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New Analytical Expresions of Concentrations in Packed Bed Immobilized-Cell Electrochemical Photobioreactor

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05 July 2023

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07 July 2023

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Abstract
In this paper, Akbari-Ganji's and Taylor series methods are applied to find analytical solutions to nonlinear differential equations that arise in an immobilized-cell photobioreactor. Approximate analytical expressions for substrate and product concentrations and both liquid and gas phases for various parameter values are derived using both methods. Efficiency, accuracy, and convergence of the two methods relative to highly accurate numerical methods are investigated to establish reliable profiles of these two methods for solving general nonlinear equations that model various physical phenomena. Numerical simulations are presented to validate the theoretical investigations.
Keywords: 
Subject: Chemistry and Materials Science  -   Electrochemistry

1. Introduction

Nonlinear systems of equations usually present real-world physical applications. Over the past three decades, the search for efficient and reliable analytical asymptotic methods to solve these systems has intensified [1]. Of the methods have received a great attention are the perturbation method (PM) [4], homotopy perturbation method (HPM) [5,6,7,8,9,10,11], variational iteration method (VIM) [12,13,14,15,16], homotopy analysis method (HAM)[17,18,19,20], differential transform method (DTM) [21,22], Adomian decomposition method (ADM) [23,24], and Green’s function iterative method [25,26].
Two-phase flow and mass transport coupled with biochemical reactions co-occur in an operating photobioreactor. Therefore, a better understanding of the complicated transport mechanism will promote the application of electrochemical photobioreactors[28,29].This communication directs our attention to the analytical and numerical method of solving nonlinear equations in immobilized-cell photobioreactor [2,3]. A comparison study between Akbari-Ganji's method (AGM) [27,28,29] and the renowned Taylors series method (see [30,31] and the references therein are presented. We aim to derive approximate analytical expressions of the concentrations of substrate and product and both liquid and gas phases for various parameter values by using these two methods. This paper will present a profile of reliability, efficiency, and convergence of both approaches.

2. Mathematical Formulation of the Problems

An immobilized-cell photo bioreactor packed with transparent gel-granules containing immobilized PSB developed and modeled by Shirejini et al. [3] is illustrated in Figure 1(a).Figure 1(b) shows a schematic diagram of mass transfer in a single gel graule, such that the mass transfer of all reactants and products is dominated by diffusion. Using Fick’s law, the mass transport equations for substrate and the hydrogen inside the gel granules are given by[32]:
Figure 1. Schematic of the entrapped-cell photobioreactor.
Figure 1. Schematic of the entrapped-cell photobioreactor.
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D granule S 1 r 2 d d r r 2 d C granule S d r = ϕ granule S
D granule H 2 1 r 2 d d r r 2 d C granule H 2 d r = ϕ granule H 2
ϕ granule S = μ X cell Y X / S * + m X cell ,     ϕ granule H 2 = α * μ X cell Y X / S * + β X cell ,   μ max = C granule S K S + C granule S
where D granule S and D granule H 2 are the significant diffusion coefficients of glucose and hydrogen in the gelgranule, C granule S and C granule H 2 are the local concentrations of glucose and hydrogen inside the gel granule, ϕ granule S is the consumption rate of glucose, ϕ granule H 2 is the generation rate of hydrogen. The parameter α * represents the growth associated kinetic constant for hydrogenproduction, β is the non-growth associated kinetic constant, X cell is the initial cell density, Y X / S * is the cell yield, and K S is a Monod constant. Furthermore, μ max denotes the maximum specific growth rate, and μ is the growth rate. The boundary conditions for the above system of Equations(1) and (2) are given by
d C granule S d r r = 0 = d C granule H 2 d r r = 0 = 0
C granule S r = R = C l S ,   C granule H 2 r = R = C g H 2
where C l S and C g H 2 are bulk solutions, and R is the radius of catalyst. The source terms   φ s , φ H 2 and φ C O 2 are defined by:
φ s = α D g r a n u l e s d C g r a n u l e s d r r = R , φ H 2 = α D g r a n u l e H 2 d C g r a n u l e H 2 d r r = R , φ C O 2 = M C O 2 2 M H 2 φ H 2
where α   is the specific area of the gel granule. The source terms of the liquid phase and gas phase are expressed by:
m l = φ s , m g = φ H 2 + φ C O 2
By introducing the dimensionless parameters
Φ 1 = X cell   μ m a x R 2 Y X S *   D granule S K S ,   Φ 2 = X cell   μ m a x R 2 C l S Y X S *   D granule S K S C g H 2 , γ 1 = X cell m   R 2   D granule S K S , γ 2 = X cell m   R 2   D granule S C l S , γ 3 = X cell m   R 2 C l S   D granule S K S C g H 2 , γ 4 = X cell m   R 2   D granule H 2 C g H 2
ζ = r R , u = C g r a n u l e s C g s ,   v = C g r a n u l e H 2 C g H 2   ,   α 1 = C l S K S
Equations (1) and (2),take the dimensionless forms:
1 ζ 2 d d ζ ζ 2 d u ( ζ ) d ζ = ( φ 1 + γ 1 ) u ( ζ ) + γ 2 ( 1 + α 1 u ( ζ ) )
1 ζ 2 d d ζ ζ 2 d v ( ζ ) d ζ = ( φ 2 + γ 3 ) u ( ζ ) + γ 4 ( 1 + α 1 u ( ζ ) )
with the dimensionless boundary conditions:
d u ( ζ ) d ζ = d v ( ζ ) d ζ = 0   at   ζ = 0
u ( ζ ) = v ( ζ ) = 1 at ζ = 1
The normalized steady-state source terms of liquid and gas phases is given by
ψ l = m l R α D g r a n u l e s C l s = d u d ζ ζ = 1
ψ g = m g R α D g r a n u l e H 2 C g H 2 = 2 + ω 2 d v d ζ ζ = 1 where ω = M C O 2 M H 2

3. Analytical expression of the concentrations using Akbari-Ganji’s method

In this section, we use AGM to derive explicit expressions for the concentrations of glucose and hydrogen. The AGM is a semi-analytical approach that has shown efficacy in solving nonlinear equations [33,34,35]. The AGM procedure begins by assuming a solution function with unknown constant coefficients, which are determined by solving a system of algebraic equations that is constructed from the differential equations and the initial conditions.

3.1. Concentration of Glucose (substrate)

Let
u ( ζ ) = a 0 + a 1 ζ + a 2 ζ 2
be a trial solution of Equation (9), where a 0 , a 1 , a 2 are constants. The boundary conditions (11) and (12) imply
1 = a 0 + a 1 + a 2 , a 1 = 0 .
Now define the function F   by
F ( ζ ) : 1 ζ 2 d d ζ ζ 2 d u ( ζ ) d ζ ( φ 1 + γ 1 ) u ( ζ ) + γ 2 ( 1 + α 1 u ( ζ ) ) = 0
then
F ( ζ = 1 ) : 2 a 1 + 6 a 2 ( φ 1 + γ 1 ) ( a 0 + a 1 + a 2 ) + γ 2 ( 1 + α 1 ( a 0 + a 1 + a 2 ) ) = 0
Using Equation (16) in Equation (18), gives
a 2 = φ 1 + γ 1 + γ 2 6 ( 1 + α 1 ) , a 0 = 1 φ 1 + γ 1 + γ 2 6 ( 1 + α 1 )
By substituting Equations (16) and (18) into Equation (15), the analytical expression for the substrate is
u ( ζ ) = 1 + φ 1 + γ 1 + γ 2 6 ( 1 + α 1 ) ( ζ 2 1 )

3.2. Concentration of Hydrogen (product)

Assume the following solution to Equation (10):
v ( ζ ) = b 0 + b 1 ζ + b 2 ζ 2
From boundary conditions (11) and (12), we obtain:
1 = b 0 + b 1 + b 2 ,   and   b 1 = 0 .
Define the G function by
G ( ζ ) : 1 ζ 2 d d ζ ζ 2 d v ( ζ ) d ζ ( φ 2 + γ 3 ) u ( ζ ) + γ 4 ( 1 + α 1 u ( ζ ) ) = 0 ,
then
G ( ζ = 1 ) : 2 b 1 + 6 b 2 ( φ 2 + γ 3 ) ( a 0 + a 1 + a 2 ) + γ 4 ( 1 + α 1 ( a 0 + a 1 + a 2 ) ) = 0
Substituting Equation (22) into Equation (24) leads to
b 2 = φ 2 + γ 3 + γ 4 6 ( 1 + α 1 ) ,   b 0 = 1 φ 2 + γ 3 + γ 4 6 ( 1 + α 1 ) ,
and substituting Equations (22) and (25) into Equation (16), the analytical expression for the product is
v ( ζ ) = 1 + φ 2 + γ 3 + γ 4 6 ( 1 + α 1 ) ( ζ 2 1 )

3.3. Normalized steady-state source terms of liquid and gas phases

The analytical expressions of normalized steady-state source terms of liquid and gas phases aregiven by:
ψ l = φ 1 + γ 1 + γ 2 3 ( 1 + α 1 )
ψ g = ( 2 + ω ) 2 φ 2 + γ 3 + γ 4 3 ( 1 + α 1 )
Remark 1. The analytical expressions given by Equations (20) and (26) for the concentrations of glucose and hydrogen, respectively, are identical to the expressions obtained by the Adomian decomposition method (ADM) [2] and the homotopy perturbation method [3].

4. Analytical expression of the concentrations using Taylor series method

The three-century-old Taylor series method (TSM) has been recently revived and exploited to accurately and efficiently solve many nonlinear differential equations representing nonlinear models in various sciences and engineering applications Equations [36,37]. In this section, we employ TSM to find the substrate and product concentrations.

4.1. Concentration of Glucose (substrate)

First, we assume that
u ( 0 ) = m
where   m   is an unknown constant to be determined. Steady state nonlinear reaction–diffusion equations can be written in the form:
ζ u ' ' ( ζ ) + 2 u ' ( ζ ) 1 + α 1 u ( ζ ) = ( φ 1 + γ 1 ) ζ u ( ζ ) + γ 2 ζ
Taking the first three derivatives of Equation (30) with respect to ' ζ ' gives
ζ u ' ' ' ( ζ ) + 3 u ' ' ( ζ ) 1 + α 1 u ( ζ ) + ζ u ' ' ( ζ ) + 2 u ' ( ζ ) α 1 u ' ( ζ ) = ( φ 1 + γ 1 ) u ( ζ ) + ζ u ' ( ζ ) + γ 2
ζ u ' ' ' ' ζ + 4 u ' ' ' ζ 1 + α 1 u ζ + 2 ζ u ' ' ' ζ + 3 u ' ' ζ α 1 u ' ζ + ζ u ' ' ζ + 2 u ' ( ζ ) α 1 u ' ' ( ζ ) = ( φ 1 + γ 1 ) 2 u ' ( ζ ) + ζ u ' ' ( ζ )
ζ u ' V ( ζ ) + 5 u ' ' ' ' ( ζ ) 1 + α 1 u ( ζ ) + 3 ζ u ' ' ' ' ( ζ ) + 4 u ' ' ' ( ζ ) α 1 u ' ( ζ ) + 3 ζ u ' ' ' ( ζ ) + 3 u ' ' ( ζ ) α 1 u ' ' ( ζ ) + ζ u ' ' ( ζ ) + 2 u ' ( ζ ) α 1 u ' ' ' ( ζ ) = ( φ 1 + γ 1 ) 3 u ' ' ( ζ ) + ζ u ' ' ' ( ζ )
For ζ = 0 , Equations (31)–(33) give the following identities:
u ' ' ( 0 ) = m ( φ 1 + γ 1 ) + γ 2 3 ( 1 + α 1 m ) u ' ' ' ( 0 ) = 0 , u ' ' ' ' ( 0 ) = m ( φ 1 + γ 1 ) + γ 2 φ 1 + γ 1 α 1 γ 2 5 ( α 1 m + 1 ) 3 , u v ( 0 ) = 0 u v i ( 0 ) = m ( φ 1 + γ 1 ) + γ 2 φ 1 + γ 1 α 1 γ 2 ( φ 1 + γ 1 ) ( 3 10 α 1 m ) 13 α 1 γ 2 7 ( α 1 m + 1 ) 5 .
The substrate concentration,using the Taylor’s series, is expressed by the expansion
  u ( ζ ) = u ( 0 ) + u ' ( 0 ) ζ 1 ! + u ' ' ( 0 ) ζ 2 2 ! + u ' ' ' ( 0 ) 3 ζ 3 ! + . . . = m + u 1 ζ 2 2 ! + u 2 ζ 4 4 ! + u 3 ζ 6 6 !
where
u 1 = m φ 1 + γ 1 + γ 2 3 α 1 m + 1 , u 2 = m φ 1 + γ 1 + γ 2 φ 1 + γ 1 α 1 γ 2 5 ( α 1 m + 1 ) 3 , u 3 = m ( φ 1 + γ 1 ) + γ 2 φ 1 + γ 1 α 1 γ 2 ( φ 1 + γ 1 ) ( 3 10 α 1 m ) 13 α 1 γ 2 7 ( α 1 m + 1 ) 5
Using the boundary conditions ζ = 1 , u ( ζ ) = 1 in Equation (35) implies that
m + u 1 1 2 ! + u 2 1 4 ! + u 3 1 6 ! = 1
from which the unknown constant m can be obtained. For the fixed values of the parameters:
φ 1 = 5 , γ 1 = 0.1 , γ 2 = 0.1   and α 1 = 5 , the numerical value of m is found to be   m = 0.85803 and from Equation (36), we obtain u 1 = 0.141015 , u 2 = 0.001159 and   u 3 = 0.000207 , and thus from Equation (35), we obtain the analytical expression of the substrate expressed by
u ( ζ ) . = 0.85803 + 0.141015 ζ 2 2 ! + 0.001159 ζ 4 4 ! 0.000207 ζ 6 6 !

4.2. Concentration of Hydrogen (product)

Similar to the approach in Section 4.1, we begin by assuming that
v 0 = l ,
where l is an unknown constant to be determined and by direct differentiation of v ( ζ ) , we obtain,
v ' ' ( 0 ) = m ( φ 2 + γ 3 ) + γ 4 3 ( 1 + α 1 m ) ,   v ' ' ' ( 0 ) = 0   , v ' ' ' ' ( 0 ) = m ( φ 1 + γ 1 ) + γ 2 φ 2 + γ 3 α 1 γ 4 5 ( 1 + α 1 m ) 3 ,   v v ( 0 ) = 0 , v v i ( 0 ) = m ( φ ` 1 + γ 1 ) + γ 2 φ 2 + γ 3 α 1 γ 4 ( φ 1 + γ 1 ) ( 1 α 1 m ) 2 α 1 γ 2 7 ( 1 + α 1 m ) 5 .
Now, the product concentration is readily obtained using Taylor’s series
v ζ = v 0 + v ' 0 ζ 1 ! + v ' ' 0 ζ 2 2 ! + v ' ' ' 0 ζ 3 3 ! +
Using the boundary condition, v 1 = 1 , in Equation (41) gives the numerical value of l. For the fixed values of the parameters φ 1 = 1 , γ 1 = 1 , γ 2 = 1 , φ 2 = 5 , γ 3 = 0.1 , γ 4 = 0.1 , α 1 = 5 , and m = 0.915769 , we obtain l = 0.8563317 . The analytical expression for the product concentration takes on the form
v ( ζ ) = 0.8563317 + 0.1425122 ζ 2 2 ! + 0.0011589 ζ 4 4 ! 0.0000581 ζ 6 6 !

4.3. Normalized steady-state source terms of liquid and gas phases

The analytical expression of the normalized steady-state source terms of liquid phases, ψ l , is obtained from the equation,
ψ l = u 1 + u 2 1 6 + u 3 1 120
Using, the values u 1 = 0.141015 , u 2 = 0.001159 and u 3 = 0.000207 , we obtain ψ l = 0.141207 . The analytical expression of normalized steady-state terms of gas phases, ψ g , is given by
ψ g = 2 + ω 2 v 1 + v 2 1 6 + v 3 1 120
where ψ g = 0.214057 when ω = 1 .

5. Numerical simulations and Discussion

Nonlinear equations in the immobilized-cell photobioreactor are analytically solved. The approximate analytical expressions of concentrations of glucose and hydrogen inside the gel and granule in addition to approximate analytical expressions of steady-state source terms of liquid and gas phases are derived using Taylor series (TSM) and Akbari-Ganji (AGM) methods.
The reaction-diffusion equations representing the packed bed photobioreactor with immobilized-cell were solved using the Adomian decomposition method (ADM) [2] and the homotopy perturbation method (HPM) [3]. Interstingly, the semi-analytical expressions of the concentrations of substrate and product obtained by the ADM, HPM, and AGM were identical (Equations (20) and (26)) for all values of parameters.
To examine the accuracy of the two proposed analytical approaches, we compared their results with numerical results obtained from the reliable MATLAB pdepe function (Appendix A) and with analytical results of other methods available in the literature. The approximate analytical and numerical concentrations of substrate and product for various parameters are summarized in Table 1, Table 2, Table 3, Table 4, Table 5 and Table 6. Even though both methods gave satisfactory results, TSM is notably more accurate. The maximum relative error average is 0.6% for the TSM and 5% for the AGM. Comparisons of normalized steady-state source terms of both liquid and gas phases for various values of parameters φ 1 , φ 2 and α 1 are given in Table 7 and Table 8.
Figures 2(a)-2(c) illustrate the behavior of the biodegradation of substrate for different values of the parameters. It is noticed that as any of the parameters ϕ 1 ,   γ 1 ,   or     γ 2 decreases, the substrate concentration increases. In contrast, Figure 2(d) confirms a direct relationship between the parameter α 1 and the substrate concentration.
The effects of all parameters on the hydrogen production profiles are shown in Figures 3(a)-3(g),where it is noticed that the concentration of hydrogen increases the parameters ϕ 2 ,   γ 3 ,   or γ 4 decreases or the parameter α i increases. However, the concentration of hydrogen is independent of any of the parameters ϕ 1 ,   γ 1 ,     and γ 2 .
Figure 2. Plot of substrate concentration for various values of parameters (Equations (20) and (35)).
Figure 2. Plot of substrate concentration for various values of parameters (Equations (20) and (35)).
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Figure 3. Plot of product concentration, v ( ζ ) , for various values of the parameters ϕ 1 ,   ϕ 2 ,   γ 1 ,   γ 2 ,   γ 3 ,   γ 4 ,   and α (Equations (26) and (41)).
Figure 3. Plot of product concentration, v ( ζ ) , for various values of the parameters ϕ 1 ,   ϕ 2 ,   γ 1 ,   γ 2 ,   γ 3 ,   γ 4 ,   and α (Equations (26) and (41)).
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Table 1. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter φ 1 when γ 1 = γ 2 = 0.1 and α 1 = 5 .
Table 1. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter φ 1 when γ 1 = γ 2 = 0.1 and α 1 = 5 .
ζ φ 1 = 10   and   m = 0.728557 φ 1 = 15   and   m = 0.610154
Num.Equation (9) AGMEq.(20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35) NumEquation (9) AGMEq.(20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35)
0 0.73 0.72 0.73 1.37 0.00 0.60 0.58 0.61 3.33 1.67
0.2 0.74 0.73 0.74 1.35 0.00 0.62 0.59 0.63 4.84 1.61
0.4 0.77 0.76 0.77 1.30 0.00 0.67 0.65 0.67 2.98 0.00
0.6 0.83 0.82 0.83 1.20 0.00 0.75 0.73 0.75 2.67 0.00
0.8 0.90 0.90 0.90 0.00 0.00 0.86 0.85 0.86 1.16 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 0.87 0.00 Average error % 2.50 0.55
Table 2. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter γ 1 when φ 1 = γ 2 = 0.1 and α 1 = 5 .
Table 2. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter γ 1 when φ 1 = γ 2 = 0.1 and α 1 = 5 .
ζ γ 1 = 7   and   m = 0.805191 γ 1 = 15   and   m = 0.610124
Num.Equation (9) AGMEq.(20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35) NumEquation (9) AGMEq.(20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35)
0 0.80 0.80 0.80 0.00 0.00 0.60 0.58 0.61 3.33 1.67
0.2 0.81 0.81 0.81 0.00 0.00 0.62 0.59 0.63 4.84 1.61
0.4 0.84 0.83 0.84 1.20 0.00 0.67 0.65 0.67 2.98 0.00
0.6 0.88 0.87 0.88 1.14 0.00 0.75 0.73 0.75 2.67 0.00
0.8 0.93 0.93 0.93 0.00 0.00 0.86 0.85 0.86 1.16 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 0.39 0.00 Average error % 2.50 0.55
Table 3. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter γ 2 when γ 1 = φ 1 = 0.1 and α 1 = 5 .
Table 3. Comparison beteween numerical and analytical results for dimensionless concentration of substrate u ( ζ ) for various values of parameter γ 2 when γ 1 = φ 1 = 0.1 and α 1 = 5 .
ζ γ 2 = 5   and   m = 0.839877 γ 2 = 7   and   m = 0.762254
Num.Equation (9) AGMEquation (20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35) NumEquation (9) AGMEq.(20) TSMEq.(35) Error % ofAGMEq.(20) Error % of TSMEquation (35)
0 0.84 0.86 0.84 2.38 0.00 0.77 0.80 0.76 3.90 1.30
0.2 0.85 0.86 0.85 1.18 0.00 0.78 0.81 0.77 3.85 1.28
0.4 0.87 0.88 0.87 1.15 0.00 0.81 0.83 0.80 2.47 1.23
0.6 0.90 0.91 0.90 1.11 0.00 0.86 0.87 0.85 1.16 1.16
0.8 0.95 0.95 0.94 0.00 1.05 0.92 0.93 0.92 1.09 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 0.97 0.17 Average error % 2.09 0.83
Table 4. Comparison beteween numerical and analytical results for dimensionless concentration of product   v ( ζ ) for various values of parameter φ 2 when γ 1 = 1 , γ 2 = 1 , γ 3 = 0.1 , γ 4 = 1 , α 1 = 5 and m = 0.915769 .
Table 4. Comparison beteween numerical and analytical results for dimensionless concentration of product   v ( ζ ) for various values of parameter φ 2 when γ 1 = 1 , γ 2 = 1 , γ 3 = 0.1 , γ 4 = 1 , α 1 = 5 and m = 0.915769 .
ζ φ 2 = 20   and   l = 0.4444703 φ 2 = 35   and   l = 0.0320751
Num.Eq.(10) AGMEq.(26) TSMEq.(41) Error% ofAGMEq.(26) Error% ofTSMEquation (41) NumEq.(10) AGMEq.(26) TSMEq.(41) Error% ofAGMEq.(26) Error% ofTSMEquation (41)
0 0.44 0.44 0.44 0.00 0.00 0.03 0.02 0.03 33.33 0.00
0.2 0.47 0.46 0.47 2.13 0.00 0.07 0.06 0.07 14.29 0.00
0.4 0.53 0.53 0.53 0.00 0.00 0.19 0.18 0.19 5.26 0.00
0.6 0.65 0.64 0.65 1.54 0.00 0.39 0.38 0.39 2.56 0.00
0.8 0.81 0.80 0.81 1.23 0.00 0.66 0.66 0.66 0.00 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 0.82 0.00 Average error % 9.24 0.00
Table 5. Comparison beteween numerical and analytical results for dimensionless concentration of product v ( ζ ) for various values of parameter γ 3 when γ 1 = 1 , γ 2 = 1 , φ 1 = 0.1 , γ 4 = 1 , α 1 = 10 and   m = 0.954173 .
Table 5. Comparison beteween numerical and analytical results for dimensionless concentration of product v ( ζ ) for various values of parameter γ 3 when γ 1 = 1 , γ 2 = 1 , φ 1 = 0.1 , γ 4 = 1 , α 1 = 10 and   m = 0.954173 .
ζ γ 3 = 40   and   l = 0.39268025 γ 3 = 65   and   l = 0.01502483
Num.Eq.(10) AGMEq.(26) TSMEq.(41) Error % ofAGMEq.(26) Error % of TSMEquation (41) NumEq.(10) AGMEq.(26) TSMEq.(41) Error % ofAGMEq.(26) Error % of TSMEquation (41)
0 0.39 0.39 0.39 0.00 0.00 0.01 0.01 0.01 0.00 0.00
0.2 0.42 0.42 0.42 0.00 0.00 0.05 0.05 0.05 0.00 0.00
0.4 0.49 0.49 0.49 0.00 0.00 0.18 0.17 0.18 5.55 0.00
0.6 0.62 0.61 0.62 1.61 0.00 0.38 0.37 0.38 2.63 0.00
0.8 0.79 0.79 0.79 0.00 0.00 0.66 0.66 0.66 0.00 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 0.27 0.00 Average error % 1.36 0.00
Table 6. Comparison beteween numerical and analytical results for dimensionless concentration of product   v ( ζ ) for various values of parameter γ 4 when γ 1 = 1 , γ 2 = 1 , γ 3 = 0.1 , φ 1 = 1 , α 1 = 5   and m = 0.915769 .
Table 6. Comparison beteween numerical and analytical results for dimensionless concentration of product   v ( ζ ) for various values of parameter γ 4 when γ 1 = 1 , γ 2 = 1 , γ 3 = 0.1 , φ 1 = 1 , α 1 = 5   and m = 0.915769 .
ζ γ 4 = 10   and   l = 0.70248543 γ 4 = 20   and   l = 0.41040946
Num.Eq.(10) AGMEq.(26) TSMEq.(41) Error % ofAGMEq.(26) Error % of TSMEquation (41) NumEq.(10) AGMEq.(26) TSMEq.(41) Error % ofAGMEq.(26) Error % of TSMEquation (41)
0 0.70 0.72 0.70 2.86 0.00 0.41 0.44 0.41 7.32 0.00
0.2 0.71 0.73 0.71 2.82 0.00 0.43 0.46 0.43 6.98 0.00
0.4 0.75 0.76 0.75 1.33 0.00 0.51 0.53 0.51 3.92 0.00
0.6 0.81 0.82 0.81 1.23 0.00 0.63 0.64 0.63 1.59 0.00
0.8 0.90 0.90 0.90 0.00 0.00 0.80 0.80 0.80 0.00 0.00
1 1.00 1.00 1.00 0.00 0.00 1.00 1.00 1.00 0.00 0.00
Average error % 1.37 0.00 Average error % 3.30 0.00
Table 7. Comparison between numerical and analytical normalized steady-state source terms of liquid phase ψ l for various values of parameter φ 1 and α 1 when γ 1 = γ 2 = 0.1 .
Table 7. Comparison between numerical and analytical normalized steady-state source terms of liquid phase ψ l for various values of parameter φ 1 and α 1 when γ 1 = γ 2 = 0.1 .
φ 1 α 1 = 0.1 α 1 = 0.5
Num.Eq.(13) AGMEq.(27) TSMEq.(43) Error% ofAGMEq.(27) Error% ofTSMEquation (43) Num.Eq.(13) AGMEquation (27) TSMEq.(43) Error% ofAGMEq.(27) Error%ofTSMEquation (43)
0 0.06 0.06 0.06 0.00 0.00 0.04 0.04 0.04 0.00 0.00
0.1 0.09 0.09 0.09 0.00 0.00 0.07 0.07 0.07 0.00 0.00
0.5 0.20 0.21 0.21 5.00 5.00 0.15 0.15 0.15 0.00 0.00
1 0.34 0.37 0.34 8.82 0.00 0.26 0.27 0.26 3.85 0.00
5 1.25 1.56 1.33 24.8 6.40 1.00 1.15 1.01 15.00 1.00
10 2.08 3.09 2.42 48.56 16.35 1.74 2.27 1.90 30.46 9.19
50 5.64 15.2 5.23 169.7 7.27 4.81 11.15 5.22 131.8 8.52
100 7.75 30.4 5.66 291.7 26.97 7.31 22.27 5.66 204.6 22.57
Average error % 68.68 7.75 Average error % 48.22 5.16
Table 8. Comparison between numerical and analytical normalized steady-state source terms of gas phase ψ g for various values of parameter φ 2 and α 1 when γ 1 = γ 2 = 1 , γ 3 = γ 4 = 0.1 , φ 1 = 1 and ω = 1 .
Table 8. Comparison between numerical and analytical normalized steady-state source terms of gas phase ψ g for various values of parameter φ 2 and α 1 when γ 1 = γ 2 = 1 , γ 3 = γ 4 = 0.1 , φ 1 = 1 and ω = 1 .
φ 2 α 1 = 0.1 α 1 = 0.5
Num.Eq.(14) AGMEq.(28) TSMEq.(44) Error % ofAGMEq.(28) Error % of TSMEquation (44) Num.Eq.(14) AGMEquation (28) TSMEquation (44) Error % ofAGMEq.(28) Error % of TSMEquation (44)
0 0.08 0.09 0.09 12.50 12.50 0.06 0.07 0.06 16.67 0.00
0.1 0.12 0.14 0.12 16.67 0.00 0.10 0.10 0.10 0.00 0.00
0.5 0.27 0.32 0.28 18.52 3.70 0.22 0.23 0.22 4.54 0.00
1 0.47 0.54 0.47 14.87 0.00 0.37 0.40 0.37 8.11 0.00
5 2.02 2.36 2.03 16.83 0.49 1.58 1.73 1.60 9.49 1.27
10 3.96 4.64 3.98 17.17 0.50 3.10 3.40 3.14 9.68 1.29
50 19.5 22.8 19.55 17.21 0.41 15.26 16.73 15.42 9.63 1.05
100 38.9 45.5 39.02 17.19 0.41 30.46 33.40 30.78 9.65 1.05
Average error % 16.37 2.25 Average error % 8.47 0.58

7. Conclusions

The objective of this research is multi-folded. First, we successfully employed two widely used analytical methods (AGM and TSM) to solve two reaction-diffusion equations representing the packed bed photobioreactor with immobilized-cell, and derive simple semi-analytical expressions of the substrate and product concentrations and analytical expressions of steady-state source terms of liquid and gas phases. Second, we studied the effect of the reaction-diffusion parameters on the concentrations of substrate and product. Third, we added to the literature some useful information about the exploitation of some of the widely used methods, in particular the AGM and TSM. As both methods appear to be effective and reliable in solving nonlinear systems, it is noticed that the AGM is more or less a modification of the Adomian decomposition method and is likely to involve some tedious algebraic computations. The TSM, on the other hand, involves less algebraic computations, gives more accurate results, and guarantees convergence if the conditions of Taylor’s theorem are met.

Author Contributions

Conceptualization, M.A. and L.R.; methodology, M.E.G.L..; software, P.J; validation, M.A., and P.J.; formal analysis, L.R.; investigation, M.E.G.L.; resources, P.J.; data curation, P.J.; writing—original draft preparation, M.A.; writing—review and editing, P.J.; visualization, L.R; supervision, M.E.G.L.; and L.R.; project administration, M.E.G.L.; All authors have read and agreed to the published version of the manuscript.

Funding

The authors have not received any funds.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The author declare no conflict of interest.

List of Symbols

Symbols Description Units
C Local substrate concentration kg/m3
R Radius of the gel granule m
D Diffusion coefficient m2/s
K Absolute permeability m2
M Molecular weight kg mol-1
H Photobioreactor height m
m Maintenance coefficient h-1
m . Source item in mass conservation equation kg m 1 s 1
φ Source item in species conservation equation kg m 1 s 1
α Specific area m2/kg
α * Growth associated kinetic constant for hydrogen production None
β Non- growthassociated kinetic constant h-1
μ Specific growth rate h-1
μ m a x Maximum specific growth rate h-1
u ( ζ ) Dimensionless substrate concentration None
v ( ζ ) Dimensionless product concentration None
α 1 Dimensionless parameter None
γ 1 , γ 2 , γ 3 , γ 4 Dimensionless parameter None
φ 1 , φ 2 Dimensionless parameter None
ψ l , ψ g Dimensionless parameter None
ω Dimensionless parameter None
ζ Dimensionless distance None
Superscripts
S Substrate
H2 Hydrogen
CO2 Carbon dioxide
Subscripts
g Gas phase
l Liquid phase

Appendix A

function pdex4
m = 2;
x = linspace(0,1);
t=linspace(0,10);
sol = pdepe(m,@pdex4pde,@pdex4ic,@pdex4bc,x,t);
u1 = sol(:,:,1);
u2 = sol(:,:,2);
%------------------------------------------------------------------
figure
plot(x,u1(end,:))
title('u1(x,t)')
xlabel('Distance x')
ylabel('u1(x,1)')
%------------------------------------------------------------------
figure
plot(x,u2(end,:))
title('u2(x,t)')
xlabel('Distance x')
ylabel('u2(x,2)')
% -----------------------------------------------------------------
function [c,f,s] = pdex4pde(x,t,u,DuDx)
c = [1; 1];
f = [1; 1] .* DuDx;
a1=10; p1=30;p2=0.1; r1=0.1; r2=0.1;r3=0.1;r4=0.1; %
F1=-(((p1+r1)*u(1)+r2)/(1+a1*u(1)));
F2= -(((p2+r3)*u(1)+r4)/(1+a1*u(1)));
s=[F1; F2];
% -----------------------------------------------------------------
function u0 = pdex4ic(x)
u0 = [0; 0];
% -----------------------------------------------------------------
function [pl,ql,pr,qr]=pdex4bc(xl,ul,xr,ur,t)
pl = [ul(1)-0; ul(2)-0];
ql = [1; 1];
pr = [ur(1)- 1; ur(2)-1];
qr = [0; 0];

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