Diffusion of Particles in Polymer Solutions

ORAL

Abstract

We use scaling theory to derive the time dependence of the mean-square-displacement $\langle\Delta r^2\rangle$ of a probe particle of size $d$ in an entangled semidilute polymer solution. Particles with size smaller than solution correlation length $\xi$ undergo ordinary diffusion ($\langle\Delta r^2 (t)\rangle \sim t$) with diffusion coefficient determined by the solvent viscosity. The motion of particles with intermediate sizes ($\xia$) at time scales shorter than the relaxation time of an entanglement strand $\tau_e$ is similar to the motion of particles with intermediate sizes. At longer time scales ($t>\tau_e$) large particles ($d>a$) are trapped by entanglement mesh and cannot move until the surrounding chains relax at the reptation time scale $\tau_{rep}$. At longer times $t>\tau_{rep}$, the motion of large particles becomes diffusive with diffusion coefficient determined by the bulk viscosity of the entangled polymer solution.

*Supported by NSF CHE-0911588 and NIH 1-R01-HL077546-03A2.

Authors

  • Liheng Cai

    • University of North Carolina at Chapel Hill
  • Michael Rubinstein

    • Department of Chemistry, The University of North Carolina, Chapel Hill, NC 27599
    • University of North Carolina
    • University of North Carolina at Chapel Hill
    • Department of Chemistry, The University of North Carolina at Chapel Hill, NC 27599-3290
    • Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599-3290, USA
    • UNC Chapel Hill