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Applied Mathematics
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(English Edition)
76A05
Introduction
A working fluid is involved in many engineering and industrial processes which is used to
transfer energy/heat from one position to another position. The enhancement in energy transfer
has been a serious issue for a long time. Nanofluid is a better candidate in this regard. Advancement in nanoparticles is acting as a new heat transfer medium which introduced new and
high potentials. The common working fluids involved in industry and engineering processes
have less thermal conductivity in comparison to metal and metal oxides. An enhancement
in heat transfer performance can be obtained by adding high conductivity materials in base
fluids[12] . The betterment in the performance of thermal conductivity without causing a pressure drop is the major advantage of nanofluids. As a consequence, the performance of various
heat transfer devices is increased, which leads to the larger capacity of operating systems. Such
fluids are looking to be very interesting in transportation, nuclear reactors, solar collectors,
car radiators, chillers, micro-electro mechanical systems, cooling of electronic devices, and in
cooling/heating of energy conversion. Having such in view, Oztop and Abu-Nada[3] discussed
the buoyancy driven flow of nanofluid filled in an enclosure. A numerical solution was presented. Turkyilmazoglu[4] presented a study to analyze the magnetohydrodynamic (MHD) flow
Received Jan. 12, 2014 / Revised Jun. 18, 2014
Project supported by the Deanship of Scientific Research (DSR), King Abdulaziz University, Jeddah,
Saudi Arabia (No. 37-130-35-HiCi)
Corresponding author S. A. SHEHZAD, Professor, Ph. D., E-mail: ali qau70@yahoo.com
70
of nanofluid with heat and mass transfer in the presence of thermal slip boundary condition.
Both exact and analytical solutions were given. The boundary flow of nanofluid over a vertical plate with convective thermal condition was examined by Rashidi et al.[5] . They used the
differential transform method to obtain the results of the velocity, the temperature, and the volumetric fraction of nanoparticles. The effect of double-stratification was numerically analyzed
on the boundary layer flow of nanofluid over a vertical flat plate by Ibrahim and Makinde[6] .
Moradi et al.[7] studied the Jeffery-Hamel flow of nanofluid with viscous dissipation. Hatami
and Ganji[8] carried out an analysis to examine the sodium alginate (SA) TiO2 non-Newtonian
nanofluid passing through a porous medium between two coaxial cylinders. Sheikholeslami et
al.[9] investigated the flow of nanofluid in a semi-porous channel. They computed the solution
expressions using the least square and Galerkin methods. The effects of the buoyancy force,
convective heating, the Brownian motion, and thermophoresis in the MHD stagnation point
flow of nanofluid were examined by Makinde et al.[10] . They obtained the numerical solution
by the Runge-Kutta fourth-order scheme.
The boundary layer flow of non-Newtonian fluid over a surface has attained considerable
attention from the recent investigators due to its broad applications in the industrial and engineering processes. More specifically, the flow and heat transfer of non-Newtonian fluids have key
importance in power engineering, petroleum production, polymer solutions, paper production,
etc. The fluid model under consideration is an Oldroyd-B fluid, which falls into the category
of rate type non-Newtonian fluid. It exhibits the characteristics of the relaxation time and the
retardation time. Very little has been said yet about the boundary layer flow of the Oldroyd-B
fluid. Sajid et al.[11] initiated the boundary layer stagnation point flow of an Oldroyd-B fluid
towards a stretching surface. They presented the results numerically. Hayat et al.[12] extended
this analysis for the three-dimensional flow of an Oldroyd-B fluid with a convective boundary
condition. The three-dimensional flow of an Oldroyd-B fluid with variable thermal conductivity and heat generation/absorption was recently addressed by Shehzad et al.[13] . Moreover, the
importance of thermal radiation is prevalent in the industrial and space technological processes
at very high temperature. Examples of such processes are glass production and furnace design,
comical flight aerodynamic rocket, space craft re-entry, plasma physics, propulsion systems, etc.
Further, the heat generation/absorption plays a vital role in disassociating fluids in packed-bed
reactors, storage of food stuffs, and heat removal from nuclear fuel debris, underground disposal
of radioactive waste material, and many others[1418] .
The present investigation deals with the two-dimensional boundary layer flow of an OldroydB fluid with nanoparticles. Mathematical formulation consists of convective heat and mass conditions. Besides these, the contributions due to thermal radiation and heat generation/absorption are also taken into account. The governing nonlinear problems are computed for the series solutions through the homotopy analysis method (HAM)[1925] . Discussion reflecting the
interpretation of sundry parameters is made. Important conclusions are presented.
Mathematical formulation
(1)
71
2u
3u
3 u u 2 u u 2 u
+
u
+v
,
2
y 2
xy 2
y 3
x y 2
y y 2
T
T
2T
C T
DT T 2
1 qr
Q
+v
= 2 + DB
+
+
(T T ),
u
x
y
y
y y
T y
(c)f y
(c)f
C
C
2C
DT 2 T
+v
= DB 2 +
.
x
y
y
T y 2
(2)
(3)
(4)
v = 0,
T T ,
C C
T
= h1 (Tf T ),
y
as y ,
DB
C
= h2 (Cf C)
y
at y = 0,
(5)
(6)
where u and v are the velocity components in the x- and y-directions, is the kinematic viscosity,
1 and 2 are the relaxation time and the retardation time, respectively, f is the density of
(c)
fluid, is the thermal diffusivity, (= (c)pf ) is the ratio of the nanoparticle heat capacity and
the base fluid heat capacity, qr is the radiative heat flux, Q is the heat source/sink parameter,
DB is the Brownian diffusion coefficient, DT is the thermophoretic diffusion coefficient, k is the
thermal conductivity, uw is the stretching velocity at the wall, and T and C are the ambient
temperature and the concentration, respectively.
The radiative heat flux qr using Rosselands approximation gives
qr =
4 T 4
,
3k y
(7)
in which is the Stefan-Boltzmann constant, and k is the mean absorption coefficient. The
temperature difference within the flow is assumed in such a manner that T 4 can be written in
the linear combination of temperature. By expanding T 4 about T in terms of Taylors series
and neglecting higher order terms, we have
4T 3 T 3T 4
(8)
T4 =
and
3
qr
16T
2T
=
.
y
3k y 2
(9)
3
T
T
2T
C T DT T 2
1 16T
2T
Q
+v
= 2 + DB
+
+
+
(T T ). (10)
x
y
y
y y T y
(c)f 3k y 2 (c)f
v = cf (),
=y
c
,
() =
T T
,
Tf T
() =
C C
.
Cf C
(11)
f + f f f 2 + 1 (f 2 f 2f f f ) + 2 (f f f 2 ) = 0,
(12)
4
1 + Tr + P rf + P rNb + P rNt 2 + P rS = 0,
3
(13)
f = 1,
0,
= Bi1 (1 (0)),
0
as
= Bi2 (1 (0))
(14)
at
= 0,
(15)
(16)
72
where 1 = 1 c is the Deborah number with respect to the relaxation time, 2 = 2 c is the
Deborah number with respect to the retardation time, P r = / is the Prandtl number, Tr =
3
4T
/(kk ) is the radiation parameter, Sc = /DB is the Schmidt number, Nb = (c)p DB (Cf
C )/((c)f ) is the Brownian motion parameter,
f T ) is the
p
p Nt = (c)p DT (Tf T )/((c)
thermophoresis parameter, and Bi1 (= (h1 /k) /a) and Bi2 (= (h2 /DB ) /a) are the Biot
numbers. The local Nusselt number and the local Sherwood number are given by
Nux =
xqw
,
k(Tf T )
Shx =
xqm
,
DB (Cf C )
(17)
where qw is the surface heat flux, and qm is the surface mass flux. The local Nusselt and local
Sherwood numbers in dimensionless forms are given below:
4
Tr (0), Shx /Re1/2
= (0),
(18)
Nux /Re1/2
=
1
+
x
x
3
where Rex = uw (x)x/ is the local Reynolds number.
(19)
akm,n k exp(n),
(20)
bkm,n k exp(n),
(21)
ckm,n k exp(n),
(22)
n=0 k=0
m () =
n=0 k=0
m () =
n=0 k=0
in which akm,n , bkm,n , and ckm,n are the coefficients. The initial guesses and auxiliary linear
operators are selected in the following forms:
f0 () = 1 exp(),
L(f ) = f f ,
0 () =
Bi1 exp()
,
1 + Bi1
L() = ,
0 () =
L() =
Bi2 exp()
,
1 + Bi2
(23)
(24)
L()(C4 e + C5 e ) = 0,
L()(C6 e + C7 e ) = 0, (25)
where Ci (i = 1, 2, , 7) are the arbitrary constants. The zeroth order problems are defined
as follows[2025] :
(1 q) L(f ) f(; q) f0 () = q~f Nf f(; q) ,
(26)
q) 0 () = q~ N f(; q), (,
q), (,
(1 q) L() (;
q) ,
(27)
q) 0 () = q~ N f(; q), (,
q), (,
(1 q) L() (;
q) ,
(28)
f (; q) = 0, (,
q) = 0, (,
q) = 0,
3 f(, q)
2 f(, q) f(, q) 2
Nf [f(, q)] =
+
f
(,
q)
3
2
3
2
2 f(, q)
(, q) f (, q) f (, q)
+ 1 f(, q)
2
f
3
2
2 f(, q) 2
4
f
(,
q)
+ 2 f(, q)
,
4
2
2
(,
q) 2
q),
+ P rS (,
+ P rNt
2
2
q)] = (, q) + Scf(, q) (, q) + Nt (, q) ,
N [(,
q), f(, q), (,
2
Nb
2
73
(29)
(30)
(31)
(32)
where ~f , ~ , and ~ are the non-zero auxiliary parameters, q [0, 1] is an embedding parameter, and Nf , N , and N are the nonlinear operators. Putting q = 0 and q = 1, one
has
(
0) = 0 (), (,
0) = 0 (),
f(; 0) = f0 (), (,
(33)
f (, q) = f0 () +
(, q) = 0 () +
m=1
m=1
fm ()q m ,
(34)
m ()q m ,
(35)
m ()q m ,
(36)
(, q) = 0 () +
m=1
1 m f (; q)
,
f
()
=
m
m!
m q=0
1 m (; q)
m () =
,
m!
m q=0
1 (; q)
.
m () =
m!
m q=0
(37)
The convergence of the above series highly depends upon the suitable values of ~f , ~ , and
~ . Considering that ~f , ~ , and ~ are selected properly such that Eqs. (34)(36) converge at
74
q = 1, we have
f () = f0 () +
() = 0 () +
m=1
m=1
fm (),
(38)
m (),
(39)
m ().
(40)
() = 0 () +
m=1
fm () = fm
() + C1 + C2 e + C3 e ,
(41)
m () = m
() + C4 e + C5 e ,
(42)
m () = m () + C6 e + C7 e ,
(43)
where fm
, m
, and m () are the special solutions.
The auxiliary parameters ~f , ~ , and ~ are important in controlling and adjusting the
convergence region of series solutions. We plot the ~-curves at the 22nd-order of HAM approximations in order to find the appropriate values. It is noted from Fig. 1 that the suitable values of
~f , ~ , and ~ are 1.45 6 ~f 6 0.10, 1.25 6 ~ 6 0.50, and 1.20 6 ~ 6 0.30, respectively. The series converge in the whole region of when ~f = ~ = ~ = 0.8 (see Table 1).
Fig. 1
Table 1
~-curves for functions f (0), (0), and (0) at 22nd-order of approximations when 1 = 2 =
0.3, S = 0.1, P r = 1.0, Sc = 0.8, Nt = 0.2, Nb = 0.3, Bi1 = Bi2 = 0.8, and Tr = 0.4
Convergence of homotopy solution for different orders of approximations when 1 = 2 =
0.2, S = 0.1, P r = 1.2, Sc = 1.0, Nt = Nb = 0.3, Bi1 = Bi2 = 0.5, Tr = 0.4, and ~f = ~ =
~ = 0.8
Order of approximation
01
05
10
20
30
35
40
45
f (0)
0.960
0.959
0.959
0.959
0.959
0.959
0.959
0.959
000
758
754
754
754
754
754
754
(0)
0.258
0.209
0.195
0.188
0.187
0.186
0.186
0.186
07
21
39
59
02
77
77
77
(0)
0.259
0.226
0.219
0.217
0.217
0.217
0.217
0.217
26
10
72
96
85
85
85
85
75
We plot Figs. 29 to examine the behaviors of the Deborah numbers 1 and 2 , the Prandtl
number P r, the Biot number Bi1 , the thermophoresis and Brownian motion parameters Nt
and Nb , the radiation parameter Tr , and the heat generation parameter S on the dimensionless
temperature (). The variations in the temperature () for different values of the Deborah
number 1 are seen in Fig. 2. Here, one can see that the temperature is lower for smaller values
of the Deborah number 1 and higher for larger values of the Deborah number. Since the
Deborah number 1 is directly proportional to the relaxation time, an increase in the value of
1 corresponds to an increase in the relaxation time. Higher relaxation time gives rise to the
temperature and the thermal boundary layer thickness. It is noted from Fig. 3 that the temperature and the thermal boundary layer thickness are reduced with an increase in the Deborah
number 2 . This is due to the fact that the Deborah number 2 is directly proportional to
the retardation time. An increase in the retardation time corresponds to lower temperature
and thinner thermal boundary layer. The comparison of Figs. 2 and 3 shows that the Deborah
numbers 1 and 2 have reverse effects on the temperature. Figure 4 depicts that both the
temperature and the thermal boundary layer thickness increase when the values of the Prandtl
number are smaller. The Prandtl number is the ratio of momentum to thermal diffusivities. A
reduction in the value of the Prandtl number implies higher thermal diffusivity and smaller momentum diffusivity. Higher thermal diffusivity and lower momentum diffusivity are responsible
for an increase in the temperature when the value of the Prandtl number decreases. Figure 5
illustrates that the temperature increases for larger Biot number Bi1 . It is seen that beyond
Bi1 = 0.8, the increase in the temperature slows down. An increase in the temperature corresponding to the Biot number Bi1 is due to the heat transfer coefficient h1 . The definition of
Bi1 involves the heat transfer coefficient h1 . The heat transfer coefficient increases when the
value of Bi1 increases. This increase in the heat transfer coefficient leads to an enhancement
in the temperature and the thermal boundary layer thickness. Variations in temperature vs.
for different values of the thermophoresis and Brownian motion parameters are examined in
Figs. 6 and 7. These figures show that the temperature is enhanced for larger values of the
thermophoresis and Brownian motion parameters. Also, we notice that the variations in the
temperature due to the thermophoresis parameter are much more than the variations due to
the Brownian motion parameter. An increase in the radiation parameter leads to an increase in
the temperature and the thermal boundary layer thickness (see Fig. 8). In fact, the increase in
the radiation parameter leads to an enhancement in the fluid temperature. Figure 9 illustrates
the variations in the temperature for various values of the heat generation parameter S. It is
found that the temperature and the thermal boundary layer thickness are increasing functions
of the heat generation parameter.
Fig. 2
Influence of 1 on temperature ()
vs. when 2 = 0.4, P r = Sc =
1.0, Bi1 = Bi2 = 0.8, Nt = Nb =
0.2, Tr = 0.5, and S = 0.2
Fig. 3
76
Fig. 4
Influence of P r on temperature ()
vs. when 1 = 2 = 0.4, Sc =
1.0, Bi1 = Bi2 = 0.8, Nt = Nb = 0.2,
Tr = 0.5, and S = 0.2
Fig. 5
Fig. 6
Influence of Nt on temperature ()
vs. when 1 = 2 = 0.4, P r = Sc =
1.0, Bi1 = Bi2 = 0.8, Nb = 0.2, Tr =
0.5, and S = 0.2
Fig. 7
Fig. 8
Influence of Tr on temperature ()
vs. when 1 = 2 = 0.4, P r = Sc =
1.0, Bi1 = Bi2 = 0.8, Nt = Nb = 0.2,
and S = 0.2
Fig. 9
To see the variations in the concentration () for different values of the Deborah numbers
1 and 2 , the Schmidt number Sc, the Biot number Bi2 , the thermophoresis parameter Nt ,
and the Brownian motion parameter Nb , Figs. 1015 are presented. Figures 10 and 11 elucidate that the Deborah numbers 1 and 2 have reverse effects on the concentration ().
The concentration () increases for higher values of 1 , while it reduces for larger values of
2 . Also, it is analyzed that the influence of 1 and 2 on the temperature () and the con-
77
Fig. 10
Influence of 1 on concentration
() vs. when 2 = 0.4, P r =
Sc = 1.0, Bi1 = Bi2 = 0.8, Nt =
Nb = 0.2, Tr = 0.5, and S = 0.2
Fig. 11
Influence of 2 on concentration ()
vs. when 1 = 0.4, P r = Sc =
1.0, Bi1 = Bi2 = 0.8, Nt = Nb = 0.2,
Tr = 0.5, and S = 0.2
Fig. 12
Influence of Sc on concentration
() vs. when 1 = 2 = 0.4, P r =
1.0, Bi1 = Bi2 = 0.8, Nt = Nb =
0.2, Tr = 0.5, and S = 0.2
Fig. 13
Table 1 is computed to see the convergent values of f (0), (0), and (0) at different
orders of HAM approximations. It is seen that the value of f (0) converges from the 10thorder of approximations, while it converges from 35th-order of deformations for (0) and
(0). It is concluded from the tabular values that 35th-order deformations are sufficient
for the convergent solutions. Table 2 is computed to examine the numerical values of the
local Nusselt and Sherwood numbers for various values of Nt , Nb , Tr , P r, Bi1 , and Bi2 when
78
1 = 2 = S = 0.1. It is seen that the values of the local Nusselt and Sherwood numbers are
reduced when the value of Nt increases. The value of the local Sherwood number increases by
increasing the value of the Brownian motion parameter.
Fig. 14
Influence of Nt on concentration
() vs. when 1 = 2 = 0.4,
P r = Sc = 1.0, Bi1 = Bi2 = 0.8,
Nb = 0.2, Tr = 0.5, and S = 0.2
Table 2
Nt
Nb
Tr
Pr
Bi1
Bi2
0.1
0.3
0.4
1.2
0.5
0.5
0.308 34
0.250 48
0.4
0.3
0.4
1.2
0.5
0.5
0.274 29
0.203 40
0.6
0.3
0.4
1.2
0.5
0.5
0.253 05
0.178 52
0.3
0.1
0.4
1.2
0.5
0.5
0.292 83
0.107 66
0.3
0.4
0.4
1.2
0.5
0.5
0.281 39
0.231 41
0.3
0.6
0.4
1.2
0.5
0.5
0.273 66
0.245 15
0.3
0.3
0.0
1.2
0.5
0.5
0.221 97
0.205 46
0.3
0.3
0.5
1.2
0.5
0.5
0.296 72
0.220 20
0.3
0.3
0.8
1.2
0.5
0.5
0.328 94
0.226 74
0.3
0.3
0.4
0.8
0.5
0.5
0.238 33
0.227 91
0.3
0.3
0.4
1.5
0.5
0.5
0.315 49
0.211 14
0.3
0.3
0.4
2.0
0.5
0.5
0.349 57
0.203 21
0.3
0.3
0.4
1.2
0.2
0.5
0.183 91
0.236 29
0.3
0.3
0.4
1.2
0.7
0.5
0.318 66
0.211 44
0.3
0.3
0.4
1.2
1.0
0.5
0.350 23
0.205 69
0.3
0.3
0.4
1.2
0.5
0.2
0.289 98
0.119 75
0.3
0.3
0.4
1.2
0.5
0.7
0.284 13
0.257 83
0.3
0.3
0.4
1.2
0.5
1.0
0.282 44
0.299 37
Conclusions
Fig. 15
Influence of Nb on concentration ()
vs. when 1 = 2 = 0.4, P r = Sc =
1.0, Bi1 = Bi2 = 0.8, Nt = 0.2, Tr = 0.5,
and S = 0.2
1/2
1/2
1/2
Nu/Rex
1/2
Sh/Rex
79
(ii) The temperature () and the concentration () are increasing functions of the Biot
numbers Bi1 and Bi2 .
(iii) Larger values of the thermophoresis and Brownian motion parameters give rise to the
temperature ().
(iv) The temperature () increases when we increase the value of the radiation parameter
Tr .
(v) The temperature () is an increasing function of the heat generation parameter S.
(vi) The concentration () is reduced for higher values of the Schmidt number Sc.
(vii) The influence of the thermophoresis and Brownian motion on the concentration ()
is quite reverse.
Acknowledgements
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