The Society of Rheology 89th Annual Meeting

October 8-12, 2017 - Denver, Colorado


MM2 


Microrheology and Microfluidics


Characterization of consecutive phase transitions in a fibrous colloidal gel using μ2rheology


October 9, 2017 (Monday) 4:10


Track 6 / Aspen

(Click on name to view author profile)

  1. Wehrman, Matthew D. (Lehigh University, Chemical and Biomolecular Engineering)
  2. Milstrey, Melissa J. (Lehigh University, Chemical and Biomolecular Engineering)
  3. Lindberg, Seth (Procter & Gamble, Process and Engineering Development)
  4. Schultz, Kelly M. (Lehigh University, Chemical and Biomolecular Engineering)

(in printed abstract book)
Matthew D. Wehrman1, Melissa J. Milstrey1, Seth Lindberg2, and Kelly M. Schultz1
1Chemical and Biomolecular Engineering, Lehigh University, Bethlehem, PA 18015; 2Process and Engineering Development, Procter & Gamble, West Chester, OH 45069


Schultz, Kelly M.


The gelation and degradation of colloidal particles is important in the design of materials used in commercial products, such as consumer and home care products. Of concern is whether the force that induces phase change can overcome processing history, particularly from shear stress. In this work, we characterize a hydrogenated castor oil (HCO) colloidal gel using μ2rheology, multiple particle tracking microrheology (MPT) in a microfluidic device. HCO is a colloidal fiber that gels and degrades in response to osmotic pressure gradients. Using μ2rheology, we determine the scaffold properties and structure during consecutive phase changes on a single sample. The microfluidic device design is a two-level device with two chambers: sample and suction chambers. Channels that deliver solvent from the second level into the sample chamber are spaced 60° around the chamber creating equal pressure around the HCO locking it in place during solvent exchange. MPT is used to characterize HCO during dynamic transitions. MPT measures the Brownian motion of particles embedded in the material and relates this movement to rheological properties using the Generalized Stokes-Einstein relation. μ2rheology measurements of consecutive phase changes of HCO start with a sheared solution of HCO (0.125 wt%) and an unsheared gel (4 wt%). Single samples are measured for 4 – 9 phase transitions. MPT measurements suggest the structure of the HCO is dependent on the starting materials shear history. When gelled, the sheared HCO solution cannot form a tightly associated, entangled network. During degradation, samples that begin as an HCO gel cannot completely degrade entanglements into single colloids. From these results, we conclude that the osmotic gradient is not a strong enough force to break or reform entanglements. Therefore, equilibrium structures depend on the shear history of the starting material, which can have important implications in end use products made with colloidal gel scaffolds.