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  • 1995-1999  (6)
  • Boger fluid  (3)
  • polymer blends  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 36 (1997), S. 97-109 
    ISSN: 1435-1528
    Keywords: Key words Polymer migration ; anomalous rheology ; Boger fluid ; normal stress ; elastic instability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The use of constant viscosity, highly elastic polymer solutions, so called Boger fluids, has been remarkably successful in elucidating the behavior of polymeric materials under flowing conditions. However, the behavior of these fluids is still complicated by many different physical processes occurring within a narrow window of observation time and applied shear rate. In this study, we investigate the long-time shear behavior of an ideal Boger fluid: a well characterized, athermal, dilute, binary solution of high molecular weight polystyrene in oligomeric polystyrene. Rheological measurements show that under an applied steady shear flow, this family of polymer solutions undergoes a transient decay of normal stresses on a timescale much longer than the polymer molecule‘s relaxation time. Rheological and flow visualization results demonstrate that the observed phenomenon is not caused by polymer degradation, phase separation, viscous heating, or secondary flows from elastic instabilities. Although the timescale is much shorter than that associated with polymer migration in the same solutions (MacDonald and Muller, 1996), the appearance of this phenomenon only at the rates where migration has been observed suggests that it may be a prerequisite for observing migration. In addition, we note that through sufficient pre-shearing of the sample, the normal stress decrease suppresses the elastic instability. These results show that there is considerable uncertainty in choosing the appropriate measure of the fluid relaxation time for consistently modeling the critical condition for the elastic instability, the decay of normal stresses, and the migration of polymer species.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1528
    Keywords: Emulsion model ; polymer blends ; drop deformation ; elongational flow ; viscoelasticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The deformation of dispersed droplets in immiscible polymer blends was studied in elongational flow, with an original method based on quenching specimens elongated in the melt. Results for high capillary numbers and different viscosity ratios were compared to the linear theory of viscoelastic emulsions of Palierne. Simple expressions for the drop deformation could be obtained for Maxwell fluids, and the influence of viscoelasticity of matrix and inclusions on the drop deformation process was discussed. With respect to the Newtonian approximation, the description of some experimental data could be improved. However, the predictions of the viscoelastic model appeared to be very sensitive to the choice of relaxation times.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 36 (1997), S. 97-109 
    ISSN: 1435-1528
    Keywords: Polymer migration ; anomalous theology ; Boger fluid ; normal stress ; elastic instability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The use of constant viscosity, highly elastic polymer solutions, so called Boger fluids, has been remarkably successful in elucidating the behavior of polymeric materials under flowing conditions. However, the behavior of these fluids is still complicated by many different physical processes occurring within a narrow window of observation time and applied shear rate. In this study, we investigate the long-time shear behavior of an ideal Boger fluid: a well characterized, athermal, dilute, binary solution of high molecular weight polystyrene in oligomeric polystyrene. Rheological measurements show that under an applied steady shear flow, this family of polymer solutions undergoes a transient decay of normal stresses on a timescale much longer than the polymer molecule's relaxation time. Rheological and flow visualization results demonstrate that the observed phenomenon is not caused by polymer degradation, phase separation, viscous heating, or secondary flows from elastic instabilities. Although the timescale is much shorter than that associated with polymer migration in the same solutions (MacDonald and Muller, 1996), the appearance of this phenomenon only at the rates where migration has been observed suggests that it may be a prerequisite for observing migration. In addition, we note that through sufficient preshearing of the sample, the normal stress decrease suppresses the elastic instability. These results show that there is considerable uncertainty in choosing the appropriate measure of the fluid relaxation time for consistently modeling the critical condition for the elastic instability, the decay of normal stresses, and the migration of polymer species.
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 301-308 
    ISSN: 1042-7147
    Keywords: polymer blends ; melt rheology ; crosslinked rubber ; structured latex ; 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
    Notes: The linear viscoelastic behavior of model rubbertoughened polymer melts has been studied. The most significant influence of the dispersed crosslinked rubber phase on the melt rheology of the blends is the existence of a secondary plateau for the storage modulus G′ at low frequencies. This behavior was ascribed to a percolation phenomenon, leading to the formation of a threedimensional network of inclusions, and contributing to the elasticity at low frequencies of the blend. Two different systems were investigated: (a) a polystyrene matrix with crosslinked and structured latex particles and (b) silicon oil matrices with homogeneous crosslinked PMMA particles. An initial shearing history was found to influence the dynamic mechanical properties of the molten blends and in particular to lower the lowfrequency plateau value for G′. During a subsequent annealing, the plateau modulus increases again. These results are in agreement with the assumption of a particle network.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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