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Process Tomography for
Multiphase Flow Visualization
May 1, 2015, Chiba, Japan
Dr. Masa TAKEI
Prof. of Chiba University, Chiba Japan
Guest Prof. of Xi’an University of Technology,
China
Chiba University
Laboratory on Multiphase
Flow and Visualization
Download web site http://www.em.eng.chiba-u.jp/~takei/ 講義 Doctor course lecture
OUTLINE Multiphase Flow System & CFD-DEM
Necessity of Flow Visualization Techniques
Application of Process Tomography
Plant & Manufacturing Process
Application of Process Tomography
Challenge to Thrombus Detection
Concluding Remarks
Liquid
Gas
Particles
Multiphase Flow Systems
G-L
L-P
G-P
GFFv
ca dt
dm
Tω
dt
dI
Gas phase (Continuum phase ) Solid phase (Discrete phase)
ia,Fuuuu
2)()(
)(egggg
ggp
t
CFD-DEM for System Design in Dense Phase
),( ipiia, uvF g
)8.0(
)1(
4
3
)8.0( 75.1)1(150)1(
7.2
2
2
e
p
D
e
p
Rd
C
Rd
43.0
Re)Re15.01(24 687.0
DC
μ
ρεduv pp Re
Ergun’s equation, 1952
Drag force
m : Mass of the particle, v : Translational velocity, ω : Rotational velocity, p : Pressure,
I : Moment of inertia, Fa : Force acting on particle exerted by surrounding air,
Fc : Contact force, G : Gravitational force, u : Velocity vector of air,
T : Torque caused by the contact force and the moment of inertia of particle,
ε : Volume fraction, ρg : Density of air, μ : Fluid viscosity, μe : Eddy viscosity ,
CD : Drag coefficient for a single particle, dp : Particle diameter, v : Particle velocity
)1000(Re
)1000(Re
Wen and Yu’s equation,
1966
u 0)(
g
g
t
cnctt
tct FFx
xF ftt ifdt
dk
cnct
t
tcnct FF
x
xFF ff if
dt
dk nn
nncn
xxF
Normal contact force
Fig. Models of contact force
Cundall and Strack 1979
Tangential contact force
kn & kt : Spring constant in the normal and tangential direction
ηn & ηt : Coefficient of viscous dissipation in the normal and tangential direction
μf : Friction coefficient
xn & xt : Particle displacement in the normal and tangential direction
Contact Force due to Particles Collision
Particle Particle
24mm
122mm 45mm
Air
Air
Air
Air
Air
FCC
FCC
FCC
FCC
Fig. New designed distributor
New Designed Distributor & Conditions
Powder circulation rate (particle flow rate) Gs [kg/m2s] 349
Center: Side
1:4
Air flow rate of center nozzle Qac [m3/s] 0.094
Total air flow rate of side nozzle Qas [m3/s] 0.378
Table Calculation conditions
T.Zhao, M.Takei, Flow Measurement and Instrumentation, (2007)
T.Zhao, M. Takei, et al., Powder Technology, (2011)
Fig. Fluidized bed test plant
Simulation Conditions
Gas phase Particle phase
Fluid type Air Particle shape spherical
Density(kg/m3) 1.2 Density(kg/m3) 1200
Bed geometry(m) 0.27
(diameter) Particle diameter(mm) 0.3
1.98(height) Number of particles 328400
Superficial velocity (m/s)
20 Spring constant (N/m) 800
Viscosity(kg/ms) 2.0×10-5 Friction coefficient 0.3
Acceleration of gravity (m/s2)
9.8 Time step (s) 10-4
k
dt
n
pp
6
)(
5
23
Time step (Y. Tsuji et al. 1992)
T. Zhao and M.Takei, Advanced Powder Technology, (2008)
T.Zhao and M.Takei, Powder Technology, (2010)
Calculation Domain and Calculation Results Particle
inlet
21
2 122
212 45
270
Particle inlet
270
Air nozzle
(Dimension in mm)
212
122
1980
h=0.33m h=0.99m h=1.65m
Fig. Simulation results of axial position
0.0% 5.0% Powder concentration
Distance from the distributor h [m]
h=300[mm]
h=400[mm]
……
……
……
……
……
……
…
h=1900[mm]
h=0[mm]
Solid
volu
me
fraction [
-]
T.Zhao, M.Takei,. Flow Measurement and Instrumentation, (2010)
T.Zhao, M.Takei, Advanced Powder Technology, (2010)
Distance from center [mm]
Part
icle
volu
me fra
ction [
-]
Calculated Profiles of Axial & Radial Volume Fraction
Fig. Profiles of axial volume fraction
Fig. Profiles of radial volume fraction
Functional particle
Nozzle spray of coating
solvent to nucleus particles
in fluidized bed
Coating Process in Powder Drug Production
Coating process
Coating solvent Nucleus particles
Functional particles
Fig. Functional particles Dry of coating solvent by
hot air
Fig. Coating process
Nucleus particles
Draft tube
Spray nozzle
Hot air supply
Hot air duct
Spray
nozzle
Apertures
plate
Bug
filter
Exhaust duct
Outer
chamber
Draft tube
Operational factors for
uniform coating
CFD-DEM & Noninvasive
monitoring technique to
visualize the uniformity of
particles fluidization
during coating process
M.Takei, et al.,Powder Technology, (2009)
CFD-DEM Simulation for Drug Production
gFFFv
Dwallcollision mdt
dm
collisionF
wallF
:Powder-powder stress
:Powder – wall stress
Powder equations of motion
Fig. Model of Particles Collision
Fig. DEM simulation results
High air velocity
Spring
dashpot
friction slider
DF :Drag force
OUTLINE Multiphase Flow System & CFD-DEM
Necessity of Flow Visualization Techniques
Application of Process Tomography
Plant & Manufacturing Process
Application of Process Tomography
Challenge to Thrombus Detection
Concluding Remarks
Simulation results look real, but they are not real !!!!!
Academic parameters of particles motion:
Coefficients of spring, dashpot and slider
Drawbacks of simulation: Perfect sphere, Same diameter particles
⇒Coefficients dependency on time & each particle
Industrial parameters of process:
Homogeneous particle concentration
Best nozzle design: Place, Number, Diameter etc.
Proper operation factor: Mass flow rate Q,
Particle supply ratio ξ, Temperature T etc., “in time”
Particle Particle
Gap between Academia and Industry for Best Design
kn & kt : Springs constant
ηn & ηt : Coefficient of viscous dissipation
μf : Friction coefficient
Happy academia: Parameter fitting with experiments
Unhappy industry: How much is the essential parameters for the
best design?
Necessity of Visualization Technique for Best Design
Flow visualization technique for best design to overcome the gap
Non destructive visualization technique
3D + time particle concentration
“What you can see “in real situation” is what you can believe”
Insufficient CFD-DEM for the best design
OUTLINE Multiphase Flow System & CFD-DEM
Necessity of Flow Visualization Techniques
Application of Process Tomography
Plant & Manufacturing Process
Application of Process Tomography
Challenge to Thrombus Detection
Concluding Remarks
Fig. Tomographic image of inside head
by medical CT
Process Tomography
Fig. Overview of PT for particle flow
Pipeline Electrode
Particle
①
②
③
⑫
⑪
⑥
⑧
④ ⑤
⑦
⑨ ⑩
①
②
③
⑫
⑪
⑥
⑧
④ ⑤
⑦
⑨ ⑩
①
②
③
⑫
⑪
⑥
⑧
④ ⑤
⑦
⑨ ⑩
From Hitachi Co Web
Fig. PT(ECT)System
10million US $ Easy handling, Low cost & high seed
10,000 US $
Governing equation of PT(ECT)
Ill posed Inverse Problem
Unknown Number > Expression
Number
Image Reconstruction
Approximate Permittivity E
0)]()([ rr V・ --(2)
jr
i
c
ji dVV
C rrr ・)()(0,
)12,,1;11,,2,1( iji
--(1)
Ci,,j:Capacitance between i and j electrodes, ε0:Vacuum permittivity, VC : Electrode voltage , r : Position vector,
ε: Relative permittivity, Vi : Potential in cross section, Γi : Area covered with electric force line
Governing Equation in the Electrostatic Field
0)]()([ rr V・ --(2)0)]()([ rr V・ --(2)
jr
i
c
ji dVV
C rrr ・)()(0,
)12,,1;11,,2,1( iji
--(1)
Ci,,j:Capacitance between i and j electrodes, ε0:Vacuum permittivity, VC : Electrode voltage , r : Position vector,
ε: Relative permittivity, Vi : Potential in cross section, Γi : Area covered with electric force line
Governing Equation in the Electrostatic Field
32 × 32 Space Resolution
Pipe inner wall
Nx =32
Ny =32
x
y
Measured Capacitance C
66 × 1
Sensitivity Matrix S e
66 × 1024
Unknown Permittivity
Distribution E
1024 × 1 C = S e E
1
12
11 10 9
8
7
6
5 4 3
2 Electrode
x
y
Sensitivity [ - ]
32 × 32 Space Resolution
Pipe inner wall
Nx =32
Ny =32
x
Nx =32
Ny =32
x
y
Measured Capacitance C
66 × 1
Sensitivity Matrix S e
66 × 1024
Unknown Permittivity
Distribution E
1024 × 1 C = S e E
1
12
11 10 9
8
7
6
5 4 3
2 Electrode 1
12
11 10 9
8
7
6
5 4 3
2 Electrode
x
y
Sensitivity [ - ]
M. Takei et al. Measurement Science and Technology (2004, 2006)
1. Two guard electrodes
Concentration of electrical line
2. High Ω Resistance
Protection of stray capacitance
3. Screen electrodes
Noise Absorption
Fig. Guard electrodes
U0=0 U1
Measured electrodes
Guard electrodes
Guard electrodes
Fig. CT sensor
Coaxial cable
Resistance
Earthed electrodes
Guard electrodes
Guard electrodes
Measured electrode
Copper wire
PT(ECT) Sensor
Noise
Fig. Screen electrode
Measured
electrodes
Nois
e a
bsorp
tion
Resistance
Noise protection method
Screen
electrode
M.Takei,et al. International Journal of Applied Electromagnetics and Mechanics, IOS Press, (2002)
M.Takei et al., Particulate Science and Technology, Taylor & Francis, (2002)
0.0 0.2
Reconstructed Images in Fluidized Bed by PT
Air
Low
Sensor position
h=0.33m
h=0.99m
h=1.65m
Case1.1 Case1.2 Case 1.3 Case 1.4
M.Takei et al. Powder Technology (2009)
M.Takei, et al., Experiments in Fluids, Springer, (2008)
Part
icle
volu
me fra
ction [
-]
Axial position h [m]
1:2
1:1
1:4 Air
Air
Air
Particle volume fraction decreased as
axial position goes downstream in both
experiment and simulation.
Low
Middle
High
Axial Volume Fraction Profiles
h=0.33m (Experiment)
h=0.99m (Experiment)
h=1.65m (Experiment)
h=0.33m (Simulation)
h=0.99m (Simulation)
h=1.65m (Simulation)
0
0.01
0.02
0.03
0.04
0.05
0.06
0.07
0 15 30 45 60 75 90 105 120 135
0
0.01
0.02
0.03
0.04
0.05
0.06
0.07
0 15 30 45 60 75 90 105 120 135
0
0.01
0.02
0.03
0.04
0.05
0.06
0.07
0 15 30 45 60 75 90 105 120 135
1:2
1:1
1:4 Air
Air
Air
Low
Middle
High Part
icle
volu
me fra
ction [
-]
Radial position r [mm]
Radial Volume Fraction Profiles
PT Images of Particle Coating
Spray time
0 min
Spray time
10 min
Spray time
20 min
Spray time
30 min
Spray time
40 min Spray time
50 min
0.0 1.0 Concentration
Fig. Instantaneous CT Images at each spray time
The high concentration particle distribution is located near the tube
Nucleus powder Crystalline cellulose Asahi Kasei Corporation Celphia 203
Nucleus powder diameter 150μm
Density of powder 870 kg/m3
Relative permittivity of Air 1.0006
Relative permittivity of Powder 2.1
Atomized coating liquid HPC (Hydroxypropyl Cellulose) Shin-Etsu Chemical Co.
Spray coating time 50 minutes
Sampling time Every 5 minutes for several seconds
Spatial Mean Concentration from Image
y xN
y
N
xoutyx
pNNN
tD1 1
1xytE
The spatial mean particle concentration at a time point
outN : the pixel number outside the pipe
Spray time 0 min
Fig. Spatial mean concentration from CT images.
Spray time 10 min Spray time 20 min
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1
Range
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1 Range
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1 Range
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1 Range
Sp
atia
l m
ean c
once
ntr
atio
n [
- ]
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1 Range
Spray time 30 min Spray time 40 min Spray time 50 min
100 200 300 400 500 Time
0.2
0.4
0.6
0.8
1 Range
×Δ t[ms]
×Δ t[ms]
Spat
ial
mea
n c
on
cen
trat
ion
[ - ]
M.Takei, et al.,Powder Technology, (2009)
T. EDA, M.TAKEI et al., Journal of Power and Energy Systems (2013)
Air
Experiments of Trickle Bed Reactor
Pulsing Bubble Trickle
(QL, Q
G)=
(13L/m
in,
70L/m
in)
(QL, Q
G)
=(6
L/m
in, 10L/m
in)
(QL, Q
G)
=(1
3L/m
in,
15L/m
in)
t=4.0
sec
z = 1020 mm,
dp = 5 mm,
x
y
t
3D Reconstructed Images
Flow Patterns in Trickle Bed
(QL, Q
G)=
(13L/m
in,
70L/m
in)
QL
QG
①
② ③
① ② ③
0.0 0.2 Normalized Conductivity [-]
Fig Experimental set up
Measurement
system
• heater
Data acquisition/
Data logger switch
unit
heater
Reference
Ceramics
beaker
Polycarb
onate
particles
Electrodes
0
1
0 1/1
6 2
/16
3/1
6 4
/16
5/1
6 6
/16
7/1
6
• heater
120[sec] 180[sec] 240[sec]
300[sec] 360[sec] 420[sec]
Fig PT temperature images
low
<-Te
mp
era
ture
->h
igh
Temperature Distribution by PT
Fig Temperature distribution by PT
ε :Relative permittivity[F/m],
M :Mol mass[kg/mol],
ρ :Density[kg/m3],
NA : Avogadro Number[-],
T :Temperature[K],
kB : Boltzmann constant[J/K],
μ :Permanent dipole moment[D]
OUTLINE Multiphase Flow System & CFD-DEM
Necessity of Flow Visualization Techniques
Application of Process Tomography
Plant & Manufacturing Process
Application of Process Tomography
Challenge to Thrombus Detection
Concluding Remarks
Artificial
valve
Artificial
heart
Artificial
lung
Artificial
vessel Stent Artificial
kidney
Artificial
liver
2) Unclear Interface multi-physics
between artificial organs and blood
1) Immature thrombus detection
measurement technique
Increase of thrombosis risk
by artificial organs
Thrombus future prediction Thrombus online measurement
Anticoagulant treatment
Anxiety for thrombosis of patient
Possibility of thrombosis prediction(When, Where, How)
However
Japanese COD: 30% Circulatory condition
Cardiac disease: 16%
Cerebrovascular disease: 12%
Others 42%
Cancer: 30%
Figure: Japanese COD
Background of Thrombus Detection
Practical use of artificial organs
COD: Cause of death
Thrombosis in VAD
impeller
Pharmaceutical Approval
of VAD
Business since 2011.4.1
「EVAHEART」「DuraHeart」
(1) Thrombus Insitu detection technique
(2) Thrombus Insilico prediction technique
(3) Thrombus Invitro validation technique
VAD accelerate the formation of thrombus
Complication of Cerebral infarction VAD impeller
Left ventricle
Blood
transmission
Blood
cannula
Aorta ascendens
Return to work &
home healthcare by
implanting VAD
Example of Ventricular Assist Device
Establishment of future prediction technique of thrombus
Our Proposal !!
Research and development of total solution
31
Blood Coagulation Process
Extrinsic reaction
Intrinsic reaction
Tissue factor
VIIa
Ca++
X Xa
IX IXa
XIa XI
XIIa XII
Polymerization
・Gelation reaction in liquid
Prothrombin
Thrombin
XIII XIIIa Ca++
Fibrin clot
Fibrin
Fibrinogen
Fibrinolysis Plasmin (Cross-link)
32
Multi-interface of Thrombus invitro
Artificial interface
Tethering
Biochemistry
factor
Gathering Rolling
G.Matsumiya et al. J Heart Lung Transplant. (2010)
Flow rate
Thrombus
structure
Mu
lti-p
hysic
s
Interface of artificial
surface and elastic
substrate Interface of blood
and endothelium Artificial interface
Interface of blood and
artificial surface
Interface of artificial
surface and
endothelium
Mimic flow
channel
032
1
AW NM
e
B
AW
Tk
NM
332
1 2
0
Polarization
Mw:Number of molecule,NA:Avogadro number,kB:Boltzmann constant,
T:Absolute temperature,ρ:Density
Clausius-Mossotti equation
Debye equation
Dielectric Spectrum Orientation
polarization
Ions polarization: Negligible
Electron
polarization
Microwave f=2.45GHz K.Asami http://www003.upp.so-net.ne.jp/asami/DS.pdf
D:Electrical flux [C/m2],
ε0 :Vacuum permittivity[F/m] ,
E :Electrical field[V/m],
P:Polarization[C/m2],
N: Number of molecule
per unit volume[-],
m: Induced dipole moment [Cm],
F: Effective electric field [V/m],
ε: Relative permittivity[-],
α : Polarizability of molecule [Cm2/V]
μ : Permanent dipole moment[Cm]
●Electrical flux and Polarization
D = ε0E + P P = Nm = NαF
Orientation & Electron
polarizations
(Polar molecule)
34
Electrical Change of RBCs Membrane Cole-Cole Plot
Electrode
R
RBCs
RBCs
R
Plasma
R
RBCs
membrane C
Electrode
R
Electrode
C
Thrombus
Re
acta
nce
[Ω]
Resistance[Ω]
Shift to upper right of
relaxation frequency
Electrode
EDL
Electrode
R
Electrode
C
Electrode
EDL
Membrane
Hemoglobin
Plasma
C
Fibrin
High
frequency
Middle
frequency
Low
frequency
Curr
ent
Curr
ent
Cu
rren
t
CPE CPE
EDL: Electrical Double Layer
0
20
40
60
80
100
120
140
160
180
200
1050 1150 1250 1350 1450
Reacta
nce X
[Ω
]
Resistance R [Ω]
t=0.0min
t=27.0min
t=45.0min
t=72.0min
t=90.0min
f =70kHz
f =1MHz
f =4MHz
Resistance increment for thrombus
formation
VoltageV 1[V]
Measurement frequency f
70kHz~4MHz
Measurement time t 90min
Measurement point 60 Point
Cole-Cole Plot
Shift on upper right
Shift of Cole-Cole plot
20Ω
Electrode
Holder
PC X
Y Z
30mm
Impedance
Analyzer
(Plasma 63%+30%CaCl2)
Reactance Change of RBCs Membrane
Thrombus formation
C Decreased
X Increased
Experimental setup
Bovine
Blood
Calcium
Chloride
Impedance
Analyzer PC
Electrode
20mm
20m
m
Z X
Y
10
mm
Photo of thrombus
formation experiment
Injection current i 4.0[mA]
Sweep AC frequency f 1[kHz]~5[MHz]
Measurement point 201[point](Log)
Calibration Open, Short
Average 5
Measurement condition
Experimental Condition
1. Estimate of RBCs relaxation frequency
2. Measurement of thrombogenic process
Addition of CaCl2
Addition of thrombin
1. Blood+CaCl2
2. Blood+PBS+CaCl2
3. Blood+PBS
4. Blood(Hematocrit change)+CaCl2
Measurement time
3.0mL+1.0mL(0.02M)
3.0mL+0.4mL+0.6mL
3.0mL+1.0mL
3.0mL(H[%]=0, 10, 20, 30)+1.0mL
t =0.0min~60.0min
PBS
PBS+Thrombin
Fibrinogen+PBS
Fibrinogen+Thrombin
4.0mL
3.5mL+0.5mL(1000units/mL)
3.5mL(2500mg/dL)+0.5mL
3.5mL(2500mg/dL)+0.5mL
Blood
Hematocrit
Blood volume
Sodium citrate
Bovine blood(H=36%)
H [%]=0,10,20,30,36,40,50,60
4.0mL
0.4mL(3.2vol%) in 4.0mL 20mm
20
mm
Z
X
Y
10
mm
Bovine
Blood Calcium
Chloride
Calibration Method
Calibration method
Calibration of cell
r0r0p CCε'Cd
Sεε'C
d
SεC 00
Cr=6.93×10-13
C0=8.85×10-14
Gε
Cρ
0
00ωρC
'ε'1
20mm
20
mm
Z
X
Y
10
mm
Relaxation
frequency
Estimate of electrode polarization and RBCs membrane
Stray
capacitance Cr
Cell constant C0
Relative permittivity and Dielectric loss
Relative
permittivity ε’ 0
rp
C
CCε'
Resistivity ρ Dielectric loss ε”
S:Electrode area[m2]
d:Distance between electrode[m]
ε0:Vacuum permittivity[F/m]
ε’: Water permittivity[F/m]
G:Conductance[S]
Cp: Measurement capacitance[F]
ω:Angular frequency[rad/s]
1E+02
1E+03
1E+04
1E+05
1E+06
1E+07
1000 10000 100000 1000000
Rela
tive p
erm
itti
vit
y ε' [-
]
Frequency f [Hz]
H=0% H=10%H=20% H=30%H=36% H=40%H=50% H=60%
0
1000
2000
3000
4000
5000
10000 100000 1000000
Die
lectr
ic l
oss ε
" [
-]
Frequency f [Hz]
H=0% H=10%H=20% H=30%H=36% H=40%H=50% H=60%
Permittivity & Dielectric Loss of RBCs
RBCs relaxation frequency
Electrode relaxation frequency:20kHz
RBCs relaxation frequency:2MHz
RBCs membrane permittivity: 250kHz
Electrode relaxation frequency
f<60kHz : Electrode polarization
60kHz<f<1MHz : RBCs membrane
permittivity
f>1MHz : RBCs dielectric relaxation
Hematocrit change
Electrode polarization
RBCs membrane permittivity
RBCs dielectric relaxation
Electric Influence of Thrombin
0.6
0.61
0.62
0.63
0.64
PBS PBS+Thrombin
Resis
tivit
y ρ
[Ω・m
]
500
520
540
560
PBS PBS+Thrombin
Rela
tive p
erm
itti
vit
y ε' [-
]
decrease
Increase
Resistivity
PBS only
PBS+Thrombin >
Relative permittivity
PBS only
PBS+Thrombin <
Thrombin decreases
the resistivity
Thrombin increases the
relative permittivity
250kHz
Electrical Influence of Fibrinogen Solution
910
930
950
970
990
1010
Fbg+PBS Fbg+Thrombin
Rela
tive p
erm
itti
vit
y ε' [-
]
0.415
0.42
0.425
0.43
0.435
0.44
0.445
Fbg+PBS Fbg+Thrombin
Resis
tivit
y ρ
[Ω・m
] Resistivity
Fibrinogen+PBS
Fibrinogen+Thrombin
>
Relative permittivity
Fibrinogen+PBS
Fibrinogen+Thrombin
<
Increase
Decrease
Fibrin formation
increases the resistivity
250kHz
Fibrin formation decreases
the relative permittivity
2500mg/dL Fibrinogen
Permittivity & Resistivity of Thrombogenic Process
Time [min] 0.0 5.0 10.0 15.0 20.0 25.0 30.0
Visual check - - - + ++ +++ +++
Time [min] 35.0 40.0 45.0 50.0 55.0 60.0
Visual check +++ +++ +++ +++ +++ +++
(a) -:Non-thrombogenic condition
(b) +:Micro thrombus formation
(c) ++:Thrombus over 1mm
(d) +++:Huge thrombus
Result of visual check
0.99
1
1.01
1.02
1.03
0.92
0.94
0.96
0.98
1
1.02
0 10 20 30 40 50 60N
orm
alized
resis
tivit
y ρ
* [-
]
No
rmalized
rela
tive
perm
itti
vit
y ε’*
[-]
Time t [min]
fec=20kHz ε' fm=250kHz ε' frc=2MHz ε' fec=20kHz ρ fm=250kHz ρ frc=2MHz ρ
(a) (b) (c)(b) (c) (d)
Relative Permittivity & Resistivity of
Thrombogenic Process of Others Conditions
Non-thrombogenic(PBS 25%) (blood 3.0mL+PBS 1.0mL)
Thrombogenic(CaCl2 15%) (blood 3.0mL+PBS 0.4mL+CaCl2 0.6mL)
The experiments showed the possibility of the real time detection of
thrombosis using the characteristics frequency of red blood cells membrane
0.99
1
1.01
1.02
1.03
1.04
1.05
1.06
0.92
0.94
0.96
0.98
1
0 10 20 30 40 50 60
No
rmalized
resis
tivit
y ρ
* [-
]
No
rmalized
rela
tive
perm
itti
vit
y ε
'* [
-]
Time t [min]
fec=20kHz ε' fm=250kHz ε' frc=2MHz ε' fec=20kHz ρ fm=250kHz ρ frc=2MHz ρ
0.99
1
1.01
1.02
1.03
1.04
0.91
0.93
0.95
0.97
0.99
1.01
0 10 20 30 40 50 60
No
rmalized
resis
tivit
y ρ
* [-
]
No
rmalized
rela
tive
perm
itti
vit
y ε
'* [
-]
Time t [min]
fec=20kHz ε' fm=250kHz ε' frc=2MHz ε' fec=20kHz ρ fm=250kHz ρ frc=2MHz ρ
Relative Permittivity & Resistivity of
Thrombus of Hematocrit Change
Addition of CaCl2
Hematocrit
Measurement time
Blood+CaCl2
H[%]=0, 10, 20, 30
t =0.0min~60.0min
3.0mL+1.0mL(0.02M)
250kHz
Only plasma was not seen of peak
of relative permittivity decrease
The phenomenon was specific to the
thrombosis, and was observed only in
the presence of red blood cells.
0.92
0.94
0.96
0.98
1
1.02
0 10 20 30 40 50 60
No
rmalized
rela
tive
perm
itti
vit
y ε
'* [
-]
Time t [min]
H=0%
H=10%
H=20%
H=30%
Visualization of Thrombogenic Process insitu Detection
Bovine
blood CaCl2
Electrode holder
(PMMA)
Data
Acquisition
System
PC
X
Y Z
30mm
30m
m
Multiplexer 10m
m
5m
m
Cross-section
X
Y
R
Electrode (SUS304)
10mm 3mm
Z
PT visualization image of thrombogenic process
Concluding Remarks
CFD-DEM calculation results in powder technology are
shown in petroleum and pharmaceutical industries.
Flow visualization technique should be played a role of
product design as well as CFD-DEM
Noninvasive PT visualization technique is useful for
pant, manufacturing & blood monitoring.
The concept is “What you can see “in real situation” is
what you can believe”