ODES-lab Research: Polymer Physics
Featuring stretched polymer physics, extensional rheology & processability
macromolecular properties: flexibility, extensibility, & segmental dissymmetry | spinnability & stringiness |
interactions: excluded volume, hydrophobic, topological, hydrodynamic, or electrostatic
STRETCHED POLYMER PHYSICS
Role of Excluded Volume, Hydrophobic, Topological and/ or Hydrodynamic Interactions
Influence of flexibility, extensibility, molecular weight, and concentration on polymer dynamics.
Extensional relaxation time displays concentration-dependent variations quite distinct from shear relaxation time.
Contributions
Extensional relaxation times measured for unentangled solutions exhibit concentration-dependence distinct from shear rheology response, or anticipated by blob models, developed for the relaxation of weakly perturbed chains.
For neutral polymers, we identified a stretched overlap concentration below which the extensional relaxation time is concentration independent.
We showed that the influence of polymer choice could be evaluated a priori, using three macromolecular parameters: flexibility, extensibility, and segmental dissymmetry, defined as the ratio of packing length to Kuhn length.
STRETCHED POLYMER PHYSICS
Role of Excluded Volume, Hydrophobic, Topological and/ or Hydrodynamic Interactions
Influence of flexibility, extensibility, molecular weight, and concentration on polymer dynamics.
Extensional relaxation time displays concentration-dependent variations quite distinct from shear relaxation time.
Contributions
Extensional relaxation times measured for unentangled solutions exhibit concentration-dependence distinct from shear rheology response, or anticipated by blob models, developed for the relaxation of weakly perturbed chains.
For neutral polymers, we identified a stretched overlap concentration below which the extensional relaxation time is concentration independent.
We showed that the influence of polymer choice could be evaluated a priori, using three macromolecular parameters: flexibility, extensibility, and segmental dissymmetry, defined as the ratio of packing length to Kuhn length.
POLYELECTROLYTES
Electrostatic and hydrophobic interactions. Influence of solvent and salt.
Shear, extensional, and interfacial rheology of proteins and charged polymers.
We presented the first comprehensive examination of the extensional rheology response of semi-dilute polyelectrolyte solutions, and found that the extensional relaxation time typically increases with concentration, with exponents distinct from those displayed by shear relaxation time.
We discovered that in glycerol/water solutions, the enhanced solvent viscosity effects do not transfer to solution shear viscosity as increasing glycerol concentration weakens the electrostatic interactions, mimicking the influence of added salt.
Graphic Abstract for Extensional Relaxation Time, Pinch-off Dynamics and Printability of Semi-Dilute Polyelectrolyte Solutions, L. N. Jimenez, J. Dinic, N. Parsi and V. Sharma*, Macromolecules, 51, 5191-5208 (2018). ExtensionalRheologySaltfreeSemidilutePolyelectrolyteSolutions
FIBER SCIENCE & ENGINEERING
Centrifugal force spinning | Spinnability | Macromolecular engineering of fiber properties | Membrane engineering
Making fibers using “the cotton candy” process.
Extensibility-enriched spinnability. Volatile-entangled spinnability.
Mechanical properties and crystallinity of fibers. Sorption.
See publications connecting our rheology and polymer physics ideas to centrifugal force spinning research carried out by our collaborators (formerly in the University of Hasselt, Belgium): Jorgo Merchiers (who finished his Ph.D. in 2021) and his advisor, Naveen Reddy. We identified two distinct mechanisms underlying spinnability: volatile-entangled and extensibility-enriched.
