Professional Documents
Culture Documents
A Thesis
Submitted to the Faculty
of
Drexel University
by
Sangho Kim
in partial fulfillment of the
requirements for the degree
of
Doctor of Philosophy
December 2002
ii
Acknowledgments
I wish to express my sincere gratitude to Dr. Young I. Cho, for his guidance
and inspiration during my entire tenure in graduate school. His experience and idea
have proven to be invaluable. I also wish to thank Dr. David M. Wootton for serving
as my co-advisor, and for his valuable suggestions and guidance on Biofluid
Dynamics.
I wish to express my appreciation to the members of my dissertation
committee, including: Dr. Ken Choi and Dr. Alan Lau from the MEM Department,
and Dr. Peter Lelkes from the School of Biomedical Engineering.
I am deeply indebted to Dr. Kenneth Kensey, Mr. William Hogenauer, and
Dr. Larry Goldstein from Rheologics, Inc. for providing valuable comments on the
test methods and data reduction procedure.
A sincere appreciation is extended to several colleagues whose friendship I
have cherished during my graduate studies, including: Dr.Wontae Kim, Dr. Sunghyuk
Lee, Chagbeom Kim, Giyoung Tak, Dohyung Lim, and Jinyong Wee.
Last but not least, I wish to thank my parents for their unbounded support
throughout my life. Their reliable provision of emotional, spiritual, and financial
support has allowed me to accomplish tasks that would have otherwise been
impossible.
iii
Table of Contents
LIST OF TABLES.....................................................................................................viii
LIST OF FIGURES ................................................................................................... x
ABSTRACT...............................................................................................................xiv
CHAPTER 1 INTRODUCTION ..............................................................................
2.2.1.1
Power-law Model...................................................................... 11
2.2.1.2
2.2.2
2.3
2.2.2.1
2.2.2.2
Casson Model............................................................................ 14
2.2.2.3
Herschel-Bulkley Model........................................................... 15
Rheology of Blood...................................................................................... 19
2.3.1
iv
2.3.1.1
Plasma Viscosity....................................................................... 20
2.3.1.2
Hematocrit................................................................................. 20
2.3.1.3
RBC Deformability................................................................... 21
2.3.1.4
2.3.1.5
Temperature .............................................................................. 22
2.3.2
2.3.2.1
2.3.2.2
Introduction................................................................................................. 30
3.2
3.2.2
Cone-and-Plate................................................................................... 35
3.3
Capillary-Tube Viscometer......................................................................... 38
3.4
3.4.1.1
3.4.1.2
3.4.2
3.5
Indirect Method.................................................................................. 42
3.5.2
v
CHAPTER 4 THEORY OF SCANNING CAPILLARY-TUBE RHEOMETER.... 49
4.1
4.2
4.1.2
Power-law Model............................................................................... 60
4.2.2
Casson Model..................................................................................... 66
4.2.3
5.4.2
5.4.3
Introduction........................................................................................104
5.6.2
Experimental Method.........................................................................106
5.6.3
vi
6.2
6.1.1
6.1.2
6.1.3
6.1.4
6.2.2
6.2.3
6.2.3.1
6.2.3.2
6.2.4
6.3
6.3.2
6.3.3
vii
APPENDIX G: REPEATABILITY STUDY WITH DISTILLED WATER ............208
APPENDIX H: EXPERIMENTAL DATA ...............................................................210
VITA ..........................................................................................................................221
viii
List of Tables
2-2. Range of shear rates of some familiar materials and processes ........................
ix
H-4. A typical experimental data set of human blood obtained by a scanning
capillary-tube rheometer with plastic riser tubes..............................................218
List of Figures
xi
xii
xiii
6-25. Test with unadulterated human blood at 37..................................................172
6-26. Wall shear stress at a capillary tube vs. shear rate............................................174
6-27. Variations of a plug-flow region at a capillary tube as a function of time
for bovine blood with 7.5% EDTA at 25.....................................................177
6-28. Velocity profiles at a capillary tube for bovine blood
with 7.5% EDTA at 25.................................................................................178
6-29. (a) Viscosity, (b) wall shear rate, and (c) wall shear stress
Plotted as a function of mean velocity at a capillary tube using
three non-Newtonian models for bovine blood with 7.5% EDTA ..................179
B-1. Falling cylinder viscometers .............................................................................199
C-1. Cross sectional view of SV352A8-01 module..................................................201
G-1. Repeatability study #1 ......................................................................................208
G-2. Repeatability study #2 ......................................................................................209
xiv
Abstract
A Study of Non-Newtonian Viscosity and Yield Stress of Blood
in a Scanning Capillary-Tube Rheometer
Sangho Kim
Professors Young I. Cho and David M. Wootton
xv
with each other as well as with the results obtained by a conventional rotating
viscometer, whereas the power-law model seemed to produce inaccurate viscosities at
low shear rates.
The yield stress values obtained from the Casson and Herschel-Bulkley
models for unadulterated human blood were measured to be 13.8 and 17.5 mPa,
respectively. The two models showed some discrepancies in the yield-stress values.
In the study, the wall shear stress was found to be almost independent of the
constitutive model, whereas the size of the plug flow region in the capillary tube
varies substantially with the selected model, altering the values of the wall shear rate
at a given mean velocity. The model constants and the method of the shear stress
calculation given in the study can be useful in the diagnostics and treatment of
cardiovascular diseases.
1
CHAPTER 1. INTRODUCTION
2
Other researchers investigated correlation between the hemorheological
parameters and stroke [Grotta et al., 1985; Coull et al., 1991; Fisher and Meiselman,
1991; Briley et al., 1994]. They reported that stroke patients showed two or more
elevated rheological parameters, which included whole blood viscosity, plasma
viscosity, red blood cell (RBC) and plate aggregation, RBC rigidity, and hematocrit.
It was also reported that both whole blood viscosity and plasma viscosity were
significantly higher in patients with essential hypertension than in healthy people
[Letcher et al., 1981, 1983; Persson et al., 1991; Sharp et al., 1996; Tsuda et al., 1997;
Toth et al., 1999].
hematocrit were elevated, whereas RBC deformability was decreased [Hoare et al.,
1976; Dintenfass, 1977; Hill et al., 1982; Poon et al., 1982; Leiper et al., 1982].
Others conducted hemorheological studies to determine the relationships
between whole blood viscosity and smoking, age, and gender [Levenson et al., 1987;
Bowdler and Foster, 1987; Fowkes et al., 1994; Ernst, 1995; Ajmani and Rifkind,
1998; Kameneva et al., 1998; Yarnell et al., 2000]. They found that smoking and
aging might cause the elevated blood viscosity. In addition, it was reported that male
blood possessed higher blood viscosity, RBC aggregability, and RBC rigidity than
premenopausal female blood, which may be attributed to monthly blood-loss
[Kameneva et al., 1998].
3
1.2. Motivation of the Present Study
The medical community has been slow in realizing the significance of whole
blood viscosity, which can be attributed partly to the lack of an uncomplicated and
clinically practical method of measuring whole blood viscosity. In most clinical
studies, mainly two types of viscometer have been available for general use:
rotational viscometers and capillary tube viscometer, as will be discussed in Chapter
3. These viscometers are used at laboratory only, and are not used in a clinical
environment. Until recently, the most immediate difficulty has been the lack of an
instrument that is specially designed for daily clinical use in measuring whole blood
viscosity.
4
experimental studies, distilled water (Newtonian fluid), bovine blood (non-Newtonian
fluid) with 7.5% EDTA, and unadulterated human blood (non-Newtonian fluid) were
used for the measurements of both viscosity and yield stress. Power-law, Casson, and
Herschel-Bulkley models were examined as constitutive models for blood in the study.
conventional rheometers that measure either the viscosity or yield stress of a fluid. In
this chapter, only rheometers that can be applicable to clinical applications are
discussed. Chapter 4 introduces the theory of a scanning capillary-tube rheometer.
Chapter 5 discusses the considerations for the experimental study, which include
unsteady effect, end effect, wall effect, temperature analysis, dye concentration effect,
and other possible factors. Chapter 6 presents the results of experimental studies
performed with a scanning capillary-tube rheometer. Chapter 6 also reports the effect
of non-Newtonian constitutive models on the rheological measurements and flow
patterns of blood in a capillary tube. Chapter 7 gives conclusions of the study and
recommendations for future study.
5
CHAPTER 2. CONSTITUTIVE MODELS
Fluid such as water, air, ethanol, and benzene are Newtonian. This means that
when shear stress is plotted against shear rate at a given temperature, the plot shows a
straight line with a constant slope that is independent of shear rate (see Fig. 2-1).
This slope is called the viscosity of the fluid. All gases are Newtonian, and common
liquids such as water and glycerin are also Newtonian. Also, low molecular weight
liquids and solutions of low molecular weight substances in liquids are usually
Newtonian. Some examples are aqueous solutions of sugar or salt.
The simplest constitutive equation is Newtons law of viscosity [Middleman,
1968; Bird et al., 1987; Munson et al., 1998]:
= &
where is the Newtonian viscosity and & is the shear rate or the rate of strain.
(2-1)
6
The Newtonian fluid is the basis for classical fluid mechanics. Gases and
liquids like water and mineral oils exhibit characteristics of Newtonian viscosity.
However, many important fluids, such as blood, polymers, paint, and foods, show
non-Newtonian viscosity.
Table 2-1 shows the wide viscosity range for common materials. Different
instruments are required to measure the viscosity over this wide range.
One
(a)
Shear stress
100
50
0
0
50
100
150
Shear rate
(b)
Viscosity
10
0
0
50
Shear rate
100
Glass
1040
Asphalt
108
Molten polymers
103
Heavy syrup
102
Honey
101
Glycerin
100
Olive oil
10-1
Light oil
10-2
Water
10-3
Air
10-5
Table 2-2. Range of shear rates of some familiar materials and processes
[Barnes et al., 1989].
Process
Range of
Shear Rates (s-1)
10-6 10-4
Medicines, paints
10-2 10-1
10-1 101
Painting, coating
Screw extruders
100 102
101 102
Foods
Dip coating
101 102
Paints, confectionery
101 103
Manufacturing liquids
Pipe flow
100 103
103 104
Rubbing
104 105
104 105
Polymer melts
103 105
Blade coating
105 106
Paper
Lubrication
103 107
Gasoline engines
Application
10
2.2. Non-Newtonian Fluid
Any fluids that do not obey the Newtonian relationship between shear stress
and shear rate are non-Newtonian. The subject of rheology is devoted to the study of
the behavior of such fluids. Aqueous solutions of high molecular weight polymers or
polymer melts, and suspensions of fine particles are usually non-Newtonian.
In the case of general non-Newtonian fluids, the slope of shear stress versus
shear rate curve is not constant.
increasing shear rate, the fluid is called shear-thinning. In the opposite case where the
viscosity increases as the fluid is subjected to a high shear rate, the fluid is called
shear-thickening.
thickening.
In general, the Newtonian constitutive equation accurately describes the
rheological behavior of low molecular weight polymer solutions and even high
molecular weight polymer solutions at very slow rates of deformation. However,
viscosity can be a strong function of the shear rate for polymeric liquids, emulsions,
and concentrated suspensions.
11
2.2.1.1. Power-law Model
One of the most widely used forms of the general non-Newtonian constitutive
relation is a power-law model, which can be described as [Middleman, 1968; Bird et
al., 1987; Munson et al., 1998]:
= m& n
(2-2)
= m& n 1
(2-3)
12
rate (see Fig. 2-2) rather than to a constant, 0 , as is often observed experimentally.
Viscosity for many suspensions and dilute polymer solutions becomes constant at a
very high shear rate, a phenomenon that cannot be described by the power-law model.
As discussed in the previous section, the power-law model does not have the
capability of handling Newtonian regions of shear-thinning fluids at very low and
high shear rates. In order to overcome this drawback of the power-law model, Cross
(1965) proposed a model that can be described as [Ferguson and Kemblowski, 1991;
Cho and Kensey, 1991; Macosko, 1994]:
= & + 0
1 + m& n
(2-4)
where
13
2.2.2. Viscoplastic Fluid
Many types of food stuffs exhibit a yield stress and are said to show a plastic
or viscoplastic behavior. One of the simplest viscoplastic models is the Bingham
plastic model, and it can be expressed as follows [Bird et al., 1987; Ferguson and
Kemblowski, 1991; Macosko, 1994]:
= m B & + y
& = 0
when y ,
when y ,
where
(2-5)
(2-6)
14
m B = a model constant that is interpreted as plastic viscosity.
Basically, the Bingham plastic model can describe the viscosity characteristics of a
fluid with yield stress whose viscosity is independent of shear rate as shown in Fig. 24. Therefore, the Bingham plastic model does not have the ability to handle the
shear-thinning characteristics of non-Newtonian fluids.
This model was originally introduced by Casson (1959) for the prediction of
the flow behavior of pigment-oil suspensions. The Casson model is based on a
structure model of the interactive behavior of solid and liquid phases of a two-phase
suspension [Casson, 1959]. The model describes the flow of viscoplastic fluids that
can be mathematically described as follows [Bird et al., 1987; Ferguson and
Kemblowski, 1991; Cho and Kensey, 1991; Macosko, 1994]:
= y + k &
& = 0
when y ,
when y ,
(2-7)
(2-8)
15
2.2.2.3. Herschel-Bulkley Model
= m& n + y
& = 0
when y ,
when y ,
(2-9)
(2-10)
16
(a)
100
Shear stress
(b)
(c)
50
0
0
50
100
150
10
Viscosity
(c)
(b)
(a)
0
0
50
100
Shear rate
150
17
Newtonian regions
0
Viscosity
(log)
Power-law region
18
100
(a)
Shear stress
(b)
50
mB
y
0
0
50
100
Shear rate
150
19
2.3. Rheology of Blood
Blood behaves like a non-Newtonian fluid whose viscosity varies with shear
rate. The non-Newtonian characteristics of blood come from the presence of various
cells in the blood (typically making up 45% of the bloods volume), which make
blood a suspension of particles [Fung, 1993; Guyton and Hall, 1996]. When the
blood begins to move, these particles (or cells) interact with plasma and among
themselves.
plasma viscosity, red cell aggregation, and red cell deformability (or rigidity).
20
2.3.1.1. Plasma Viscosity
Plasma is blood from which all cellular elements have been removed. It has
been well established that plasma behaves like a Newtonian fluid. Careful tests
conducted using both rotating and capillary tube viscometers over a range of shear
rates (i.e., from 0.1 to 1200 s-1) found no significant departures from linearity.
Therefore, its viscosity is independent of shear rate. Figure 2-5 illustrates this clearly
in the horizontal viscosity line for plasma [Dintenfass, 1971; Dinnar, 1981]. Since
blood is a suspension of cells in plasma, the plasma viscosity affects whole blood
viscosity, particularly at high shear rates.
2.3.1.2. Hematocrit
Hematocrit is the volume percentage of red blood cells in whole blood. Since
studies have shown normal plasma to be a Newtonian fluid [Fung, 1993], the nonNewtonian features of human blood undoubtedly come from suspended cells in blood.
The rheological properties of suspensions correlate highly with the concentrations of
suspended particles. In blood, the most important suspended particles are the red
blood cells (RBC). Hematocrit is the most important determinant of whole blood
viscosity [Benis et al., 1970; Thurston, 1978; Fung, 1993; Picart et al., 1998; Cinar et
al., 1999]. The effect of hematocrit on blood viscosity has been well documented.
All studies have shown that the viscosity of whole blood varies directly with
21
hematocrit at all cell concentrations above 10%. In general, the higher the hematocrit,
the greater the value of whole blood viscosity [Dintenfass, 1971; Dinnar, 1981; Chien
et al., 1987; Guyton and Hall, 1996].
Since red cells do not have a nucleus, they behave like a fluid drop [Dinnar,
1981]. Hence, when a number of red cells cluster together as in the flow of a low
shear rate, they aggregate together. Accordingly, human RBCs have the ability to
22
form aggregates known as rouleaux. Rouleaux formation is highly dependent on the
concentration of fibrinogen and globulin in plasma. Note that bovine blood does not
form rouleaux because of absence of fibrinogen and globulin in plasma [Fung, 1993].
Various degrees and numbers of rouleaux in linear array and branched network are
pictured in Fig. 2-7.
Figure 2-8 shows the relationship between blood viscosity and rouleaux
formation. Rouleaux formation of healthy red cells increases at decreasing shear
rates. As red cells form rouleaux, they will tumble while flowing in large vessels.
The tumbling disturbs the flow and requires the consumption of energy, thus
increasing blood viscosity at low shear [Fung, 1993]. As shear rate increases, blood
aggregates tend to be broken up, resulting in drop in blood viscosity (see Fig. 2-8). In
short, rouleaux formation increases blood viscosity, whereas breaking up rouleaux
decreases blood viscosity.
2.3.1.5. Temperature
It is
23
preferable and is a standard in hemorheologic studies to carry out blood viscosity
measurements at body temperature of 37. Typically, blood viscosity increases less
than 2% for each decrease in temperature [Barbee, 1973].
24
yield stress include blood, ketchup, salad dressings, grease, paint, and cosmetic
liquids.
The magnitude of the yield stress of human blood appears to be at the order of
0.05 dyne/cm2 (or 5 mPa) [Schmid- Sch&o&nbein and Wells, 1971; Walawender et al.,
1975; Nakamura and Sawada, 1988; Fung, 1993; Stoltz et al., 1999] and is almost
independent of temperature in the range of 10-37 [Barbee, 1973].
25
shear rates. In their study, the first step was from the no-flow condition to a shear
rate of 10 s-1.
approximately 20 seconds at the shear rate of 10 s-1 before the final state was attained.
Next, when the shear rate stepped from 10 to 100 s-1, almost no time was required to
reach the microstructual equilibrium after the change of shear rate.
Gaspar-Rosas and Thurston (1988) also investigated on erythrocyte aggregate
rheology by varying shear rate from 500 s-1 to zero. Based on their results, it can be
concluded that the recovery of quiescent structure requires approximately 50 seconds
while the high shear rate structure is attained in a few seconds. In other words, in
order to minimize the effect of the thixotropic characteristic of blood on the viscosity
measurement between the shear rates of 500 and 1 s-1, at least 50 seconds should be
allowed during the test to have the fully aggregated quiescent state at a shear rate near
1 s-1.
Viscosity (cP)
26
Whole blood
Plasma
1
10
400
100
-1
Shear rate (s )
27
Relative viscosity
10
Normal blood
1
0.2
0.4
0.6
0.8
Fig. 2-6. Variation of the relative viscosity of blood and suspension with rigid spheres
at a shear rate > 100 s-1 [Goldsmith, 1972].
28
Fig. 2-7. Rouleaux formation of human red blood cells photographed on a microscope
slide showing single linear and branched aggregates (left part) and a network (right
part). The number of cells in linear array are 2, 4, 9, 15 and 36 in a, b, c, d, and f,
respectively. [Fung, 1993; Goldsmith, 1972]
Relative viscosity
29
10
Normal blood
1
1
10
Shear rate (s-1)
400
Fig. 2-8. Elevated blood viscosity at low shear rates indicates RBC aggregation
(rouleaux formation). Blood viscosity decreases with increasing shear rates as RBC
aggregations breaks up to individual red cells.
30
CHAPTER 3. CONVENTIONAL RHEOMETRY: STATE-OF-THE-ART
3.1. Introduction
Numerous types of rheometers have been used to measure the viscosity and
yield stress of materials [Tanner, 1985; Ferguson and Kemblowski, 1991; Macosko,
1994]. In the present study, rheometer refers to a device that can measure both
viscosity and yield stress of a material, whereas viscometer can measure only the
viscosity of the material. In addition, only shear viscometers will be discussed in the
study since the other type, extensional viscometers, are not very applicable to
relatively low viscous fluids, such as water and whole blood.
Typically, shear viscometers can be divided into two groups [Macosko, 1994]:
drag flows, in which shear is generated between a moving and a stationary solid
surface, and pressure-driven flows, in which shear is generated by a pressure
difference over a capillary tube. The commonly utilized members of these groups are
31
shown in Fig. 3-1. Numerous techniques have been developed for determining the
yield stress of fluids both directly and indirectly.
Most of these viscometers can produce viscosity measurements at a specified,
constant shear rate. Therefore, in order to measure the viscosity over a range of shear
rates, one needs to repeat the measurement by varying either the pressure in the
reservoir tank of capillary tube viscometers, the rotating speed of the cone or cup in
rotating viscometers, or the density of the falling objects. Such operations make
viscosity measurements difficult and labor intensive. In addition, these viscometers
require anticoagulants in blood to prevent blood clotting. Hence, the viscosity results
include the effects of anticoagulants, which may increase or decrease blood viscosity
depending on the type of anticoagulant [Rosenblum, 1968; Crouch et al., 1986;
Reinhart et al., 1990; Kamaneva et al., 1994].
Drag-flow type of viscometers includes a falling object (ball or cylinder)
viscometer and a rotational viscometer. However, the falling object viscometer is not
very convenient to use for clinical applications. In the case of the falling object
viscometer, the relatively large amount of a test fluid is required for the viscosity
measurement. In addition, since the testing fluid is at a stationary state initially, the
type of viscometer is not very applicable to a thixotropic fluid like whole blood. The
principle of the falling object viscometer is provided in Appendix B.
For the yield measurement of blood, most researchers have used indirect
methods rather than direct methods for practical reasons [Nguyen and Boger, 1983;
de Kee et al., 1986; Magnin and Piau, 1990]. Thus, the details of direct methods will
32
not be discussed in this chapter.
extrapolation using constitutive models are introduced and discussed in this chapter.
33
Rheometers
Yield Stress
Measurements
Viscosity
Measurements
Drag
Flows
PressureDriven Flows
CapillaryTube
Viscometer
Falling/
Rolling
Object
Viscometer
Indirect
Methods
Data
Extrapolation
Rotational
Viscometer
Direct
Methods
Extrapolation
using
Constitutive
Models
34
3.2. Rotational Viscometer
geometrical dimensions. By changing the speed of the rotating element, one is able to
collect different torques, which are used for the determination of the shear stressshear rate curve. Figure 3-2 shows a typical coaxial-cylinder system that has a fluid
confined within a narrow gap (
Ri
0.99 ) between the inner cylinder rotating at
Ro
( Ri ) =
Mi
Mo
or ( Ro ) =
2
2Ri H
2Ro2 H
(3-1)
35
& ( Ri ) & ( Ro ) =
R
Ro Ri
when 1 >
Ri
0.99
Ro
(3-2)
where
Ri + Ro
2
3.2.2. Cone-and-Plate
3M
and & =
.
3
2R
(3-3)
36
Ri
Ro
37
Fluid
Cone
Plate
38
3.3. Capillary-Tube Viscometer
39
Figure 3-4 shows the schematic diagram of a typical capillary-tube viscometer,
which has the capillary tube with an inner radius of Rc and a length of Lc . It is
assumed that the ratio of the capillary length to its inner radius is so large that one
may neglect the so-called end effects occurring in the entrance and exit regions of the
capillary tube. Then, the shear stress at the tube wall can be obtained as follows:
rPc
2 Lc
w =
Rc Pc
2 Lc
(3-4)
(3-5)
where
It is of note that the shear stress distribution is valid for fluids of any rheological
properties.
In the case of a Newtonian fluid, the shear rate at tube wall can be expressed
by taking advantage of the well-known Hagen-Poiseuille Equation as:
& w =
4Q 4V
=
Rc3 Rc
where
Rc4 Pc
= Rc2 V = volumetric flow rate (Hagen-Poiseuille Equation)
8 Lc
V = mean velocity.
(3-6)
40
Compressed
air
Air
Test fluid
Reservoir
tank
Capillary tube
Lc
2 Rc
Collected
test fluid
Balance
41
3.4. Yield Stress Measurement
independent assessment of yield stress as the critical shear stress at which the fluid
yields or starts to flow.
The value obtained by the extrapolation of a flow curve is known as
extrapolated or apparent yield stress, whereas yield stress measured directly,
usually under a near static condition, is termed static or true yield value.
42
3.4.1. Indirect Method
The
One of most common procedures is to extend the flow curve at low shear rates
to zero shear rate, and take the shear stress intercept as the yield stress value. The
technique is relatively straightforward only if the shear stress-shear rate data are
linear. With nonlinear flow curves, as shown in Fig. 3-5, the data may have to be
fitted to a polynomial equation followed by the extrapolation of the resulting curve fit
to zero shear rate. The yield stress value obtained obviously depends on the lowest
shear rate data available and used in the extrapolation. This shear rate dependence of
the extrapolated yield stress has been demonstrated by Barnes and Walters (1985)
with a well-known yield stress fluid, Carbopol (carboxylpolymethylene).
They
concluded that this fluid would have no detectable yield stress even if measurement
was made at very low shear rates of 10-5 s-1 or less. This finding should be viewed
with caution, however, since virtually all viscometric instruments suffer wall slip and
43
other defects which tend to be more pronounced at low shear rates especially with
yield stress fluids and particulate systems [Wildermuth and Williams, 1985; Magnin
and Piau, 1990]. Thus, it is imperative that some checking procedure should be
carried out to ascertain the reliability of the low shear rate data before extrapolation is
made.
1
2
1
2
44
data available. Several studies have shown that a given fluid can be described equally
well by more than one model and hence can have different yield stress values
[Keentok, 1982; Nguyen and Boger, 1983; Uhlherr, 1986].
Various techniques have been introduced for measuring the yield stress
directly and independently of shear stress-shear rate data. Although the general
principle of the yield stress as the stress limit between flow and non-flow conditions
is often used, the specific criterion employed for defining the yield stress seems to
vary among these techniques. Furthermore, each technique appears to have its own
limitations and sensitivity so that no single technique can be considered versatile or
accurate enough to cover the whole range of yield stress and fluid characteristics.
Usually, the direct methods are used for fluids having yield stresses of greater than
approximately 10 Pa [Nguyen and Boger, 1983]. Therefore, as mentioned earlier, the
direct method is not very convenient to use for the yield stress measurement of blood
since the yield stress of human blood is approximately 1 to 30 mPa [Picart et al.,
1998].
45
Fig. 3-5. Determination of yield stress by extrapolation [Nguyen and Boger, 1983].
46
3.5. Problems with Conventional Viscometers for Clinical Applications
Over the years, rotational viscometers have been the standard in clinical
studies investigating rheological properties of blood and other body fluids. Despite
their popularity, rotational viscometers have some drawbacks that limit their clinical
applicability in measuring whole blood viscosity. They include the need to calibrate a
torque-measuring sensor, handling of blood, surface tensions effects, and the range of
reliability.
The torque-measuring sensor can be a conventional spring or a more
sophisticated electronic transducer. In either case, the sensor requires a periodic
calibration because repeated use of the sensor can alter its spring constant. The
calibration procedure is often carried out at manufacturers laboratory because it
requires an extremely careful and elaborate protocol, requiring the viscometer unit to
be returned for service.
Another concern is the need to work with contaminated blood specimens.
After each measurement, the blood sample must be removed from the test section,
and the test section must be cleaned manually. Not only is this procedure timeconsuming, but also it poses a potential risk for contact with contaminated blood.
Surface tension effects arise in the use of the coaxial-cylinder viscometer
because surface tension is relatively high for blood and macromolecular solutions.
The contact area between the blood and an inner cylinder is not uniform along the
47
periphery. The bob (inner cylinder) is pulled in different directions and revealed in
fluctuating torque readings, introducing serious errors in viscosity measurement.
Another inherent difficulty in measuring whole blood viscosity using
rotational viscometers is the limited shear rate range. In the extremes of the reputed
range (whether high shear or low shear, depending on the instrument), the detected
torque values do not have sufficient accuracy. Usually, manufacturers recommend
discarding viscosity data if the torque is less than 10% of the maximum value of the
sensor. This restriction is a major concern. For example, in the case of Brookfield
rotational viscometer, the minimum shear rate is often limited at approximately 30-50
s-1 due to the 10% restriction.
There are other clinical, practical considerations in using the rotational
viscometer. For example, it is usually necessary to treat the blood sample with a
measurable amount of anticoagulant, such as ethylenediaminetetraacetic acid (EDTA)
or heparin, to prevent coagulation during viscosity measurements. The reason for this
is that the contact area among blood, rotational viscometer component, and air is
relatively large for the size of the blood sample, and it usually takes a relatively long
time to complete viscosity measurements over a range of shear rates. Treating blood
with such anticoagulants results in an altered sample, and subsequent viscosity
measurements do not reflect the intrinsic values of unadulterated blood.
48
3.5.2. Problems with Capillary-Tube Viscometers
After the
measurement at one shear rate, the pressure at the reservoir tank must be readjusted to
either increase or decrease shear rate. Then, the next shear rate case resumes. Thus,
anticoagulants must be added to whole blood for the viscosity measurement over a
range of shear rates.
49
CHAPTER 4. THEORY OF SCANNING CAPILLARY-TUBE RHEOMETER
50
the density of the falling object has to be changed in order to vary shear rate as
mentioned in Chapter 3. Such operations can make viscosity measurements time
consuming and labor intensive. Because of the time required to measure viscosity
over a range of shear rates, it is necessary to add anticoagulants to blood to prevent
clotting during viscosity measurements with these conventional viscometers. The
present study introduces an innovative concept of a new capillary tube rheometer that
is capable of measuring yield stress and viscosity of whole blood continuously over a
wide range of shear rates without adding any anticoagulants.
Figure 4-1 shows a schematic diagram of a U-shaped tube set, which consists
of two riser tubes, a capillary tube, and a stopcock. The inside diameter of the riser
tubes in the present study is 3.2 mm. The inside diameter and length of the capillarytube are 0.797 and 100 mm, respectively. The small diameter of the capillary tube,
compared with that of the riser tubes, was chosen to ensure that the pressure drops at
the riser tubes and connecting fittings were negligibly small compared to the pressure
drop at the capillary tube [Kim et al., 2000a, 2000b, and 2002].
Furthermore, the inside diameter of the capillary tube was chosen to minimize
the wall effect which is often known as Fahraeus-Lindqvist effect [Fahraeus and
Lingqvist, 1931]. The details of the wall effect will be discussed in Chapter 5. In the
present study, the wall effect was found to be negligibly small.
51
The length of the capillary tube (i.e., Lc = 100 mm) in the U-shaped tube set
was selected to ensure that the end effects would be negligible [Kim et al., 2000a,
2000b, and 2002]. The end effects at the capillary tube will be also reported in
Chapter 5. In addition, the capillary-tube dimensions in the SCTR were selected to
complete one measurement within 2-3 min, a condition that is desirable when
measuring the viscosity of unadulterated whole blood in a clinical environment.
Figure 4-2 shows sketches of the fluid levels in the U-shaped tube set as time
goes on. The fluid level in the right-side riser tube decreases whereas that in the leftside riser tube increases. As time goes to infinity, the two fluid levels never become
equal due to the surface tension and yield stress effects as shown in Fig. 4-2(c) (i.e.,
ht = > 0). While a test fluid travels through the capillary tube between riser tubes 1
and 2, the pressure drop caused by the friction at the capillary tube can be obtained by
measuring the fluid levels at riser tubes 1 and 2. In Fig. 4-3, a typical fluid-level
variation measured by the SCTR is shown. Points (a), (b), and (c) represent the three
moments indicated in Fig. 4-2 (i.e., at t = 0 , t > 0, and t = , respectively).
Figure 4-4 shows the liquid-solid interface condition for each fluid column of
a U-shaped tube. A falling column (right side) always has a fully wet surface
condition, while a rising column (left side) has an almost perfectly dry surface
condition at the liquid-solid interface during the entire test. Therefore, the surface
52
tension at the right side was consistently greater than that at the left side since the
surface tension of a liquid is strongly dependent on the wetting condition of the tube
at the liquid-solid interface [Jacobs, 1966; Mardles, 1969; Kim et al., 2002]. The
height difference caused by the surface tension at the two riser tubes was one order of
magnitude greater than the experimental resolution desired for accurate viscosity
measurements. Thus, it is extremely important to take into account the effect of the
surface tension on the viscosity measurement using the disposable tube set.
The mathematical model of the flow analysis began with the equation of the
conservation of energy in the form of pressure unit, where the surface-tension effect
was considered between the two top points of the fluid columns at the riser tubes (see
Fig. 4-4). Assuming that the surface tension for the liquid-solid interface at each riser
tube remains constant during the test, one may write the governing equations as [Bird
et al., 1987; Munson et al., 1998]:
P1 +
s 2 V
1
1
V12 + gh1 = P2 + V22 + gh2 + Pc + ght = +
ds ,
s
1
2
2
t
where
P1 and P2 = static pressures at two top points
= density of fluid
g = gravitational acceleration
V1 and V2 = flow velocities at two riser tubes
h1 and h2 = fluid levels at two riser tubes
(4-1)
53
V = flow velocity
t = time
s = distance measured along streamline from some arbitrary initial point.
In Eq. (4-1), the energy emitted from LEDs was ignored since the energy transferred
from the LEDs, which can affect the temperature of a test fluid, was negligible small.
In order to ensure that the amount of the heat emitted from the LEDs is very small,
the temperature of bovine blood was measured during a room-temperature test. The
results showed no changes in temperature during the test, indicating that the energy
emitted from LEDs might be negligibly small.
For the convenience of data-reduction procedure, the unsteady term in Eq. (41),
s2
s1
V
ds , may be ignored under the assumption of a quasi-steady state. In order
t
to make the assumption, one should make sure that the pressure drop due to the
unsteady effect is very small compared with that due to the friction estimated from
the steady Poiseuille flow in a capillary tube.
The unsteady term can be broken into three integrations that represent the
pressure drops due to the unsteady flow along the streamlines at riser tube 1, capillary
tube, and riser tube 2 as [Munson et al., 1998]:
s2
s1
V
ds =
t
s1
s1
s 2 dV
s2 dV
dVr
c
r
ds +
ds +
ds ,
s
s
1
2
dt
dt
dt
(4-2)
where Vr and Vc are mean flow velocities at riser and capillary tubes, respectively.
Since the term of
V
is independent of streamlines, one can simplify the equation as:
t
54
s2
s1
V
ds =
t
dV r
dV
dV
dV
dV
l1 + c Lc + r l 2 = Lc c + (l1 + l 2 ) r ,
dt
dt
dt
dt
dt
(4-3)
where l 1 and l 2 are lengths of the liquid columns whereas Lc is the length of the
capillary tube as shown in Fig. 4-5. Using the mass conservation, Rc2 Vc = Rr2 Vr ,
the pressure drop due to the unsteady effect can be reduced as:
Punsteady =
s2
s1
R
V
ds = Lc r
t
Rc
2
dV
+ l1 + l 2 r ,
dt
(4-4)
where
dVr
dh1 (t )
dh2 (t )
and
. In order to calculate the term of
from the
dt
dt
dt
experimental values, one could use the following central differential method:
(4-5)
For the comparison of Punsteady with Pc , Punsteady was estimated through a curvefitting process. In order to obtain a smooth curve from raw data, the following
exponential equation was used.
2
dV
Error = r a e bt .
dt
(4-6)
55
Two constants, a and b , were obtained through a curve-fitting process, a leastsquare method, which minimized the sum of error for all experimental data points
obtained in each test.
Typical results showed that the magnitude of the pressure drop due to the
unsteady flow, Punsteady , was always less than 1% of that of pressure drop at capillary
tube, Pc , over the entire shear-rate range. This confirms that the assumption of a
quasi-steady state could be used for the present data procedure. The details of
experimental results will be discussed in Chapter 5.
Assuming a quasi-steady flow behavior, one may rewrite Eq. (4-1) as follows
[Bird et al., 1987; Munson et al., 1998]:
P1 +
1
1
V12 + gh1 (t ) = P2 + V22 + gh2 (t ) + Pc (t ) + ght = .
2
2
(4-7)
Pc (t ) = g [h1 (t ) h2 (t ) ht = ] .
(4-8)
Note that h at t = contains a height difference due to the surface tension, hst ,
and an additional height difference due to the yield stress, h y , for the case of blood
(i.e., see Fig. 4-3).
56
Open to air
3.2 mm
Riser tubes
Capillary tube
0.797 mm
100 mm
Stopcock
57
Riser tube 2
Riser tube 1
(a) at t = 0
(b) at t > 0
ht =
(c) at t =
58
Height
h1 (t )
ht =
h2 (t )
(a)
(b)
Time
(c)
59
Wet surface
condition
l1
Dry surface
condition
l2
2'
Lc
1'
Fig. 4-4. Liquid-solid interface conditions for fluid columns of a U-shaped tube set.
60
Casson and
It is well known that power-law model does not have the capability to handle
yield stress. As provided in Chapter 2, the relation among shear stress, shear rate, and
viscosity in power-law fluids may be written as follows:
61
= m& n ,
(4-9)
= m& n 1 .
(4-10)
Since n < 1 for pseudo-plastics, the viscosity function decreases as the shear rate
increases. This type of behavior is characteristic of high polymers, polymer solutions,
and many suspensions including whole blood.
We consider the fluid element in the capillary tube at time t as is shown in
Fig. 4-5. The Hagen-Poiseuille flow may be used to derive the following relationship
for the pressure drop at the capillary tube as a function of capillary tube geometry,
fluid viscosity, and flow rate [Fung, 1990; Munson et al., 1998]:
2 Lc
2 Lc & w 8Lc Q 8Lc Rr2 dh
2l
,
w =
Pc = =
=
=
r
Rc
Rc
dt
Rc4
Rc4
(4-11)
where
r = radial distance
l = length of fluid element
& w =
4Q
= wall shear rate
Rc3
dh1
dh
dh
= Rr2 2 = Rr2
= volumetric flow rate.
dt
dt
dt
The above relationship is valid for Newtonian fluids whose viscosities are
independent of shear rate. For non-Newtonian fluids, the viscosities vary with shear
62
rate. However, the Hagen-Poiseuille flow within the capillary tube still holds for a
quasi-steady laminar flow. When applying a non-Newtonian power-law model to
whole blood, the pressure drop at the capillary tube can be described as follows
[Middleman, 1968; Bird et al., 1987; Fung, 1990]:
2 w Lc& w 2mLc & wn 2mLc
Pc =
=
=
Rc
Rc
Rc
3n + 1 Q
3
n Rc
,
=
2mLc
Rc
3n + 1 Rr2 dh
3
n Rc dt
(4-12)
where
& w =
It is of note that if n = 1 , Eq. (4-12) yields to Eq.(4-11). Applying Eqs. (4-8), (4-11),
and (4-12), one can rewrite the energy conservation equation as follows:
g {h1 (t ) h2 (t ) ht = } =
8Lc Rr2 dh
for Newtonian fluids,
dt
Rc4
2mLc
g {h1 (t ) h2 (t ) ht = } =
Rc
3n + 1 Rr2 dh
3
n Rc dt
(4-13)
(4-14)
(4-15)
63
1
n
(4-16)
where
dh
d dh1 dh2
=
= 2 2
dt
dt
dt
dt
gRc4
4 Lc Rr2
1
gRc n
2mLc
=
.
2
3n + 1 Rr
3
n 2 Rc
The above equations are the first-order linear differential equations. Since and
are constants, these equations can be integrated as follows:
(t ) = (0) e t
(4-17)
n 1
n 1 n 1
(t ) = (0) n
t
n
(4-18)
index, m . A least-square method was used for the curve fitting. The data reduction
procedure adopted is as follows:
1. Conduct a test and acquire all data, h1 (t ) and h2 (t ) .
2. Guess values for m , n , and ht = .
3. Calculate the following error values for all data points:
64
(4-19)
& w =
Rc
gRc
Pc =
(t )
2 Lc
2 Lc
1
(4-20)
R
n gRc
n
& w = c Pc =
(t )
2mLc
2mLc
(4-21)
When n becomes 1 ( 0.001), is equal to m , whereas when 0< n <1, the viscosity
is calculated from Eq. (4-10).
In order to obtain the velocity profile at the capillary tube, which changes with
time, using a power-law model, Eq. (4-21) can be used to derive it. Since & =
dV
,
dr
r
n
dV (t , r )
=
Pc (t ) ,
dr
2mLc
1
P (t ) n
P (t ) n
V (t , r ) = c r n dr = c
2mLc
2mLc
r
n + 1
n +1
n
+C ,
(4-22)
65
1
P (t ) n n nn+1
C = c
Rc .
2mLc n + 1
(4-23)
Finally, the velocity profile within the capillary tube can be expressed as follows:
1
n Pc (t ) n
Vc (t , r ) =
n + 1 2mLc
n +1
nn+1
Rc r n
(4-24)
n h1 (t ) h2 (t ) ht =
=
2mLc
n + 1
1
n
n +1
nn+1
Rc r n
(4-25)
In order to determine the mean flow velocity at the riser tube, one has to find
the flow rate at the capillary tube first. The flow rate can be obtained by integrating
the velocity profile over the cross-sectional area of the capillary tube as follows:
Q(t ) = 2
Rc
0
Vc (t , r )rdr
1
3 n +1
n Pc (t ) n n
R
=
c
3n + 1 2mLc
(4-26)
1
n
3 n +1
n g [h1 (t ) h2 (t ) ht = ]
n
=
Rc
2mLc
3n + 1
Since Q(t ) = Rr2Vr (t ) , the mean flow velocity at the riser tube can be determined by
the following equation:
66
1
3 n +1
n Pc (t ) n Rc n
Vr (t ) =
2
3n + 1 2mLc Rr
(4-27)
1
3 n +1
n
c
2
r
n g [h1 (t ) h2 (t ) ht = ] n R
=
R
2mLc
3n + 1
The Casson model can handle both yield stress and shear-thinning
characteristics of blood, and can be described as follows [Barbee and Cokelet, 1971;
Benis et al., 1971; Reinhart et al., 1990]:
= y + k &
when y ,
when y ,
& = 0
(4-28)
(4-29)
where
w =
y =
Pc (t ) Rc
,
2 Lc
Pc (t ) ry (t )
2 Lc
(4-30)
(4-31)
67
where ry is a radial location below which the velocity profile is uniform as shown in
Fig. 4-6, i.e., plug flow, due to the yield stress. Now, for the Casson model, Eq. (4-8)
becomes Pc (t ) = g [h1 (t ) h2 (t ) hst ] , indicating that the effect of the surface
tension is isolated from the pressure drop across the capillary tube. Using Eqs. (4-28)
and (4-29), one can obtain the expressions of shear rate and velocity profile at the
capillary tube as follows:
Pc (t ) ry (t )
dV
1 Pc (t ) r
,
& = c =
dr
k
2 Lc
2 Lc
Vc (t , r ) =
(4-32)
3
3
1 Pc (t ) 2
8 12
2
2
2
R
r
r
(
t
)(
R
r
) + 2ry (t )( Rc r )
c
y
c
4k
3
Lc
for ry (t ) r Rc , (4-33)
Vc (t ) =
1 Pc (t )
1
( Rc ry (t ) ) 3 ( Rc +
ry (t ) )
4k
3
Lc
for ry (t ) r .
(4-34)
For the purpose of simplicity, one may define two new parameters,
C (r ) =
ry (t )
r
, so that Eqs. (4-33) and (4-34) become as follows:
and C y (t ) =
Rc
Rc
1 Pc (t ) 2 r
Rc 1
Vc (t , r ) =
4k
R
Lc
c
1
2
8 ry 2 r
1
3 Rc R c
r
2
+ 2 y
Rc
r
1
Rc
1
3
Rc2 Pc (t )
8 2
2
=
1 C (r ) C y (t )1 C 2 (r ) + 2C y (t )(1 C (r ) )
4kLc
3
for ry (t ) r Rc , (4-35)
68
Pc (t )
Vc (t ) =
Rc
4kLc
( )
r
1 y
Rc
1 ry
Rc 1 +
3
R
c
for ry (t ) r ,
(4-36)
3
Rc2 Pc (t )
1
1 C y (t ) 1 +
C y (t )
4kLc
3
where C y (t ) =
ry (t )
Rc
y
w (t )
P ()
.
P(t )
In order to determine the mean flow velocity at the riser tube, one has to find
the flow rate at the capillary tube first. The flow rate can be obtained by integrating
the velocity profile over the cross-sectional area of the capillary tube as follows:
Rc
Q(t ) = 2 Vc r dr
0
Rc4 Pc (t )
8k
[(
Lc
16 2 y 12 Pc (t ) 1 2
(
) (
)
Rc
Lc
7
4 2 y
1 2 y 4 Pc (t ) 3
(
) (
) (
) ]
Lc
3 Rc
21 Rc
(4-37)
1 y 4
16 y 12 4 y
1 ( ) + ( ) ( )
21 w
3 w
7 w
Rc4 Pc
8kLc
Rc4 Pc
8kLc
16 12 4
1
4
Cy + Cy Cy
7
3
21
Since Q(t ) = Rr2Vr (t ) , the mean flow velocity at the riser tube can be determined by
the following equation:
69
Vr (t ) =
Rc4 Pc (t ) 16 2 y 1 2 Pc (t ) 1 2
[(
) (
) (
)
7
Lc
Rc
Lc
8kRr2
+
4 2 y
1 2 y 4 Pc (t ) 3
) (
(
) (
) ]
3 Rc
21 Rc
Lc
(4-38)
Rc4 Pc
16 1
4
1
[1 C y 2 + C y C y4 ]
2
7
3
21
8kRr Lc
1
Rc4 g
16
[(h1 (t ) h2 (t ) hst ) (h y (h1 (t ) h2 (t ) hst )) 2
2
7
8kRr Lc
4
1
+ h y h y4 (h1 (t ) h2 (t ) hst ) 3 ]
3
21
where C y (t ) =
h y
P ()
=
.
P(t ) h1 (t ) h2 (t ) hst
(4-39)
70
dh1 (t )
dh (t )
must be equal to 2 . Therefore, it was more
dt
dt
convenient and accurate to use the difference between the velocities at the two riser
tubes, i.e.,
d (h1 (t ) h2 (t ))
dh (t )
dh (t )
, than to use 1
and 2
directly. In order to get
dt
dt
dt
the difference between the two velocities from the experimental values, one could use
the central differential method as follows:
d (h1 (t ) h2 (t ) ) [h1 (t + t ) h2 (t + t )] [h1 (t t ) h2 (t t )]
=
.
dt
2 t
(4-40)
Using Eq. (4-39), the derivative of the velocity difference can be determined
theoretically as follows:
d (h1 (t ) h2 (t ) )
= 2Vr (t )
dt
=
1
Rc4 g
16
[(h1 (t ) h2 (t ) hst ) (h y (h1 (t ) h2 (t ) hst )) 2
2
7
4kRr Lc
4
1
h y h y4 (h1 (t ) h2 (t ) hst ) 3 ]
3
21
(4-41)
71
fluids and Newtonian fluids regardless of the existence of the yield stress. The data
reduction procedure adopted is as follows:
1. Conduct a test and acquire all data, h1 (t ) and h2 (t ) .
2. Guess values for the unknowns, k , hst , and h y .
3. Calculate the following error values for all data points.
(4-42)
& w (t ) =
w (t ) =
gRc
2kLc
h1 (t ) h2 (t ) hst h y
(4-43)
(4-44)
Note that when h y becomes approximately zero (i.e., resolution of 8.3 10 5 ), the
non-Newtonian viscosity, , is reduced to k , a Newtonian viscosity. Furthermore,
the relation between wall viscosity and shear-rate can be obtained from Eqs. (4-43)
and (4-44) as follow:
w (t ) = k +
y
& w (t )
4k y
& w (t )
(4-45)
gRc h y
2 Lc
=k+
& w (t )
2kgRc h y
Lc
& w (t )
where k and h y are the fluid properties to be determined using the Casson model.
72
Yield stress could be also determined through the curve-fitting method from
the experimental data of h1 (t ) and h2 (t ) by using the Casson model. Since the
pressure drop across the capillary tube, Pc (t ) , could be determined using Eq. (4-8),
Pc () represents the effect of the yield stress on the pressure drop. The relationship
between the yield stress, y , and Pc () can be written by the following equation:
y =
Pc () Rc gh y Rc
.
=
2 Lc
2 Lc
(4-46)
Therefore, once h y is obtained using a curve-fitting method, the yield stress can be
automatically determined.
For a Herschel-Bulkley (H-B) model, the shear stress at the capillary tube can
be described as follows [Tanner, 1985; Ferguson and Kemblowski, 1991; Macosko,
1994]:
= m& n + y
& = 0
when y ,
when y ,
where
(4-47)
(4-48)
73
Since the H-B model reduces to the power-law model when a fluid does not have a
yield stress, the H-B model is more general than the power-law model.
For the H-B model, wall shear stress and yield stress can also be defined as
follows:
w =
y =
Pc (t ) Rc
,
2 Lc
Pc (t ) ry (t )
2 Lc
(4-49)
Pc () Rc gh y Rc
,
=
2 Lc
2 Lc
(4-50)
where ry is a radial location below which the velocity profile is uniform due to the
yield stress (see Fig. 4-7). Using Eqs. (4-47)-(4-50), one can obtain the expressions
of shear-rate outside of the core region as:
Pc
dV
& = c =
dr 2mLc
1
n
(r ry ) n
for ry (t ) r Rc .
(4-51)
The velocity profile outside of core region can be obtained by integrating Eq. (4-51)
as:
1
n +1
n +1
n Pc (t ) n
n
n
(
)
(
)
Vc (t , r ) =
R
r
(
t
)
r
r
(
t
)
c
y
y
n + 1 2mLc
for ry (t ) r Rc .
(4-52)
Since the velocity profile inside of the core region is a function of time, t , only, the
profile can be obtained using a boundary condition, Vc (t , r ) = Vc (t ) at r = ry .
1
n +1
n Pc (t ) n
n
(
)
Vc (t ) =
R
r
(
t
)
c
y
+
n
1
2
mL
for ry (t ) r .
(4-53)
74
Again, for the purpose of simplicity, one may define two new parameters, C (r ) =
and C y (t ) =
ry (t )
Rc
r
Rc
1
n +1
n +1
n +1
n Rc Pc (t ) n ry (t ) n r ry (t ) n
Vc (t , r ) =
Rc
Rc
n + 1 2mLc
Rc
n +1
n +1
n +1
n Rc Pc (t ) n
n
n
(
)
(
)
1
C
(
t
)
C
(
r
)
C
(
t
)
=
y
y
n + 1 2mLc
for ry (t ) r Rc , (4-54)
1
n +1
n Rc Pc (t ) n
Vc (t ) =
n + 1 2mLc
ry (t )
1
Rc
n +1
n
for ry (t ) r .
(4-55)
1
n
n +1
n +1
n Rc Pc (t )
(1 C y (t ) ) n
=
n + 1 2mLc
In order to determine the mean flow velocity at the riser tube, one has to find
the flow rate at the capillary tube first. The flow rate can be obtained by integrating
the velocity profile over the cross-sectional area of the capillary tube as follows:
Rc
Q(t ) = 2 Vc r dr
0
Pc
=
2mLc
2 n +1
n +1
n n 2
n
n
(
)
(
)
(
)
[
r
R
r
+
R
+
r
r
y c y
c
y
c
y
n + 1
n
2
ry (Rc ry )
2n + 1
2 n +1
n
n
2
(Rc ry )
3n + 1
3 n +1
n
]
(4-56)
75
Pc
=
2mLc
2R
= R
3 n +1
n
c
3 n +1
ry
n n
[ Rc n
n + 1
Rc
3 n +1
n
c
n ry
2n + 1 Rc
n Pc
n + 1 2mLc
ry (t )
Rc
1 y
Rc
1 y
Rc
2 n +1
n
n +1
n
2R
+R
3 n +1
n
c
3 n +1
n
c
r
r
1 + y 1 y
Rc R c
ry
n
1
3n + 1 Rc
3 n +1
n
2 n +1
n
2 n +1
n +1
n 2
n
[C y (1 C y ) + (1 + C y ) (1 C y ) n
n
2
C y (1 C y )
2n + 1
where C y (t ) =
2 n +1
n
y
w (t )
3 n +1
n
n
2
(1 C y )
3n + 1
h y
P ()
=
.
P (t ) h1 (t ) h2 (t ) hst
Since Q(t ) = Rr2Vr (t ) , the mean flow velocity at the riser tube can be
determined by the following equation:
3 n +1
R n n Pc
Vr (t ) = c 2
Rr n + 1 2mLc
n +1
2 n +1
n 2
[C y (1 C y ) n + (1 + C y ) (1 C y ) n
n
2
C y (1 C y )
2n + 1
2 n +1
n
(4-57)
3 n +1
n
n
2
(1 C y )
3n + 1
Equation (4-57) can be rewritten to clearly display the unknowns and the observed
variables as follows:
76
3 n +1
R n n g [h1 (t ) h2 (t ) hst ] n
Vr (t ) = c 2
2mLc
Rr n + 1
h y
[
h1 (t ) h2 (t ) hst
h y
h y
1
h1 (t ) h2 (t ) hst
+ 1 +
h1 (t ) h2 (t ) hst
h y
n +1
n
1
h1 (t ) h2 (t ) hst
h y
n
2
2n + 1 h1 (t ) h2 (t ) hst
2 n +1
n
h y
1
h1 (t ) h2 (t ) hst
h y
n
2
1
3n + 1 h1 (t ) h2 (t ) hst
3 n +1
n
(4-58)
2 n +1
n
Note that Eq. (4-58) contains two independent variables, i.e., h1 (t ) and h2 (t ) , and
one dependent variable, i.e., Vr (t ) .
determined through the curve fitting in Eq. (4-58), namely m , n , hst , and h y .
Once the equation for the mean flow velocity, Vr (t ) , was derived, one could
determined the unknown parameters using the experimental values of h1 (t ) and h2 (t )
by using the same curve-fitting method of determining unknowns as in the case of the
Casson model. In the case of the H-B model, there were four unknown values, which
were m , n , hst , and h y . Note that the unknown values were assumed to be
constant for the curve-fitting method.
Using Eq. (4-58), the derivative of the velocity difference can be determined
theoretically as follows:
77
d (h1 (t ) h2 (t ) )
= 2Vr (t )
dt
3 n +1
2 Rc n n g [h1 (t ) h2 (t ) hst ] n
2mLc
Rr2 n + 1
h y
[
h1 (t ) h2 (t ) hst
h y
1
h1 (t ) h2 (t ) hst
h y
+ 1 +
h1 (t ) h2 (t ) hst
n +1
n
h y
1
h1 (t ) h2 (t ) hst
h y
n
2
2n + 1 h1 (t ) h2 (t ) hst
2 n +1
n
h y
1
h1 (t ) h2 (t ) hst
h y
n
2
1
3n + 1 h1 (t ) h2 (t ) hst
3 n +1
n
2 n +1
n
]
(4-59)
where Vr (t ) is the mean flow velocity at the riser tube. In order to execute the curvefitting procedure, one needs to have a mathematical equation of Vr for the H-B model.
Eq. (4-58) and (4-59) were used for the curve fitting of the experimental data to
determine the unknown constants, i.e., n , m , hst , and h y . Note that Eq. (4-59)
could be applicable for H-B fluids, Shear-thinning fluids, and Newtonian fluids
regardless of the existence of the yield stress.
After iterations for the determination of the unknowns that minimize the sum
of the error, wall shear rate and viscosity for all data points can be calculated as
follows:
gRc
& w (t ) =
2mLc
n
(h1 (t ) h2 (t ) hst ) h y
1
n
(4-60)
78
w (t ) =
(4-61)
Note that when h y becomes approximately zero (i.e., resolution of 8.3 10 5 ), the
H-B model is reduced to power-law model. In addition, when n becomes 1, the
mathematical form of the H-B model yields to Bingham plastic [Tanner, 1985], which
can be described as follows:
= m B & + y
& = 0
when y ,
(4-62)
when y ,
(4-63)
where
Similar to the Casson model, the relationship between wall viscosity and
shear-rate using the H-B can be expressed as follows:
w (t ) = m& w (t ) n 1 +
y
& w (t )
(4-64)
gRc h y
2 Lc
n 1
= m& w (t ) +
& w (t )
where m , n , and h y are the fluid properties to be determined using the H-B model.
79
Capillary tube
Rc
l
(a) Motion of a cylindrical fluid element within a capillary tube.
2rl
Pr 2
Flow direction
( P P)r 2
80
Capillary tube
ry
Rc
81
CHAPTER 5. CONSIDERATIONS FOR EXPERIMENTAL STUDY
82
5.1. Unsteady Effect
assumption of a quasi-steady state could be used for the present data reduction
procedure.
(a)
83
Punsteady
3
2
1
0
0
10
20
30
(b)
Time (s)
400
Pc
300
200
100
0
0
10
20
30
Time (s)
Fig. 5-1. Pressure drop estimation for distilled water. (a) Pressure drop due to an
unsteady flow in a test with distilled water. (b) Pressure drop at a capillary
tube in a test with distilled water.
84
Punsteady
Time (s)
Punsteady (Pa)
Pc (Pa)
0.5
2.89
245.46
1.18
2.61
222.08
1.18
1.56
132.60
1.18
0.93
79.40
1.17
10
0.26
22.98
1.13
15
0.07
6.85
1.02
20
0.02
2.02
0.99
Pc
100 (%)
(a)
85
0.8
Punsteady
0.4
0
0
30
60
90
120
150
(b)
Time (s)
800
Pc
600
400
200
0
0
30
60
90
120
150
Time (s)
Fig. 5-2. Pressure drop estimation for bovine blood. (a) Pressure drop due to an
unsteady flow in a test with bovine blood. (b) Pressure drop at a capillary
tube in a test with bovine blood.
86
Time (s)
Punsteady (Pa)
Pc (Pa)
0.5
0.54
705.21
0.08
0.52
688.11
0.08
0.39
535.93
0.07
10
0.28
399.14
0.07
30
0.067
139.24
0.05
60
0.008
42.63
0.02
120
15.27
Pc
100 (%)
87
5.2. End Effect
Figure 5-3 shows the flow-pattern changes due to end effects at both (a)
entrance and (b) exit of a capillary tube. Due to the sudden contraction and expansion,
additional pressure drops can occur at the both ends. The most common method used
to estimate these minor pressure drops is to use the loss coefficient, K L , which is
defined as [Munson et al., 1998]:
KL =
PEnd
1
Vc 2
2
(5-1)
so that
PEnd = K L
1
Vc 2
2
(5-2)
where PEnd is the pressure drop due to the end effects and Vc is the mean velocity at
the capillary tube.
With the present experimental set-up, the velocity in the capillary tube was
approximately 16 times greater than that in the riser tube. Therefore, the energy loss
by secondary flow patterns or eddies in the entrance and exit of the capillary tube
may appear to be significant in a high shear zone. In the case of a laminar flow, the
loss coefficient was reported to be approximately 2.24 [Ferguson and Kemblowski,
1991]. Using the value of the loss coefficient, the pressure loss due to the sudden
changes in geometry, PEnd , became only 1.79 Pa (for distilled water) and 1.88 Pa
(for bovine blood) for the maximum shear rate of 400 s-1 at a corresponding velocity
of 0.04 m/s. In contrast, the pressure drops across the capillary tube at the maximum
88
shear rate were 245 Pa (for distilled water) and 705 Pa (for bovine blood), indicating
that the loss due to the secondary flow patterns or eddies at both entrance and exit
could be neglected.
In these end regions (see Fig. 5-3), the flow is changing from (or to) its
previous (or future) distribution outside the capillary tube. The length of an end
region is generally a function of tube geometry and some dynamic parameters. The
entrance length, the length of tube required to achieve the fully developed simple
shear flow, can be estimated by using the following equation [Middleman, 1968]:
Le
0.035 Re
D
(5-3)
where Le is the entrance region, D ( 0.8 mm) is the inner diameter of a capillary
tube, and Re is the Reynolds number. The maximum Reynolds number from a
typical run in the present study was approximately 28.6. The entrance length in the
capillary tube used for the present study was estimated to be 0.0008 m using the
above equation. Generally, the ratio of the entrance length to the capillary-tube
length,
Le
, should be the order of 0.01 in order to assume the effect of entrance
Lc
length to be negligible [Middleman, 1968]. Since the ratio was 0.008 in the present
study, it is reasonable to assume that the entrance length effect is negligibly small.
89
Fig. 5-3. Flow-pattern changes due to end effects [Munson et al., 1998].
90
5.3. Wall Effect (Fahraeus-Lindqvist Effect)
91
apparent viscosity of blood decreases to a value close to plasma viscosity if the
diameter of the capillary tube decreases below 0.1 mm [Benis et al., 1970].
In order to check whether or not the present capillary tube diameter (with
0.797 mm ID) was large enough to prevent the wall effect, two additional capillary
tubes, whose diameters were 1.0 mm (with length = 130 mm) and 1.2 mm (with
length = 156 mm), were used for the viscosity measurements of bovine blood with
7.5% EDTA at a room temperature of 25. As shown in Fig. 5-6, the experiments
performed with three different capillary tubes with ID of 0.797 mm (the standard size
of the SCTR), 1.0 mm, and 1.2 mm provided almost identical viscosity results,
confirming that the wall effect was negligibly small for the present capillary tube with
ID equal to 0.797 mm.
92
Arterial wall
Flow
RBCs
Cell-free region
Fig. 5-4. Migration of cells toward to the center of lumen (wall effect).
93
1
10
100
400
800
94
Viscosity (cP)
100
0.797 mm
1.0 mm
1.2 mm
10
1
1
10
100
-1
Shear rate (s )
1000
Fig. 5-6. Viscosity measurements for bovine blood with three different capillary tubes
with ID of 0.797 mm (with length = 100 mm), 1.0 mm (with length = 130 mm), and
1.2 mm (with length = 156 mm).
95
5.4. Other Effects
Since the small diameter of a capillary tube was selected to make sure that the
pressure drop at the capillary tube could be dominant, the pressure drops at riser tubes
should be negligibly small. It has been suggested that the pressure drop in the
reservoir should be estimated by using a power-law model as [Marshall and Riley,
1962; Metzger and Knox, 1965; Macosko, 1994]:
Pr =
Pc Lr
R
Lc ( r )
Rc
(5-4)
n +3
n
where
Pr = pressure drop in reservoir
generally provides almost identical viscosity results with both Casson and HerschelBulkley models at the shear rates between approximately 300 and 30 s-1.
The
viscosity results of blood obtained with those models will be discussed in Chapter 6
in detail. Typically, the power-law index, n , for healthy human blood is 0.75-0.85 at
a body temperature of 37.
96
Considering the reservoir in Eq. (5-4) as the riser tubes in the present system
and n = 0.8 for human blood, one can obtain the following relation between pressure
drops at capillary and riser tubes using Eq. (5-4).
Pr
1
Pc
500
(5-5)
Therefore, in the case of human blood, the sum of the pressure drops at riser tubes is
approximately 0.2 Pa at a shear rate of 30 s-1 while the pressure drop at the capillary
tube is approximately 93 Pa.
It could be argued that Casson or Herschel-Bulkley model would have a larger
pressure drop than the power-law model at a lower shear rate. Therefore, we want to
examine whether or not the pressure drop at the riser tube is still negligibly small for
Casson or Herschel-Bulkley model compared to that at the capillary tube at a very
low shear rate by looking at the upper bound of the error. It is rather obvious that the
pressure drop at the riser tube at a low shear rate (i.e., below 30 s-1) should be smaller
than 0.2 Pa. Lets consider a shear rate of 1 s-1. The pressure drop at the capillary
tube at & = 1 s-1 is approximately 15 Pa. Therefore, the pressure drop at the riser tube
is less than 1.33% (i.e.,
0.2
= 0.0133 ). Hence, it is reasonable to assume that the
15
pressure drops at the riser tubes can be ignored compared to the pressure drop at the
capillary tube.
97
In order to measure the viscosity of blood by using the SCTR, one needs to
know the density of blood. However, in the case of human blood, it is not very
convenient to measure the density of blood for each viscosity measurement.
Therefore, the following relation [Chien et al., 1987] between hematocrit (Hct as a
dimensionless fraction) and blood density ( in kg/m3) was used for the estimation
of the density of human blood.
= 1026 + 67 Hct
(5-6)
98
It is reasonable to assume that the 60-second period is long enough to cause
aggregations if the aggregations were going to take place. To further validate the
above assumption, a longer capillary tube (125-mm length) was used. Since the test
duration increased in the longer capillary tube, an anticoagulant (7.5% EDTA) was
added to avoid the blood clotting. As shown in Fig. 5-7, the viscosity results obtained
by using the longer capillary tube showed excellent agreements with those obtained
by using the capillary tube with 100-mm length (also with 7.5% EDTA). Therefore,
it is concluded that, in the present system, the thixotropic effect of blood on the
viscosity measurement is negligibly small.
99
Density
(kg/m3)
35
1049.5
40
1052.8
45
1056.2
50
1059.5
100
100
Viscosity (cP)
100 mm
125 mm
10
1
1
10
100
1000
-1
Shear rate (s )
Fig. 5-7. Viscosity results for human blood with two different capillary tubes with
length of 100 mm (with ID = 0.797 mm) and 125 mm (ID = 0.797 mm).
101
102
Capillary Surface
Thermocouple
Exit
Thermocouple
Entrance
Thermocouple
Thermometer
Fig. 5-8. Schematic diagram of a U-shaped tube set for temperature measurement.
103
Temperature ()
40
38
36
Entrance
Exit
Capillary Surface
34
32
30
0
50
100
150
200
Time (s)
Fig. 5-9. Temperature measurement at a capillary tube during a viscosity test.
104
5.6.1. Introduction
t = 0, the fluid begins to fall from the riser tube with the high level to the riser tube of
low level by gravity. Since the flow rate depends on the pressure head between the
two fluid levels, the flow rate gradually decreases with time as the difference between
the two fluid level decreases with time. Since the flow rate can be estimated from the
time rate of change of the fluid level, one can estimate both flow rate and pressure
drop from the measurement of two fluid levels. Then, one can calculate shear rate
from the flow rate data and shear stress from the pressure drop data, respectively.
From the shear rate and shear stress, one can determine the viscosity of the liquid.
Thus, the most important experimental variable in the operation of the SCTR
is the measurement of two fluid levels in the riser tubes. As shown in Fig. 5-10, the
present SCTR uses an optical detector (i.e. CCD sensors and LED array) to measure
the fluid-level variations in the riser tubes. The optical detector works as follows: as
an opaque fluid level rises in the riser tube, the opaque fluid blocks the passage of the
light emitted by the LED. Accordingly, the number of the CCD sensors that receive
105
the light from the LED becomes smaller. Computer software records the changes in
the number of CCD sensors that receive the light from the LED. Since the number of
the CCD sensors that dont receive the light from the LED is directly proportional to
the fluid level, one can determine the fluid level. In other words, the instantaneous
fluid levels are recorded in the form of pixel numbers (i.e., CCD sensors) versus time
in a computer data file through an analog-to-digital dataacquisition system. The
fluid level data from the two riser tubes were analyzed to determine the viscosity of
the fluid.
Therefore, it is essential to have an opaque fluid for the present SCTR
operation so that the light from the LED can be blocked by the opaque fluid as the
fluid level increases, and vice versa. Of course, one can use a laser light so that a
transparent fluid can be used as demonstrated by Kim et. al. (2000b). However, the
cost of a SCTR using such a laser-based system became prohibitively expensive,
making such a system economically unattractive.
In order to use the SCTR using CCD-LED arrangements for the viscosity
measurement of a transparent fluid, one may add dye to the fluid in order to make the
fluid opaque. However, the addition of a dye to a transparent fluid may alter the
viscosity of the fluid. Furthermore, the addition of the dye may make a transparent
Newtonian fluid such as water a non-Newtonian fluid if the concentration of the dye
is sufficiently large [Kim and Cho, 2002].
Therefore, the objective of the study is to investigate the effect of dye
concentration on the viscosity of distilled water in the SCTR. More specifically, the
106
present study plans to determine the maximum concentration of dye below which the
viscosity of the dye-water solution is not altered.
Although distilled water is a Newtonian fluid, the aqueous solution of dyewater may exhibit the non-Newtonian characteristics for a sufficiently large dye
concentration. Thus, in order to investigate the viscosity characteristics of a dyewater solution, the present study used a non-Newtonian model to reduce experimental
data. In the previous chapters, various non-Newtonian models have been introduced
for the determination of blood viscosity with the SCTR, which include power-law
model, Casson model, and Herschel-Bulkley (H-B) model.
However, it is not very convenient to use the Casson model when a fluid
shows only shear-thinning characteristics without yield stress. The H-B model is
reduced to a power-law model for the case of fluids with no yield stress. Thus, in the
present study, a power-law model was used for the viscosity analysis of the dye-water
solution. The procedure of data reduction with power-law model will be discussed in
Chapter 6. Therefore, only the experimental results will be provided and discussed in
the next section.
107
108
on the viscosity of the dye-water solution was negligibly small when the amount of
dye used was less than 2% by volume.
Figure 5-12 shows the viscosity data for the dye-water solution with six
different dye concentrations.
concentrations (i.e., 3, 4, 7%) of dye, the results showed that the effect of dye
concentration on the viscosity of water was very small. However, at low shear-rates
such as 1 and 10 s-1, the viscosity of the dye-water solution dramatically increased
with increasing dye concentration.
In the present experiment, the maximum concentration of dye, under which
the viscosity of the dye-water solution did not change, was approximately 2% by
volume. Compared with the reference data for water at 25 [Munson et al., 1998],
the test results obtained with 0.5%, 1%, and 2% of dye concentrations gave less than
2% error in the entire shear-rate range.
109
LED array
CCD 1
Riser tube 1
Riser tube 2
CCD 2
Computer
system
for data
collection
Test fluid
Capillary tube
Three-way stopcock
1.04
1.8
1.6
1.4
0.96
1.2
0.92
0.88
0.8
0.84
0.6
0
2 3 4 5
6 7
Dye concentration (%)
Consistency index, k
(cPs n-1 )
Power-law index, n
110
Fig. 5-11. Variations of both power-law index and consistency index of dye-water
solution due to the effects of dye concentrations.
111
2.5
at 500 1/s
at 100 1/s
at 10 1/s
at 1 1/s
Viscosity (cP)
2
1.5
1
0.5
0
0
Fig. 5-12. Viscosity data for dye-water solution with 6 different dye concentrations
at 25.
112
CHAPTER 6. EXPERIMENTAL STUDY WITH SCTR
Chapter 6 presents the results of viscosity and yield stress measurements with
the scanning capillary-tube rheometer (SCTR). Experimental tests were performed
with mineral oil, distilled water, bovine blood with 7.5% EDTA, and unadulterated
human blood.
Section 6.1 provides the viscosity results of both mineral oil and human blood
produced with the SCTR (with precision glass riser tubes) using the power-law model
for data reduction.
Section 6.2 gives the test results of distilled water, bovine blood, and human
blood obtained with the SCTR (with plastic riser tubes). Casson and HerschelBulkley models were used for data reduction to handle the yield stress of blood.
Section 6.3 reports the effect of the three models on the viscosity and yieldstress measurements of blood with the SCTR as well as on the flow patterns of blood
such as velocity profile and wall shear stress in a capillary tube.
constitute the majority of the cellular content and account for almost one half of the
113
blood volume. The presence of such a high volume of red blood cells makes blood a
non-Newtonian fluid whose viscosity varies with shear rate. Whole blood viscosity
decreases
as
shear
rate
increases,
phenomenon
called
shear-thinning
114
used in the present tests were 3 mm. The inside diameter and length of the capillary
tube were 0.797 mm and 100 mm, respectively.
The essential feature in the scanning capillary-tube rheometer is the use of an
optical detector (i.e., CCD sensors and LED array) to measure the fluid level
variations in the riser tubes, h1 (t ) and h2 (t ) , every 0.02 s. The instantaneous fluid
Typical tests are conducted as follows: The system was turned on and
connected to a computer.
115
immediately transferred to the sample cup of the Brookfield rotating viscometer that
was maintained at a constant temperature of 37 by a water bath connected to the
cup.
The viscosity measurements with the rotating viscometer were completed
within approximately 1 minute from the time when the blood left the human body.
Blood clotting rapidly developed inside the cone-and-plate test section. The rate of
blood clotting with time critically depends on the thrombotic tendency of a particular
individuals blood. As soon as blood began to clot, the rotating viscometer flashed an
EEEE sign indicating an overloaded torque, and thus tests were stopped. This
usually happened within 2 minutes of the test. During the viscosity measurement
with the Brookfield rotating viscometer, hematocrit values were determined with a
microhematocrit centrifuge (International Clinical Centrifuge).
Immediately following the removal of the syringe, the experiment with the
scanning capillary-tube rheometer was continued with the second stopcock turned to
a position to allow blood flow to both the capillary tube and riser tube 2. When blood
reached a predetermined height of 300 pixels in the riser tube 2, the second stopcock
was shut to stop further blood flow into the riser tube 2, and the first stopcock was
then turned to direct blood flow into the riser tube 1 up to a height of 1000 pixels. At
t = 0, the data acquisition system was enabled, and both stopcocks were adjusted to
allow blood to flow from the riser tube 1 to tube 2 as driven by the gravity head. Of
note is that the initial pixel difference of 700 was chosen to produce the maximum
shear rate of approximately 400 s-1. If a higher shear rate is desired, an initial pixel
difference greater than 700 can easily be selected.
116
For the purpose of calibration, the present study used the scanning capillarytube rheometer to measure the viscosity of mineral oil, which had a standard
Newtonian viscosity of 9.9 cP at 25. In the tests with human blood and mineral oil,
the capillary tube and major portions of the transfer tube in which test fluids were
actually flowing through the capillary tube were placed in a water bath maintained at
37 and 25, respectively.
The mathematical procedure for data reduction using a power-law model was
discussed in Chapter 4. The least-square method was used for curve fitting of the
experimental data and Eq. (4-18) in order to determine the power-law index, n , and
the consistency index, m . A standard software package (Excel-Solver, Microsoft;
see Appendix E), which has a formula known as a Newtons method (see Appendix
F) [Microsoft Corporation, 57926-0694; Harris, 1998; John, 1998; Brown, 2001], was
used for iterations to determine the values of n and m that minimize the sum of error
(see Eq. (4-19)).
The analysis of data reduction for a mineral oil is introduced in Fig. 6-2.
Figure 6-2(a) shows both experimental values of (t ) and theoretical values of (t )
that were obtained with initial guesses of the two unknowns, whereas Figure 6-2(b)
shows the curve-fitting result after iterations to minimize the sum of error. The initial
guesses for n and m were 0.8 and 8 (cPsn-1), respectively, in the case of the mineral
117
oil (see Fig. 6-2(a)). The resulting values of n and m were determined to be 1 and
9.91 (cPsn-1), respectively, by the iterations using the Excel-Solver.
The analysis of data reduction for human blood is shown in Fig. 6-3. For the
human blood case, initial guesses of the two unknowns of n and m were 0.8 and 6
(cPsn-1), respectively (see Fig. 6-3(a)). After iterations to minimize the sum of error,
the unknowns, n and m , were determined to be 0.83 and 9.27 (cPsn-1), respectively
(see Fig. 6-3(b)). The initial guesses and resulting values of n , m , and ht = for
both mineral oil and human blood were reported in Table 6-1.
Both mineral oil and unadulterated human blood were used in the present
study. The former was specially ordered as a dyed viscosity-standard fluid (i.e., 9.9
cP at 25) from Cannon Instrument Company (State Park, PA), and the latter was
obtained from donors. For comparison purpose, the viscosity of the human blood was
also measured by using a cone-and-plate rotating viscometer (Brookfield model DVIII) at 37. The rotating viscometer used in the present study had an LV-type spring
torque with a CP-40 spindle. In order to maintain the preset temperatures, a water
bath (PolyScience model 2LS-M) was used, which controlled the temperature with an
accuracy of 0.1.
Figures 6-4 and 6-5 show test results obtained with the mineral oil at 25.
Figure 6-4 shows the fluid level variations in the riser tubes, h1 (t ) and h2 (t ) . Both
118
fluid levels converge gradually from the initial fluid level difference and eventually
reach an equilibrium fluid level. In the case of mineral oil, 14.5 mm of an initial fluid
level difference was used to ensure that viscosity measurements at a low shear rate
range were accurate. It is of note that, for mineral oil, ht = was found to be zero.
Figure 6-5 shows viscosity results for the mineral oil at 25 obtained with
the SCTR. The power-law index of the mineral oil was determined to be 1.0 by a
computer program (Excel-solver), confirming that it was a Newtonian fluid. Based
on the present viscosity measurement method, the viscosity of the mineral oil was
found to be between 9.86 and 9.91 cP at 25, which was a 0.5% difference in the
whole range of shear rates from the standard viscosity of 9.9 cP at the same
temperature.
Figure 6-6 shows height variations in each riser tube as a function of time for
fresh human blood at 37. In the case of human blood, about 58 mm of initial fluid
level difference was used for the viscosity measurement so that one could obtain the
accurate viscosity of human blood over a wide shear rate range as low as 1 s-1. In
order to finish a test without using anticoagulants, the test should be completed within
3-4 minutes. Otherwise, blood may begin to clot. In the present study, one test run
took less than 2 minutes. For human blood, the trends of fluid level variations were
very similar to those for mineral oil. However, ht = for human blood was not zero
but a finite value, which depended on the individual donor. The minimum and
maximum values of ht = were found to be 3.86 mm and 6.22 mm, respectively,
119
among 8 donors. These values of ht = represent the thixotropic characteristics of
blood that result in the yield stress.
Figure 6-7 shows the viscosity of unadulterated human blood at 37, which
was measured with both the SCTR and the cone-and-plate rotating viscometer (RV).
Closed circle symbols indicate viscosity data measured with the SCTR while triangle
symbols indicate those measured with the RV. The viscosity of the unadulterated
human blood measured with the present SCTR was based on a calculation method
that determined the power-law index, n , and consistency index, m . In the case
shown in Fig. 5, the values of n and m were 0.828 (dimensionless) and 9.267
(cP s n -1 ) , respectively.
Compared with the measured data using the RV, the present test results from
the SCTR gave excellent agreement with those measured by the RV (i.e., less than
5% difference) in a shear rate range between 30 and 375 s-1. However, as the shear
rate decreased below 30 s-1, the RV was not recommended by Brookfield for the
measurement of blood viscosity. More specifically, the shear stress should vary from
a minimum of 10% to 100% of the full range of the torque sensor used in the
rotational type viscometer at a given shear rate for reasonably accurate viscosity
measurements [Brookfield, 1999]. Therefore, the minimum shear rate at which the
RV could be used for the viscosity measurement of human blood was 30 s-1.
Blood clotting in the RV was the other reason that one could not obtain more
than 7 data points. One could see the effects of blood clotting on viscosity as testing
time passed beyond 1 minute with the RV. Since only 0.5 ml was used for the RV
test, the blood contact area with the surface of the cone-and-plate was much bigger
120
than that in the case of the SCTR, a condition that might have caused rapid blood
clotting.
Figure 6-8 shows the viscosity of unadulterated human blood for two different
donors at 37, whose hematocrits were Hct = 41 and 46.5. Furthermore, human
blood from 8 donors was tested for viscosity measurements in the present study.
Every result using SCTR gave good agreement with that from the RV at high shear
rates but had a different slope with respect to shear rate individually. The viscosity
for the case with Hct = 46.5 was consistently greater than that for the case with Hct =
41. The difference between the two viscosity data was very small at high shear rates
greater than 300 s-1 whereas the difference was significant (i.e., greater than 200%) at
a low shear range, indicating the significance of low shear viscosity data.
In fact, it is well known that slip at the wall occurs in the flow of two-phase
systems because of the displacement of the disperse phase away from solid surfaces
[Barnes, 1995; Picart et al., 1998a, 1998b]. In the case of blood, a significant amount
of slip appears at low shear rates when the size of RBC (red blood cells) is relatively
large compared to wall roughness. For a smooth geometry like a glass tube, however,
the slip effect begins to be considerable from as low as 0.5 s-1 [Picart et al., 1998a].
Therefore, whole blood that was used in the present study did not show large slip
effects since the lowest shear rate data used was 1 s-1. In order to get reliable
viscosity data below 0.5 s-1, it may be necessary to use a rough surface capillary.
121
LED Array
CCD
Riser tube 2
CCD
Riser tube 1
First
stopcock
Computer
system
Transfer tube
Water bath
Capillary tube
Fig. 6-1. Schematic diagram of the scanning capillary-tube rheometer with precision
glass riser tubes.
122
16
Experimental data
12
Theoretical data
(mm) 8
n = 0.8
m = 8 (cPsn-1)
4
0
0
20
40
60
80
100
120
Time (s)
16
Experimental data
12
Theoretical data
(mm) 8
n =1
m = 9.91 (cPsn-1)
4
0
0
20
40
60
80
100
120
Time (s)
Fig. 6-2. Curve-fitting procedure with power-law model for mineral oil.
123
60
Experimental data
40
Theoretical data
(mm)
n = 0.8
m = 6 (cPsn-1)
20
0
0
20
40
60
80
100
120
Time (s)
60
Experimental data
Theoretical data
40
(mm)
n = 0.83
m = 9.27 (cPsn-1)
20
0
0
20
40
60
80
100
120
Time (s)
(b) With final resulting values
Fig. 6-3. Curve-fitting procedure with power-law model for human blood.
124
Table. 6-1. Comparison of initial guess and resulting value using power-law model.
Distilled Water
Human Blood
Initial Guess
n = 0.8
m = 8 (cPsn-1)
ht = = 0.03 mm
n = 0.8
m = 6 (cPsn-1)
ht = = 3 mm
Resulting Value
n =1
m = 9.91 (cPsn-1)
ht = = 0.0271 mm
n = 0.83
m = 9.27 (cPsn-1)
ht = = 3.86 mm
125
60
Height (mm)
Riser tube 1
40
Riser tube 2
20
0
0
50
100
150
Time (s)
Fig. 6-4. Height variation in each riser tube vs. time for mineral oil (9.9 cP viscositystandard oil).
126
Viscosity (cP)
12
10
SCTR
8
6
0
20
40
60
Fig. 6-5. Viscosity measurement for mineral oil at 25 with a scanning capillarytube rheometer (SCTR).
Height (mm)
127
100
90
80
70
60
50
40
30
20
10
0
Riser tube 1
Riser tube 2
50
100
150
Time (s)
Fig. 6-6. Height variation in each riser tube vs. time for human blood at 37.
128
Viscosity (cP)
100
Hematocrit : 40.5
SCTV
RV
10
1
1
10
100
1000
Fig. 6-7. Viscosity measurement (log-log scale) for human blood at 37 with
rotating viscometer (RV) and scanning capillary-tube rheometer (SCTR).
129
Viscosity (cP)
100
SCTV
RV
Hematocrit : 46.5
10
Hematocrit : 41
1
1
10
100
1000
130
Since inexpensive
disposable capillary-riser tube sets should be used for clinical applications, it may not
be easy to strictly control the surface quality of riser tubes within a certain limit.
Therefore, the effects of the surface tension at the riser tubes as well as the properties
of a testing fluid had to be considered in the viscosity and yield stress measurements
with the SCTR.
The resistance associated with air-liquid interfaces in plastic riser tubes of a
small diameter in the SCTR can be a significant part of the pressure head applied to
131
the SCTR, particularly at low shear rates [Jacobs, 1966; Mardles, 1969; Einfeldt and
Schmelzer, 1982]. The meniscus resistance depends on the surface tension of the
fluid-air interface and on the reciprocal of the internal radius of the riser tube.
Throughout the development of a U-shaped scanning capillary-tube rheometer
concept, the focus has been on how to isolate the effects of surface tension and yield
stress in obtaining low-shear-rate viscosity for non-Newtonian fluids like blood. This
study attempted to measure the viscosity of unadulterated blood at a body temperature
of 37.
selected for the viscosity and yield stress measurements of blood since both models
have a yield stress term.
Figure 6-9 shows a photograph of the SCTR with plastic riser tubes, which
consists of two charge-coupled devices (CCD 1 and CCD 2) that are positioned
vertically, two light-emitting diodes (LEDs), two riser tubes made of acrylic plastic
and a capillary tube made of glass, a stopcock, and a data-acquisition system. The
inside diameter of the riser tubes used in the study was 3.2 mm. The inside diameter
and length of the capillary tube were 0.797 mm and 100 mm, respectively. The small
diameter of the capillary tube, compared with that of the riser tubes, was chosen to
ensure that the pressure drop at the capillary tube was significantly greater than those
at the riser tubes and connecting fittings.
132
Tests with distilled water and bovine blood were performed at the room
temperature of 25.
Riser tube 1 was first filled with the test fluid to the
133
extra blood was collected for hematocrit measurements, which were determined with
a microhematocrit centrifuge (International Clinical Centrifuge) for both bovine
blood and human blood.
Viscosities of distilled water (a Newtonian fluid), bovine blood containing
7.5% EDTA, and unadulterated human blood were measured over a range of shear
rates. Because the CCD sensor requires an opaque fluid, dye was added to the
distilled water.
The amount of dye used for distilled water was less than 1%
concentration by volume, and the dye-effect on the viscosity of distilled water was
negligibly small at this concentration. Bovine blood was purchased from Lampire
Biological Laboratories, Inc., and human blood was obtained from two healthy male
donors who were 29 and 51 years of age. For comparison purposes, a reference value
was used for the distilled water while the viscosity of the bovine blood was
independently checked by using the cone-and-plate rotating viscometer.
The fluid level data from the two riser tubes were analyzed to determine the
viscosities of distilled water (a Newtonian fluid) and blood (a non-Newtonian fluid).
In order to measure blood viscosity using a U-shaped SCTR, one needs to isolate the
effects of both surface tension and yield stress on the viscosity of blood. The details
of mathematical procedure for curve-fitting using the Casson model have already
134
been introduced in Chapter 4. Thus, in this section, the procedure to determine the
unknown values for the Casson model is discussed.
As discussed in Chapter 4, there are three unknown values, i.e., k , hst , and
h y , to be determined through the iterations using the same software package (Excel
Solver; see Appendix E) used in the power-law model case. The least-square method
was used for curve fitting of the experimental data and Eq. (4-41) to obtain the three
unknowns involved in the Casson model.
The procedure of data reduction for distilled water is shown in Fig. 6-11.
Figure 6-11(a) shows mean-velocity variations at a riser tube which were obtained
experimentally and theoretically. In the case of theoretical values, the initial guesses
for the three unknowns were used to estimate the values. In Fig. 6-11(b), the curvefitting results after iterations to minimize the sum of error that were calculated by Eq.
(4-42) are shown. The initial guesses and final values of k , hst , and h y for
distilled water are shown in Table 6-2.
Figures 6-12 and 6-13 show the curve-fitting procedures for human blood
obtained from two donors. As shown in Table 6-2, the same initial guesses of the
three unknowns were used for the two different bloods. However, the resulting
values of the three unknowns in the Casson model for the two donors were very
different, validating the present curve-fitting method.
135
Figures 6-14 and 6-15 show test results obtained with distilled water at 25.
Figure 6-14 shows the fluid-level variations in the two riser tubes, h1 (t ) and h2 (t ) .
Both fluid levels converged gradually from the initial difference to an equilibrium
state. Even for the distilled water, ht = was not zero due to the difference in the
surface tension between the two riser tubes. Unless the wetting conditions of the
liquid-solid interface at the two riser tubes are exactly same, the surface-tension
difference always exists.
Figure 6-15 shows viscosity results from two tests for distilled water at 25
obtained with the SCTR, together with the reference data for comparison. The values
of hst were determined to be approximately 4 mm for both tests whereas the values
of h y were determined to be zero by a computer program (Microsoft Excel-solver),
validating the data reduction procedure involving the yield stress. Based on this
viscosity measurement method, the viscosity of the distilled water was found to be
between 0.876 and 0.878 cP at 25. The solid line indicates the viscosity of the
distilled water calculated by using the so-called Andrades equation. Since the water
viscosity data are given in the literature as a function of temperature, the exact
viscosity of water at 25 was calculated using the Andrades equation [Munson et al.,
1998]:
= De
(6-1)
136
where D and B are given as 9.93 10 4 mPas and 2026.57 K, respectively, for water
in a temperature range between 20 and 30.
Based on Eq. (6-1), the water viscosity was estimated to be 0.892 cP at 25.
The test results obtained with the SCTR gave less than 2% error in the entire shear
rate range, validating the test methods and data reduction procedure. Thus, it is
concluded that it is extremely important to consider the effect of the surface tension
on the viscosity measurement using a gravity driven, U-shaped capillary-tube system.
Figure 6-16 shows height variations at the two riser tubes as a function of time
for bovine blood with 7.5 % EDTA at a room temperature of 25. The trends of
fluid-level variations for the bovine blood were very similar to those for the distilled
water. As expected, ht = for the bovine blood was not zero but a finite value that is
slightly greater than that for the distilled water. The height difference due to surface
tension, hst , and the height difference due to yield stress, h y , were determined to
be in the range of 5.7-6.1 mm and 0.52-0.59 mm, respectively. The hematocrit of the
bovine blood was measured to be 35 percent.
Figure 6-17 shows the viscosity of the bovine blood with 7.5% EDTA at 25,
which was measured with both the SCTR (indicated by circles and triangles) and the
rotating viscometer (RV; indicated by diamonds). Compared with the measured data
using the RV, the test results from the SCTR gave excellent agreement within 3% in a
shear rate range between 15 and 300 s-1. However, as the shear rate decreased below
15 s-1, the viscosity data measured from the RV seemed to be incorrect. More
specifically, the torque for viscosity measurements with the RV should be greater
than 10% of the full scale (as suggested by Brookfield) at a given shear rate for
137
reasonably accurate viscosity measurements. In the case of the bovine blood, the
minimum shear rate that Brookfield recommended, based on the 10% criterion, was
approximately 30 s-1. In contrast, the SCTR gave a consistent viscosity measurement
over a range of shear rates as low as a shear rate of 1 s-1. Related to the uncertainty in
measuring blood viscosity at low shear rates, wall slip is an issue.
Since the
minimum shear rate in this study was 1 s-1, as discussed earlier, one could assume that
the slip effect was negligibly small [Picart et al., 1999a].
Figures 6-18 and 6-19 show test results of fresh, unadulterated human blood at
a body temperature of 37. The test was completed within 2-3 min to avoid blood
clotting, which might have altered the viscosity of the blood. Figure 6-18 shows
height variations in the two riser tubes as a function of time for the fresh human blood
at 37. The value of ht = for the fresh human blood had a finite value, which
depended on individual donors. The values of hst for donors 1 and 2 were found to
be approximately 8.5 and 9.6 mm, respectively.
In the use of the SCTR, two phenomena of particular importance should be
pointed out in regards to clinical hemorheology: one is the carry-over effect and the
other is the surface tension effect. First, at the completion of a measurement, a thin
layer of the test blood sample was always retained on the tube wall, unless the tube
was very carefully washed and dried. This residual layer can be called carry-over.
Hence, for unadulterated blood-viscosity measurements, it was necessary to use
disposable capillary-riser tube sets to avoid the carry-over phenomenon. Second, the
difference between surface tensions at the two riser tubes may vary from one
138
disposable set to another. Although the riser tubes were made of the same material
(acrylic plastic), the surface tensions were slightly different from set to set.
The values of h y representing the effect of the yield stress for donors 1 and 2
were found to be 0.7 and 0.2 mm, respectively. These results were consistent with
hematocrit data for donors 1 and 2, which were 42 and 35 percent, respectively.
Donor 2 (a physician) practices therapeutic bloodletting periodically, which explains
why the hematocrit of donor 2 was unusually low. It is of note that the value of h y
represents the thixotropic characteristics of fresh human blood that is closely related
to the yield stress.
A thixotropic blood exhibits a high viscosity when first sheared from rest.
The viscosity continues to decrease as shearing continues. Thixotropy is usually a
result of the partial destruction, by shearing, of the internal liquid structure. While at
rest, the internal structure made of suspended cells and plasma may form to create
aggregations of RBCs, for example. This phenomenon is generally referred to as
structure viscosity.
In fact, the phenomenon of RBCs aggregations at low shear rates is well
known but not well understood so far. The forces leading to aggregations are weak,
so if a sample of normal blood is subjected to increasing shear rate, the aggregates
progressively break up and are generally monodispersed at a shear rate greater than
10 s-1. However, it is important to note that there could be two kinds of yield stresses:
a start-up yield stress and a stopping yield stress [Cho and Choi, 1993]. The yield
stress determined in this study was the stopping yield stress, an important
phenomenon in clinical hemorheology and studies of cardiovascular disease. In the
139
viscosity measurement with whole blood, a typical test duration in which the shear
rate decreased from 10 to 1 s-1 was longer than 60 seconds. It is reasonable to assume
that the 60-second period is long enough to cause aggregations if the aggregations
were going to take place.
Figure 6-19 shows the viscosities of the two donors at 37 measured with the
SCTR. The viscosities for donor 2 were significantly lower than those for donor 1
due to the difference in hematocrit. In addition, the viscosity curve for donor 2 was
flatter than that for donor 1 since donor 2 had a smaller value of h y and a lower
hematocrit. Figure 6-20 shows shear stress variations against shear rate for both
donors. Like the case of viscosity, shear stress for donor 2 was significantly lower
than that for donor 1 due to differences in hematocrit and yield stress. The values of
the yield stress determined from Casson model were approximately 14 mPa and 5
mPa for donor 1 and 2, respectively. The difference between the viscosity data
increased as the shear rate decreased indicating that the viscosity was more influenced
by hemorheological parameters such as hematocrit and yield stress at low shear rates
than at high shear rates.
The detailed mathematical procedure for curve-fitting using a HerschelBulkley (H-B) model was provided in Chapter 4. As in the case of the Casson model,
the H-B model can also handle the yield stress of blood. However, in the data
140
reduction with the H-B model, there are four unknown values to be determined
through the curve-fitting technique, whereas the Casson model has only three
unknowns.
The four unknown values, i.e., m , n , hst , and h y , are to be determined
through a least-square method using the same software package (Excel-Solver,
Microsoft; see Appendix E) that uses the formula of Newtons method. In the
process of curve fitting, Eq. (4-59) was used for theoretical values. In the case of the
H-B model, the experimental data of bovine blood with 7.5% EDTA were used to
validate the method of data reduction.
Figure 6-21(a) shows mean-velocity values at a riser tube which were
obtained both experimentally and theoretically. In the case of theoretical values, the
initial guesses for the four unknowns, which are shown in Table 6-3, were used. In
Fig. 6-21(b), the curve-fitting results after the iterations to determine the four
unknowns are shown. The initial guesses and final values of m , n , hst , and h y
for bovine blood with 7.5% EDTA using the H-B model are shown in Table 6-3.
Figure 6-22 shows the viscosity of the bovine blood with 7.5% EDTA at 25,
which was measured with the SCTR. Three consecutive tests were performed with
bovine blood.
repeatable results. The final values of four unknowns for each test are reported in
Table 6-4.
141
CCD-LED arrays
Riser tube 1
Test Fluid
Stopcock
Riser tube 2
Capillary tube
142
Rheometer
System
Heating
Pad
Fig. 6-10. Heating pad for a test with unadulterated human blood.
143
0.025
Experimental data
Theoretical data
0.02
2Vr 0.015
(m/s)
0.01
0.005
0
0
10
20
30
40
Time (s)
0.02
Theoretical data
2Vr
0.015
(m/s)
0.01
0.005
0
0
10
20
30
40
Time (s)
Fig. 6-11. Curve-fitting procedure with Casson model for distilled water.
144
Table. 6-2. Comparison of initial guess and resulting value using Casson model.
Initial Guess
Resulting Value
Distilled Water
Human Blood
k = 1 (cPs)
h y = 0.5 mm
k = 1 (cPs)
h y = 0.5 mm
hst = 3 mm
hst = 5 mm
k = 0.878 (cPs)
h y = 0.00
hst = 4.02 mm
Donor 1
Donor 2
k = 2.743 (cPs)
h y = 0.74 mm
k = 2.121 (cPs)
h y = 0.16 mm
hst = 8.47 mm
hst = 9.58 mm
145
0.008
2Vr
(m/s)
Experimental data
Theoretical data
0.006
0.004
0.002
0
0
20
40
60
80
100
120
Time (s)
0.006
2Vr
(m/s)
0.004
0.002
0
0
20
40
60
80
100
120
Time (s)
146
0.008
Experimental data
0.006
2Vr
(m/s)
Theoretical data
0.004
0.002
0
0
20
40
60
80
100
120
Time (s)
(a) With initial guess values
0.008
Experimental data
2Vr
(m/s)
Theoretical data
0.006
0.004
0.002
0
0
20
40
60
80
100
120
Time (s)
(b) With final resulting values
147
0.1
Height (m)
0.08
Riser tube 1
0.06
0.04
Riser tube 2
0.02
0
0
50
100
150
Time (s)
Fig. 6-14. Height variation in each riser tube vs. time for distilled water at 25.
148
Viscosity (cP)
1.5
Test 1
Test 2
Reference
1.3
1.1
0.9
0.7
0.5
0
100
200
300
-1
Shear rate (s )
400
149
0.1
Riser tube 1
Height (m)
0.08
0.06
0.04
Riser tube 2
0.02
0
0
30
60
90
Time (s)
120
150
Fig. 6-16. Height variation in each riser tube vs. time for bovine blood with 7.5%
EDTA at 25.
150
Viscosity (cP)
100
Test 1
Test 2
RV
10
1
1
10
100
-1
Shear rate (s )
1000
Fig. 6-17. Viscosity measurement for bovine blood with 7.5% EDTA at 25 using
both rotating viscometer (RV) and scanning capillary-tube rheometer (SCTR).
Hematocrit was 35. 1 cP = 1 mPas.
Height (m)
151
0.1
0.09
0.08
0.07
0.06
0.05
0.04
0.03
0.02
0.01
0
A : Donor 1
B : Donor 2
B
A
30
60
90
Time (s)
120
150
Fig. 6-18. Height variation in each riser tube vs. time for human blood at 37.
152
Viscosity (cP)
100
Donor 1
Donor 2
10
1
1
10
100
1000
-1
Shear rate (s )
Fig. 6-19. Viscosity measurement for human blood (2 different donors) at 37.
Hematocrits for donors 1 and 2 were 42 and 35, respectively. 1 cP = 1 mPas.
153
10000
1000
100
10
Donor 1
Donor 2
1
1
10
100
1000
Fig. 6-20. Shear-stress variation vs. shear rate for human blood (from 2 different
donors) at 37.
154
0.005
2Vr
(m/s)
Experimental data
0.004
Theoretical data
0.003
0.002
0.001
0
0
40
80
120
Time (s)
(a) With initial guess values
0.005
Experimental data
0.004
Theoretical data
2Vr
(m/s) 0.003
0.002
0.001
0
0
40
80
120
Time (s)
(b) With final resulting values
Fig. 6-21. Curve-fitting procedure with Herschel-Bulkley model for bovine blood.
155
Initial Guess
n = 0.8
m = 5 (cPsn-1)
h y = 1 mm
hst = 6 mm
Resulting Value
n = 0.875
m = 8.6 (cPsn-1)
h y = 1.2 mm
hst = 5.8 mm
156
Viscosity (cP)
100
Test #1
Test #2
Test #3
10
1
1
10
100
1000
157
Test #2
Test #3
n = 0.875
m = 8.6 (cPsn-1)
h y = 1.2 mm
n = 0.876
m = 8.7 (cPsn-1)
h y = 1.2 mm
n = 0.872
m = 8.76 (cPsn-1)
h y = 1.24 mm
hst = 5.8 mm
hst = 5.8 mm
hst = 5.8 mm
158
159
Figures 6-23(a) and 6-23(b) show the calibration results obtained in the SCTR
with distilled water at 25. Figure 6-23(a) shows the fluid-level variations in the
two riser tubes, h1 (t ) and h2 (t ) . Both fluid levels converged gradually from the
initial difference to an equilibrium state. Even for the distilled water, the difference
in the two fluid-levels at t = , ht = , was not zero due to the difference in the
surface tension between the two riser tubes.
Figure 6-23(b) shows viscosity results for distilled water at 25 obtained
with the SCTR using the three different non-Newtonian constitutive models, together
with the reference data for comparison. The values of hst were determined to be
approximately 3.3-3.4 mm for the three models, whereas the values of h y were
determined to be zero for all models, validating the data reduction procedure
involving the yield stress. The viscosity of distilled water was found to be between
0.884 and 0.905 cP at 25 for all three models. As shown in Table 6-6, the test
results obtained with the SCTR gave less than 2% error over the entire shear rate
range, validating the experimental procedure and data reduction method using the
three non-Newtonian constitutive models. Furthermore, the viscosity measurement of
water confirmed that one needs to consider the effect of the surface tension on the
viscosity measurement in the SCTR.
Figures 6-24(a) and 6-24(b) show test results obtained with bovine blood at
25. Figure 6-24(a) shows height variations at two riser tubes as a function of time
160
for the bovine blood with 7.5% EDTA as an anticoagulant. The trends of fluid-level
variations for the bovine blood were very similar to those for the distilled water. As
expected, ht = for the bovine blood was not zero, but a finite value that is slightly
greater than that for the distilled water. The hematocrit of the bovine blood was
measured to be 35%.
Figure 6-24(b) shows the viscosity of the bovine blood at 25, which was
measured with both the SCTR and a rotating viscometer (RV). The SCTR results
obtained by using the three constitutive models showed very good agreement among
themselves at shear rates higher than approximately 30 s-1. However, the power-law
model maintained the rate of the viscosity change (the slope of a viscosity curve)
constant whereas both the Casson and H-B models increased the rate of viscosity
change as shear rate decreased, indicating the existence of yield stress in the bovine
blood. Moreover, the viscosity results using the Casson model showed very good
agreement with those using the H-B model.
The test results from the SCTR using the three non-Newtonian models gave
excellent agreement with the measured data using the RV within 5% in a shear-rate
range between 30 and 300 s-1. However, as the shear rate decreased below 30 s-1, the
viscosity data measured from the RV seemed to be incorrect. More specifically, the
torque for viscosity measurements with the RV should be greater than 10% of the full
scale (as suggested by Brookfield) for reasonably accurate viscosity measurements.
In the case of the bovine blood, the minimum shear rate that Brookfield
recommended, based on the 10% criterion, was approximately 30 s-1. In contrast, the
SCTR gave a consistent viscosity measurement over a range of shear rate as low as a
161
shear-rate of 1 s-1. In addition, the viscosities measured using both the Casson and HB models in the SCTR seemed to be more accurate than the power-law viscosity at
low shear rates. Table 6-7 provides the viscosity results at the several shear rates,
which were produced by using the three non-Newtonian constitutive models.
Figures 6-25(a) and 6-25(b) show test results of fresh, unadulterated human
blood at a body temperature of 37. The test was completed within 2-3 minutes to
avoid blood clotting, which might have altered the viscosity of the blood. Figure 625(a) shows height variations in the two riser tubes as a function of time for the fresh
human blood at 37. The value of ht = for the fresh human blood was measured to
be approximately 8.5 mm. The hematocrit of this donors blood was 42%.
Figure 6-25(b) shows the viscosity of the human blood at a body temperature
of 37, which was measured with the SCTR. The SCTR results obtained by using
the three constitutive models showed very good agreement among themselves at
shear rates higher than approximately 20 s-1. However, like the bovine blood case,
the power-law model maintained the rate of the viscosity change constant whereas
both the Casson and H-B models increased the rate of viscosity change as shear rate
decreased, indicating the existence of yield stress in the human blood. Table 6-8
shows the viscosity results of the unadulterated human blood for the three constitutive
models.
For cases of the bovine blood and fresh human blood, the power-law model
maintained constant slopes in the viscosity curve, while both the Casson and H-B
models showed rapid increases in the viscosity as the shear rate decreased. However,
162
the viscosities obtained from the three different constitutive models gave good
agreement at a high shear rate zone.
Over the years, many researchers have reported on the yield stress of blood.
The measurements of the rheological properties of fluids having yield stress are
summarized by Nguyen et al. (1983). According to their classifications, the yieldstress measurement with the SCTR can be classified as indirect methods rather than
direct methods since the yield stress of a fluid can be obtained in the SCTR by using
constitutive models. Bingham plastic, Casson, and H-B models were used in their
study to describe the rheological behavior of yield-stress fluids.
Figures 6-26(a), 6-26(b), and 6-26(c) show the results of shear stress versus
shear rate for distilled water, bovine blood, and human blood, respectively. In the
case of the distilled water, the shear stresses obtained using the three different nonNewtonian models were almost identical.
described as the intersecting point where the shear stress-shear rate curve meets with
the y-axis (i.e., at zero shear rate). Table 6-9 shows the yield-stress results together
with the model constants of the three constitutive models. As expected, the distilled
water shows no yield stress, while both the bovine and human bloods show finite
values of the yield stress for the cases of Casson and H-B models. Note that the yield
163
stress values for the Casson and H-B models were calculated using the following
equation:
y =
gh y Rc
2 Lc
(6-2)
The yield stress of the human blood was consistently greater than that of the
bovine blood although the human blood was tested at a high temperature of 37. It
might be due to both the difference in hematocrit and the RBC aggregations of the
human blood at low shear rates. The yield stress values of the human blood with
hematocrit of 42% were measured to be 13.8 and 17.5 mPa for the Casson and H-B
models, respectively. Note that the yield stress measured in the present study was the
stopping yield stress, an important phenomenon in clinical hemorheology and
treatments of cardiovascular disease. The yield stress values vary from 1 mPa to 30
mPa for normal human blood with hematocrit of 40% [Chen et al., 1991; Picart et al.,
1999a], supporting the validity of the method of the present yield-stress measurement
using the SCTR.
The yield stress obtained with the H-B model was consistently greater than
that obtained with the Casson model in the cases of both bovine and human bloods as
shown in Table 6-9. In order to evaluate which model produces more accurate yield
stress results, the experimentally measured values of ht = were compared with those
of hst + h y determined analytically through the curve-fitting procedure for the
bovine and human bloods (see Table 6-10). The value of the fluid-level difference in
riser tubes 1 and 2 at a time of 180 seconds was taken as a measure of ht = . Hence,
164
the experimental values (i.e., ht = ) should be bigger than those (i.e., hst + h y ) to
be obtained analytically.
As shown in Table 6-10, the values of hst + h y obtained with the Casson
model were consistently smaller than the experimentally measured values while the
values obtained with H-B model were bigger. Based on the comparison, one may
conclude that the Casson model does a better job in determining the yield stress of
blood than the H-B model. However, it is of note that both models produced almost
identical values of hst , thus almost identical surface tensions, for the bovine and
human blood.
Figure 6-27 shows the variations of C y (t ) for the bovine blood with 7.5%
EDTA, indicating that the plug-flow region grows at the capillary tube with
increasing time. Due to the difference in yield stress values for the Casson and H-B
models, the size of the plug-flow region estimated from the two models start to differ
after approximately 30 seconds. Note that the H-B model predicts a much larger
plug-flow region than the Casson model.
Figures 6-28(a), 6-28(b), and 6-28(c) show velocity profiles at the capillary
tube for the bovine blood at room temperature of 25, which were plotted at three
mean velocities of 3, 0.3, and 0.03 cm/s, respectively. At a relatively high velocity of
3 cm/s, the three constitutive models predicted identical velocity profiles. However,
165
as the mean velocity (i.e., shear rate) decreased, the clear deviation among the three
models started to appear near the center of the tube at 0.3 cm/s and became bigger at
0.03 cm/s, a phenomenon which can be attributed to the difference in yield stress
values. Therefore, it can be concluded that the yield stress plays an important role in
the determination of both the blood viscosity and velocity profiles in a blood flow.
Figure 6-28(c) also shows that the size of the plug-flow region at the center of the
tube for the H-B model is much larger than that for the Casson model at
approximately 0.03 cm/s.
The shear rate, viscosity, and shear stress obtained with both the Casson and
H-B models for the bovine blood were plotted as a function of the mean velocity at
the capillary tube in Figs. 6-29(a), 6-29(b), and 6-29(c), respectively. Wall shear
stress represents the friction exerted on the vessel wall by moving blood. It has been
shown in a number of studies that wall shear stress may play an important role in
endothelial cell morphology and functions influencing the production of substances
such as nitric oxide, prostacyclin, and endothelin [Baldwin and Thurston, 1995;
Usami et al., 1995; Fung, 1996; Mitsumata et al., 1996; Samijo et al., 1998; Frame et
al., 1998; Cotran et al., 1999; Kensey and Cho, 2001].
As shown in Fig. 6-29(c), the value of the wall shear stress is almost
independent of the selection of a constitutive model. Due to the difference in the size
of the plug-flow regions, the wall shear rates for the Casson model at low mean
velocities were much lower than those for the H-B model, resulting in consistently
higher wall viscosity for the Casson model as shown in Fig. 6-29(b). Since the wall
shear stress can be calculated from the product of viscosity (shown in Fig. 6-29(b))
166
and wall shear rate (shown in Fig. 6-29(a)) at a given mean velocity, the difference in
the wall shear stress between the two models is very small.
167
Power-law
Casson
Herschel-Bulkley
x
x
x
168
100
(a)
Height (mm)
80
Riser tube1
60
40
Riser tube 2
20
0
0
30
60
90
120
150
Time (s)
1.5
(b)
power-law
H-B
Casson
Reference
Viscosity (cP)
1.3
1.1
0.9
0.7
0.5
0
100
200
300
400
Fig. 6-23. Test with distilled water at 25. (a) Fluid-level variations in two riser
tubes. (b) Viscosity results.
169
Viscosity (cP)
*Error
Power-law
0.905
1.46%
Herschel-Bulkley (H-B)
0.884
0.90%
Casson
0.886
0.68%
170
100
(a)
Height (mm)
80
Riser tube 1
60
40
Riser tube 2
20
0
0
30
60
90
120
150
Time (s)
100
Viscosity (cP)
(b)
power-law
H-B
Casson
RV
10
1
1
10
100
1000
-1
Shear rate (s )
Fig. 6-24. Test with bovine blood at 25. (a) Height variations in riser tube vs. time
for bovine blood with 7.5% EDTA. (b) Viscosity measurement for bovine blood with
7.5% EDTA using a rotating viscometer (RV) and a scanning capillary-tube
rheometer (SCTR).
171
Viscosity
(cP)
from RV
Power-law
Casson
H-B
300
4.43
4.39
4.49
4.28
150
4.78
4.75
4.84
4.71
90
5.11
5.03
5.18
5.09
45
5.75
5.44
5.85
5.71
30
6.25
5.7
6.38
6.2
15
8.81
6.16
7.7
7.21
7.5
17
6.67
9.7
8.9
7.4
14.5
12.8
Lower than 3
8.38
(at 1 s-1)
22.5
(at 1.35 s-1)
18.55
(at 1.55 s-1)
172
(a)
100
Height (mm)
80
Riser tube 1
60
40
Riser tube 2
20
0
0
30
60
90
120
150
Time (s)
(b)
Viscosity (cP)
100
power-law
H-B
Casson
10
1
1
10
100
-1
Shear rate (s )
1000
Fig. 6-25. Test with unadulterated human blood at 37. (a) Height variations in riser
tubes vs. time. (b) Viscosity results.
173
Power-law
Casson
H-B
300
3.89
4.11
4.09
150
4.45
4.47
4.57
90
4.93
4.85
4.97
45
5.67
5.59
5.63
30
6.15
6.16
6.15
15
7.06
7.65
7.3
7.5
8.12
9.95
9.1
Lower than 5
9.76
(at 3 s-1)
14.73
(at 3.33 s-1)
12.9
(at 3.3 s-1)
Lower than 3
12.17
(at 1 s-1)
27.26
(at 1.18 s-1)
21.9
(at 1.32 s-1)
174
(a)
1000
power-law
H-B
Casson
100
10
1
1
10
100
1000
Shear stress (mPa)
(b)
W ater
Bovine Blood
100
power-law
H-B
Casson
10
1
1
10
100
(c)
1000
Human Blood
100
power-law
H-B
Casson
10
1
1
10
Shear rate (s -1)
100
Fig. 6-26. Wall shear stress at a capillary tube vs. shear rate. (a) for distilled water at
25. (b) for bovine blood at 25. (c) for human blood at 37.
175
Table. 6-9. Comparison of model constants, h y , and y . (Note that [m] = cPsn-1)
Power-law
H-B
n =1
m = 0.905
h y = 0
n =1
m = 0.884
h y = 0
y=0
y=0
Bovine blood
(25)
n = 0.8866
m = 8.3771
h y = 0
n = 0.8753
m = 8.599
h y = 0.8 mm
h y = 0.52 mm
y=0
y = 16.4 mPa
y = 10.7 mPa
Human blood
(37)
n = 0.7991
m = 12.171
h y = 0
n = 0.8601
m = 8.9721
h y = 0.85 mm
h y = 0.67 mm
y=0
y = 17.5 mPa
y = 13.8 mPa
Distilled water
(25)
Casson
k = 0.886 cP
h y = 0
y=0
k = 3.7302 cP
k = 3.2896 cP
176
Bovine blood
(25)
Human blood
(37)
H-B
Casson
6.5 mm
6.5 mm
6.6 mm
( hst = 5.8 mm
6.26 mm
( hst = 5.74 mm
h y = 0.8 mm)
h y = 0.52 mm)
ht =
(experimental)
9.13 mm
9.13 mm
hst + h y
9.25 mm
( hst = 8.4 mm
9.07 mm
( hst = 8.4 mm
h y = 0.85 mm)
h y = 0.67 mm)
ht =
(experimental)
hst + h y
(analytical)
(analytical)
177
1
Casson
H-B
0.8
Cy
0.6
0.4
0.2
0
0
50
100
Time (s)
150
200
Fig. 6-27. Variations of a plug-flow region at a capillary tube as a function of time for
bovine blood with 7.5% EDTA at 25.
178
6
3 cm/s
Velocity (cm/s)
(a)
4
power-law
Casson
H-B
2
0
0
0.01
0.02
0.03
0.04
(b)
Velocity (cm/s)
0.6
0.3 cm/s
0.4
power-law
0.2
Casson
H-B
0
0
0.01
0.02
0.03
0.04
(c)
Velocity (cm/s)
0.06
0.03 cm/s
0.04
power-law
Casson
H-B
0.02
0
0
0.01
0.02
0.03
0.04
Radius (cm)
Fig. 6-28. Velocity profiles at a capillary tube for the bovine blood with 7.5% EDTA
at 25: (a) at a mean velocity of 3 cm/s. (b) approximately 0.3 cm/s.
(c) approximately 0.03 cm/s.
179
-1
(a)
1000
100
10
Casson
H-B
1
0.1
0.01
0.1
10
(b)
Viscosity (cP)
1000
Casson
H-B
100
10
1
0.01
0.1
10
(c)
100
10
1
0.1
0.01
0.01
Casson
H-B
0.1
1
Mean velocity (cm/s)
10
Fig. 6-29. (a) Wall shear rate, (b) Viscosity, and (c) Wall shear stress. Plotted as a
function of mean velocity at a capillary tube using three non-Newtonian models for
bovine blood with 7.5% EDTA. Note that 1 dyne/cm2 = 102 mPa.
180
CHAPTER 7. CONCLUSIONS AND RECOMMENDATIONS
181
The effect of the surface tension was taken into account by using an additional
term, hst , while the effect of the yield stress was considered as a model constant in
either Casson or Herschel-Bulkley model. For the SCTR using gravity as a driving
force, it was necessary to consider the effect of the surface tension even for
Newtonian fluids. Furthermore, in the case of a thixotropic liquid like whole blood,
the surface-tension effect should be isolated from the yield-stress effect to obtain
accurate viscosity data over a range of shear rates using the SCTR. In order to avoid
the influence of the carry-over phenomenon on viscosity measurements, disposable
tube sets were used for tests with fresh human blood.
The present study also investigated the effect of dye concentration on the
viscosity of a dye-water solution using a SCTR. In the experiment, six different
concentrations (0.5, 1, 2, 3, 4, and 7% by volume) of dye were used at 25C. When
the dye concentration was greater than 2%, the viscosity of the dye-water solution
could be significantly altered particularly at low shear rates. Based on the experiment
with the SCTR, one can conclude that the maximum 2% concentration of dye by
volume can be used to make a transparent aqueous solution opaque for the operation
of the SCTR.
The present study investigated the effects of three non-Newtonian constitutive
models on the viscosity and yield stress measurements in a scanning capillary-tube
rheometer: power-law, Casson, and Herschel-Bulkley models.
For a Newtonian fluid (i.e., distilled water), all three models produced
excellent viscosity results.
bloods), both Casson and H-B models gave viscosity results which are in good
182
agreement with each other as well as with the results obtained by a conventional
rotating viscometer, whereas the power-law model seemed to produce inaccurate
viscosities at low shear rates due to its inability to handle the yield stress of blood.
The yield stress values obtained from the Casson and H-B models for the
human blood were measured to be 13.8 and 17.5 mPa, respectively. The two models
showed some discrepancies in the yield-stress values. The results from the Casson
model seemed to be more accurate than those from the H-B model.
The ability to estimate the wall shear stress in various arterial vessels could be
a significant step in clinical hemorheology. In the present study, the wall shear stress
was found to be almost independent of a constitutive model, whereas the size of the
plug flow region varies substantially with the selected model, altering the values of
the wall shear rate at a given mean velocity. The model constants and the method of
the shear stress calculation given in the study can be useful in the diagnostics and
treatment of cardiovascular diseases.
The present study developed a new rheometer that was specially designed for
measuring unadulterated human blood. However, the measurement was not
strictly in vivo. It would be very useful to develop a method to measure the
viscosity of human blood in vivo.
183
-
The present study measured the viscosity and yield stress of human blood
without adding any anticoagulants. The study on the effect of thrombotic
tendency of each individual person on both viscosity and yield stress of blood
should be conducted.
The two yield stress models, Casson and Herschel-Bulkley models, gave
different yield stresses for blood in the present study. It is not very clear
which model is more accurate.
184
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APPENDIX A. Nomenclature
English Letters
dimensionless radius at = y , r
Cy
dimensionless radius at = y ,
height [m]
KL
loss coefficient
torque [Nm]
power-law index
pressure [Pa]
radius [m]
ry
R
R
195
R
ry
Re
Reynolds number
time [s]
Greek Letters
&
density [kgm-3]
196
angle [rad]
Subscripts
atm
atmosphere
capillary tube
entrance
End
end effects
fluid
inner cylinder
loss
needle
outer cylinder
st
surface tension
time
unsteady
unsteady state
wall
yield stress
infinity
197
Falling Cylinder/Needle
( n f ) gR
(B-1)
2
( n f ) gR 2
2v
(1 + ln )
where
n = density of needle
f = density of fluid
g = gravitational acceleration
(B-2)
198
199
200
Description
Key Features
201
Cover Glass
Plastic Housing
Rod Lens
LED Light Source
Connector
Sensor Array
PCB Substrate
202
For the experiment with unadulterated human blood, capillary tubes used in a
SCTR have been coated with biocompatible materials. The coating work was carried
out by a company called Biocompatibles in Farnham, Surrey (U.K.). The following
procedure was employed to coat the inner surface of the capillary tube:
1. Prepare 100 ml of a 10mg/ml PC1036 solution in 99% Hexane and 1%
Ethanol.
2. Clean the capillary tube lumen by using a 20ml syringe to pull and push the
Hexane through the lumen vertically.
3. Pass compressed air vertically through both ends of the capillary tube lumen
for 2 seconds at a flow rate of 30-35 liters per minute to remove any
remaining traces of Hexane.
4. Coat the capillary tube by using a 20 ml syringe to pull and push the PC1036
polymer solution through the lumen vertically.
5. Immediately after coating, pass compressed air vertically through both ends of
the capillary tube lumen for 2 seconds at a flow rate of 30-35 liters per minute
to remove any remaining traces of PC1036 polymer solution.
6. Place the capillary tube horizontally in an incubator preheated to 70 for 4
hours to allow the coating to cure.
203
The capillary tube lumen was reported to be free from blockage after the coating
procedure. In addition, the thickness of the polymer coating cured on the inner
surface of the capillary tube was reported approximately 1 m.
204
Solver is well-known and widely used in scientific researches [Harris, 1998; John,
1998; Brown, 2001]. The procedure and its mode of operation are very easy and
obvious.
205
2. Add a further column containing a chosen model.
The parameters
(unknowns) of the chosen model are estimated and located in any free cells.
These are the Change cells.
3. Add a further column which expresses the squared error between the known
206
The Newton method is one of the most widely used methods for root finding.
It can be used for the problem to find solutions of a system of non-linear equations
[Young and Gregory, 1988; Isaacson and Keller, 1994; Hildebrand, 1987]. Consider
the general problem of fitting a function of the following type:
y = f ( X ; A)
(F-1)
E ( A) = f ( X ( j ) ; A) y ( j )
(F-2)
j =1
satisfied:
E
E
E
= 0,
= 0 , , and
= 0.
a1
a 2
a m
(F-3)
Note that some or all of the equations in Eq. (F-3) may be non-linear. Applying the
chain rule to the definition of the error function E , one may rewrite Eq. (F-3) in the
following forms:
207
[f (X
( j)
[f (X
( j)
; A) y ( j )
j =1
l
] f ( Xa
; A)
] f ( Xa
; A)
( j)
=0
; A) y ( j )
j =1
( j)
=0
(F-4)
[f (X
l
( j)
; A) y ( j )
j =1
] f ( Xa
( j)
; A)
=0
Considering the non-linear cases, the standard form for these problems is Eq. (F-4).
F1 ( A) = 0
F2 ( A) = 0
i.e.,
Fm ( A) = 0
F ( A) = 0
(F-5)
(F-6)
(F-7)
The above equation is a linear system of equations, so one can solve it for A1 A0 .
208
Viscosity (cP)
1
0.98
0.96
0.94
0.92
0.9
Test #1
Test #2
Test #3
Test #4
Test #5
Reference (0.892 cP)
0.88
0.86
0.84
0.82
0.8
0
100
200
300
Shear rate (s -1)
400
500
Viscosity (cP)
209
1
0.98
0.96
0.94
0.92
0.9
0.88
0.86
0.84
0.82
0.8
Test #1
Test #2
Test #3
Test #4
Test #5
Reference (0.892 cP)
100
200
300
400
500
210
Table H-1. A typical experimental data set of human blood obtained by a scanning
capillary-tube rheometer with precision glass riser tubes. One out of 100 data points
is selected from an original data set.
Time (s)
0.00
2.00
4.00
6.00
8.00
10.00
12.00
14.00
16.00
18.00
20.00
22.00
24.00
26.00
28.00
30.00
32.00
34.00
36.00
38.00
40.00
42.00
44.00
46.00
48.00
50.00
52.00
54.00
56.00
58.00
60.00
211
212
213
Table H-2. A typical experimental data set of distilled water obtained by a scanning
capillary-tube rheometer with plastic riser tubes. One out of 100 data points is
selected from an original data set.
Time (s)
0.00
2.00
4.00
6.00
8.00
10.00
12.00
14.00
16.00
18.00
20.00
22.00
24.00
26.00
28.00
30.00
32.00
34.00
36.00
38.00
40.00
42.00
44.00
46.00
48.00
50.00
52.00
54.00
56.00
58.00
60.00
62.00
64.00
66.00
68.00
70.00
214
215
Table H-3. A typical experimental data set of bovine blood obtained by a scanning
capillary-tube rheometer with plastic riser tubes. One out of 100 data points is
selected from an original data set.
Time (s)
0
2
4
6
8
10
12
14
16
18
20
22
24
26
28
30
32
34
36
38
40
42
44
46
48
50
52
54
56
58
60
62
64
66
68
70
216
217
218
Table H-4. A typical experimental data set of human blood obtained by a scanning
capillary-tube rheometer with plastic riser tubes. One out of 100 data points is
selected from an original data set.
Time (s)
0.00
2.00
4.00
6.00
8.00
10.00
12.00
14.00
16.00
18.00
20.00
22.00
24.00
26.00
28.00
30.00
32.00
34.00
36.00
38.00
40.00
42.00
44.00
46.00
48.00
50.00
52.00
54.00
56.00
58.00
60.00
62.00
64.00
66.00
68.00
70.00
219
220
221
VITA
Sangho Kim
Education
Drexel University
Doctor of Philosophy in Mechanical Engineering
Master of Science in Mechanical Engineering
Kyungpook National University
Bachelor of Science in Mechanical Engineering
Philadelphia, PA
12/2002
Taegu, Korea
02/1997
Journal Publications
S. Kim, Y.I. Cho, K.R. Kensey, R.O. Pellizzari and P.R. Stark
A scanning dual-capillary-tube viscometer
Review of Scientific Instruments, Vol. 71, No. 8, August 2000, 3188-3192
S. Kim, Y.I. Cho, A.H. Jeon, B. Hogenaeur and K.R. Kensey
A new method for blood viscosity measurement
J. Non-Newtonian Fluid Mechanics, 94 (2000) 47-56
S. Kim, Y.I. Cho, W.N. Hogenaeur and K.R. Kensey
A method of isolating surface tension and yield stress effects in a U-shaped scanning
capillary-tube viscometer using a Casson model
J. Non-Newtonian Fluid Mechanics, 103 (2002) 205-219
S. Kim and Y.I. Cho
The effect of dye concentration on the viscosity of water in a scanning capillary-tube
viscometer
J. Non-Newtonian Fluid Mechanics, 2002 (submitted)
S. Kim, Y.I. Cho, and W.N. Hogenaeuer
Non-Newtonian constitutive models for the viscosity and yield-stress measurements of
blood using a scanning capillary-tube rheometer
Biorheology, 2002 (submitted)
Conference Publications
US Patents
U.S. Patent No. 6,428,488
U.S. Patent No. 6,412,336
U.S. Patent No. 6,322,524
U.S. Patent No. 6,402,703
U.S. Patent No. 6,450,974