers on the whiskers. In the procedure, styrene co-acrylonitrile polymer is used as a processing aid and is later extracted. The procedure allows for the generation of polyamide layers less than 30 nm thick. Crystallinity in these thin layers was suppressed. An expression has been developed to characterize the crystallinity gradient in the interphase of the whisker surface. The equation shows that the initial 1.4 nm of polymer is fully amorphous and produces excellent evaluations of the crystallinity gradient to layer thicknesses of 70 nm. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2457-2464, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 51-56 
    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: Inverse gas chromatography of alkanes has been used to assess the degree of fusion of rigid polyvinyl chloride (PVC) extrudates. The relative degree of fusion is provided by ratios of the retention volumes of the alkane probe molecules in the bulk of the PVC. This method is nonintrusive and can be used to measure degree of fusion quantitatively if a completely fused reference material can be provided. The present analysis involves evaluations of the contributions to the overall retention volume of the alkane probes, resulting from adsorption and from bulk diffusion. The diffusivity of the alkanes was clearly dependent on the processing history of the PVC extrudate. A direct variation was observed between the size of the diffusing molecules and their residence time as adsorbates on the polymer surface. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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