Author/Authors :
M. Tokuyama، نويسنده , , Y. Enomoto، نويسنده , , Y. Enomoto and I. Oppenheim ، نويسنده ,
Abstract :
The coupled diffusion equations recently proposed by Tokuyama for concentrated hard-sphere suspensions are numerically solved, starting from nonequilibrium initial configurations. The most important feature of those equations is that the self-diffusion coefficient DS(Φ) becomes zero at the glass transition volume fraction φg as DS(Φ) D01−Φ(x,t)/φgγ with γ=2 where Φ(x,t) is the local volume fraction of colloids, D0 the single-particle diffusion constant, and . This dynamic anomaly results from the many-body correlations due to the long-range hydrodynamic interactions. Then, it is shown how small initial disturbances can be enhanced by this anomaly near φg, leading to long-lived, spatial heterogeneities. Those heterogeneities are responsible for the slow relaxation of nonequilibrium density fluctuations. In fact, the self-intermediate scattering function is shown to obey a two-step relaxation around the β-relaxation time tβ 1−φ/φg−1, and also to be well approximated by the Kohlrausch–Williams–Watts function with an exponent β around the α-relaxation time tα 1−φ/φg−η, where η=γ/β, and φ is the particle volume fraction. Thus, the nonexponential α relaxation is shown to be explained by the existence of long-lived, spatial heterogeneities