Colloidal electrolyte friction and sedimentation: A mode-coupling approach

Citation
M. Kollmann et G. Nagele, Colloidal electrolyte friction and sedimentation: A mode-coupling approach, J CHEM PHYS, 113(17), 2000, pp. 7672-7688
Citations number
68
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF CHEMICAL PHYSICS
ISSN journal
00219606 → ACNP
Volume
113
Issue
17
Year of publication
2000
Pages
7672 - 7688
Database
ISI
SICI code
0021-9606(20001101)113:17<7672:CEFASA>2.0.ZU;2-P
Abstract
Using a simplified mode-coupling scheme (MCS) for multicomponent Brownian d ispersions, we calculate the effect of mobile salt and counterions on the t racer diffusion and sedimentation of a suspended colloidal macroion. In thi s scheme, potential forces and also the leading far-field hydrodynamic inte ractions (HI) between macroion and small electrolyte ions forming its ion a tmosphere are accounted for on the basis of the many-body Smoluchowski equa tion. The static pair correlation functions, which are needed as input, are treated in a first step within the Debye-Huckel approximation. In this way , analytical results are derived for the time-dependent friction function, the long-time tracer diffusion coefficient, and the sedimentation velocity of the macroion as functions of the electrolyte concentration, electrolyte ion mobilities, and macroion charge. Onsager's limiting law for simple elec trolytes is recovered from the MCS in the limit of vanishing macroion radiu s. The results of our theoretical treatment are compared with experimental data on electrolyte friction and predictions of other existing theories. Go od agreement with experimental data on tracer diffusion and with Booth's th eory of electrolyte friction is observed. The inclusion of HI between macro ion and microions is shown to be essential for a proper description of the electrolyte friction effect. (C) 2000 American Institute of Physics. [S0021 -9606(00)51241-0].