How do polymers stretch in capillary-driven extensional flows?
arXiv:2403.04103 · doi:10.1021/acs.macromol.4c01604
Abstract
Measurements of the capillary-driven thinning and breakup of fluid filaments are widely used to extract extensional rheological properties of complex materials. For viscoelastic (e.g., polymeric) fluids, the determination of the longest relaxation time depends on several assumptions concerning the polymeric response to the flow that are derived from constitutive models. Our capillary thinning experiments using polymeric fluids with a wide range of extensibility, suggest that these assumptions are likely only valid for highly extensible polymers but do not hold in general. For polymers with relatively low extensibility, such as polyectrolytes in salt-free media, conventional extrapolation of the longest relaxation time from capillary thinning techniques leads to a significant underestimation.
References in corpus (7)
- Single Polymer Dynamics for Molecular Rheology
- Decoupling the effects of shear and extensional flows on the alignment of colloidal rods
- Dynamically Heterogeneous Relaxation of Entangled Polymer Chains
- Universal solvent quality crossover of the zero shear rate viscosity of semidilute DNA solutions
- Dependence of DNA persistence length on ionic strength of solutions with monovalent and divalent salts: a joint theory-experiment study
- Effects of particle stiffness on the extensional rheology of model rod-like nanoparticle suspensions
- Effects of polydispersity and concentration on elastocapillary thinning of dilute polymer solutions