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Effect of charged boundary on electrophoresis: Sphere in spherical cavity at arbitrary potential and double-layer thickness

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Effect of charged boundary on electrophoresis: Sphere in spherical cavity at

arbitrary potential and double-layer thickness

Jyh-Ping Hsu

, Zheng-Syun Chen, Ming-Hong Ku, Li-Hsien Yeh

Department of Chemical Engineering, National Taiwan University, Taipei, 10617 Taiwan Received 10 April 2007; accepted 15 May 2007

Available online 20 June 2007

Abstract

The boundary effect on electrophoresis is investigated by considering a spherical particle at an arbitrary position in a spherical cavity. Our previous analysis is extended to the case where the effect of double-layer polarization can be significant. Also, the effect of a charged boundary, which yields an electroosmotic flow and a pressure gradient, thereby making the problem under consideration more complicated, is investigated. The influences of the level of the surface potential, the thickness of double layer, the relative size of a sphere, and its position in a cavity on the electrophoretic behavior of the sphere are discussed. Some results that are of practical significance are observed. For example, if a positively charged sphere is placed in an uncharged cavity, its mobility may have a local minimum as the thickness of the double layer varies. If an uncharged sphere is placed in a positively charged cavity, the mobility may have a local minimum as the position of the sphere varies. Also, if the size of a sphere is fixed, its mobility may have a local minimum as the size of a cavity varies. These provide useful information for the design of an electrophoresis apparatus.

©2007 Elsevier Inc. All rights reserved.

Keywords: Electrophoresis; Boundary effect; Electroosmotic flow; Sphere in spherical cavity; Double-layer polarization

1. Introduction

Electrophoresis is one of the most important analytical tools in various fields such as colloidal, biological, biomedical, and biochemical sciences [1,2], to name a few. It is also a basic technique for the separation/processing of particles of colloidal size in practice. Recent research and development in biochip technology and electrokinetic phenomena in microchannels are also related closely to electrophoresis. In these cases, the effect of the presence of a boundary on the electrophoretic behavior of a particle becomes important and the classical result, which is based on an isolated particle in an infinite fluid, needs be modified accordingly. A considerable amount of work has been devoted to the analysis of boundary effects of various types

[3–18]. Among these, a rigid sphere at the center of a spherical cavity, considered by Zydney[6]and Lee et al.[7,8], is a

repre-* Corresponding author. Fax: +886 2 23623040.

E-mail address:jphsu@ntu.edu.tw(J.-P. Hsu).

sentative one. Although this geometry is of a one-dimensional nature, thereby considerably simplifying relevant mathematical treatments, the key influence of the presence of a boundary on the electrophoretic behavior of an entity can be taken into ac-count. However, because the cavity surface was assumed to be uncharged in these studies, the effect of electroosmosis, an ef-fect of practical significance, was neglected.

In a previous study, Hsu et al. [9] considered the elec-trophoresis of a rigid sphere at an arbitrary position in a spher-ical cavity under conditions of weak applied electric field and low surface potential, where the effect of double-layer polar-ization, an effect of fundamental significance, can be neglected. The same problem was also analyzed by Hsu et al.[10]for the case in which the cavity surface can be charged. In the present study, these analyses are further extended to the case of arbi-trary surface potential and double-layer thickness; that is, the effect of double-layer polarization can be significant. Here, both the surface of a sphere and that of a cavity can be charged; that is, the effect of the electroosmotic flow arising from the pres-ence of the latter is taken into account.

0021-9797/$ – see front matter © 2007 Elsevier Inc. All rights reserved.

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Fig. 1. Schematic representation of the problem where a sphere of radius a is placed in a spherical cavity of radius b. An electric field E parallel to the z-axis is applied. The center of the particle is at z= m and that of the cavity at z = 0.

2. Theory

The problem under consideration is illustrated in Fig. 1, where a nonconducting sphere of radius a is placed at an ar-bitrary position in a spherical cavity of radius b. Let ζaand ζb

be respectively the surface potential of the sphere and that of the cavity. Spherical coordinates (r, θ, ϕ) are adopted, with the origin located at the center of the cavity. The center of the par-ticle is at z= m, and that of the cavity at z = 0. A uniform electric field E in the z-direction is applied. The cavity is filled with an aqueous Newtonian fluid containing z1:z2electrolyte; z1and z2are respectively the valence of cations and that of

an-ions, with α= −z2/z1. Let ε be the permittivity of the liquid

phase, ρ the space charge density, e the elementary charge, nj

and Dj the number concentration and the diffusivity of ionic

species j respectively, kBand T the Boltzmann constant and

the absolute temperature respectively, φ the electrical potential, and v, η, and p be the velocity, the viscosity, and the pressure of the liquid phase respectively. Then the phenomenon under consideration can be described by

(1) ∇2φ= −ρ ε = − 2  j=1 zjenj ε , (2) ∇ ·  −Dj  ∇nj+ zje kBT nj∇φ  + njv  = 0, (3) ∇ · v = 0, (4) −∇p + η∇2 v+ ρ∇φ = 0,

where∇2and∇ are respectively the Laplace operator and the gradient operator.

Following the treatment of O’Brien and White[19], we let φ= φ1+ φ2, where φ1and φ2are respectively the equilibrium

potential or the potential in the absence of E and a perturbed potential arising from E. Also,

(5) nj= nj0exp  −zje(φ1+ φ2+ gj) kBT  ,

where gjis a perturbed potential that simulates the deformation

of the double layer.

Suppose that the applied electric field is weak compared with that established by the sphere and/or the cavity. Then the ex-pressions for the distortion of the double layer, the electrical potential, and the flow field near a sphere can be linearized. Using Eqs.(1), (2), and (5)and the relation φ= φ1+ φ2and

neglecting terms involving the product of two perturbed terms, it can be shown that the concentration and the electric fields can be described by (6) ∇∗2φ1∗= − 1 (1+ α) (κa)2 φr  exp−φrφ∗1 − expαφrφ1∗ , (7) ∇∗2φ2∗− (κa) 2 (1+ α)  exp−φrφ∗1 + α expαφrφ∗1 φ2 = (κa)2 (1+ α)  exp−φrφ1∗ g1∗+ expαφrφ1∗ αg2, (8) ∇∗2g1− φr∇∗φ1∗· ∇∗g∗1= φr2Pe1v∗· ∇∗φ1∗, (9) ∇∗2g2+ αφr∇∗φ1∗· ∇∗g∗2= φr2Pe2v∗· ∇∗φ1∗ (10) n1= expφrφ∗1  1− φr  φ2+ g1, (11) n2= expαφrφ1∗  1+ αφr  φ2+ g2.

In these expressions, ∇∗= a∇ is the scaled gradient op-erator, ∇∗2= a2∇2 is the scaled Laplace operator, and φr = ζkz1e/kBT is the scaled surface potential, where ζk = ζa if ζa= 0, and ζk= ζbif ζa= 0. nj= nj/n10, φj= φj/ζk, Pej= ε(zje/kBT )2/ηDj, which is the electrical Péclet number of

ion species j , and gj= gj/ζk, j= 1, 2; κ = [ 2j=1nj0(ezj)2/ εkBT]1/2is the reciprocal Debye length; v= v/UE; and UE= (εζk2/ηa)is the magnitude of the velocity of the particle pre-dicted by the Smoluchowski theory when an electric field of strength (ζk/a)is applied.

In terms of the scaled symbols, the flow field can be de-scribed by (12) ∇ · v= 0, (13) −∇p+ η∇2 v∗+ ∇2φ∇φ= 0, where p= p/prefand pref= εζk2/a2.

Suppose that both the sphere and the cavity surface are non-conductive, nonslip, and impermeable to ionic species, and the concentration of ionic species reaches the bulk value on the cavity surface. Then the boundary conditions associated with Eqs.(6)–(9) and (12)–(13)can be expressed as

(14) φ1= ζa/ζk on the sphere surface,

(15) φ1= ζb/ζk on the cavity surface,

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n· ∇∗φ2= 0 on the sphere surface,

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n· ∇∗φ2= −Ezcos θ on the cavity surface,

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(19) gj= −φ2, j= 1, 2 on the cavity surface,

(20)

v= (v/UE)ez on the sphere surface,

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v∗= 0 on the cavity surface.

In these expressions, Ez= Ez/(ζk/a)is the scaled strength of

the applied electric field, n is the unit normal vector directed into the liquid phase, and ezis the unit vector in the z-direction.

Following the treatment of O’Brien and White [19], the present problem is decomposed into two subproblems. In the first subproblem, a sphere moves at a constant velocity in the absence of E, and in the second subproblem the sphere is fixed in the space when E is applied. Let Fibe the total force acting on a sphere in subproblem i, and let Fi be its magnitude; then F1= χVand F2= βEz, where χ is independent of V∗and β is independent of Ez, and V= v/UEis the scaled velocity.

The fact that the sum of F1and F2 must vanish at the steady

state yields (22) μm=VEz = − β χ,

where μm is the scaled mobility of a sphere. For the present problem, the total force acting on a sphere in the z-direction F, includes the electrical force Feand the hydrodynamic force Fd. If we let Fei and Fdi be respectively the z-components of Fe, and Fdin subproblem i, then

(23) Fi= Fei+ Fdi, i= 1, 2. Feican be evaluated by[20] (24) Fei= S E· n) · ezdS,

where S denotes the spherical surface, E = −∇φ, σEε(EE−12E2I) is the Maxwell stress tensor, and I is the unit

ten-sor. It can be shown that, in terms of scaled symbols, Eq.(24)

Fig. 2. Variation of the scaled mobility μmas a function of κa at various levels of the scaled surface potential φrfor the case where a positively charged sphere is in an uncharged cavity. Solid curves: results based on the present method; dashed curves: results based on a pseudo-spectral method (8). Parameters used are Pe1= Pe2= 0.1, α = 1, and λ = 0.5. leads to[20,21] (25) Fei∗= Fei εζk2a2= S ∂φ1∂n ∂φ2∂z∂φ1∂t ∂φ2∂t dS,

where n and t are the magnitude of the unit normal vector and that of the unit tangential vector, respectively. Fdi can be

eval-uated by[22] (26) Fdi= S H· n) · ezdS,

where σH≡ −pI + η[∇v + (∇v)T] and the superscript T de-notes matrix transpose. In terms of the scaled symbols, Eq.(26)

can be rewritten as (27) Fdi∗ = Fdi εζk2a2 = S (σ∗H· n) · ezdS.

3. Results and discussions

FlexPDE[23], a commercial program based on a finite ele-ment method, is adopted to solve the governing equations and

Fig. 3. Variation of the scaled mobility μmas a function of κa for various values of the position parameter P for the case where a positively charged sphere is in an uncharged cavity at λ= 0.5. (a) φr= 1, (b) φr= 5.

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Fig. 4. Contours of the scaled net ionic concentration CD (= n1− n2) at two levels of κa for the case where a positively charged sphere is in an uncharged cavity at λ= 0.5 and φr= 5. (a) κa = 0.7, (b) κa = 1.5.

the associated boundary conditions, and the results obtained are used to calculate the mobility of a particle; the detailed procedure can be found in[8,19]. Our previous experience in-dicates that this program is efficient and sufficiently accurate for the resolution of the boundary value problem of the present type [24]. Its applicability is further justified by reanalyzing the problem considered by Lee et al.[8], the electrophoresis of a sphere at the center of a spherical cavity, where a pseudo-spectral method based on Chebyshev polynomials is adopted for the resolution of the governing equations and the associated boundary conditions.Fig. 2shows that the performance of the present numerical scheme is satisfactory.

In subsequent discussion, numerical simulations are con-ducted to examine the electrophoretic behavior of a sphere

under various conditions. For illustration, we consider two typ-ical cases, namely, a positively charged sphere in an uncharged cavity and an uncharged sphere in a positively charged cavity. Also, we assume Pe1= Pe2= 0.1 and z1= z2; that is, α= 1.

For convenience, a position parameter P = 100m/(b − a)% is defined; if P = 0%, a sphere is at the center of a cavity, and P = 100% if a sphere touches the north pole of a cavity. 3.1. Positively charged sphere in uncharged cavity

Let us consider first the case in which a positively charged sphere is placed in an uncharged cavity.Fig. 3a shows the vari-ation of the scaled mobility of a sphere μm as a function of double-layer thickness κa at various values of the position

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para-Fig. 5. Flow fields for the case ofFig. 4.

meter P for the case of a low scaled surface potential (φr = 1),

and that for the case of a high scaled surface potential (φr= 5)

is presented inFig. 3b.Fig. 3a reveals that if φr is low μm

in-creases monotonically with the increase in κa. This is because the smaller the κa the thinner the double layer, and the larger the absolute value of the potential gradient on the sphere sur-face, leading to a higher surface charge density, and therefore, the greater the electric force acting on the sphere.Fig. 3a also reveals that if κa is fixed, the larger the P the smaller the μm. This is because the closer a sphere is to a cavity, the greater the viscous retardation arises from the latter. As can be seen in

Fig. 3b, the qualitative behavior of μmwhen φris high becomes

different from that when it is low. Here, μmhas a local mini-mum when κa varies. This phenomenon was also observed by O’Brien and White[19]for the electrophoresis of a sphere in an

infinite fluid. The presence of the local minimum in μmarises

from the fact that when κa is small the electrical driving force in subproblem 2 declines with the increase in κa due to double-layer polarization, but the hydrodynamic force Fd2 increases

with κa, and the rate of the former is higher than that of the latter. The effect of double-layer polarization becomes unim-portant when κa is sufficiently large (thin double layer).Figs. 4 and 5show some typical results for the contours of the scaled net ionic concentration, CD (= n1− n2), and the flow field, re-spectively. As can be seen inFig. 4, the thicker the double layer the more serious the effect of double-layer polarization, that is, the more asymmetric the contours of CD. Under the conditions assumed, a sphere moves upward and the concentration of an-ions (counteran-ions) near its bottom is higher than that near its top. The asymmetric distribution of CD yields an internal

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elec-Fig. 6. Variation of the scaled mobility μm(a), and β (b), as a function of the position parameter P at various levels of the scaled surface potential φrfor the case where a positively charged sphere is in an uncharged cavity at κa= 1 and λ= 0.5.

tric field, the direction of which is opposite to that of the applied electric field, thereby reducing the mobility of the sphere.Fig. 5

shows that a clockwise (counterclockwise) vortex is generated on the right- (left)-hand side of a sphere. Also, the fluid flow at a thicker double layer can be faster than that at a thinner double layer, which was not observed for the case in which the surface potential of a sphere is low.

Fig. 6a shows that the scaled mobility of a sphere μm declines with the increase in the position parameter P , which is expected. This figure also reveals that μmdecreases with the increases in the scaled surface potential φr. This is because for

the value of κa considered, the effect of double-layer polariza-tion is important and the strength of the corresponding induced electric field increases with the level of the surface potential of a particle. This phenomenon can also be explained by the varia-tion of β, which is a measure of the net force acting on a sphere in the second subproblem, illustrated inFig. 6b, where β de-creases with the increase in φr.

The influence of the cavity wall on the electrophoretic be-havior of a sphere is presented inFig. 7. Here, the value of a is fixed, and therefore, the larger the λ (= a/b) the smaller the cavity and the more significant the wall effect, which leads to a smaller scaled mobility μm. For a fixed λ, μmdeclines with

Fig. 7. Variation of the scaled mobility μmas a function of λ (= a/b) for various levels of the scaled surface potential φrfor the case where a positively charged sphere is in an uncharged cavity at P= 95% and κa = 1.

the increase in scaled surface potential φr due to the effect of

double-layer polarization.

3.2. Uncharged sphere in positively charged cavity

Fig. 8shows the variation of scaled mobility μm as a func-tion of double-layer thickness κa at various values of the po-sition parameter P for the case when an uncharged sphere is placed in a positively charged cavity. This figure indicates that, if μm<0,m| decreases with the increase in κa, but the re-verse is true if μm>0. Also, if κa is fixed, m| decreases with the increase in P , and if P is fixed,|μm| increases with the increase in φr. This is because negative charge is induced

on the sphere surface as it approaches a positively charged cav-ity. Therefore, the sphere moves in the −z-direction; that is, μm<0. As κa increases, the thickness of the double layer near the cavity surface decreases and the amount of induced charge on the sphere surface declines accordingly. Since the cavity is positively charged, an electroosmotic flow is generated when E is applied; a clockwise vortex appears on the right-hand side of a sphere and a counterclockwise vortex appears on its left-hand side. In this case, the sphere experiences a drag force in the z-direction. Therefore, the mobility of the sphere may become positive as κa increases.

Fig. 9shows that, in general, if the surface potential of a cav-ity is not high, μm<0, andm| decreases with the increase

in P . However, if the surface potential of the cavity is suffi-ciently high (φr = 5), μm>0 if P is small and μm<0 if P is

large. Also, μmhas a local minimum as P varies. These can be

explained by the fact that if φr is not high, the movement of a

sphere is dominated by the electrical driving force Fe2, which is

in the−z-direction, since negative charge is induced on its sur-face, and therefore, μm is negative. As P increases, although

both|Fd2| and |Fe2| increase, the rate of increase in the former

is higher than that in the latter, and therefore,m| decreases. If φr is sufficiently high, because the hydrodynamic force acting

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Fig. 8. Variation of the scaled mobility μmas a function of κa for various values of the position parameter P for the case where an uncharged sphere is in a positively charged cavity at λ= 0.5. (a) φr= 1, (b) φr= 5.

Fig. 9. Variation of the scaled mobility μmas a function of the position para-meter P at various levels of the scaled surface potential φrfor the case where an uncharged sphere is in a positively charged cavity at κa= 1 and λ = 0.5.

the sphere toward the z-direction, is greater than Fez, μmis

pos-itive. As P increases, since the amount of charge induced on the spherical surface increases,|Fe2| increases, and μmdeclines

ac-Fig. 10. Variation of the scaled mobility μm as a function of λ (= a/b) at various levels of the scaled surface potential φrfor the case where an uncharged sphere is in a positively charged cavity at P= 95% and κa = 1.

cordingly and becomes negative when P exceeds about 40. If a sphere is close to a cavity, Fdzdominates, and the nonslip

con-dition of the cavity surface requires that μm must approach to zero, and therefore, μmhas a local minimum.

Fig. 10shows the variation of scaled mobility μmas a func-tion of λ (= a/b) at various levels of the scaled surface po-tential φr. A comparison betweenFigs. 7 and 10indicates that

althoughm| declines with the increase of λ in both cases due

to the hydrodynamic retardation of the cavity, μmmay have a

local minimum as λ varies if φr is sufficiently low inFig. 10.

The presence of the local minimum arises from the fact that if λis small, Fe2dominates, and Fd2dominates if λ is large. If λ

is small, the rate of increase in Fe2as λ increases is faster than

that of Fd2, but the reverse is true if λ is large.

4. Conclusions

The electrophoretic behavior of a sphere at an arbitrary po-sition in a spherical cavity for the case in which the effect of double-layer polarization can be important is investigated the-oretically. If a positively charged sphere is in an uncharged cavity, we conclude the following. (i) If the surface potential is low, the mobility increases monotonically with the decrease in the thickness of double layer. (ii) For a fixed double-layer thickness, the closer a sphere is to a cavity the smaller the mo-bility is. (iii) If the surface potential is high, the momo-bility has a local minimum when the thickness of the double layer varies. (iv) The mobility declines with increases in the surface poten-tial. If an uncharged sphere is placed in a positively charged cavity we conclude the following. (i) If the mobility is negative, its absolute value declines with the decrease in the thickness of the double layer, but the reverse is true if it is positive. (ii) The absolute value of the mobility increases with the increase in the surface potential. (iii) In general, if the surface potential is not high, the mobility is negative, and its absolute value declines with the decrease in the separation distance between a sphere and a cavity. However, if the surface potential is sufficiently high, the mobility is positive if a sphere is away from a cavity,

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and is negative if it is close to a cavity. (iv) The mobility has a local minimum as the position of a sphere varies. For a fixed sphere size, its mobility may have a local minimum as the size of a cavity varies if the surface potential is sufficiently low.

Acknowledgment

This work is supported by the National Science Council of the Republic of China.

References

[1] H. Shintani, J. Polonsky, Handbook of Capillary Electrophoresis Applica-tions, Blackie Academic & Professional, London, 1997.

[2] P.D. Grossman, J.C. Colburn, Capillary Electrophoresis: Theory and Prac-tice, Academic Press, San Diego, 1992.

[3] F.A. Morrison, J.J. Stukel, J. Colloid Interface Sci. 33 (1969) 88. [4] H.J. Keh, J.L. Anderson, J. Fluid Mech. 153 (1985) 417. [5] A.A. Shugai, S.L. Carnie, J. Colloid Interface Sci. 213 (1999) 298.

[6] A.L. Zydney, J. Colloid Interface Sci. 169 (1995) 476.

[7] E. Lee, J.W. Chu, J.P. Hsu, J. Colloid Interface Sci. 196 (1997) 316. [8] E. Lee, J.W. Chu, J.P. Hsu, J. Colloid Interface Sci. 205 (1998) 65. [9] J.P. Hsu, S.H. Hung, C.Y. Kao, Langmuir 18 (2002) 8897.

[10] J.P. Hsu, L.H. Yeh, Z.S. Chen, J. Colloid Interface Sci. 310 (2007) 281. [11] H.J. Keh, S.B. Chen, J. Fluid Mech. 194 (1988) 377.

[12] H.J. Keh, L.C. Lien, J. Chin. Inst. Chem. Eng. 20 (1989) 283. [13] H.J. Keh, L.C. Lien, J. Fluid Mech. 224 (1991) 305. [14] H.J. Keh, J.Y. Chiou, Am. Inst. Chem. Eng. J. 42 (1996) 1397. [15] H.J. Keh, J.S. Jan, J. Colloid Interface Sci. 183 (1996) 458. [16] J. Ennis, J.L. Anderson, J. Colloid Interface Sci. 185 (1997) 497. [17] J.W. Chu, W.H. Lin, E. Lee, J.P. Hsu, Langmuir 17 (2001) 6289. [18] H.J. Keh, K.D. Horng, J. Kuo, J. Fluid Mech. 231 (1991) 211.

[19] R.W. O’Brien, L.R. White, J. Chem. Soc. Faraday Trans. 2 74 (1978) 1607.

[20] J.P. Hsu, L.H. Yeh, M.H. Ku, J. Colloid Interface Sci. 305 (2007) 324. [21] J.P. Hsu, L.H. Yeh, J. Chin. Inst. Chem. Eng. 37 (2006) 601.

[22] J. Happel, H. Brenner, Low-Reynolds Number Hydrodynamics, Nijhoff, Boston, 1983.

[23] PDE Solutions, FlexPDE, Version 2.22.

數據

Fig. 1. Schematic representation of the problem where a sphere of radius a is placed in a spherical cavity of radius b
Fig. 2. Variation of the scaled mobility μ ∗ m as a function of κa at various levels of the scaled surface potential φ r for the case where a positively charged sphere is in an uncharged cavity
Fig. 4. Contours of the scaled net ionic concentration CD ( = n ∗ 1 − n ∗ 2 ) at two levels of κa for the case where a positively charged sphere is in an uncharged cavity at λ = 0.5 and φ r = 5
Fig. 5. Flow fields for the case of Fig. 4.
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