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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 34 (1995), S. 586-600 
    ISSN: 1435-1528
    Keywords: Non-aqueous drag reducers ; steady and dynamic shear properties ; temperature and concentration effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The steady and dynamic shear properties of two non-aqueous drag-reducers (a medium molecular weight polyisobutylene and a commercial organic drag-reducer) in kerosene solutions over a wide range of temperature and concentration were presented. The intrinsic and zero-shear viscosity results were used to identify the concentrate regimes of these solutions. A characteristic time constant λ0, which was based on the spring-bead model for dilute solutions, was employed as the scaling parameter for both steady-shear and dynamic data over a wide range of concentration and temperature. The inadequacy of the Graessley reduced-variable method in the dilute region was illustrated. The shear-thinning behaviour of these polymer solutions could be described by the Carreau model. The dynamic data followed the Zimm and Rouse-like behaviour in the low and high frequency limits. The Cox-Merz rule was obeyed in the low shear rate and frequency regions. The Carreau and the zero-frequency Maxwell time constants appeared to be related to λ0 by a constant factor over a wide range of polymer concentrations. The finding provides a method for extrapolating viscoelastic information into the drag reduction regime, and could be useful for interpretation of drag reduction results.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 34 (1995), S. 384-396 
    ISSN: 1435-1528
    Keywords: Direct simulation ; molecular dynamics ; FENE fluids ; flow between parallel plates ; flow in sudden expansion and contraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Direct simulations of macromolecular fluids are carried out for flows between parallel plates and in expanding and contracting channels. The macromolecules are modeled as FENE dumbbells with soft disks or Lennard-Jones dumbbell-dumbbell interactions. The results are presented in terms of profiles and contour plots of velocity, pressure, temperature, density, and flow fields. In addition the data for potential energy, shear stress, and the normal components of the stress tensor are collected. In general, an excellent agreement is found between the simulated profiles and the well-known flow structures, such as flow separation and formation of viscous eddies, indicating that micro-hydrodynamics is a viable tool in linking macroscopic phenomena with the underlying physical mechanisms. The simulations are performed in the Newtonian regime, for medium-size systems comprising up to 3888 dumbbells. This number is sufficiently large to control boundary and particle number effects. The flow is induced by gravity. The traditional stochastic (thermal) and periodic boundary conditions are employed. Also, diffusive boundary conditions, which could include a stagnant fluid layer and repulsive potential walls, are developed. The scaling problems, which are related to the application of a large external force in a microscopic system (of the size of the order 100 Å), result in extreme pressure and temperature gradients. In addition, the viscosity and thermal conductivity coefficients obtained from velocity and temperature profiles of the channel flow are presented. These results are confirmed independently from modeling of Couette flow by the SLLOD equations of motion and from the Evans algorithm for thermal conductivity.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1528
    Keywords: Blends ; linear viscoelasticity ; emulsion models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The linear viscoelastic properties of several molten blends with immiscible components of different viscosity ratio have been investigated. All the blends show a morphology of emulsion type. At low frequencies, the behaviors of these blends are essentially governed by the interface. The Palierne (1990) model is shown to well predict the linear behavior of all the blends. The Lee and Park model (1994), developed to take into account the relationship between the rheological behavior and morphological changes under large strain flows, is also shown to well describe the storage and loss moduli of the blends by adjusting a single fitting parameter. Based on the weighted relaxation spectra, a comparison of both model predictions is made focussing on the time associated to the interface. An approximate method is then proposed to evaluate the interface parameter introduced in the Lee and Park model. At high frequency, discrepancies are observed for the Lee and Park predictions when the viscoelastic properties of both components are considerably different. The description of the bulk properties of the blend, i.e., the mixing rule used by Lee and Park, is modified to obtain a better description of the high frequency data.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 391-391 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 600-608 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Mechanical and rheological properties of blends of a thermotropic liquid crystalline polyester with a polycarbonate have been investigated. The blends are fibrillar in character and exhibit great hardness and toughness due to high degree of molecular orientation which develops during the melt blending and processing steps. Increases of the Young modulus by 100 percent are observed for blends containing only 10 percent of liquid crystalline polymer, LCP. Time-dependent behavior of the blends was investigated by performing solid state relaxation measurements and the relaxation modulus was also found to increase by the addition of LCP. The effect is relatively small in the glassy zone of viscoelastic response, but increases through the transition and viscous flow regions. The melt viscosity of the polycarbonate is slightly shear thinning whereas that of the unblended LCP increases rapidly with decreasing shear rate at low shear rate. This suggests the presence of yield stresses as confirmed by measurements on the Rheometics RSR in the stress sweep mode. The melt viscosity of the blends was found to be similar to that of the unblended polycarbonate, but more shear-thinning and less viscous. Preliminary results of scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) are also presented.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1876-1885 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Thermal, rheological, morphological, and mechanical properties of a thermotropic liquid crystalline polymer, TLCP (copolyester Vectra A-950 from Hoechst), blended with a polycarbonate (PC), a polyethylene glycol terephthalate (PETG), and a blend of PC and PETG (20/80) are presented and discussed. Important supercooling effects are observed for the TLCP. For the blends the glass transition temperature of the matrix is shown to decrease slightly, suggesting partial miscibility of the components. A finer dispersion is observed for the TLCP/PC blends, at least for TLCP concentrations lower than 20%, for which the mechanical properties are quite good. For higher TLCP concentrations, as well as for the other two matrices, the mechanical properties follow more or less the mixing rule, and the morphology of the blends suggests poor adhesion. We were unable to obtain fibrillar structures by extruding the blends through a capillary rheometer; in the TLCP/PC blends, the TLCP domains were too small, and for the other blends the extrudates had not enough melt strength.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 669-676 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: The exit flow from a capillary is analyzed with the help of macroscopic mechanical energy and momentum balances. The analysis shows that primary normal stress differences cannot be determined from the exit pressures under the assumption that the flow is viscometric down to the exit. This assumption and the second one (made by Han [9]) that both slit and capillary exit pressures are the same would lead to unacceptable results. Published exit pressure data for polyethylene melts are shown to be unreliable because of large hole-pressure errors in the pressure measurements. Pressure profiles obtained with a thin tube technique for the flow of a poly(isobutylene) solution indicate that the flow does not remain fully developed near the exit. Moreover, it is shown that for this polymer solution the excess viscous dissipation at the exit contributes to approximately 90 percent of the exit pressure.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 293-308 
    ISSN: 0887-6266
    Keywords: polymer blends ; morphology ; stability ; co-continuity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphological stability of polystyrene high-density polyethylene (PS/PE) blend is investigated in the region of dual-phase continuity. The effect of the addition of a triblock SEBS copolymer to the blends on the stability of these morphologies, is examined. The results show that the morphology of the unmodified blends changes from co-continuous to droplet matrix for PS-rich blends whereas the morphology of a 50/50 blend maintains continuity but coarsened significantly upon annealing at 200°C. In the presence of the copolymer, these morphologies are much more stable. Selective solvent extraction of polystyrene in di-ethyl ether reveals that the level of PS continuity in the 50/50 blend is higher for the unmodified system than for the modified one. Upon annealing, the level of PS continuity significantly increases for the unmodified 50/50 PS/PE blend. The effect of the copolymer content in the blend on the interfacial tension between the two components is also investigated using the breaking thread method. The interfacial tension is found to be reduced from 5.6 to 1.1 mN/m by the addition of 20 parts of the copolymer to the blend. © 1997 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1965-1968 
    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: The critical molecular weight Mc of 36 flexible and semirigid polymers has been studied. A unique correlation between the critical end-to-end distance 〈Rc〉 for entanglements and the average polymer chain diameter D is found. This correlation is discussed in the light of the reptation concept.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 1544-1550 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Plastic profile die design is a complex task because of cross section area and shape changes occurring after die exit. Dimensions of the profile are increased by the extrudate swell phenomenon and decreased by drawdown and shrinkage. An experimental study on the effect of processing conditions on extrudate swell and on the shape of a rectangular profile was done for rigid poly(vinyl chloride), PVC, and high density polyethylene, HDPE, resins. Extrudate swell was found to be a strong decreasing function of residence time in the die and also, for short dies, of entrance geometry. For PVC, equilibrium swell increased with melt temperature. The differences in swelling for the two polymers are explained with the help of creep/recovery data obtained on a stress rheometer. Drawdown, die land length, and melt temperature were shown to have an important effect on the shape of a rectangular profile. Decreasing the die land and increasing the melt temperature had the effect of increasing preferably the thickness while drawdown, by inhibiting the swelling, decreased the thickness.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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