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  • 1995-1999  (3)
  • 1996  (3)
  • Boger fluid  (1)
  • eutrophication
  • polymer blends
  • 1
    ISSN: 1573-5117
    Keywords: acidic water ; alkaline water ; autoecology ; bioindication ; macrophyte community ; eutrophication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two bioindication scales of the degree of eutrophication based on aquatic macrophyte communities were established in two types of running waters free of organic matter, the one in acidic “soft” waters (pH 5.5–7.0, conductivity 40–110 μS.cm−1), the other in alkaline hard waters (pH 7–8, conductivity 500–900 μS.cm−1). We show that the main determining factor of the macrophyte distribution is the nutrient level (trophy), especially the level of phosphate and ammonia. The acidic scale, with increasing pH, includes four stages ranging from oligotrophic to eutrophic level (traces to 300 μg.l−1 N-NHinf4p+ and P-PO4 3−), while the alkaline scale at constant pH comprises six stages of a trophic gradient. For the most part, the floristic composition found in the two sequences is different and depends on conductivity and alkalinity variation. However, some species occur in the two scales and may reflect differences in the trophic level, depending on whether the waters are alkaline or acidic. This change of trophic level for these species is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 35 (1996), S. 369-381 
    ISSN: 1435-1528
    Keywords: Melt rheology ; linear and non-linear viscoelasticity ; polymer blends ; reinforced polymers ; morphology ; Cox-Merz rule ; aggregation ; percolation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Viscoelastic behavior, phase morphology and flow conditions relationships in polymer/rubber blends have been investigated. The importance of such correlations is illustrated on polymethylmethacrylate (PMMA)/rubber blends subjected to different flow conditions both under small and large deformations. In small-amplitude oscillatory shear (the morphology does not change during the flow) the elastic modulus G′ of the concentrated blends shows a secondary plateau, G′ p , in the low frequency region. This solid-like behavior appears for rubber particle contents beyond the percolation threshold concentration (15%). Morphological observations revealed that for concentrations higher than 15%, the particles are dispersed in a three-dimensional network-type structure. In capillary flow it was found that the network-type structure was destroyed and replaced by an alignment of particles in the flow direction. This morphological modification resulted in a decrease in both viscosity and post-extrusion swell of the blends. Morphological observations revealed that the ordered structure in the flow direction was concentrated only in the skin region of the extrudate, where the shear stress is higher than the secondary plateau, G′ p . A simple kinetic mechanism is proposed to explain the observed morphology. Similarly, steady shear measurements performed in the cone-and-plate geometry revealed alignment of particles in the flow direction for shear stress values higher than G′p.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 181-192 
    ISSN: 0887-6266
    Keywords: ternary solutions ; solvent quality ; polystyrene-dioctyl phthalate ; light scattering ; Boger fluid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymer solvent interactions in the ternary system high molecular weight polystyrene (HMPS), low molecular weight polystyrene (LMPS), and dioctyl phthalate (DOP) have been characterized by means of intrinsic viscometry (IV), dynamic light scattering (DLS), and static light scattering (SLS). Excluded volume exponents have been extracted from the scaling of intrinsic viscosity and translational diffusivity with polymer molecular weight for a mixed solvent of 13 wt % LMPS/87 wt % DOP. The value of the excluded volume exponent, v = 0.45, indicates that HMPS in the mixed solvent DOP/LMPS has apparently assumed a reduced conformation relative to the theta condition. However, SLS measures of the second virial coefficient (A2) confirm that DOP is a theta solvent at our experimental temperature of 22°C and indicate that the addition of LMPS increases A2. SLS also suggests that neither solvent component is strongly preferentially adsorped into the HMPS coil. Our system then is a mixture of a theta solvent and a good solvent that exhibits poor solvent scaling behavior. We believe this to be the first demonstration of such behavior in a system that does not exhibit appreciable preferential adsorption. We conclude by examining our observations in the context of current descriptions of mixed solvent thermodynamics. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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