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Polyelectrolyte-driven flocculation of suspended particulate in solution is an important process in a variety of industrial processes such as drinking water treatment and composite material synthesis. Flocculation depends on a wide variety of physicochemical and hydrodynamic properties, which affect floc size, growth rate, and floc morphology. Floc formation and growth behavior is explored here using two different molecular weights of a cationic polyacrylamide flocculant and anisotropic Na-bentonite clay particles under a variety of solution ionic strengths. A Taylor–Couette cell with radial injection capabilities was used to study the effects of solution ionic strength and polyelectrolyte molecular weight on floc size, growth rate, and floc morphology during the flocculation process with a constant global velocity gradient. The floc size generally decreased with increasing ionic strength whereas the floc growth rate initially increased then decreased. This likely occurred due to charge screening effects, where increased bentonite aggregate size and a less expanded polyelectrolyte conformation at higher ionic strengths results in a decreased ability for the polyelectrolyte to bridge multiple bentonite aggregates. The densification of bentonite aggregates at higher ionic strengths resulted in floc morphologies that were more resistant to shear-induced breakage. With the exceptions of optimal dose concentration and dispersion coefficients, there were no clear differences in the floc growth rate behaviors for the two molecular weights studied. This work contributes to an improved understanding of the physicochemical complexities of polyelectrolyte-driven flocculation that can inform dosing requirements for more efficient industrial operations. 

Methylcellulose solutions are known to form microfibrils at elevated temperatures or in the presence of salt. The fibrils have a significant impact on the solution's rheological properties. Here, the shear and extensional properties of methylcellulose solutions with added salt are measured using hyperbolic microfluidic channels, allowing for new characterization at lower molecular weights and higher shear and strain rates that are difficult to access by macroscale rheology studies. 1 and 2 wt% methylcellulose solutions with molecular weight of 150 kg mol −1 with NaCl content between 0 to 5 wt% have been characterized. All solutions were found to be shear thinning, with power law thinning behavior at shear rates above 100 s −1 . The addition of NaCl up to 5 wt% had only small effects on shear viscosity at the shear rates probed (100 s −1 and 10 000 s −1 ). Extensional viscosities as low as 0.02 Pa s were also measured. Unlike the results for shear viscosity, the addition of 5 wt% NaCl caused significant changes in extensional viscosity, increasing by up to 10 times, depending on extension rate. Additionally, all solutions tested showed apparent extensional thinning in the high strain rate regime (>100 s −1 ), which has not been reported in other studies of methylcellulose solutions. These findings may provide insight for those using methylcellulose solutions in process designs involving extensional flows over a wide range of strain rates.