1. Introduction
Numerical simulation of biological fluids in the presence of magnetic fields (biomagnetic fluid dynamics (BFD)) has attracted considerable attention over the last decades. Numerous research studies have been published, mainly related to bioengineering (e.g., development of magnetic devices for cell separation, development of magnetic tracers) and medical applications (e.g., targeted transport of drugs using magnetic particles as drug carriers) [
1,
2]. The majority of biological fluids are considered as biomagnetic, mainly because they contain ions which interact with the applied magnetic field. Blood in particular, has erythrocytes that have the tendency to orient with their disk plane parallel to the magnetic field direction [
3], and behaves as a diamagnetic material when oxygenated and as a paramagnetic material when deoxygenated [
4].
The first mathematical model that described BFD flow under the action of an applied magnetic field was developed by Haik et al. [
1]. In Haik’s model, biofluids were modelled as isothermal, electrically non-conducting magnetic fluids (ferrofluids). Blood was modelled as a magnetic fluid, with its erythrocytes (due to erythrocytes blood exhibits polarization) being magnetic dipoles and the plasma the liquid carrier. Additionally, the ions in the blood plasma interact with an applied magnetic field. Therefore, blood can be modelled as an electrically conducting fluid which exhibits magnetization, such that magnetohydrodynamics (MHD) [
5] could also be incorporated into the mathematical model.
In theoretical hydrodynamics the study of a fluid with inner microstructure is considered as an interesting and challenging topic. The concept of microfluids introduced by Eringen [
6] to characterize concentrated suspensions of neutrally buoyant deformable particles in a viscous fluid. In micropolar fluids (a subclass of microfluids), rigid particles which are contained in a small representative volume element can rotate about the center of the volume, and their motion is by the microrotation vector [
7,
8]. The local rotation of the particles is independent of the mean fluid flow and the local vorticity flow field [
8]. Micropolar flow theory describes the non-Newtonian behavior of a category of fluids, such as liquid crystals, ferro-liquids, colloidal fluids, liquids with polymer additives, animal blood carrying deformable particles (platelets), clouds with smoke, suspensions, liquid crystals [
8,
9]. Additionally, micropolar fluids exhibit micro-rotational and micro-inertial effects. Therefore, the main advantage of using a micropolar fluid model to study the blood flow over non-Newtonian fluid models is that micropolar models incorporates the rotation of the fluid particles by means of an independent kinematic vector called the microrotation vector.
Fluid flow is different in micro scale compared to macro scale. In fact, there are flows where the Navier–Stokes equations, as derived through classical continuum theory, become incapable of explaining the micro scale fluid transport phenomena [
10]. Micropolar theories, which account for the microstructure of the fluid, appear as an alternative approach to numerically solve micro scale fluid dynamics, which are more computationally efficient than molecular dynamics (MD) simulations. Apart from the theoretical studies on micropolar fluid flow, there are studies that use micropolar theories to explain experimental observations in microchannels [
11,
12,
13,
14]. These experiments demonstrated the difference in flow regime of microflows and highlighted that in microscale fluid flows several effects, which are typically excluded from the macroscale (e.g., micro-rotational effects due to rotation of molecules), become important.
There are many physiological fluids that behave like suspensions of deformable or rigid particles in a Newtonian fluid. For example, blood is a suspension of red cells, white cells and platelets in plasma. Blood is a fluid that can be modelled as a micropolar fluids [
6,
9]. The experimental study of Bugliarello and Sevilla [
15] showed that blood plasma can be modelled like a Newtonian fluid and the erythrocytes like a Non-Newtonian core fluid region. Several theoretical studies [
16,
17,
18] on blood flow have assumed that blood behaves either as a Newtonian or as a non-Newtonian fluid. However, these studies fail to provide an estimate of the motion of red cells, white cells and platelets in plasma. It is therefore crucial to study the rheological properties of red and white cells and platelets to determine blood flow resistance in arteries and in vessels. Blood is a typical biomagnetic fluid due to the interaction of intercellular protein, cell membrane and hemoglobin.
In this study, we consider the biomagnetic fluid flow (blood flow), under the action of a magnetic field, for a two-dimensional duct with constriction. The micropolar/biofluid is considered to be viscous, incompressible and Newtonian, with the flow being laminar. The flow is subjected to an external magnetic field, which is generated with a magnet placed at a point in the proximity of the lower plate. The fluid is assumed to be poor conductor so that the induced magnetic field inside the fluid can be neglected. Under this assumption the flow is affected only by the magnetization of the fluid. The momentum equation takes into account the magnetization of the fluid, since the biomagnetic fluid flow is affected by the magnetization of the fluid due to the presence of the magnetic field. Although the fluid exhibits electrical conductivity, it may be taken as a poor conductor in which Lorentz force arising in magneto-hydrodynamics is much smaller in comparison to the magnetization force. Finally, it is also assumed that the magnetization of the biomagnetic fluid is varying linearly with the temperature of the fluid and the strength of the magnetic field.
We numerically solve the governing equations using the well-established meshless point collocation (MPC) method. The MPC method has been successfully applied to numerous problem in science and engineering involving fluid and solid mechanics applications, such as elasticity [
19], crack propagation [
20], heat transfer [
21], flow in porous media [
22], transport phenomena, to name a few. In particular, the proposed meshless scheme has been applied to a number of biomedical applications, such as tumor ablation [
23], neurosurgery [
24], soft tissue deformation [
25] and electrophysiology [
26]. This paper is organized as follows: in
Section 2 we present the governing equations, while in
Section 3 we briefly describe the discretization correction particle strength exchange (DC PSE) differentiation method and we discuss the solution procedure. issues related to the accuracy and the computational cost of the proposed scheme. In
Section 4 we verify the accuracy of our algorithm by comparing our results to finite element solutions. In
Section 5 we demonstrate the accuracy, efficiency and the ease of use of the proposed scheme using numerical examples. Finally,
Section 6 contains discussion and conclusions.
2. Governing Equations
We consider the laminar incompressible flow of a homogeneous, micropolar, Newtonian and electrically conducting fluid (blood). The micropolar fluid flows under the influence of a magnetic field. Two major forces act on the fluid, magnetization and Lorenz force. The first, applies due to the orientation of the erythrocytes along the magnetic field, while the second arises due to the electric current generating from the moving ions in the plasma. The biofluid under investigation (blood) is subjected to equilibrium magnetization, and its apparent viscosity due to magnetic field is negligible. Additionally, the contribution of the Lorentz force is incorporated in the mathematical model adopting flow principles of magnetohydrodynamics (MHD).
The following assumptions are made regarding of the blood flow: blood is an electrically conducting biomagnetic Newtonian fluid [
27,
28,
29]; the flow is laminar and the viscosity due to the magnetic field is considered to be negligible; the rotational forces acting on the erythrocytes when they enter and exit the magnetic field are discarded (equilibrium magnetization); the walls of the channel are electrically nonconducting and the electric field is considered negligible. Under these assumptions the governing flow equations are extended as:
where
is the velocity vector,
is the pressure,
T* is the fluid temperature and
N* is the microrotation vector,
is the density of the electric current,
is the magnetic induction,
is the electrical conductivity of the fluid,
is the Stokes tensor,
is the magnetization,
is the magnetic field intensity. Additionally, we assume that fluid mass density
, dynamic viscosity
, specific isobaric heat per unit mass
, heat conduction
and all micropolar fluid properties such as vortex viscosity coefficient
and microinertia
, are constant parameters.
is the dissipation function which for the three-dimensional case has the form (dropping the terms for the
z- component of velocity, and spatial derivatives with respect of
z we obtain the expression in two dimensions):
We consider flow in two dimensions and we write the governing equations in their velocity–vorticity formulation. We solve the steady-state N–S equations and therefore we drop the transient terms form the governing equations. For the case of two-dimensional plane flow the governing equations, in the velocity–vorticity formulation, are written as:
The term
represents the thermal power per unit volume due to the magnetocaloric effect. The term
in Equation (8) represents the Lorentz force per unit volume and arises due to the electrical conductivity of the fluid, where the same term in Equation (10) represents the Joule heating. The magnetization
is a function of the magnetic field intensity
and temperature
, following the formula
derived experimentally in [
11], with
is a constant and
is the Curie temperature. The components
and
of the magnetic field intensity
are given as
where
is the location (point) where the magnetic wire (current-carrying conductor) is placed, and
is the magnetic field strength at this point
. The magnitude
of the magnetic field intensity is given by:
We use the following non-dimensional parameters:
with
being the maximum velocity at the inlet of the channel,
and
the temperature at the upper and lower wall, respectively, and
. The non-dimensional form of the governing equations as:
with the non-dimensional parameters defined as
(Reynolds number),
(Eckert number),
(Temperature number),
(Prandtl number),
(Magnetic number from ferro-hydrodynamics),
(Magnetic number from magneto-hydrodynamics). The magnitude
of the magnetic field intensity is given by the relation
. The boundary conditions defined as
For the velocity–vorticity flow equations, we compute the updated vorticity values [
30] using the velocity field values and the strong form meshless discretization-corrected particle strength exchange (DC PSE) operators of the first order spatial derivative (see Equation (29)) as
.
4. Algorithm Verification
We verify the accuracy of the proposed scheme by comparing our numerical findings with those reported in [
27,
29]. We consider the biomagnetic fluid flow under the influence of an externally applied magnetic field in a channel with an unsymmetrical single stenosis and in a channel with irregular multi-stenoses (
Figure 1).
We assign values to the dimensionless parameters described in the governing equations based on the values reported in [
27,
29]. We set
,
and
. The length
and the width
of the unconstricted channel are taken as
and
, respectively. We use the iterative solution procedure, described in
Section 3.2, to obtain a steady-state solution for all the flow cases considered herein. To reach a steady-state solution, we set the convergence tolerance to
for the vorticity, microrotation and the temperature at each node of the flow domain.
4.1. Unsymmetrical Stenosis
As a first verification example we consider flow in a flow domain with an unsymmetrical stenosis downstream [
29] (
Figure 1a). The lower and upper walls of the channel are defined as:
The positive constants A1, A2 control the degree of constriction of the channel, while B1, B2 are the constants controlling the length of the stenosed area. The stenosed parts at the lower and the upper plates are positioned at sites with coordinates x1 and x2, respectively. Herein, we considered A1 = 0.5, A2 = 0.4, B1 = 6 and B2 = 4, while the stenosed sites were positioned at x1 = 3 and x2 = 4.
We consider a fixed location of the magnetic source
and we use different values for the magnetic numbers
and
. To represent the flow domain, we use a uniform Cartesian nodal distribution embedded into the flow domain (see
Figure 2). The nodal distribution applies by generating a grid that covers the symmetrical stenosis and identifying only those nodes that lie inside the geometry (nodes are also used on the boundaries). We use successively denser computational grids (point clouds) to ascertain a grid independent solution. The coarsest grid (Cloud 1) consists of 56,118 nodes (corresponding to
node spacing), and the densest (Cloud 4) of 298,176 nodes (corresponding to
0.0057 node spacing).
Table 1 lists the grid configurations used in the simulations.
To ensure a grid independent numerical solution we project the velocity, vorticity, temperature and stream function values computed using Cloud 1, 2 and 3 into Cloud 4. The results obtained with the finest grid are taken as reference. We apply the projection using the modified moving least s(MMLS) method [
38]. The accuracy of the proposed meshless scheme increases with increasing number of nodes and Cloud 3 offers a converged solution (see
Table 2).
Table 3 lists the computational time (in seconds) for computing the spatial derivatives for the grid resolutions listed in
Table 2, and for the numerical solution of governing equations (for each time iteration) in the case of
and
. It takes roughly 350 iterations to reach a normalized root mean square error of order
. The efficiency of the proposed scheme appears to be superior to finite element solvers used to numerically solve the steady-state Navier–Stokes equations [
39].
Figure 3 shows the stream function, vorticity and temperature contour plots for
and
and
and
, respectively. The numerical results obtained using the proposed meshless scheme are in a very good agreement with the numerical results reported in [
27].
4.2. Irregular Multi-Stenoses
In the second verification example, the flow domain is a channel with irregular multi-stenotic regions (see
Figure 1b). The flow domain narrows downstream with a symmetric stenosis close to the inlet and recovers its initial width. Then, a severe constriction follows which is unsymmetrically spread in the middle of the channel. After the recovery of the second stenosis, the channel narrows down gradually so that the exit diameter is less than the entrance diameter. The lower and upper walls of the channel are defined as:
with
being a positive constant (
), and the piecewise constant-valued functions
,
and
defined as:
To represent the flow domain, we use regular (uniform) nodal distribution embedded into the flow domain. The nodal distribution applies by generating a uniform Cartesian grid that covers the unsymmetrical stenosis and identifying only those nodes that lie inside the geometry (nodes are also used to represent the boundaries). We use a grid that consists of 56,118 nodes (corresponding to node spacing as in Cloud 3), which offers a converged solution. We consider a fixed location of the magnetic source and we use different values for the magnetic numbers and .
Figure 4 shows the streamlines, vorticity contours and isotherms for
,
and
,
, respectively.
Figure 5 shows the profile plots for the stream function (
), vorticity (
) and temperature (
) at different location of the flow domain, namely at
and 9. The numerical results obtained using the proposed meshless scheme are in a very good agreement with the results presented in [
27].
5. Numerical Results
In this section we investigate the influence of microrotation number (K) and Reynolds number on the flow regime. The fluid properties, the boundary conditions and external magnetic field, are identical to the previous cases.
We examine the biomagnetic fluid flow under the influence of an externally applied magnetic field in a channel with a single unsymmetrical stenosis, and with irregular multi-stenoses. Numerical studies on Newtonian [
11] and non-Newtonian [
17] blood flow through stenosed arteries demonstrated that the shape of the stenosis (single or multiple, symmetrical or unsymmetrical) affects the flow regime, and hence deserve special attention.
For the problems considered in this section, we assign flow (dimensionless) parameters directly related to blood flow. The density and dynamics viscosity of the blood are
and
, respectively, while the blood flows into the vessel with maximum velocity
and height (in the unconstricted region) of
. Furthermore, we consider a magnetic field strength of 8 T, and we set the temperature at the upper and lower wall of the vessel to
°C and
°C. In our study, we consider the Prandtl number
to be constant, despite that the dynamic viscosity
, the specific heat under constant pressure
and the thermal conductivity
are temperature dependent. Therefore, for the temperature range considered in this study, we set the specific heat to
and the thermal conductivity to
. For the aforementioned values
,
and
[
29]. The length and the width of the unconstricted channel are taken as
and
, respectively.
5.1. Dependence on Microrotation Number
In this section, we investigate the influence of the microrotation number (
K) on the flow regime (flow dynamics). We consider fluid flow in a channel with a unsymmetrical single stenosis and with irregular multi-stenoses (see
Figure 1).
For the unsymmetrical stenosis, we used A1 = 0.5, A2 = 0.4, B1 = 6 and B2 = 4, while the stenosed sites were positioned at x1 = 3 and x2 = 4. We consider a fixed location of the magnetic source . For the multiple stenosis flow case, we used A1 = 0.5, A2 = 0.4, B1 = 6 and B2 = 4, while the lower and the upper plates are positioned at x1 = 3 and x2 = 4, respectively. We consider a fixed location of the magnetic source
We use a uniform Cartesian grid, embedded into the irregular geometry, to represent the flow domain. In the unsymmetrical stenosis flow case, a grid of 151,703 nodes (corresponding to node spacing) is used, while in the channel with multiple stenosis we use a grid of 127,427 nodes (corresponding to node spacing). Both grid ensure grid independent numerical solutions. In our simulations, we set , , and and .
Figure 6 shows the streamlines, vorticity and microrotation contours, along with isotherms for the unsymmetrical stenosis flow case for different Reynolds numbers. It is well observed that the streamlines, vorticity and microrotation contours and the isotherms are distorted from being straight lines in the region after the stenosis. A vortex following the circulation is formed downstream of the stenosis close to the upper wall in both streamlines and isotherm profiles. As the microrotation number increases, the re-attachment length of the vortex decreases (the vortex is actually compressed). Additionally, the vortex formed at the upper wall of the stenosis is also compressed when microrotation number increases. The same pattern appears to vorticity, microrotation and temperature filed values.
Figure 7 shows the streamlines, vorticity and microrotation contours, along with isotherms obtained for the unsymmetrical stenosis flow case. In our simulations, we set
,
,
and
and
.
5.2. Dependence on Reynolds Number
In this section, we investigate the influence of the Reynolds number (
Re) on the flow regime. We consider flow in a channel with a unsymmetrical single stenosis, and with irregular multi-stenoses (see
Figure 1). For the unsymmetrical stenosis, we used
A1 = 0.5,
A2 = 0.4,
B1 = 6 and
B2 = 4, while the stenosed sites were positioned at
x1 = 3 and
x2 = 4. We consider a fixed location of the magnetic source
. For the multiple stenosis flow case, we used
A1 = 0.5,
A2 = 0.4,
B1 = 6 and
B2 = 4, while the lower and the upper plates are positioned at
x1 = 3 and
x2 = 4, respectively. We consider a fixed location of the magnetic source
.
We use a uniform Cartesian grid, embedded into the irregular geometry; to represent the flow domain, we use regular (uniform) nodal distribution embedded into the flow domain. In the case of the unsymmetrical stenosis, a grid of 151,703 nodes (corresponding to node spacing) is used, while in the channel with multiple stenosis we use a grid of 127,427 nodes (corresponding to node spacing). Both grid ensure grid independent numerical solutions. In our simulations, we set , , and and .
Figure 8 shows the streamlines, vorticity and microrotation contours, and isotherms for the unsymmetrical stenosis flow case for different Reynolds numbers. It is well observed that the streamlines, vorticity contours and the isotherms are distorted from being straight lines in the region after the stenosis. A vortex following the circulation is formed downstream of the stenosis close to the lower wall in both streamlines and isotherm profiles. As Reynolds number increases, a second vortex is formed in the upper wall just after the stenosis. For the microrotation, as the Reynolds number increases the iso-contour lines that form a vortex in the lower wall are stretched downstream and towards the upper wall. Additionally, a secondary vortex appears close to the upper wall.
Figure 9 shows the streamlines, vorticity and microrotation contours, and isotherms for the unsymmetrical stenosis flow case for different Reynolds numbers. It is well observed that the streamlines, vorticity contours and the isotherms are distorted from being straight lines in the region after the stenosis downstream. The vortex which is formed downstream of the stenosis close to the upper wall in both streamlines and isotherm profiles. As the Reynolds number increases, a second vortex is formed in the upper wall just after the stenosis. For the microrotation, as the Reynolds number increases the iso-contour lines that form a vortex in the lower wall are stretched downstream and towards the upper wall. Additionally, a secondary vortex appears close to the upper wall.