1971
DOI: 10.1021/ma60020a015
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Dynamic Viscoelastic Properties of Polystyrene in High-Viscosity Solvents. Extrapolation to Infinite Dilution and High-Frequency Behavior

Abstract: The storage (O') and loss (G") shear moduli of solutions of four polystyrenes with narrow-distribution weightaverage molecular weights (M) from 19,800 to 860,000 have been measured over a frequency range frpm 0.02 to 634 Hz. The solvents were two Aroclors (chlorinated diphenyls) with a viscosity range from 2 to 7000 P over a temperature range from -

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Cited by 68 publications
(49 citation statements)
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“…Recently, Manke and Williams [8] studied the behaviour of a monodisperse polystyrene in two solvent blends of low molecular weight polystyrene and styrene monomer. Their experimental results confirmed the previous work of Massa et al [9] that polymer behaviour may also be affected under certain conditions by the internal viscosity of the polymer. This property has been found to be dependent on the structure of the polymer and of the solvent as well as the solvent viscosity [10][11][12].…”
Section: Introductionsupporting
confidence: 90%
“…Recently, Manke and Williams [8] studied the behaviour of a monodisperse polystyrene in two solvent blends of low molecular weight polystyrene and styrene monomer. Their experimental results confirmed the previous work of Massa et al [9] that polymer behaviour may also be affected under certain conditions by the internal viscosity of the polymer. This property has been found to be dependent on the structure of the polymer and of the solvent as well as the solvent viscosity [10][11][12].…”
Section: Introductionsupporting
confidence: 90%
“…is independent of the molecular weight M and the solvent viscosity ~ as has been observed by Ferry et al (4,5). …”
Section: General Expression For the Limiting Viscositysupporting
confidence: 63%
“…This suggests that their [tl~]/[tl0] ~ 0.8 was not the true rheological limit, either. [14]. These workers used good viscous solvent (Aroclors) for polystyrene, so r/s was even larger for their systems (,-~ 7 P a ' s ) than in ours ( 1 .…”
Section: Discussionmentioning
confidence: 58%
“…The polymer coil is severely deformed in the [t/oo] limit while negligibly deformed in the [r/~o] limit, but if these limits both represent the summed contributions of independent chain segments, the overall chain configuration may not be a dominant factor. In fact, the use of Aroclor in the dynamic experimënts [14] expands the polystyrene chain relative to the use of a theta solvent, perhaps to the extent (though not with the same symmetry) that shear extends the chain in the latter case.…”
Section: Discussionmentioning
confidence: 99%