Optical measurements of the shear response of semidilute dispersions of polymer-dispersed multiwalled carbon nanotubes are presented. For a weakly elastic polymer melt, the data suggest that the semiflexible tubes orient along the direction of flow at low shear stress, with a transition to vorticity alignment above a critical shear stress, σc, corresponding to a critical Deborah number of approximately 0.15. In contrast, data for a highly elastic polymer solution suggest that the tubes orient with the flow field at high shear rates, in the limit of large Deborah number. The measurements are in qualitative agreement with previous experimental and theoretical studies of fiber orientation in elastic fluids under simple shear flow.
We describe an optical metrology for measuring shear-induced structure and orientation in dilute dispersions of multiwalled carbon nanotubes. Small-angle polarized light scattering and optical microscopy are combined in situ to quantify the structural anisotropy of multiwalled carbon nanotubes in semidilute, surfactant-stabilized aqueous suspensions under simple shear flow. Measurements performed as a function of the applied shear rate are used to demonstrate the capabilities and limitations of the experimental technique, which should be suitable for probing the shear response of polymer-nanotube melts and solutions.
A ubiquitous domain pattern is observed in two-phase viscoelastic fluids falling within the simple paradigm of soft viscoelastic domains suspended in a less viscoelastic fluid under shear flow. Three strikingly different complex fluids exhibit the same shear-induced domain structure, which we relate to the elasticity of the dispersed phase via an approximate Weissenberg number. We suggest a physical mechanism for the formation of this pervasive pattern, independent of the dynamic origin of the elasticity of the suspended phase.
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