Di Du

Generating an in situ tunable interaction potential for probing 2-D colloidal phase behavior

We present a novel method to tune the interaction potential from 5kBT to 40kBT in situ between micron-sized superparamagnetic colloids. The potential is composed of a highly tunable long-range attraction induced via a rotating magnetic field and a short-range electrostatic repulsion. Various 2-D thermodynamic phases are observed in a colloidal suspension at different field strengths. Quantitative agreement is found between theory and experiments for dipolar interactions. A theory to account for the induced dipole due to neighboring particles is also presented. The effective three-body potential of a dilute trimer system is measured to account for many-body effects in the system. These results demonstrate an ideal model to study the phase behavior in 2-D systems.

Modified Mason number for charged paramagnetic colloidal suspensions

The dynamics of magnetorheological fluids have typically been described by the Mason number, a governing parameter defined as the ratio between viscous and magnetic forces in the fluid. For most experimental suspensions of magnetic particles, surface forces, such as steric and electrostatic interactions, can significantly influence the dynamics. Here we propose a theory of a modified Mason number that accounts for surface forces and show that this modified Mason number is a function of interparticle distance. We demonstrate that this modified Mason number is accurate in describing the dynamics of a rotating pair of paramagnetic colloids of identical or mismatched sizes in either high or low salt solutions. The modified Mason number is confirmed to be pseudoconstant for particle pairs and particle chains undergoing a stable-metastable transition during rotation. The interparticle distance term can be calculated using theory or can be measured experimentally. This modified Mason number is more applicable to magnetorheological systems where surface forces are not negligible.