American Journal of Computational and Applied Mathematics
p-ISSN: 2165-8935 e-ISSN: 2165-8943
2014; 4(4): 141-153
doi:10.5923/j.ajcam.20140404.04
Nabil T. M. Eldabe 1, Ahmed M. Sedki 2, 3, I. K. Youssef 3
1Mathematics Department, Faculty of Education, Ain Shams University, Heliopolis, Cairo, Egypt
2Mathematics Department, Faculty of Science, Jazan University, Jazan, Saudi Arabia
3Mathematics Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, Egypt
Correspondence to: Ahmed M. Sedki , Mathematics Department, Faculty of Science, Jazan University, Jazan, Saudi Arabia.
| Email: | ![]() |
Copyright © 2014 Scientific & Academic Publishing. All Rights Reserved.
An analysis is made to study the mass transfer in boundary layer flow past a moving permeable flat plate embedded in porous medium with variable wall concentration in presence of chemical reaction. The governing nonlinear partial differential equations are transformed into a set of ordinary differential equations by using similarity transformations. The numerical computations are carried out for several values of physical parameters involved in the transformed equations. The resulting nonlinear system of partial differential equations are solved numerically by both Keller-Box method which is an implicit finite difference method and by the numerical method based on fourth order Runge-Kutta iteration scheme with shooting method. The features of the flow and mass transfer characteristics for different values of the governing parameters are analyzed and discussed. To support the accuracy of the numerical results, a comparison is made with known results from the open literature for some particular cases of the present study and the results are found to be in excellent agreement for the used numerical methods. It is found that the existence of dual solutions exists when the surface and the fluid move in opposite directions. The results indicate that the increase of porous parameter decreases the variation of a velocity profiles and the variation of a skin friction coefficient while it increases both concentration profiles and concentration gradient at the surface. It is due to the presence of a porous medium which increases the resistance to flow resulting in decrease in the flow velocity and increase in the solute concentration.
Keywords: Mass transfer, Chemical reaction, Moving permeable plate, Variable wall concentration, Porous medium, Similarity transformations, Keller box method
Cite this paper: Nabil T. M. Eldabe , Ahmed M. Sedki , I. K. Youssef , Numerical Solutions for Boundary Layer Fluid Flow with Mass Transfer over a Moving Permeable Flat Plate Embedded in Porous Medium with Variable Wall Concentration in Presence of Chemical Reaction, American Journal of Computational and Applied Mathematics , Vol. 4 No. 4, 2014, pp. 141-153. doi: 10.5923/j.ajcam.20140404.04.
, Variation of a skin friction coefficient
, Concentration profiles φ (η) and concentration gradient at the surface φ′ (0) for different values of the governing parameters are discussed and analyzed.![]() | (1) |
![]() | (2) |
![]() | (3) |
is the kinematic viscosity where ρ is the density and
is the dynamic viscosity of the fluid. C is the concentration, D is the diffusion coefficient and C0 is the concentration in the free stream. R(x) is the variable reaction rate of the solute and is given as
, L is the reference length and R0 is constant. The boundary conditions for the velocity components and the concentration are ![]() | (4) |
![]() | (5) |
the free stream velocity is
is the variable plate concentration and C0 is a positive solute constant. n is a power-law exponent which signifies the change of amount of solute in the x-direction.
is the variable suction or injection through the permeable plate and is given by
,
is a constant with
for suction and
for injection. The stream function ψ (x, y) that satisfies the continuity equation and is related to the velocity components in the usual way as ![]() | (6) |
![]() | (7) |
![]() | (8) |
![]() | (9) |
![]() | (10) |
![]() | (11) |
is the local Reynolds number and ƞ is the similarity variable defined as
where U is the composite velocity defined as U=U∞+Uw (Afzal et al. [15]).
is the dimensionless stream function and φ is the dimensionless concentration function. Substituting in equations (6-9) to obtain the set of ordinary differential equations![]() | (12) |
![]() | (13) |
is the porous parameter,
is the Schmidt number and
is the chemical reaction rate number. The boundary conditions finally become ![]() | (14) |
![]() | (15) |
,S > 0 ( i.e.
< 0) corresponds to suction and S < 0 (i.e.
> 0 ) corresponds to injection. The physical quantities of interest in this problem are the local skin-friction coefficient
and rate of mass transfer -
which are defined as![]() | (16) |
![]() | (17) |
, say
. We set the following first order system: ![]() | (18) |
![]() | (19) |
![]() | (20) |
and
but no such values are given in the boundary conditions. The initial guess values for
and
are chosen and applying fourth order Runge –Kutta method then solution is obtained. To get accurate solution, it is important for shooting method to choose the appropriate finite value of
. In order to determine
for the initial value problem (18-20), we start with some initial guess values for some particular set of the physical parameters to obtain
and
. The solution procedure is repeated with another value of
until two successive values of
and
differ only by the specified significant digit. The last value of
is finally chosen to be the most appropriate value of the limit
for that particular set of parameters. The value of
may change for another set of physical parameters. After determining the value
, we compare the calculated values of
and
at
with the given boundary conditions
and
and adjust the values of
and
using Secant method to give better approximation for the solution. The step size is taken as
. The process is repeated until we get the results correct up to the desired accuracy 10-6 level. 
where
is the
- spacing and
is the
-spacing. Here i and j are just sequence of numbers that indicate the coordinate location, not tensor indices or exponents. The derivatives in the
-direction are replaced by finite difference, for example the finite- difference form for any points are 
,
We start by writing the finite difference of equations for the midpoint
using centered –difference derivatives, we get

If we assume
,
,
,
,
to be known for
, then we have to obtain the solution of the unknown (
,
,
,
,
) for
. The system can be written as![]() | (21a) |
where
We note that
and
involves only known quantities if we assume that the solution is known on
. The transformed boundary layer thickness
is to sufficiently large so that it is beyond the edge of the boundary layer [29, 30]. The boundary conditions at
yields ![]() | (21b) |
After dropping the quadratic and higher order terms in 

,
and
. We have also dropped the superscript (k) for simplicity. This procedure yields the following linear tri-diagonal system. 

![]() | (22a) |

where










To complete the system (22a), we recall the boundary condition (21b), which can be satisfied exactly with no iteration. So, to maintain these correct values in all the iterates, we take![]() | (22b) |
That is:![]() | (23) |


, 

To solve the system (23), we assume that A is nonsingular and can factorized into
, where
Now we have
, if we define![]() | (24) |
![]() | (25) |
can be solved from equation (25)
Where
the step in which
,
and
are calculated, is usually referred to as the forward sweep. Once the elements of
are found, equation (24) then gives the solution
in the so called backward sweep, in which the elements are obtained by the following relations:
these calculations are repeated until some convergence criterion is satisfied and calculations are stopped when
, where
is small prescribed value.
for various of q with previously reported by Ishak [12] and excellent agreement are found for the used numerical methods as shown in Table 1. The numerical computations are carried out for several values of parameters involved in the equations viz. the suction or injection parameter (s), the Schmidt number (sc), the chemical reaction rate parameter (B), the power –law exponent (n), porous parameter (N) and the velocity ratio parameter (q).
|
, Variation a skin friction coefficient
, Concentration profiles φ(η) and concentration gradient at the surface φ′(0) for different values of the each parameter and physical meaning are also given.The external suction or injection parameter (S) effects are demonstrated in Figures (1-6), it is found that at fixed
,variation of a velocity profiles
and variation of a skin friction coefficient
increase with the increase of the suction (S) while both Concentration profiles φ(η) and concentration gradient at the surface φ′(0) reduce. It is due to the fact that the momentum as well as concentration boundary layer thicknesses decrease with suction.![]() | Figure 1. for different values of s |
![]() | Figure 2. for different values of s |
![]() | Figure 3. against for different values of s |
![]() | Figure 4. for different values of s |
![]() | Figure 5. φ(η) for various values of s |
![]() | Figure 6. φ′ (0) for different values of s |
and variation of a skin friction coefficient
decrease and Concentration profiles φ (η) and concentration gradient at the surface φ′ (0) increase. It is due to the injection, both momentum and boundary layer thicknesses increase. The Schmidt number (Sc) effects are displayed in Figures (7-8), it is observed that The Schmidt number has major effects on the distribution of solute. At fixed ƞ the increase of Schmidt Sc reduces quickly both concentration profiles φ(η) and concentration gradient at the surface φ′(0). This is due to the fact that the rate of solute transfer from the surface increases when the Schmidt number increases. The negative value of the concentration profile for large Sc is because of substantial increase in the rate of solute transfer from the plate to the fluid in the chemical reaction. It is observed that the magnitude of the concentration gradient initially increases with Sc, but for greater values of
it decreases with Sc.![]() | Figure 7. φ (η) for various values of Sc |
![]() | Figure 8. φ′ (0) for different values of sc |
reduces both the concentration profiles φ (η) and concentration gradient at the surface φ′(0) and thus the chemical reaction enhances the mass transfer. ![]() | Figure 9. φ(η) for various values of B |
![]() | Figure 10. φ′(0) for different values of B |
. While the concentration profile increases with the increase in the magnitude of n with n < 0 and for large negative values of n, the overshoot of solute is observed near the surface. The magnitude of the concentration gradient at the surface φ′ (0) increases with the increase in positive n but decreases with the increase in the magnitude of n. with n < 0. Thus, the effect of increase of n when the surface concentration is
which is completely opposite to the effect of the increase of n when the surface concentration is
. Note that, the wall concentration is constant when n=0.![]() | Figure 11. φ(η) for various values of n |
![]() | Figure 12. φ′(0) for different values of n |
, variation of a velocity profiles
and variation of a skin friction coefficient
decrease with the increase in porous parameter while the increase of N increase both concentration profiles φ(η) and concentration gradient at the surface φ′(0). Also it is shown in Figures (1-3, 5, 13) that the presence of a porous medium increases the resistance to flow resulting in decrease in the flow velocity and increase in the solute concentration which increases the solute boundary layer thickness.![]() | Figure 13. for different values of N |
![]() | Figure 14. for different values of N |
![]() | Figure 15. φ(η) for various values of N |
![]() | Figure 16. φ′(0) for different values of N |
, variation of a skin friction coefficient
decreases with the increasing in q > 0 while variation of a velocity profiles
increases but far away from the plate
decreases. The increase of q > 0 reduce both concentration profiles φ(η) and concentration gradient at the surface φ′(0). ![]() | Figure 17. for different values of q |
![]() | Figure 18. for different values of q |
![]() | Figure 19. φ(η) for various values of q |
![]() | Figure 20. φ′(0) for different values of q |
changing the nature, it decreases. It is shown in table (1) that the values of f ′′(0) are positive when q < 0.5, and they become negative when the value of q exceeds 0.5. The concentration profiles φ(η) and concentration gradient φ′(0) for some values of the chemical reaction rate parameter (B) are presented in Figures 23 and 24 respectively. These profiles satisfy the boundary conditions (13), which support the numerical results besides supporting the dual nature of the solutions presented in Figures (21-23). They show that φ(η) increases for both solutions with the decreasing of B in any point while Figure 24 shows that the concentration gradient φ′(η) for both solutions initially decreases with the increasing of B but far away from the plate it increases. ![]() | Figure 21. for different negative values of q |
![]() | Figure 22. for different negative values of q |
![]() | Figure 23. for different negative values of B |
![]() | Figure 24. for different negative values of B |
and variation of a skin friction coefficient
decrease with the increasing in porous parameter N while both concentration profiles φ(η) and concentration gradient at the surface φ′(0) increase. The increasing of the velocity ratio parameter (q), suction or injection parameter S, the reaction rate parameter B , the Schmidt number Sc and the power–law exponent (n) reduce both Concentration profiles φ(η) and concentration gradient at the surface φ′(0). The increasing of velocity ratio parameter (q) increases the variation of a velocity profiles
but far away from the plate it decreases. Dual solutions are found to exist when q < 0 i.e. the plate and the free stream move in the opposite directions. Consequently, the solute boundary layer thickness is found to increase with the increase of magnitude of q for the upper branch and in the lower branch it decreases. It is found that both φ(η) and the concentration gradient φ′(η) increase for dual solutions with the decreasing of B in any point but far away from the plate the concentration gradient φ′(η) decreases for dual solutions.