609308 Color, Structure, and Rheology of a Diblock Bottlebrush Copolymer Solution

Friday, November 20, 2020
Materials Engineering and Sciences Division (08) (PreRecorded+)
Matthew Wade1, Dylan Walsh1, Johnny Ching-Wei Lee1, Elizabeth G. Kelley2, Kathleen Weigandt2, Damien Guironnet1 and Simon Rogers1, (1)Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, (2)National Institute of Standards and Technology, Center for Neutron Research, Gaithersburg, MD

A structure-property-process relation is established for a diblock bottlebrush copolymer solution, through a combination of rheo-neutron scattering, imaging, and rheological measurements. Polylactic acid-b-polystyrene diblock bottlebrush copolymers were dispersed in toluene with a concentration of 175 mg/ml, where they self-assembled into a lamellar phase. All measurements were carried out at 5 ˚C. The solution color, as observed in reflection, is shown to be a function of the shear rate. Under equilibrium and near-equilibrium conditions, the solution has a green color. At low shear rates the solution remains green, while at intermediate rates the solution is cyan. At the highest rates applied the solution is indigo. The lamellar spacing is shown to be a decreasing function of shear rate, partially accounting for the color change. The lamellae are oriented ‘face-on’ with the wall under quiescence and low shear rates, while a switch to ‘edge-on’ is observed at the highest shear rates, where the reflected color disappears. The intramolecular distance between bottlebrush polymers does not change with shear rate, although at high shear rates, the bottlebrush polymers are preferentially aligned in the vorticity direction within the lamellae. We therefore form a consistent relation between structure and function, spanning a wide range of length scales and shear rates.

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