
A single blood vessel surrounded by the biological tissue with a tumor is considered. The influence of the heating technique (e.g. ultrasound, microwave, etc.) is described by setting a fixed temperature for the tumor which is higher than the blood and tissue temperature. The temperature distribution for the blood sub-domain is described by the energy equation written in the dual-phase lag convention, the temperature distribution in the biological tissue with a tumor is described also by the dual-phase lag equation. The boundary condition on the contact surface between blood vessel and biological tissue and the Neumann condition are also formulated using the extended Fourier law. So far in the literature, the temperature distribution in a blood vessel has been described by the classical energy equation. It is not clear whether the Fourier's law applies to highly heated tissues in which a significant thermal blood vessel is distinguished, therefore, taking into account the heterogeneous inner structure of the blood, the dual-phase lag equation is proposed for this sub-domain. The problem is solved by means of the implicit scheme of the finite difference method. The computations were performed for various values of delay times, which were taken from the available literature, and the influence of these values on the obtained temperature distributions was discussed.
Citation: Ewa Majchrzak, Mikołaj Stryczyński. Dual-phase lag model of heat transfer between blood vessel and biological tissue[J]. Mathematical Biosciences and Engineering, 2021, 18(2): 1573-1589. doi: 10.3934/mbe.2021081
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A single blood vessel surrounded by the biological tissue with a tumor is considered. The influence of the heating technique (e.g. ultrasound, microwave, etc.) is described by setting a fixed temperature for the tumor which is higher than the blood and tissue temperature. The temperature distribution for the blood sub-domain is described by the energy equation written in the dual-phase lag convention, the temperature distribution in the biological tissue with a tumor is described also by the dual-phase lag equation. The boundary condition on the contact surface between blood vessel and biological tissue and the Neumann condition are also formulated using the extended Fourier law. So far in the literature, the temperature distribution in a blood vessel has been described by the classical energy equation. It is not clear whether the Fourier's law applies to highly heated tissues in which a significant thermal blood vessel is distinguished, therefore, taking into account the heterogeneous inner structure of the blood, the dual-phase lag equation is proposed for this sub-domain. The problem is solved by means of the implicit scheme of the finite difference method. The computations were performed for various values of delay times, which were taken from the available literature, and the influence of these values on the obtained temperature distributions was discussed.
Modeling of the tissue heating process during thermal therapy is most often based on the well-known Pennes equation [1]. It is the classical Fourier's equation in which the source functions describing the blood perfusion and the metabolic heat generation are introduced. The form of this equation results from the assumption of instantaneous propagation of the thermal wave in the domain considered. In recent years, this model is often replaced by the Cattaneo-Vernotte equation [2,3] or the dual-phase lag equation [4]. In the Cattaneo-Vernotte equation the phase lag called the relaxation time τq appears. This parameter takes into account the effect of the finite value of the thermal wave velocity and it is the lag time of the heat flux in relation to the temperature gradient. In the dual-phase lag equation the additional parameter called the thermalization time τT is introduced, which takes into account the delay time of the temperature gradient in relation to the heat flux. The thermalization time takes into account the small-scale response in space while the relaxation time takes into account the small-scale response in time [4].
The thermally significant blood vessels can affect the temperature distribution in the heated tissue during thermal therapy, e.g. [5,6,7,8,9]. On the other hand, the influence of a strongly heated tumor region on the temperature distribution of blood flowing through the vessel is also interesting. The mathematical models of this type of phenomena used so far are based on the Fourier-Kirchhoff equation for the blood sub-domain and one of the equations mentioned above for the tissue sub-domain. In this paper the energy equation for the blood sub-domain is assumed in the convention of the dual-phase lag model and the temperature distribution in the tissue domain is also described by the dual-phase lag equation. The model is supplemented by the appropriate boundary and initial conditions. These conditions are formulated here on the basis of the extended Fourier law in which the relaxation and thermalization times appear [10,11,12]. To the best of our knowledge, the extended energy equation with two lag times is presented here for the first time. The problem formulated is solved using the implicit scheme of the finite difference method. In the final part of the paper the results of computations are shown and the conclusions are presented.
Heat conduction for the macroscale problems is described by the Fourier law
q(X,t)=−λ∇T(X,t) | (1) |
where λ is the thermal conductivity of the material, ∇T(X,t) is the temperature gradient, q (X, t) is the heat flux, X, t are the geometrical co-ordinates and time. Introducing the formula (1) to the Fourier-Kirchhoff equation [13]
cρ[∂T(X,t)∂t+w⋅∇T(X,t)]=−∇⋅q(X,t)+Q(X,t) | (2) |
one obtains equation in the form
cρ[∂T(X,t)∂t+w⋅∇T(X,t)]=∇[λ∇T(X,t)]+Q(X,t) | (3) |
where c is the specific heat, ρ is the mass density, w is the velocity vector and Q (X, t) is the capacity of internal heat sources.
The generalization of the Fourier is presented by Tzou [4], in particular
q(X,t+τq)=−λ∇T(X,t+τT) | (4) |
where τq and τT are the phase lags.
Using the Taylor series expansions, the following first-order approximation of Eq (4) is obtained
q(X,t)+τq∂q(X,t)∂t=−λ[∇T(X,t)+τT∂∇T(X,t)∂t] | (5) |
From Eq (5) it follows that
−q(X,t)=τq∂q(X,t)∂t+λ[∇T(X,t)+τT∂∇T(X,t)∂t] | (6) |
Introducing this formula to the Eq (2) one has
cρ[∂T(X,t)∂t+w⋅∇T(X,t)]=τq∂∂t[∇⋅q(X,t)]+∇[λ∇T(X,t)]+τT∇[λ∂∇T(X,t)∂t]+Q(X,t) | (7) |
Because (c.f. Eq (2))
∇⋅q(X,t)=−cρ[∂T(X,t)∂t+w⋅∇T(X,t)]+Q(X,t) | (8) |
thus
cρ[∂T(X,t)∂t+w⋅∇T(X,t)]=τq∂∂t{−cρ[∂T(X,t)∂t+w⋅∇T(X,t)]+Q(X,t)}+∇[λ∇T(X,t)]+τT∇[λ∂∇T(X,t)∂t]+Q(X,t) | (9) |
or
cρ[∂T(X,t)∂t+w⋅∇T(X,t)]+τq∂∂t[cρ[∂T(X,t)∂t+w⋅∇T(X,t)]]=∇[λ∇T(X,t)]+τT∂∂t[∇[λ∇T(X,t)]]+Q(X,t)+τq∂Q(X,t)∂t | (10) |
For the constant thermophysical parameters the Eq (10) takes a form
cρ[∂T(X,t)∂t+w⋅∇T(X,t)+τq∂2T(X,t)∂t2+τq∂[w⋅∇T(X,t)]∂t]=λ∇2T(X,t)+λτT∂[∇2T(X,t)]∂t+Q(X,t)+τq∂Q(X,t)∂t | (11) |
It should be noted that in the case of the dual-phase lag model the boundary conditions should be formulated in a different way than in the Fourier model [10,11,12]. For example, the Neumann boundary condition has the following form
qb(X,t)+τq∂qb(X,t)∂t=−λ[n⋅∇T(X,t)+τT∂[n⋅∇T(X,t)]∂t] | (12) |
where n is the normal outward vector and qb (X, t) is the known boundary heat flux.
Under the assumption that for t = 0: ∇T(X,t)=0 and ∇⋅q(X,t)=0 (Eq (2)), the initial conditions are the following [14]
t=0:T(X,t)=Tp,∂T(X,t)∂t|t=0=Q(X,0)cρ | (13) |
where Tp is the initial temperature.
A single blood vessel and surrounding biological tissue with a tumor region, as shown in Figure 1, is considered (axisymmetric problem). As in the paper [8], it is assumed that the influence of the heating technique (e.g. ultrasound, microwave, etc.) is described by setting a fixed temperature for the tumor which is higher than the blood and tissue temperature.
Blood temperature is described by the equation (c.f. Eq (11))
cbρb(∂Tb∂t+v∂Tb∂z+τqb∂2Tb∂t2+τqbv∂2Tb∂t∂z)=λb∇2Tb+τTbλb∂(∇2Tb)∂t+Qmetb | (14) |
where
∇2Tb=1r∂∂r(r∂Tb∂r)+∂2Tb∂z2=1r∂Tb∂r+∂2Tb∂r2+∂2Tb∂z2 | (15) |
and v is the blood flow velocity in the axial direction, Qmet b is the metabolic heat source (constant value of Qmet b is assumed here), while Tb = Tb(r, z, t).
Temperature field in the tissue with a tumor is described by equation
cρ(∂T∂t+τq∂2T∂t2)=λ∇2T+λτT∂(∇2T)∂t+Q+τq∂Q∂t | (16) |
where
Q=wbcb(Ta−T)+Qmet | (17) |
while wb is the blood perfusion rate, Ta is the arterial blood temperature, Qmet is the metabolic heat source (constant value of Qmet is assumed here) and T = T(r, z, t).
On the contact surface between blood vessel and biological tissue the continuity condition of temperature and heat flux is assumed
(r,z)∈Γc:{Tb=Tqb=q | (18) |
On the outer surface of the tissue the constant temperature (body core temperature) is accepted. For z = 0, z = Z and r = 0 the no-flux conditions are assumed.
The initial conditions are also known (c.f. Eq (13))
t=0:Tb=T=Tp,∂Tb∂t|t=0=Qmetbcbρb,∂T∂t|t=0=wbcb(Ta−Tp)+Qmetcρ | (19) |
It should be noted that in the condition (18) the dependence (12) must be taken into account. After mathematical manipulations one has [12]
(r,z)∈Γc:{Tb=T−λbn⋅∇Tb−λb(τTb+τq)∂(n⋅∇Tb)∂t−λbτqτTb∂2(n⋅∇Tb)∂t2=−λn⋅∇T−λ(τT+τqb)∂(n⋅∇T)∂t−λτqbτT∂2(n⋅∇T)∂t2 | (20) |
The problem formulated is solved using implicit scheme of the finite difference method. Let Tfi,j=T(ri,zj,fΔt) where ∆t is the time step, ri = ih, zj = jk (Figure 2) and f = 0, 1, …, F. Taking into account the initial conditions (19) one has: T0i,j=Tp, for blood subdomain: T1i,j=Tp+QmetbΔt/(cbρb), for tissue sub-domain: T1i,j=Tp+[wbcb(Ta−Tp)+Qmet]Δt/(cρ+τqwbcb).
For transition tf → tf+1(f ≥ 1) the following approximate form of Eq (14) resulting from the introduction of adequate differential quotients is used
cbρbTf+1i,j−Tfi,jΔt+cbρbτqbTf+1i,j−2Tfi,j+Tf−1i,j(Δt)2=λb(∇2Tb)f+1i,j+λbτTbΔt[(∇2Tb)f+1i,j−(∇2Tb)fi,j]+Qb−cbρbvTf+1i,j+1−Tf+1i,j−12k−cbρbτqbvΔt(Tf+1i,j+1−Tf+1i,j−12k−Tfi,j+1−Tfi,j−12k) | (21) |
or
cbρbTf+1i,j−Tfi,jΔt+cbρbτqbTf+1i,j−2Tfi,j+Tf−1i,j(Δt)2=λb(Δt+τTb)Δt(∇2Tb)f+1i,j−λbτTbΔt(∇2Tb)fi,j+Qb−cbρbv(Δt+τqb)(Tf+1i,j+1−Tf+1i,j−1)2kΔt+cbρbτqbv(Tfi,j+1−Tfi,j−1)2kΔt | (22) |
where
(∇2Tb)pi,j=1ri,jTpi+1,j−Tpi−1,j2h+Tpi−1,j−2Tpi,j+Tpi+1,jh2+Tpi,j−1−2Tpi,j+Tpi,j+1k2 | (23) |
while p = f or p = f+1.
After mathematical manipulations one has
Tf+1i,j=λb(Δt+τTb)DΔt(1ri,jTf+1i+1,j−Tf+1i−1,j2h+Tf+1i−1,j+Tf+1i+1,jh2+Tf+1i,j−1+Tf+1i,j+1k2)−λbτTbDΔt(1ri,jTfi+1,j−Tfi−1,j2h+Tfi−1,j−2Tfi,j+Tfi+1,jh2+Tfi,j−1−2Tfi,j+Tfi,j+1k2)+QbD−cbρbv(Δt+τqb)(Tf+1i,j+1−Tf+1i,j−1)2kΔtD+cbρbτqbv(Tfi,j+1−Tfi,j−1)2kΔtD+cbρb(Δt+2τqb)D(Δt)2Tfi,j−cbρbτqbD(Δt)2Tf−1i,j | (24) |
where
D=cbρb(Δt+τqb)(Δt)2+2λb(Δt+τTb)h2Δt+2λb(Δt+τTb)k2Δt | (25) |
Approximate form of Eq (16) is the following
cρTf+1i,j−Tfi,jΔt+cρτqTf+1i,j−2Tfi,j+Tf−1i,j(Δt)2=λ(∇2T)f+1i,j+λτTΔt[(∇2T)f+1i,j−(∇2T)fi,j]+wbcb(Ta−Tf+1i,j)+Qmet−τqwbcbTf+1i,j−Tfi,jΔt | (26) |
or
(cρ+τqwbcb)Tf+1i,j−Tfi,jΔt+cρτqTf+1i,j−2Tfi,j+Tf−1i,j(Δt)2=λ(Δt+τT)Δt(∇2T)f+1i,j−λτTΔt(∇2T)fi,j+wbcb(Ta−Tf+1i,j)+Qmet | (27) |
and after mathematical manipulations one has
Tf+1i,j=λ(Δt+τT)EΔt(1ri,jTf+1i+1,j−Tf+1i−1,j2h+Tf+1i−1,j+Tf+1i+1,jh2+Tf+1i,j−1+Tf+1i,j+1k2)−λτTEΔt(1ri,jTfi+1,j−Tfi−1,j2h+Tfi−1,j−2Tfi,j+Tfi+1,jh2+Tfi,j−1−2Tfi,j+Tfi,j+1k2)+(cρ+τqwbcb)Δt+2cρτqE(Δt)2Tfi,j−cρτqE(Δt)2Tf−1i,j+wbcbTa+QmetE | (28) |
where
E=(cρ+τqwbcb)Δt+cρτq(Δt)2+2λ(Δt+τT)h2Δt+2λ(Δt+τT)k2Δt+wbcb | (29) |
The second part of boundary condition (20) is approximated with respect to time in the following way
−λb(n⋅∇Tb)f+1−λb(τTb+τq)1Δt[(n⋅∇Tb)f+1−(n⋅∇Tb)f]−λbτqτTb1(Δt)2[(n⋅∇Tb)f+1−2(n⋅∇Tb)f+(n⋅∇Tb)f−1]=−λ(n⋅∇T)f+1−λ(τT+τqb)1Δt[(n⋅∇T)f+1−(n⋅∇T)f]−λτqbτT1(Δt)2[(n⋅∇T)f+1−2(n⋅∇T)f+(n⋅∇T)f−1] | (30) |
or
A1(n⋅∇Tb)f+1−A3(n⋅∇Tb)f+A5(n⋅∇Tb)f−1=A2(n⋅∇T)f+1−A4(n⋅∇T)f+A6(n⋅∇T)f−1 | (31) |
where
A1=λb(Δt)2+Δt(τTb+τq)+τqτTb(Δt)2,A2=λ(Δt)2+Δt(τT+τqb)+τqbτT(Δt)2A3=λbΔt(τTb+τq)+2τqτTb(Δt)2,A4=λΔt(τT+τqb)+2τqbτT(Δt)2,A5=λbτqτTb(Δt)2,A6=λτqbτT(Δt)2 | (32) |
Let (s, j) is the node located on the contact surface. Taking into account the first part of boundary condition (20), one obtains
A1Tf+1s,j−Tf+1s−1,jh−A3Tfs,j−Tfs−1,jh+A5Tf−1s,j−Tf−1s−1,jh=A2Tf+1s+1,j−Tf+1s,jh−A4Tfs+1,j−Tfs,jh+A6Tf−1s+1,j−Tf−1s,jh | (33) |
or
Tf+1s,j=A1A1+A2Tf+1s−1,j+A2A1+A2Tf+1s+1,j+A3A1+A2(Tfs,j−Tfs−1,j)−A4A1+A2(Tfs+1,j−Tfs,j)−A5A1+A2(Tf−1s,j−Tf−1s−1,j)+A6A1+A2(Tf−1s+1,j−Tf−1s,j) | (34) |
The no-flux boundary condition (c.f. Eq (12))
n⋅∇T(X,t)+τT∂[n⋅∇T(X,t)]∂t=0 | (35) |
is approximated with respect to time, namely
(n⋅∇T)f+1+τTΔt[(n⋅∇T)f+1−(n⋅∇T)f]=0 | (36) |
For the nodes with the coordinate z = 0 one has
Δt+τTΔtTf+1i,1−Tf+1i,0k−τTΔtTfi,1−Tfi,0k=0 | (37) |
and then
Tf+1i,0=Tf+1i,1−τTΔt+τT(Tfi,1−Tfi,0) | (38) |
Similarly, for nodes with the coordinate z = Z one obtains
Δt+τTΔtTf+1i,n−Tf+1i,n−1k−τTΔtTfi,n−Tfi,n−1k=0 | (39) |
and then
Tf+1i,n=Tf+1i,n−1+τTΔt+τT(Tfi,n−Tfi,n−1) | (40) |
For each transition tf → tf+1(f ≥ 1) the system of Eqs (24), (28), (34), (38) and (40) is solved using the iterative method.
The thermally significant blood vessel of dimensions R = 0.001 m, Z = 20R = 0.02 m is considered. The blood flow velocity is equal to v = 0.2 m/s [6,15]. The outer radius of the domain considered is R1 = 5R. The heating target volume (tumor) is specified as 1.5R ≤ r ≤ 2.5R, 1.5Z/4 ≤ z ≤ 3Z/4 (Figure 1). The following values of thermophysical parameters are assumed: thermal conductivities λb = 0.488 W/(m K), λ = 0.5 W/(m K), specific heats cb = 3770 J/(kgK), c = 4000 J/(kgK), mass densities ρb = 1060 kg/m3, ρ = 1000 kg/m3, metabolic heat sources Qmetb = 245 W/m3, Qmet = 245 W/m3, blood perfusion rate wb = 0.5 kg/(m3 s), arterial blood temperature Ta = 37 ℃ [16].
The values of phase lags reported in literature vary greatly from one to another. For example, in the papers [9,17] the relaxation and thermalization times are of the order of 10 s. On the other hand, in the paper [18] it is found that the phase lag times for heat flux and temperature gradient for the living tissues are very close to each other and are within the range [0.464 s, 6.825 s]. Due to the lack of precise data, in this work the extreme values of time delays, namely τqb = τq = τTb = τT = 0.464 s and τqb = τq = τTb = τT = 6.825 s are considered and as suggested by Zhang [18], the same values of these delay times are accepted.
The initial temperature of tissue and blood is equal to Tp = 37 ℃, on the outer surface of the tissue the boundary temperature equals 37 ℃, while in the tumor region the constant temperature 45 ℃ is accepted.
The computations have been done under the assumption that m = 50, n = 200, m1 = 15, m2 = 25, n1 = 50, n2 = 150 (Figure 2) and Δt = 0.005 s.
In Figures 3 and 4 the temperature distribution after 5 second is shown. Figures 5 and 6 illustrate the temperature history at the points A (0.0014 m, 0.01 m), B (0.003 m, 0.01 m) obtained using the DPL model and the classical ones. As one can see, for small values of time delays (Figure 5) the temperature values in the domain stabilize quite quickly and the system reaches the steady state conditions, while for large values of time delays (Figure 6), this process takes much longer. The differences between the courses of thermal processes are great especially in the initial stage of heating. After reaching the steady state, the curves coincide, of course. As expected, the heating process is slower for the model with lag times and the longer delay times prolong the duration of the tissue heating process.
Figures 7–9 illustrate the temperature distribution in the radial direction for z = Z/2 = 0.01 m for DPLM and models based on the Fourier-Kirchhoff equations, respectively. The curves correspond to times of 1, 2, 3, 4 and 5 s. In the blood sub-domain (r ≤ 0.001 m), a slight increase in temperature is observed only near the blood vessel wall. The introduction of delay times slows down the changes of instantaneous and local temperatures in the sub-domains considered.
As can be seen in the previous Figures, the temperature in the blood vessel does not change much. Figures 10 and 11 show the changes in the temperature of the blood vessel wall along the z axis for times 1, 2, 3, 4 and 5 s. The influence of the increased temperature in the tumor region on the changes in the wall temperature is clearly visible. Outside of this region, its temperature varies to a small extent. For low values of delay times (Figure 7), after about five seconds the system reaches steady state conditions, while for large values of delay times (Figure 8) it is just the beginning of the heating process.
It should be noted that the influence of the blood flow direction on the computations results is clearly visible. As it approaches the heated tumor, the blood warms up more and more, and it cools more slowly as it leaves the heated sub-domain.
As mentioned before, in this paper the energy equation for the blood sub-domain is assumed in the convention of the dual-phase lag model. Therefore, it should be checked whether the introduction of delay times to the equation describing the temperature field in the blood sub-domain significantly changes the computations results. For this purpose, calculations were made for τqb = τq = 3 s, τTb = τT = 1 s [19] (the same relaxation time and thermalization time for both sub-domains) and τqb = τTb = 0, τq = 3 s, τT = 1 s, respectively (mixed model).
The results of the comparison are presented in the form of heating curves at the points A and B (Figure 12) and additionally at the point C (0.0009 m, 0.01 m) located in the blood sub-domain and at the point D (0.001m, 0.01 m) located on the blood vessel wall (Figure 13).
As can be seen, the differences are slight and do not exceed 0.5 ℃ on the blood vessel wall (point D) and are practically invisible in the blood vessel sub-domain (point C) as well as in the tissue sub-domain (points A and B). Summing up, the introducing the delay times into the equation describing the temperature distribution in the blood vessel has a relatively small impact on the results (for the assumed values of relaxation and thermalization times, of course).
The single blood vessel surrounded by the biological tissue with a tumor has been considered. A constant temperature of 45 ℃ has been assumed in the heated tumor region. The temperature fields have been described by dual-phase lag equation both for the blood region as well as for the tissue with a tumor. For comparison, the classical models have been also considered. Additionally, computations were made for the 'mixed' model, in which the temperature field in the tissue sub-domain is described by the DPL equation, while the temperature field in the blood vessel by the classical model. For such formulated mathematical description, an algorithm based on FDM in an implicit form was presented. The numerous numerical computations concerning the different variants of the basic model have been made. It turned out (which could of course be expected) that the visible differences between the solutions can be observed. The limit results of all variants for the steady state coincide, which confirms the correctness of the assumed numerical algorithm.
It should be noted that for all variants of computations and assumed delay times, the temperature in the blood vessel did not rise much (about 1 ℃), mostly near the blood vessel wall. Comparison of the calculation results obtained by the DPL model and mixed model in which the classical equation for the blood sub-domain has been assumed showed slight changes in temperature.
Obviously, the results are closely related to the adopted relaxation and thermalization times, and there is a need for further experimental studies to more accurately estimate these delay times.
Here, a constant temperature of the tumor region has been assumed. In future, the heating schemes should be taken into account, this means the external heating power density and heating duration [6,7].
The research is financed from financial resources from the statutory subsidy of the Faculty of Mechanical Engineering, Silesian University of Technology in 2021.
Authors declare no conflicts of interest in this paper.
[1] |
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