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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
Study of Electrohydrodynamic Micropumping
Through Conduction Phenomenon
Seyed Reza Mahmoudi, Kazimierz Adamiak, Fellow, IEEE, G. S. Peter Castle, Life Fellow, IEEE, and Mehdi Ashjaee
Abstract—In the present paper, a single-stage axisymmetric
conduction micropump in the vertical configuration has been
proposed. This micropump consists of four components: highvoltage ring electrode, grounded disk-shaped electrode, insulator spacer, and inlet/outlet ports. The high-voltage electrode and
grounded electrode of the device were patterned on the two separate commercial LCP substrates with 30 µm copper cladding
using standard lithographic techniques. The final spacing between
two electrodes and the overall size of the device were measured to
be 286 µm and 50 mm × 70 mm × 5 mm, respectively. The static
pressure generation of the micropump was measured at different
applied voltage using three different dielectric liquids, 10-GBN
Nynas and Shell Diala AX transformer oils, and N-hexane. The
range of applied voltages was between 300 and 1500 VDC, and
maximum pressure generation up to 100 Pa was achieved at
1500 VDC applied voltage. To further verify the experimental
results, a numerical simulation was also performed. The pressure
head generation was predicted numerically and compared with
experimental results at different applied voltages.
Index Terms—Dielectric liquids, electrohydrodynamics, finite
element method, micropumps, space charge.
I. I NTRODUCTION
HE OPERATION of electrohydrodynamic (EHD) micropumps is based on the interaction between electric fields
and electric charges in a dielectric fluid. The electric body force
f in a dielectric liquid, which results from an imposed electric
can be expressed as [1]
field, E,
T
1 2
∂ε
1
2
f = ρc E − E ∇ε + ∇ E ρ
2
2
∂ρ T
(1)
where ρc is volume charge density, ε is the fluid permittivity,
and ρ is the fluid density, T is the fluid temperature.
Manuscript received November 8, 2010; revised April 29, 2011; accepted
May 17, 2011. Date of publication July 14, 2011; date of current version
September 21, 2011. Paper 2010-EPC-450.R1, presented at the 2010
Industry Applications Society Annual Meeting, Houston, TX, October 3–7,
and approved for publication in the IEEE T RANSACTIONS ON I NDUSTRY
A PPLICATIONS by the Electrostatic Processes Committee of the IEEE Industry
Applications Society.
S. R. Mahmoudi, K. Adamiak, and G. S. Peter Castle are with the
Department of Electrical and Computer Engineering, University of Western Ontario, London, ON N6A 5B9, Canada (e-mail: smahmou3@uwo.ca;
kadamiak@eng.uwo.ca; pcastle@eng.uwo.ca).
M. Ashjaee is with the Department of Mechanical Engineering, Faculty
of Engineering, University of Tehran, 14174 Tehran, Iran (e-mail: Ashjaee@ut.ac.ir).
Color versions of one or more of the figures in this paper are available online
at http://ieeexplore.ieee.org.
Digital Object Identifier 10.1109/TIA.2011.2161970
The first term on the right-hand side of (1) is the electrophoretic, or Coulombic, force that results from the net free
space charges in the fluid. The second term, known as the
dielectrophoretic force, arises from the permittivity gradient.
The last term, called the electrostrictive force, is important only
for compressible fluids. Free space charges in dielectric liquids
can be generated by three different mechanisms: I) Induction:
occurs in dielectric liquid with variable electrical conductivity,
which can be caused due to the presence of a thermal gradient, or in two or multiphase flows; II) Conduction: through
imbalanced dissociation–recombination reactions in the areas
adjacent to the electrodes; III) Injection: by direct charge injection from the solid/liquid interface. These three distinctive
mechanisms for free space charge generation can be exploited
to create induction, conduction, and injection EHD pumping
effects [4].
For an isothermal single-phase dielectric liquid, the last two
terms of (1) vanish and EHD pumping operation require the
existence of net space charge in the presence of an electric
field to produce a net Coulombic force. Because the induction
EHD pumps require a fluid nonhomogeneity for its operation,
it cannot be utilized for isothermal single phase liquid pumping
purposes. Therefore, there are only two possibilities to produce
free space charge: ion injection and dissociation mechanisms.
Ion drag pumps are based on direct ion injection from a charged
electrode surface to the liquid. As a main disadvantage, these
pumps cause degeneration of the working fluid and its electrical
properties; thus, they are not reliable for long-term operation
[2]. The typical electrode life time in ion injection pump was
reported to be less than 1 h [3]. The chemical reactions cause serious electrode damages which affect the static head generation
produced by the micropump. In contrast, conduction pumping
is based on interaction between the electric field and charge
carriers, which result from the imbalance rate of dissociation–
recombination reactions around the electrodes submerged in
a low conductivity dielectric liquid. A similar effect in liquids with high electrical conductivity, such as electrolytes, is
called electroosmosis. The feasibility of conduction pumps has
been proven for nonisothermal liquids and two phase flow
applications [4]. Elimination of the direct ion injection and
their operation in both isothermal and nonisothermal dielectric
liquids makes them potentially attractive in many applications.
The conduction mechanism in weakly conductive dielectric
liquids is a complicated phenomenon. When a relatively small
electric field (below 0.1 V/μm) is established between a low
potential and a high potential electrodes immersed in a dielectric liquid, the ion injection is negligible, but the liquid
impurities adjacent to the electrodes may begin to dissociate.
0093-9994/$26.00 © 2011 IEEE
MAHMOUDI et al.: STUDY OF ELECTROHYDRODYNAMIC MICROPUMPING THROUGH CONDUCTION PHENOMENON
The process of dissociation of the neutral species and recombination of the created ion pairs can be schematically written as
follows [5]:
Kd
−→ +
A + B−.
A B
←−
Kr
+
−
(2)
By increasing the applied voltage, but before reaching some
threshold value of electric field (approximately 0.1 V/μm),
the rate of neutral species dissociation and the rate of generated ions recombination are in equilibrium everywhere. By
increasing the electric field above this threshold, depending on
the liquid properties, the rate of dissociation in the vicinity of
the electrodes exceeds that of recombination. The nonequilibrium dissociation–recombination process near the electrodes
creates a layer with charges, having polarity opposite to the
electrode voltage, in which the dissociation is dominant over
recombination and is called the heterocharge layer. The attraction between the electrodes and the charges results in a
net fluid flow from the blunt electrode toward the electrode
having smaller radii of curvature. The conduction mechanism
in this regime is mainly due to the ionic dissociation and is
referred to as EHD conduction pumping. Further increasing of
the electric field (in the order of 10 V/μm, depending on the
liquid characteristics and impurity concentration), results in ion
injection from the liquid/metal interface and produces a reverse
pressure. Beyond this threshold, the ion-injection pumping
mechanism will be dominant [6], and the pumping direction is
reversed.
The concept of the charge generation through the dissociation phenomenon has been known for long time [1], but the
idea of using this phenomenon for pumping dielectric liquids is
comparatively new [20]. Several theoretical [6], [17], numerical
[12], [15], [18], [19] and experimental works [5], [13], [16],
[21] were carried out to determine the feasibility of EHD pumping through the conduction phenomenon. In all of the previous
studies, commercial refrigerants R-123, R-134a, and N-Hexane
were introduced as working fluids to a single or multistage
pump with the electrode spacing in the order of millimeter
and the steady-state static pressure generation of the pump
was determined. Furthermore, several geometries for highvoltage electrodes were investigated to increase pressure generation [21]. The initiation of a typical macroscale conduction
pumping for R-123 was observed for voltages in the order of
5 kV DC.
The main motivation in miniaturization of the EHD pumps
is to shrink the separation between the electrodes to generate
an intense electric field over a small volume of the working
fluid even with reduced applied voltage for lab-on-a-chip applications. In this article, an EHD micropump is referred to a
device with an electrode spacing d in the order of d ≤ 10−4 m.
Typically, scaling down an EHD pump electrode spacing from
macro- to microscale reduces the level of applied voltage
required for the operation as much as one or even two orders
of magnitude. This significant change in the operating voltage
eliminates the need for a bulky high-voltage power supply.
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Moreover, EHD pumping of the dielectric liquids used for heat
transfer, such as high Prandtl number liquids (transformer oils),
fluorinert dielectric liquids [10] with low boiling temperature,
and high latent heat of vaporization, cryogenic liquids [32] and
other commercial refrigerants, shows promising performance
in recent advanced cooling systems. Accordingly, scaling of
the EHD pumps to smaller sizes can be potentially attractive
in microfluidic devices.
A survey of the literature for microscale EHD pumps shows
that the miniaturization of ion drag pumps has been the subject of many investigations [28], [33]. Bart et al. [7] and
Richter et al. [8] proposed preliminary designs for an ion
injection micropump. Ahn [9] studied an ion drag micropump
with 30-mm channel length and a planar electrode pair on glass
substrate. Two different design with emitter-collector spacing
of 100 and 200 μm were fabricated. The device was operated
in the range of applied voltages between 20 and 130 V DC.
Static pressure heads up to 200 Pa at 110 V applied voltage
was achieved with 100 μm gap spacing using ethylene glycol.
Darabi et al. [10] developed an ion drag pump consisting of
50–90 pumping stages with 100 μm electrode gaps fabricated
on an alumina substrate. They used HFE-7100 (3M Co.) as a
dielectric working fluid and obtained static pressure heads up
to 700 Pa at 300 V applied voltage. Recently, several attempts
were carried out to find a suitable high resistivity material to
protect the electrodes and working fluid against oxidation and
aging due to the ion injection at the solid–liquid interface.
Yang et al. [3] fabricated an ion drag micropump with indiumtin oxide (ITO) as a material resistant against corrosion for
the electrodes instead of using conventional electrode materials
such as evaporated Cr/Au [10]. More stable operation of the
micropump without visible damages of the ITO electrodes
was initially observed and looked promising. However, in
subsequent tests, the lifetime of the electrodes at 15 V DC
applied voltage was only 6 min. This short lifetime of the
electrodes and deterioration of the thermophysical properties of
the working fluid due to the significant electrochemical effects
during the operation [2] are the main disadvantages of the ion
drag micropumps, and recently fewer investigations have been
carried out to improve such designs.
Although there have been these several attempts to scale
down the ion injection pumps and decrease the operating voltage level, there were no similar attempts to miniaturize the
conduction pumps mainly because they have been proposed
just recently. Also, to the best of the authors’ knowledge, few
investigations have been carried out to match the experimental results and the numerical simulations for the conduction
pumping [14]. Moreover, in all of the numerical and experimental studies, the effect of conduction pumping has been
reported with only three dielectric liquids, R-123, R-134a, and
N-Hexane, as working fluid [15]–[21]. In the present work, an
axisymmetric single-stage microscale conduction pump in the
vertical configuration was designed, fabricated, and tested using
three different working fluids: 10-GBN Nynas and Shell Diala
AX transformer oils, and N-hexane. At steady-state operation
and in the absence of the fluid flow, the static generated pressure
and electric current of the device were measured at different
applied voltages. To find an estimate for the charge density
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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
Fig. 1. Qualitative description of electrode design.
distribution and the electric field variation in the micropump,
and further verify the experimental results, a numerical study
based on the double-species bipolar conduction model was
performed. The pressure generation was predicted numerically
and compared with experimental results at different applied
voltages.
II. E LECTRODE D ESIGN FOR A C ONDUCTION M ICROPUMP
To exploit charge carriers generated by the conduction mechanism for pumping purposes, the electrode geometry should
be designed properly to form an effective heterocharge layer.
For conduction pumping, high-voltage electrodes are needed
to provide large projected area perpendicular to the flow direction or pressure gradient [21]. Moreover, to mitigate the
ion injection effect at the metal/liquid interface, sharp edges
should be avoided. If an imposed electric field is applied to a
pair of parallel plates, a heterocharge layer is formed adjacent
to both electrodes. The Coulombic forces exerted on the heterocharge layers near both electrodes are balanced. Therefore,
net flow cannot be produced in this geometry [6]. However, by
implementing some small changes in the configuration of the
electrodes, one may increase the projected area and achieve a
conduction pumping effect. For example, the high-voltage electrode may have the form of a series of concentric annuli, fixed
parallel to the planar grounded electrode, which is immersed
in a dielectric liquid, as shown in Fig. 1. Heterocharge layers,
adjacent to each electrode, are formed, and the nonuniform
field distribution near the high-voltage electrode creates an
attraction toward the upper electrode. In this particular configuration, the radial component of the electric force exerted on
the heterocharge layer is balanced, and the axial component
of the electric force generates a pressure gradient, eventually
causing a net flow in the axial direction. Since the electric field
is more intense near the edges of the annuli, the thickness of the
corresponding heterocharge layer will be larger, and the static
pressure across it will be high. Therefore, the flow direction
in the micropump is from the grounded electrode toward highvoltage electrode.
In this study, the proposed conduction micropump consists of
four components: high-voltage electrode, grounded electrode,
insulator spacer, and inlet/outlet ports. The printed circuit board
technology (PCB) was adapted to pattern the electrode geometries for the micropump. The PCB technology was recently
Fig. 2. Top view of (a) high-voltage annulus electrodes and (b) grounded
electrode patterned on two separate substrates. (Not scaled).
implemented to fabricate several devices such as a magnetic
fluxgate sensor [23], RF switch [35], and microfluidic devices
[22], [34]. The schematic configuration of the high-voltage
electrode and grounded electrode of the micropump patterned
on the two substrates are presented in Fig. 2. The high-voltage
electrode, shown in Fig. 2(a), consists of a series of concentric
annulus rings patterned on a commercial liquid crystal polymer
(LCP) substrate coated with copper cladding using standard
lithographic techniques. A total of 75 concentric annuli each
25 μm wide and spaced 75 μm apart were electrically connected together. Considering the 75 ring structures with a thickness of 30 μm as a high-voltage electrode provides the projected
area perpendicular to the axial direction in the order of 1 cm2 .
Furthermore, this radial symmetric electrode design helps to
minimize the number of sharp points and edges, which are
usually encountered in a rectangular planar electrode design,
thus minimizing any undesired ion injection. A disc-shaped
grounded electrode was patterned on another piece of LCP
substrate with the cladding using the same technique. A 230 μm
thick annulus LCP spacer was utilized to position the two
substrates parallel to each other. To seal the micropump, a layer
of resin epoxy was used on both sides of the spacer. The final
spacing between the two electrodes and the total volume of the
fluid in the micropump was measured to be d = 286 μm and
0.8 μL, respectively. Comparing the electrode separation of this
device (d < 0.3 mm) with previous macroscale design (d ∼
2 mm), the current device is expected to operate at one order of
magnitude smaller applied voltage. Two identical holes on both
substrates, 2 mm in diameter, serve as inlet/outlet ports. The
details of the geometry and dimensions are shown in Fig. 3. The
MAHMOUDI et al.: STUDY OF ELECTROHYDRODYNAMIC MICROPUMPING THROUGH CONDUCTION PHENOMENON
Fig. 3.
Details of packaged conduction micropump.
performance of EHD micropumps is temperature dependent.
Temperature rise in pumping volume can be induced by Joule
heating of working fluid particularly at higher applied voltages.
Therefore, one should be cautious about the thermal effects
which may significantly affect the performance of EHD pump.
For the presented packaged device, since the total surface area
of the pump is comparatively large (∼60 cm2 ) with respect
to the total volume of the micropump, the temperature rise in
working fluid is expected to be small. Therefore, in the present
work, the variation of ion mobility, permittivity, and electrical
conductivity of the working fluid due to thermal effects was
assumed to be negligible.
III. E XPERIMENTAL A PPARATUS AND P ROCEDURE
The packaged micropump was investigated using three different working fluids. The two transformer oils mentioned
earlier were selected due to their low electrical conductivity.
Commercial grade normal hexane (N-hexane) was also used,
and it was chosen because it showed no significant pumping effect in the previous macroscale studies. The V –I characteristics
and the magnitude of generated pressure for this micropump
were obtained for each of the different working fluids. The electrical and thermophysical properties of the fluids are tabulated
in Table I.
The charge relaxation time of the dielectric liquids used in
this study is typically long. Therefore, the mobility of ions [11],
charge density distribution, electric field variation, and resultant
2227
pressure of the device may be affected by even a weak stream of
the fluid. The vertical positioning of the micropump enabled us
to minimize the impact of disturbance and to measure the static
pressure generation in the absence of fluid flow. The grounded
side of the micropump was positioned at the bottom of a bath of
working fluid, and the HV side of the pump with the patterned
ring structures was positioned at the top.
The micropump was completely submerged in the bath of
working fluid, and a hypodermic syringe was used to fill it. A
variable 0–3600 V DC power supply with a resolution of 10 V
was connected to the upper electrode to provide the necessary
voltage for the operation of the micropump. A microammeter
was connected between the lower electrode and ground to
measure the electric current. In the present work, only the
static operation of the micropump at steady-state condition has
been investigated; therefore, no mass flow rate measurement
was carried out. To measure the generated static pressure at
different values of applied voltage, a transparent tube 2 mm
in diameter and 20 mm long was perpendicularly connected
to the pump outlet. After reaching the steady-state condition,
the column of working fluid is at a position where the electric
body force is balanced with the weight of the column. Both
the column rise due to the capillary action and conduction
pumping were measured for different working fluids at different
applied voltages with a CCD camera. Before starting the image
processing, the measurement system was calibrated using an
external object with known sizes. Its size in pixels, both in
vertical and horizontal directions, was obtained at a specific
focal length. To minimize the optical aberration, the liquid
column is adjusted to be at the center of the image. A MATLAB
code was used to convert the number of pixels directly to
the liquid height and static pressure. To find the net liquid
column rise due to EHD conduction pumping, the experimental
column rise due to the capillary action was subtracted from the
generated head (H = hgenerated − hc ). The total static pressure
generation was calculated from the equation P = ρgH. The
measured column rise due to the capillary action was approximately 2 mm, 3 mm, and 3.5 mm for N-hexane, Shell Diala
AX, and 10-GBN Nynas, respectively. To verify the experimental observation of liquid column rise due to the capillary
forces, the height of liquid was calculated for a narrow tube
from the relation hc = 2γ/ρgr, where γ is the surface tension
and r is radius of the tube. The comparison showed consistency between experimental observation and the formula with
±0.5 mm difference.
The experimental uncertainty of the calculated pressure generation was mainly due to the column level measurement.
Although the conduction pressure generation relies on the electrical and thermophysical properties of the working fluid which
may vary significantly with small changes in concentration of
contaminants, in the present study, the numerical values of
these properties were obtained from the literature (Table I).
The uncertainties associated with the measured parameters are
summarized in Table II. The electrical permittivity of other
materials used in this study is presented in Table III. Each
experiment was repeated three times to ensure the repeatability
of experiments, and error bars are affixed to all the data in the
graphs presented.
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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
TABLE I
E LECTRICAL AND T HERMOPHYSICAL P ROPERTIES OF THE W ORKING F LUIDS U SED IN T HIS S TUDY AT 296.7 K
TABLE II
U NCERTAINTY OF E ACH Q UANTITY W HICH WAS
M EASURED IN THE P RESENT W ORK
dicates thermal equilibrium condition. The momentum balance
equation can be expressed as
−
→
−
→
(7)
−∇∗ P ∗ + Co ρ∗c E ∗ + ρ∗ g ∗ = 0
where ρ∗ and P ∗ are dimensionless mass density and the
generated pressure, respectively.
The definition of dimensionless parameters appearing in the
above equations are
z
z∗ = ,
d
p∗ =
TABLE III
E LECTRICAL P ERMITTIVITY OF M ATERIALS
n
n∗ =
neq
IV. N UMERICAL A NALYSIS
A. Governing Equations
In this study, the system of governing equations is formulated
−
→
based on the previous assumptions [12]. The electric field E ∗
around the electrodes, which is responsible for the charge generation, is distorted by the net free charges ρ∗c in the dielectric
liquid and is governed by Poisson’s equation
−
→
∇∗ · E ∗ = Co ρ∗c
(3)
∗ = −∇∗ ϕ∗
ρ∗c = p∗ − n∗ and E
(4)
where
where p∗ and n∗ are positive and negative charge densities,
respectively.
The charge transport equations of positive and negative
charge carriers for the simplest conduction model [5] are
−
→
∇∗ · (p∗ E ∗ − α∇∗ p∗ ) = 2Co (1 − p∗ n∗ )
−
→
−∇∗ · (n∗ E ∗ + α∇∗ n∗ ) = 2Co (1 − p∗ n∗ ).
p
,
neq
(5)
(6)
Co in (5) and (6) is a nondimensional conduction parameter
which can be interpreted as ratio of charge relaxation time,
τT = ε/σ, to charge transit time, τ = d/bE, Co = (τT /2τ ) ≈
(neq d2 )/(εV ) = (σeq d2 )/(2bεV )(τT /2τ . The subscript eq in-
E∗ =
E
V
d
P∗ =
ρ∗ g ∗ =
,
r∗ =
ε·
P
V 2 ,
ε·
r
,
d
ϕ∗ =
ϕ
V
d
ρg
V 2 1 .
d
(8)
d
The diffusion coefficient α in (5) and (6) is equal to D/bV =
(kT /eV ) ≈ (1/40 V).
The order of magnitude analysis shows that the contribution of the hydrodynamic convection and diffusion terms are
negligible comparing with that of the electric body force at
steady-state condition and static operation of the device. This
assumption is consistent with the previous numerical model
proposed by Atten and Yagoobi [5], and Jeong et al. [12].
Therefore, the charge convection terms in (5) and (6) can be
neglected. The applied boundary conditions are summarized in
Table IV.
An unstructured triangular mesh with increased mesh density in the area of the intense electric field around the highvoltage electrodes and in the heterocharge layer region around
the grounded electrodes was applied. To ensure that the numerical results are independent of the computational grid, a
grid sensitivity analysis was performed for different working
fluids at different applied voltages. The criterion for the grid
independency analysis was that the total pressure generation
calculations were to be constant to the second decimal.
V. R ESULTS AND D ISCUSSION
Fig. 4 shows a photograph of the micropump submerged in
a bath of 10-GBN Nynas transformer oil during its operation.
By increasing the applied voltage and before reaching the
steady-state conditions, the electric current passing through the
micropump increases and a liquid column rise is generated in
the vertical direction. In all experiments before reaching steadystate conditions, the direction of the net flow in this particular
design of the micropump was from the grounded side (blunt
MAHMOUDI et al.: STUDY OF ELECTROHYDRODYNAMIC MICROPUMPING THROUGH CONDUCTION PHENOMENON
2229
TABLE IV
S UMMARY OF B OUNDARY C ONDITIONS
Fig. 4. Demonstration of the column rise for a conduction micropump in a
bath of 10-GBN Nynas transformer oil at (a) V = 0 and (b) V = 1500 VDC
applied voltages.
electrode) toward the high-voltage electrode. The direction of
the net flow from blunt electrode toward high-voltage electrode
which is a visible feature of the conduction pumping effect confirms that the current micropump predominantly operates based
on conduction phenomenon. It takes a few seconds, depending
on the magnitude of applied voltage, to reach the steady-state
conditions. At the steady-state condition, the electric current
of the micropump shows no measurable fluctuation and the
liquid column rise in the capillary tube remains static. Both
the electric current and static pressure generation measurements
presented in this paper were performed at the steady-state
conditions.
The presented device was tested at 1500 VDC for a 14-h continuous operation, and the static generated pressure and electric
current were monitored frequently. No appreciable change was
observed in the pressure and electric current during the time.
This suggests that the chemical reaction in the electrode/liquid
interface due to the direct ion injection is not appreciable, and
the electrodes remain relatively unchanged during this period.
Comparing the direct ion injection micropump and conduction
pumping, one can conclude that the conduction micropumps are
remarkably reliable and suitable for long-term operations.
By increasing the applied voltage, the current through the
conduction micropump increases. Fig. 5 shows V –I characteristics for the micropump with 10-GBN Nynas and Shell Diala
AX transformer oils. At the fixed gap spacing between the
electrodes of 286 μm, the level of applied voltage for initiation
of the conduction pumping is reduced to a few hundred volts.
Changing the working fluid results in only small variations
in the V –I characteristics, because the electrical properties of
these two fluids are very similar.
Fig. 5. V –I characteristic for conduction micropump measured for two
different working fluids.
Fig. 6. Distribution of equipotential lines for microscale conduction pumping
for 10-GBN Nynas at 1500 VDC applied voltage. Potential difference between
two adjacent lines is 50 V.
The numerically calculated equipotential lines for the conduction micropump submerged in the bath of 10-GBN Nynas
transformer oil are depicted in Fig. 6. Potential difference
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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
Fig. 7. Calculated positive and negative charge densities in microscale conduction pump with 10-GBN Nynas oil transformer.
Fig. 8. Axial electric field in microscale conduction pump calculated for
different working fluids.
between two adjacent lines is 50 V. The equipotential lines are
distorted by the charge distribution near to the electrodes, and
they are closer to each other adjacent to the high-voltage and
grounded electrodes.
The solution of the charge transport equations yields the
spatial variation of charge carriers. Fig. 7 shows the numerical results for the concentration of positive and negative
charges at 300 and 1500 VDC applied voltage with 10-GBN
Nynas transformer oil as the working fluid. Because the thermophysical properties of the two transformer oils are very
similar, the distribution of charges for Shell Diala AX is not
presented. It can be seen that the heterocharge layers extend
into entire the gap spacing at both lowest and highest applied
voltages.
Fig. 8 shows the electric field distribution between the electrodes for 10-GBN and N-hexane. The integration of electric
field along a given path between the two electrodes should be
Fig. 9. Comparison of calculated and experimental static pressures for conduction micropump using 10-GBN Nynas oil transformer.
equal to the electric potential difference V because the applied
voltage is constant. Therefore, the model predicts electric field
enhancement in the whole space over the electrode gap particularly adjacent to the electrodes due to the existence of charge
excluding a depression in a narrow band in the equilibrium
region. A much smaller enhancement of the electric field near
both electrodes can be observed for N-hexane due to its lower
concentration of heterocharges.
The comparison between the numerical results and experimental pressure generation for 10-GBN Nynas as the working
fluid is presented in Fig. 9. The conduction pumping effect was
started at the average field strength of 1 V/μm, and a maximum
101 Pa pressure generation was achieved at the average field
strength of 5.24 V/μm. The comparison between numerical
prediction and experimental results for pressure generation
shows a good agreement with an average 8% deviation. The
numerical results fall in the band of experimental uncertainty
except at highest applied voltage. It is of interest to note
that at 1500 VDC, the pressure generation of the device is
overestimated. This corresponds to the average field strength of
5.24 V/μm, a condition where the ion injection phenomenon
may produce a back pressure, reducing the pressure generated
by the conduction micropump. This interpretation is confirmed
when it is realized that the local field strength around the highvoltage electrode is approximately twice as that of the average
value of field strength and is in the order of the theoretical
threshold, 10 V/μm, where ion injection can occur.
Fig. 10 shows the comparison between the experimental and
numerical results for the pressure generation of the micropump
using Shell Diala AX indicating a good agreement with an
average deviation of 12%. Similar to the 10-GBN Nynas,
the numerical model overestimates the pressure generation.
Comparing the numerical results of the pressure generation in
microscale for 10-GBN Nynas and Shell Diala AX shows that
there is a small difference between the experimental and numerical results. The main reason for this difference is believed to be
the uncertainty associated with the ion mobility calculation. In
MAHMOUDI et al.: STUDY OF ELECTROHYDRODYNAMIC MICROPUMPING THROUGH CONDUCTION PHENOMENON
2231
Fig. 10. Comparison of calculated and experimental static pressures for
conduction micropump using Shell Diala AX oil transformer.
this study, the ion mobilities of negative and positive charges
were assumed to be identical and calculated based on Walden’s
rule, which relates the ion mobility to dynamic viscosity.
Referring to the thermophysical and electrical properties of
these two working fluids shows that the electrical properties of
the fluids are very similar, whereas there is appreciable difference between their dynamic viscosities and ion mobilities. It
should be noted that the dynamic viscosity of both transformer
oils are exponential function of temperature and small changes
in temperature may significantly change their viscosity and ion
mobility [24], [26]. It should be noted that in the present numerical analysis, the field enhancement coefficient was assumed to
be negligible. This assumption is particularly valid at low-field
regimes (E < 4 V/μm). However, it was shown that neglecting
the field enhancement coefficient for even moderate electric
fields (4–6 V/μm) still provides good agreements between
experimental and numerical pressure generation [6].
By submerging the micropump in the bath of N-hexane and
applying the voltage, an electric current was measured, but
no appreciable pressure generation was produced. A similar
effect has been reported in the literature for a macroscale
conduction pump with N-hexane as working fluid using various
configurations of the electrodes [5]. Because of its shorter
relaxation time, thicker heterocharge layer, and the associated
enhancement of the electric field in the gap, one should expect
higher numerical pressure generation for N-hexane based on
the thermophysical properties tabulated in Table I. However,
N-hexane is proven to be particularly sensitive to the effect
of contaminations, and the electrical conductivity of values on
the order of 10−8 to 10−17 (nine orders of magnitude difference) can be found throughout the literature [5], [25], [31].
Implementing the tabulated value of conductivity, σ = 63.9 ×
10−12 S/m, agreement between experimental and numerical
pressure generation cannot be achieved. To obtain agreement,
a numerical value of σ = 1 × 10−12 S/m for electrical conductivity of N-hexane must be assumed. The dimensionless
positive and negative charge densities and the electric field
Fig. 11. Distribution of positive and negative charge densities in microscale
conduction pump calculated for N-hexane.
were calculated and shown in Fig. 11. The charge distribution is very similar to that of 10-GBN Nynas, but N-hexane
charge distribution profile is more diffusive due to its two
order of magnitude higher ion mobility. Assuming the numerical value for electrical conductivity σ = 1 × 10−12 S/m,
the thermal equilibrium charge density for N-hexane, neq =
4.17 × 10−5 C/m3 , becomes two order of magnitude lower
than neq = 1.91 × 10−4 C/m3 for 10-GBN Nynas. With this
assumed value of electrical conductivity for N-hexane, the
numerical solution predicts pressure generations about 10−1 Pa
at applied voltages up to 1500 kV, which is consistent with the
experimental observations of negligible column rise.
A typical distribution of charge density over the microscale
gap for a given dielectric fluid spacing slightly differs from that
of macroscale spacing. By increasing the applied voltage, the
weakly conductive liquid around the electrodes experiences the
bipolar ionization, and heterocharge layers develop. By further
increasing the electric field strength, the heterocharge layers
extend over the entire gap spacing. Generally, at macroscale, the
gap is larger than the thickness of the heterocharge layer. The
conduction parameter Co determines the regime of charge concentration distribution. The different regimes of heterocharge
layer distribution are demonstrated in Fig. 12. To show the
impact of Co on the charge distribution patterns, the growth
of the heterocharge layer is qualitatively demonstrated at different scales of Co for macroscale gap spacing [Fig. 12(a)
and (b)] and for microscale gap spacing [Fig. 12(c) and (d)].
The conduction parameter is a function of the electric field
strength, thermophysical properties of dielectric fluid, and the
square of electrode spacing. By decreasing the gap space
from order of centimeters to micrometers, Co becomes very
small. Thus, depending on the dielectric fluid properties, the
heterocharge layers around the opposite polarity electrodes
extend to the gap spacing, and no definitive equilibrium region
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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
Fig. 12. Space charge density and electric field in macro- and microgaps. (a) and (b). Impact of space averaged conduction parameter on formation of heterocharge layers in parallel plate geometry filled with a low conductive dielectric liquid. (c) Extension of heterocharge to the length of gap spacing for microscale
gap spacing in parallel plate geometry filled with low conductive electrodes at comparatively lower applied voltages. (d) Heterocharge extension for microscale
gap spacing in parallel plate geometry filled with low conductive electrodes at comparatively higher applied voltages.
can be identified. For the operating voltage of 300–1500 VD,
the Co varies between 10−4 < Co < 10−3 for transformer oils
and 1 × 10−2 < Co < 5 × 10−2 for N-hexane. Therefore, the
operation of the device falls in the regime depicted in Fig. 12(d).
Moreover, by shrinking the distance between the electrodes,
the required voltage to initiation of the conduction pumping
effect decreases. Because the diffusion coefficient is inversely
proportional to the applied voltage, it becomes one or two order
of magnitude higher for the microscale device.
It should be noted that the theoretical static pressure generation obtained for macroscale conduction pump overestimates
the resulted static pressure generation of the micropump. The
quadratic relation between the pressure generation and the electric field P = 0.85εV 2 /d2 was derived by Feng and Yagoobi
[6] for a conduction pump with macrospace separation between
the electrodes, where λ ≪ d. This cannot be applied for the
device tested here with microscale gap spacing, where λ is in
the order of ∼d. This equation can be applied only for the conduction macropump, where the thickness of the heterocharge
layer near the electrode is smaller (or much smaller) than the
electrode spacing [see Fig. 12(a)]. In the present conduction
micropump with an electrode gap spacing in the order of
few hundreds micrometers, the heterocharge layers, formed
around two opposite charged electrodes, extend to the entire gap
spacing [compare Fig. 12(a) and (d)]. Therefore, the theoretical
analysis based on the simplifications due to the small heterocharge layer thickness is not applicable to the present study.
Furthermore, in the previous theoretical model, it has been
assumed that ion diffusion has a negligible contribution in the
carrier transport process. According to the discussion given by
Atten and Yagoobi [5], the ion diffusion term should be taken
into account for V < 2500 VDC. Therefore, P = 0.85εV 2 /d2
cannot describe the static pressure generation at microscale
gap spacing with heterocharge layers extended to the length of
electrode separation.
VI. C ONCLUSION
In this paper, an axisymmetric EHD conduction micropump with 286 μm gap spacing between electrodes was proposed. The micropump was tested in the vertical configuration
with three different working fluids: two transformer oils and
N-hexane. The static pressure generation due to the conduction
pumping was measured at different applied voltages. As an
important result, the initiation of conduction pumping was
reduced to 300 VDC applied voltage, which is one order of
magnitude lower than that of the typical macroscale conduction
pumps. To verify the experimental results, the 2-D axisymmetric model of the micropump was developed based on a double species conduction model. The static pressure generations
were calculated and compared with the experimental results
in steady-state static operation at different applied voltages.
The numerical static pressure generations of the device are
generally in a good agreement with the experimental data
except for an overestimation at 10 V/μm local field strength
(1500 VDC). This overestimation is believed to be related to
MAHMOUDI et al.: STUDY OF ELECTROHYDRODYNAMIC MICROPUMPING THROUGH CONDUCTION PHENOMENON
the reversed pressure generation due to the initiation of the
direct ion injection at the corresponding field strength threshold
predicted by the theory.
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Seyed Reza Mahmoudi is currently working toward
the Ph.D. degree in the Department of Electrical and
Computer Engineering at the University of Western
Ontario (UWO), London, ON, Canada.
From 2003 to 2008, he was with the Laser Diagnostics Research Laboratories in the Department
of Mechanical Engineering, University of Tehran,
Tehran, Iran, working on visualization of electrohydrodynamic natural convection heat transfer enhancement using a Mach-Zehnder interferometer and
also investigating conduction pumping effect in dielectric liquids. In 2009, he joined the UWO Applied Electrostatics Research
Center where his current research focuses on liquid/vapor phase change phenomenon in the presence of corona discharge. He has coauthored about 15
peer-reviewed conference and journal publications.
Kazimierz Adamiak (M’87–SM’06–F’09) was
born in Poland in 1951. He received the M.Sc.
and Ph.D. degrees in electrical engineering from
Szczecin University of Technology, Szczecin,
Poland, and the D.Sc. degree (habilitation) from
Gdansk University of Technology, Gdansk, Poland,
in 1974, 1976, and 1983, respectively.
From 1984 to 1986, he was an Assistant Professor in the Department of Electrical Engineering,
Kielce University of Technology, Kielce, Poland. He
was then a Visiting Professor at Queen’s University,
Kingston, ON, Canada, the University of Minnesota, Minneapolis, and the
University of Wisconsin, Madison. During 1989–1990, he was associated with
Quantic Laboratories Inc., Winnipeg, MB, Canada. In 1990, he joined the
Department of Electrical and Computer Engineering, University of Western
Ontario, London, ON, Canada, where he is currently a Professor and a member
of the Applied Electrostatics Research Centre. His research interests include
applied electrostatics, electrohydrodynamics, and computational electromagnetics. He is the author or coauthor of numerous published technical papers.
Dr. Adamiak is a Registered Professional Engineer in the Province of
Ontario, Canada.
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IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, VOL. 47, NO. 5, SEPTEMBER/OCTOBER 2011
G. S. Peter Castle (S’61–M’68–SM’77–F’92–
LF’05) received the B.E.Sc. and Ph.D. degrees
in electrical engineering from the University of
Western Ontario, London, ON, Canada, in 1961
and 1969, respectively, and the M.Sc. (Eng) degree and DIC from Imperial College, University of
London, London, U.K., in 1963.
He is Professor Emeritus and Adjunct Research
Professor in the Department of Electrical and Computer Engineering, University of Western Ontario,
London, ON, Canada. He has been active in research
in the field of applied electrostatics for over 45 years, having published
extensively in the areas of electrostatic precipitation, electrostatic painting and
coating, electrophotography, and electrostatic separation.
Mehdi Ashjaee received the Ph.D. degree from the
University of Wisconsin, Madison, in 1986.
He is a Professor of thermal-fluid science at the
University of Tehran, Tehran, Iran. His main research
interest is visualization of transport phenomena
through optical techniques such as interferometry
and holography. He has also contributed to the field
of spray and atomization. He has published more
than 100 articles in well-recognized journals and
proceedings.