Abstract

The dynamics of concentrated, charge-stabilized colloidal silica suspensions was studied over a wide range of wave-vectors. The short-time diffusion coefficient, D(Q), was measured for concentrated suspensions up to their solidification points by photon correlation spectroscopy with coherent X-rays and compared to free particle diffusion D0, studied by Dynamic Light Scattering (DLS) in the dilute case. Small angle X-ray scattering (SAXS) was used to determine the static structure factor S(Q). D0/D(Q) peaks for Q values corresponding to the maximum of the static structure factor showing that the mostly likely density fluctuations decay the slowest. The data allow one to estimate the diffusion coefficient D(Q) in the Q → 0 and Q → ∞ limits. Thus, hydrodynamic functions can be derived free from any modeling of the static or dynamic properties. The effects of hydrodynamic interactions on the diffusion coefficient in charge-stabilized suspensions are presented for volume fractions 0.075 < Φ < 0.28.

URL

https://doi.org/10.1107/S0021889800099994

Authors

G. Grübel, D. L. Abernathy, D. O. Riese, W. L. Vos, and G. H. Wegdam

Year of publication

2000

Date published

01/2000

Journal

J. Appl. Cryst.

Volume

33

Pages

424-427

DOI number

10.1107/S0021889800099994

Keywords

colloidal suspensions, dynamic scattering, small-angle x-ray scattering, x-ray scattering