Analytical analysis reveals enhanced rheological properties and shrinkage in active polar polymers, suggesting implications for material design.
The conformational and rheological properties of active polar linear polymers under linear shear flow are studied analytically. We describe a discrete active polar linear polymer as an inextensible flexible Gaussian bead–spring chain supplemented by active forces along the bonds. The linear, non-Hermitian equations of motion are solved by an eigenfunction expansion in terms of a biorthogonal basis set. The model reveals an intimate coupling between activity and shear flow, which implies activity-enhanced polymer conformational and rheological properties. Compared to a passive polymer, we find a significantly enhanced shrinkage transverse to the flow direction with increasing shear rate, with a power-law exponent of −4/3, compared to the passive value of −2/3. This conformational change is tightly linked with a strongly amplified shear-thinning behavior, where the shear viscosity exhibits the same power law. The characteristic shear rate for the onset of these effects is determined by the activity. In the asymptotic limit of large activities, the shear-induced features become independent of activity and equal to those of passive polymers.
No takes yet. Share an insight, caveat, or question.
Panda et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: