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@ARTICLE{Abade:21654,
author = {Abade, G.C. and Cichocki, B. and Ekiel-Jezewska, M.L. and
Nägele, G. and Wajnryb, E.},
title = {{D}iffusion, sedimentation, and rheology of concentrated
suspensions of core-shell particles},
journal = {The journal of chemical physics},
volume = {136},
issn = {0021-9606},
address = {Melville, NY},
publisher = {American Institute of Physics},
reportid = {PreJuSER-21654},
pages = {104902},
year = {2012},
note = {The work of G.C.A. was supported by CAPES
Foundation/Ministry of Education of Brazil. M.L.E.J. and
E.W. were supported in part by the Polish Ministry of
Science and Higher Education Grant No. N501 156538. G.N.
thanks M. Heinen for helpful discussions and the Deutsche
Forschungsgemeinschaft (SFB-TR6, project B2) for financial
support. Numerical simulations were done at NACAD-COPPE/UFRJ
in Rio de Janeiro, Brazil, and at the Academic Computer
Center in Gdansk, Poland.},
abstract = {Short-time dynamic properties of concentrated suspensions
of colloidal core-shell particles are studied using a
precise force multipole method which accounts for
many-particle hydrodynamic interactions. A core-shell
particle is composed of a rigid, spherical dry core of
radius a surrounded by a uniformly permeable shell of outer
radius b and hydrodynamic penetration depth κ(-1). The
solvent flow inside the permeable shell is described by the
Brinkman-Debye-Bueche equation, and outside the particles by
the Stokes equation. The particles are assumed to interact
non-hydrodynamically by a hard-sphere no-overlap potential
of radius b. Numerical results are presented for the
high-frequency shear viscosity, η(∞), sedimentation
coefficient, K, and the short-time translational and
rotational self-diffusion coefficients, D(t) and D(r). The
simulation results cover the full three-parametric
fluid-phase space of the composite particle model, with the
volume fraction extending up to 0.45, and the whole range of
values for κb, and a/b. Many-particle hydrodynamic
interaction effects on the transport properties are
explored, and the hydrodynamic influence of the core in
concentrated systems is discussed. Our simulation results
show that for thin or hardly permeable shells, the
core-shell systems can be approximated neither by no-shell
nor by no-core models. However, one of our findings is that
for κ(b - a) ≳ 5, the core is practically not sensed any
more by the weakly penetrating fluid. This result is
explained using an asymptotic analysis of the scattering
coefficients entering into the multipole method of solving
the Stokes equations. We show that in most cases, the
influence of the core grows only weakly with increasing
concentration.},
keywords = {Colloids: chemistry / Computer Simulation / Diffusion /
Hydrodynamics / Models, Chemical / Particle Size / Rheology
/ Solvents: chemistry / Surface Properties / Colloids (NLM
Chemicals) / Solvents (NLM Chemicals) / J (WoSType)},
cin = {ICS-3},
ddc = {540},
cid = {I:(DE-Juel1)ICS-3-20110106},
pnm = {BioSoft: Makromolekulare Systeme und biologische
Informationsverarbeitung},
pid = {G:(DE-Juel1)FUEK505},
shelfmark = {Physics, Atomic, Molecular $\&$ Chemical},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22423856},
UT = {WOS:000301664600036},
doi = {10.1063/1.3689322},
url = {https://juser.fz-juelich.de/record/21654},
}