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Mobility of an axisymmetric particle near an elastic interface

Published online by Cambridge University Press:  07 December 2016

Abdallah Daddi-Moussa-Ider*
Affiliation:
Biofluid Simulation and Modeling, Fachbereich Physik, Universität Bayreuth, Universitätsstraße 30, Bayreuth 95440, Germany
Maciej Lisicki
Affiliation:
Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Wilberforce Rd, Cambridge CB3 0WA, UKInstitute of Theoretical Physics, Faculty of Physics, University of Warsaw, Pasteura 5, 02-093 Warsaw, Poland
Stephan Gekle
Affiliation:
Biofluid Simulation and Modeling, Fachbereich Physik, Universität Bayreuth, Universitätsstraße 30, Bayreuth 95440, Germany
*
†Email address for correspondence: abdallah.daddi-moussa-ider@uni-bayreuth.de

Abstract

Using a fully analytical theory, we compute the leading-order corrections to the translational, rotational and translation–rotation coupling mobilities of an arbitrary axisymmetric particle immersed in a Newtonian fluid moving near an elastic cell membrane that exhibits resistance towards stretching and bending. The frequency-dependent mobility corrections are expressed as general relations involving separately the particle’s shape-dependent bulk mobility and the shape-independent parameters such as the membrane–particle distance, the particle orientation and the characteristic frequencies associated with shearing and bending of the membrane. This makes the equations applicable to an arbitrary-shaped axisymmetric particle provided that its bulk mobilities are known, either analytically or numerically. For a spheroidal particle, these general relations reduce to simple expressions in terms of the particle’s eccentricity. We find that the corrections to the translation–rotation coupling mobility are primarily determined by bending, whereas shearing manifests itself in a more pronounced way in the rotational mobility. We demonstrate the validity of the analytical approximations by a detailed comparison with boundary integral simulations of a truly extended spheroidal particle. They are found to be in a good agreement over the whole range of applied frequencies.

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Papers
Copyright
© 2016 Cambridge University Press 
Figure 0

Figure 1.Illustration of a spheroidal particle located at $z=z_{0}$ above an elastic cell membrane. The short and long axes are denoted by $a$ and $c$, respectively. The unit vector $\boldsymbol{u}_{1}$ is pointing along the spheroid symmetry axis and $\boldsymbol{u}_{2}$ is the unit vector perpendicular to the plane of the figure. The unit vector $\boldsymbol{u}_{3}$ is defined to be orthogonal to both $\boldsymbol{u}_{1}$ and $\boldsymbol{u}_{2}$.

Figure 1

Figure 2.The scaled translational mobility correction components versus the scaled frequency. The spheroid is located above the membrane at $z_{0}=2c$ inclined at an angle $\unicode[STIX]{x1D703}=\unicode[STIX]{x03C0}/3$ from the vertical. The analytical predictions of the real and imaginary parts of the translational mobility corrections are shown as dashed and solid lines, respectively. The corrections due to shearing and bending are shown respectively in green (bright grey in a black and white printout) and red (dark grey in a black and white printout). Horizontal dotted lines represent the hard-wall limits from Lisicki et al. (2016). BIM simulations are marked as squares and circles for the real and imaginary parts, respectively. For the membrane parameters we take a reduced bending modulus $E_{B}:=\unicode[STIX]{x1D705}_{B}/(c^{2}\unicode[STIX]{x1D705}_{S})=2/3$ and the Skalak parameter $C=1$.

Figure 2

Figure 3.The scaled coupling mobility corrections versus the scaled frequency. Black and blue symbols refer to the $tr$ and $rt$ components, respectively, obtained from BIM simulations. The other colours are the same as in figure 2.

Figure 3

Figure 4.The scaled rotational mobility correction component versus the scaled frequency. Black and blue symbols refer to the 13 and 31 components, respectively, obtained from BIM simulations. The colour code is the same as in figure 2.

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