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ISSN: 1696-8352
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ABSTRACT
This study aimed to simulate the heat and mass transfer process of a spiral tubular Lithium
Bromide/Water (LiBr/H2O) absorber based on a non-linear mathematical model
developed in MATLAB program, using an iterative numerical method and experimental
data from the literature for calibration and validation. For this, the absorber was simplified
as a descending film flat plate and the simulation considered three different cases of
cooling water temperature variation: 21.5°C, 23.5°C, 25.6°C. The effective mass transfer
coefficient, Kef, was obtained from the literature, and the overall heat transfer coefficient,
U, was calculated using the overall thermal resistance within the absorber. The
distributions for the temperature and concentration of the solution and cooling water,
obtained by the model, showed good agreement when compared to the literature. It was
found that the heat and mass transfer increased when varying the absorber length up to
14.25 m, and from this value on, they remained nearly constant. Increasing the mass flow
rate of the cooling water inlet decreases the temperature and concentration of the
LiBr/H2O. In addition, copper and aluminum proved to be more suitable for use in the
absorber tube than stainless steel.
RESUMO
Este estudo teve como objetivo simular o processo de transferência de calor e massa de
um absorvedor tubular de brometo de lítio/água (LiBr/H2O) baseado em um modelo
matemático não-linear desenvolvido no programa MATLAB, usando um método
numérico iterativo e dados experimentais da literatura para calibração e validação. Para
isso, o absorvedor foi simplificado como uma placa plana de filme descendente e a
simulação considerou três casos diferentes de variação da temperatura da água de
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1 INTRODUCTION
In recent years, there has been a growing concern related to the need for changes
in energy matrices and gas emissions that are responsible for the degradation of the
environment, bringing the exposed facts to the real world. The demand for room cooling
is inserted in this context, and an alternative to conventional thermal cooling equipment’s
is absorption refrigeration system. They can be used to take advantage of renewable
thermal sources or waste heat from industrial processes, reducing environmental impacts
from refrigeration (Garcia-Hernando and Vega, 2019).
The absorber has a recognized prominence among the basic components of an
absorption refrigeration system (Jaballah et al., 2019). In the absorber, the concentrated
liquid solution absorbs the refrigerant vapor from the evaporator. As a result, the capacity
of the absorber determines the amount of refrigerant that constantly circulates through the
cycle; thus, the greater the mass and heat transfer in the process in this equipment, the
greater the capacity of the system to remove heat from the fluid, which will be refrigerated
(Giannetti et al., 2017).
In this way, the design of absorbers for absorption refrigeration systems is still
subject to numerous uncertainties since its process involves, simultaneously, heat and
mass exchanges, in addition to the systemic interactions of the absorption of the
refrigerant vapor, requiring greater understanding and demanding of numerous scientific
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studies, mainly because it is known that the performance of these devices is influenced
by their geometry and by the absorption methods employed (Olbricht and Luke 2019).
Olbricht and Luke (2019) carried out an experimental analysis of heat and mass
transfer in a falling film LiBr/H2O absorber of tube bundles aiming to generate
correlations that would improve the design of this equipment. They found that heat
transfer and mass transfer are more significant depending on the Reynolds number of the
fluids that raise the refrigerant's temperature. However, a comparison with literature
correlations revealed a strong deviation between experimental and calculated results.
Toppi et al. (2015) performed modeling and experimental validation of heat and mass
transfer in a tube-in-tube absorber, considering the pressure drop along the equipment.
Arshi and Sudharsan (2020) carried out a detailed experimental study on a
horizontal tube falling film absorber used in a LiBr/H2O system, considering the
influence of the cooling water flow rate, its inlet temperature and spray density on the
temperatures and solution concentrations, heat and mass fluxes, and heat transfer
coefficients. They found, among other things, the better performance in absorption, the
higher the flow of cooling water, while the increase in the temperature of this water
caused the opposite. Nabil et al. (2014) compared a simplified non-linear model and a
simplified linear model to evaluate the overall heat and mass transfer in a spiral tubular
absorber of a LiBr/H2O absorption chiller.
Thus, considering the scarcity in the literature of simulation of the absorption
process in spiral tubular absorbers, this study used a non-linear mathematical model to
simulate heat and mass transfer in a spiral tubular absorber applied in systems that use
the fluid of LiBr/H2O, cooled with counter-current water, to obtain the distributions of
the temperature and concentration of the solution, and of the cooling water.
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copper tubes. Each row consists of 17 tubes with a developed length of 1.9m and an outer
diameter of 19 mm. Both rows are contained within a steel envelope. Therefore, the only
measurable quantities are represented by the inlet and outlet of the absorber. In Figure 1b,
the concentrated LiBr/H2O solution and water vapor are sprayed from the top of the
absorber, forming a film with the water vapor onto the spiral tubes. The cooling water
enters from the bottom of the absorber and flows into the tubes, and the absorption process
takes place outside the tubes.
Since the outside diameter of the absorber spiral tubes is much smaller than the
length, the heat and mass transfer process that takes place inside the absorber can be
simplified as a vertical flat plate, where the absorbing solution and the cooling fluid are
in a counterflow, Figure 1c. Inside the absorber, the concentration of the LiBr/ H2O
solution decreases along the flow direction of the solution because of water vapor
absorption. The heat of absorption that is generated in the vapor absorption by the
LiBr/H2O solution is coupled with the heat transferred between the LiBr/H2O solution
and cooling water, yielding the temperature variation along the longitudinal axis in both
fluids.
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ii.The solution film is treated as a semi-infinite medium for heat and mass transfer;
iii.The steam is considered to be single-phase;
iv.The solutions in the system are Newtonian and the physical properties constant
with temperature and concentration;
v.The descending film is considered laminar flow;
vi.Equilibrium pressure exists at the vapor-solution interface;
vii.The vapor continues with uniform pressure (which is the absorption pressure) and
temperature;
viii.Vapor drag in the descending film is negligible;
ix.The heat transferred from the solution to the vapor is negligible.
The heat transfer coefficient from the LiBr/ H2O solution to the tube wall is hi,
and the heat transfer coefficient from the tube wall to the cooling water is ha. The overall
heat transfer coefficient between the solution and the cooling water is represented by the
variable U. To study the mass and the heat transfer within the absorber, three independent
variables were considered: the temperature of the cooling water, Ta, the temperature of
the LiBr/H2O solution, Ts and the concentration of LiBr in the solution, s.
Figure 2. (a) Schematic of the control volumes. (b). Energy balance at the liquid-vapor interface
Source: Adapted from (Tsai and Blaco, 1998) and (Patnaik et al., 1193).
The energy and mass balance were constructed using the control volume of length
dX, section ABCD of the descending film of the LiBr/H2O solution, figure 2a, with the
equation for the heat of absorption d𝑄𝑠𝑎 expressed by the product of the overall heat
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transfer coefficient, U with the temperature difference between the solution and the
coolant, based on the external surface area, expressed as:
𝑑ℎ𝑠 𝑑𝑚𝑣
𝑀𝑠 = ℎ𝑣𝑠 − 𝑈(𝑇𝑠 − 𝑇𝑎 ) (1)
𝑑𝐴 𝑑𝐴
ℎ𝑣𝑠 = ℎ𝑣 − ℎ𝑠 (2)
The enthalpy of the LiBr/H2O solution, hs, 𝑖s a function of Ts, and s. Therefore,
the equation for conservation of energy on the solution side o'f LiBr/ H2O can be
expressed as:
The change in vapor absorption rate, dmv, can be expressed in terms of the mass
transfer coefficient, Km, as:
For an infinitesimal control volume of length dX, involving the interface (figure
2.b), the energy conservation equation for the interface, can be expressed as:
hpv, depends on the temperature and the interface concentration, Tif e 𝜔𝑖𝑓 .
The condition at the liquid-vapor interface can be expressed through equations (6)
and (7), as:
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The enthalpy of absorption in the liquid, hab, must be evaluated at the average
temperature. It was assumed that the if, and Ts, are in equilibrium at the interface at the
same constant vapor pressure, Pv, and the relationship between temperature and
concentration at equilibrium is approximately linear (Ibrahim and Vinnicombe, 1993),
expressed as:
The constants “a” and “b”, can be considered for the working pressure range of
the LiBr/H2O system from 0.8 kPa to 2 kPa, where 𝑎 is constant at equilibrium ratio and
𝑏 is a coefficient at equilibrium ratio [K-1]
𝑃 −0.188
𝑎 = 0.37794 (𝑃 ) (9)
0
𝑃 −0.06574
𝑏 = 4.8688 × 10−3 (𝑃 ) (10)
0
where:
The condition at the liquid-vapor interface, the equilibrium ratio, and the
concentration at the interface, if, can be expressed as:
𝜆(𝑎+𝑏𝑇𝑠 )+𝑏𝜔𝑠
𝜔𝑖𝑓 = (11)
𝜆+𝑏
ℎ0
𝜆=ℎ (12)
𝑎𝑏 𝐾𝑚 𝜌𝑠
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Equations 13 and 14 express the change in mass flow rate of the LiBr/H2O solution
relative to the absorption area differential, dA, as:
𝑑𝑀𝑠
= 𝐾𝑒𝑓 𝜌𝑠 (𝜔𝑠 − (𝑎 + 𝑏𝑇𝑠 )) (13)
𝑑𝐴
1 1 𝑏ℎ𝑎𝑏 𝜌𝑠
=𝐾 + (14)
𝐾𝑒𝑓 𝑚 ℎ0
The mass of the absorbent, LiBr salt, in the solution is assumed constant:
𝑀
𝑀𝑠 = 𝜔 𝑙 (15)
𝑠
𝑑𝜔𝑠 𝐾𝑒𝑓 𝜌𝑠 𝑀𝑙
=− (𝜔𝑠 − (𝑎 + 𝑏𝑇𝑠 )) (16)
𝑑𝐴 𝑀𝑠2
The temperature profiles of the solution, Ts, and the cooling water, Ta, are
represented by differential equations 17 and 18, as:
𝑑𝑇𝑠 ℎ 𝐶 𝑀 𝑈
= 𝐾𝑒𝑓 𝜌𝑠 (𝑀 𝑣𝑠𝐶 + 𝑀𝑤2 𝐶 𝑙) (𝜔𝑠 − (𝑎 + 𝑏𝑇𝑠 )) − 𝑀 𝐶 (𝑇𝑠 − 𝑇𝑎 ) (17)
𝑑𝐴 𝑠 𝑠 𝑠 𝑠 𝑠 𝑠
𝑑𝑇𝑎 𝑈
= −𝑀 (𝑇𝑠 − 𝑇𝑎 ) (18)
𝑑𝐴 𝑎 𝐶𝑝𝑎
The above set of governing equations allows predicting the behavior of the
concentration, temperature of the solution, and the cooling water temperature Ts, s and
Ta, for the analyzed absorber.
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𝑇𝑠 𝑖 −𝑇𝑠 𝑖−1 ℎ 𝐶 𝑀 𝑈
= 𝐾𝑒𝑓 𝜌𝑠 (𝑀 𝑣𝑠𝐶 + 𝑀𝑤2 𝐶 𝑙) (𝜔𝑠 − (𝑎 + 𝑏𝑇𝑠 𝑖 )) 𝐿 − 𝑀 𝐶 (𝑇𝑠 𝑖 − 𝑇𝑎 𝑖 )𝐿 (20)
𝑑𝑋 𝑠 𝑠 𝑠 𝑠 𝑠 𝑠
In the case of the cooling water temperature, Ta, the first derivative approximation
by progressive finite differences was used; taking into account that the water flow is in
countercurrent with the flow of the LiBr/H2O, solution, so the new value of the cooling
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water temperature evaluated at xi, will depend on the previous value of the cooling water
temperature that is at xi+1, as shown in figure 3.
𝑇𝑎 𝑖+1 −𝑇𝑎 𝑖 𝑈
= −𝑀 (𝑇𝑠 𝑖 − 𝑇𝑎 𝑖 )𝐿 (21)
𝑑𝑋 𝑎 𝐶𝑝𝑎
ℎ 𝐶𝑤 𝑀 𝑈
𝑇𝑠 𝑖−1 +[𝐾𝑒𝑓 𝜌𝑠 ( 𝑣𝑠 + 2 𝑙 )(𝜔𝑠 −𝑎)]𝐿𝑑𝑋+ 𝑇 𝐿𝑑𝑋
𝑀𝑠 𝐶 𝑠 𝑀𝑠 𝐶 𝑠 𝑀𝑠 𝐶 𝑠 𝑎 𝑖
𝑇𝑠 𝑖 = ℎ 𝐶𝑤 𝑀 𝑈
(23)
1+[𝐾𝑒𝑓 𝜌𝑠 𝑏( 𝑣𝑠 + 2 𝑙 )]𝐿𝑑𝑋+ 𝐿𝑑𝑋
𝑀𝑠 𝐶 𝑠 𝑀𝑠 𝐶 𝑠 𝑀𝑠 𝐶 𝑠
𝑈𝐿
𝑇 𝑑𝑋+𝑇𝑎 𝑖+1
𝑀𝑎 𝐶𝑝𝑎 𝑠 𝑖
𝑇𝑎 𝑖 = 𝑈 (24)
1+ 𝐿𝑑𝑋
𝑀𝑎 𝐶𝑝𝑎
The amount of vapor mass absorbed, mv, the change in lithium bromide (LiBr)
concentration at the interface, if, and the change in the mass flow rate of the if, and the
change in the mass flow rate of the LiBr/H2O solution, (Ms), were calculated using the
discrete equations (25), (26) e (27):
𝜆(𝑎+𝑏𝑇𝑠 )+𝑏𝜔𝑠
𝜔𝑖𝑓 = (25)
𝜆+𝑏
Figure 4 shows the flowchart of the model developed to calculate the temperature
and concentration profiles of the LiBr/H2O solution, Ts, and s and the temperature profile
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of the cooling water, Ta, inside the absorber. The subroutine approach starts by entering
the initial data, the properties of the LiBr/H2O solution, and cooling water, such as
density, specific heats, flow rates, the required enthalpies, the operating pressure of the
absorber, and the reference pressure. Also needed are the values of the heat and mass
transfer coefficients. It was necessary to solve the equation system (17, 18 e 20) through
the Gauss-Seidel method, using an initial value of the solution temperature (𝑇𝑠𝑣 ), the
solution concentration (𝑣𝑠 ) and the cooling water temperature (𝑇𝑎𝑣 ) to initialize the
iterative procedure.
The program determines the new values of the solution temperature (𝑇𝑠𝑁 ), solution
concentration (𝑁 𝑁
𝑠 ), and cooling water temperature (𝑇𝑎 ), all from the equation system,
from the initial values, and calculates the error between the old value and the new value
against the stopping criterion, the precision error (e). If the error exceeds the precision
error value, the values of the solution temperature, solution concentration, and cooling
water temperature are updated to determine the new values. If the error does not exceed
the error allowed, the obtained values represent the solution temperatures and
concentration. Finally, the program visualizes the values of the solution temperature, the
solution concentration, and the cooling water temperature.
Also included in the program were the equations for determining the flow rate of
the LiBr/H2O solution, Ms, the absorbed vapor flow rate, mv, and the concentration at the
interface, if, through the equations. In the end, the profiles of the LiBr solution
temperature and concentration, 𝑇𝑠 and 𝜔𝑠 , as well as the cooling water temperature,𝑇𝑎 are
determined.
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Figure 4. Flowchart of the numerical model developed for the heat and mass transfer process inside an
absorber using the MATLAB computational platform.
Table 1. Characteristics of the spiral absorber. Adapted from Nabil et al. [8]
Item Characteristics Symbol Unit Value
2
01 Total absorber area At m 3.86
02 Outer tube diameter d m 0.019
03 Length of spiral tube X m 1.9
Source: The authors (2023)
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Table 2 shows the operating conditions of the absorber, which were obtained from
the experimental data performed (Nabil et al. 2014).
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Figure 6. Physical mesh elements variation. a) Temperature profile of the LiBr/H 2O solution at the outlet
of the absorber b) Relative error of the temperatures of the LiBr/H2O solution at the absorber.
41,0 1,604%
39,0
37,0 1,204%
Ts [°C]
Error
35,0
33,0 0,804%
31,0
29,0 0,404%
0,0 0,4 0,8 1,1 1,5 1,9
nodes=5
Absorber length nodes=15
nodes=10
[m] 0,004%
nodes=20 nodes=25 nodes=30 5 20 35 50 65 80 95 110 125
nodes=35 nodes=40 nodes=45 Physical mesh elements
Source: The authors (2023)
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therefore the LiBr/H2O solution temperature decreases faster with absorber length, as
there is greater heat transfer between both fluids. The maximum relative errors found
between the values of the developed model and the values taken from the literature were
1.2% and 2.01%, corroborating the ability of the numerical model to predict the behavior
of the solution temperature along the absorber.
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Figure 7. Temperature of the LiBr/H2O solution in the absorber. Left) Tae= 21°C. Right) Tae= 25.6°C
On the other hand, the figure 8 shows the comparison between the values of the
temperature distribution of the LiBr/H2O solution and the results extracted from Nabil et.
al (2014) by using a coupled nonlinear model, where the effective mass transfer
coefficient, Kef, and the overall heat transfer coefficient, U, and the heat flux were
calculated by linearizing the model. It can be observed that the distribution obtained in
Nabil et. al. (2014) increases at the inlet of the absorber but decreases right after growth
since the absorption heat generated in the vapor absorption process cannot be completely
removed in the cooling process, which increases the temperature of the solution. The
results obtained using the proposed model show a solution temperature distribution with
a negative temperature gradient along the length of the absorber, i.e., the temperature
decreases with the length of the absorber. However, there is no increase in the solution
temperature at the inlet of the absorber due to the difference in the values of the solution
properties, where for the specific heat, enthalpy, and density the values were considered
constant, according to what was proposed by Islam et al. (2004), but Nabil et al. (2014)
used a variation of the enthalpy value and the specific heat as a function of temperature.
Despite this simplification, the maximum relative errors were insignificant, with values
less than 3.00%.
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Islam et al. (2004), It is observed that the variation of the LiBr concentration rate in the
solution had a decreasing behavior along the absorber length, indicating that the water
vapor absorption process by the solution was more relevant at the inlet of the absorber.
In figure 8, it can be seen that the concentration of LiBr in the solution was reduced
as the temperature of the cooling water was also decreased, i.e. more of the heat generated
by the process of water vapor absorption by the solution was removed through the cooling
water, optimizing the absorptive process.
Figure 8. LiBr concentration in the solution inside the absorber. Left) Tae= 21°C. Right) Tae= 25.6°C
The almost linear distribution of the LiBr concentration in the LiBr/H2O solution
is a result of the small variation of the mass flow of absorbed water vapor from the inlet
to the outlet of the absorber.
Comparing the distributions of the simulations for the temperature of the
LiBr/H2O solution (fig. 7), with the distribution of the LiBr concentration in the LiBr/H2O
solution inside the absorber (fig. 8), for the three tests, it can be observed that in the initial
sections of the absorber the temperature distribution of the solution presents a larger
gradient than the concentration of the solution, because of the thermal diffusivity (Dt =
1.427e-7 m2/s), which represents an order of magnitude larger than the mass diffusivity
(Dm= 1.352e-9 m2/s) of the LiBr/H2O solution. The results found for LiBr concentration
were 0.5501, 0.5602, 0.5660, with maximum relative errors of 1.77%, 2.79%, and 3.11,
respectively, with the experimental data.
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Figure 9. Cooling water temperature variation inside the absorber. Left) Tae= 21°C. Right) Tae= 25.6°C
30 30
Experimental
25 Simulation
Simulação 25
T [°C]
T [°C]
20 20 Experimental
Simulação
15 15
0 0,38 0,76 1,14 1,52 1,9 0 0,38 0,76 1,14 1,52 1,9
Absorber length [m] Absorber length [m]
Source: The authors (2023)
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Figure 10. Vapor flow absorbed in the absorber considering Tae = 23.5 °C
Therefore, while the concentration gradient across the film increases with length,
the diffusion resistance on the liquid side forces the concentration profile to follow the
same trend as the cooling fluid, in this case, water. The maximum errors found for the
mass flow rate of the absorbed vapor were 6% and 5% lower than the values found in the
literature.
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subsequent simulations, until reaching a length of 23.75 m with 1000 nodes in the ab-
sorber tube. Figure 11a represents the variation of the temperature of the LiBr/ H2O solu-
tion at the outlet of the absorber as the length of the tube increases. Considering that the
flow rate and the inlet temperatures of the solution and cooling water remain constant,
and varying the length of the tube, there is an increase in the total absorption area, and, in
this sense, the overall heat transfer coefficient, U, tends to decrease, leading to an increase
in the amount of heat of the solution to be removed by the cooling water, and finally, the
temperature of the LiBr/H2O solution at the absorber outlet is reduced. The variation of
the LiBr/H2O solution concentration in the absorber as a function of increasing absorber
tube is shown in figure 12b. The concentration is represented in the mole fraction of LiBr
in the LiBr/H2O solution.
As observed in Fig. 11b, increasing the length of the absorber tube provides a
direct increase in the total area leading to a greater absorption heat exchange from the
solution, and therefore allowing greater absorption of the vapor into the solution, decreas-
ing the concentration of LiBr at the outlet of the absorber. Moreover, from the value of
9.5 m of tube length, it is observed that the LiBr/H2O solution temperature tends to be
stabilized, almost constant, due to the consideration of constant operating parameters,
causing the longer tube lengths to have thicker thermal boundary layers at the end of the
length, entailing a lower temperature gradient on the wall, and consequently a lower heat
exchange by conduction, corresponding to a lower convection heat coefficient. This leads
to a decrease in heat and mass exchange inside the absorber (Ochoa et al., 2017; Lima et
al., 2021), and therefore less steam will be absorbed for the absorption process of the
absorption cooling system, a fact observed in fig. 11b.
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Figure 11. a) LiBr/H2O solution outlet temperature varying of the absorber tube length. b) Solution con-
centration varying of the absorber tube length.
45 0,60
40
0,52
30
0,54 14,25;
0,52
25
20 0,51
0 4,75 9,5 14,25 19 23,75 0 4,75 9,5 14,25 19 23,75
Absorber length [m] Absorber length [m]
Source: The authors (2023)
Figure 12. a) Heat transferred within the absorber considering the cooling water inlet temperature at the
absorber outlet. b) LiBr/H2O solution temperature considering the cooling water inlet temperature at the
absorber outlet.
44
14
12 40
10
Heat [KW]
36
8
Ts [°C]
6 32
4
28
2
0 24
0 0,38 0,76 1,14 1,52 1,9 0 0,38 0,76 1,14 1,52 1,9
Absorber length [m]]
Ta=10.5 Ta=14.5 Ta=18.5 Absorber length [m]
Ta=10.5 Ta=14.5 Ta=18.5
Ta=22.5 Ta=26.5 Ta=30.5
Ta=22.5 Ta=26.5 Ta=30.5
Source: The authors (2023)
It is observed that by decreasing the inlet cooling water temperature, at the outlet
of the absorber, there is an increase in heat exchange due to the increased difference in
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the temperatures of the cooling water and the LiBr/H2O solution. Since the arrangement
in the absorber, between the LiBr/H2O solution and the cooling water, is countercurrent,
there is a greater heat transfer in the final sections of the absorber. Figure 12b shows the
variation of the LiBr/H2O solution temperature inside the absorber with the variation of
the cooling water inlet temperature at the absorber outlet. It can be seen that by increasing
the cooling water inlet temperature, the absolute value of the gradient of the solution tem-
perature inside the absorber with the absorber length decreases, the heat transfer is lower,
there is less vapor absorption at the interface, and a higher solution temperature at the
absorber outlet.
Figure 13 shows the variation of the concentration of the LiBr/ H2O solution inside
the absorber with the variation of the cooling water inlet temperature at the absorber out-
let.
The concentration is given in the fraction of LiBr within the LiBr/ H2O solution.
It can be seen that by increasing the inlet temperature of the cooling water, the absolute
value of the gradient of the concentration of the solution inside the absorber with the
length of the absorber decreases, there is less vapor absorption at the interface, and at the
exit of the absorber the LiBr concentration is not decreased.
Figure 13. LiBr/H2O solution concentration considering the cooling water inlet temperature at the ab-
sorber outlet.
0,6
LiBr mass fraction
0,58
Ta=10°.5C Ta=14.5°C
0,56 Ta=18.5°C Ta=22.5°C
Ta=26.5°C Ta=30.5°C
0,54
0 0,38 0,76 1,14 1,52 1,9
Absorber length [m]
Source: The authors (2023)
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Figure 16. a) LiBr/H2O solution temperature considering the cooling water inlet flow rate at the absorber
outlet. b) LiBr/H2O solution concentration considering the cooling water inlet flow rate at the absorber
outlet.
44
0,59
LiBr mass fraction
41
38
0,57
35
T [°C]
32
0,55
29 0 0,38 0,76 1,14 1,52 1,9
0 0,38 0,76 1,14 1,52 1,9
Absorber length [m]
Absorber length [m] Ma=0.199 kg/s Ma=0.398 kg/s
Ma=0.796 kg/s Ma=1.596 kg/s
Ma=0.199 kg/s Ma=0.398 kg/s
Ma=0.796 kg/s Ma=1.592 kg/s Ma=3.1834 kg/s Ma=6.368 kg/s
It is observed that by increasing the cooling water flow rate, the solution temper-
ature at the outlet of the absorber decreases. This is due to the effect of increasing the
cooling water flow rate, directly increasing the Reynolds number of the cooling water
flow, and the heat transfer coefficient on the cooling water side (h), and therefore its
overall heat transfer coefficient, U. This leads to a decrease in the LiBr concentration at
the absorber outlet, as can be seen in Figure 16b.
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ISSN: 1696-8352
heat transfer coefficients, U, were calculated based on the type of tube material. In Figure
17 it is observed that the use of Copper and Aluminum showed very similar LiBr/H2O
solution temperature profile values, as a function of the overall absorber heat transfer
coefficient, which was similar (487.8 and 482.6 W/m.K).
The absolute value of the gradient of the solution temperature with the length of
the absorber with copper and aluminum was higher than that shown by the absorber tube
with Steel, due to having a lower overall heat transfer coefficient, U, i.e., there is less heat
transfer between the cooling water and the solution.
Figure 19. Temperature behavior of the LiBr/H2O solution varying the absorber tube material. Figure 20.
LiBr/H2O solution concentration varying the absorber tube material.
The behavior of the solution concentration, Figure 20, using Copper or Aluminum
was similar since the heat transfer between the cooling water and solution was similar,
i.e., the vapor absorption by the solution was similar with both materials. Furthermore,
the absolute value of the gradient of the solution concentration with the absorber length,
𝑑𝜔𝑠
𝑑𝑋
, with these materials (Copper and Aluminum) was higher than the absolute value
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presented by the Steel absorber tube, which allowed less heat transfer between the cooling
water and the solution temperature, and therefore less mass transfer at the interface.
7 CONCLUSIONS
A study of the heat and mass transfer process within a lithium bromide and water
tubular spiral absorber, simplified as a flat downward film plate, in one dimension at
steady state with the fluids in countercurrent, is developed using a nonlinear mathematical
model. Three different cases were simulated by varying the cooling water temperature by
21.5°C, 23.5°C, 25.6°C, where the values of the average overall transfer coefficient were
491, 470 and 423.74 W/(m.K).
For the temperature distribution, which showed good agreement when compared
to literature data, it is observed that in the initial sections thermal diffusion governs the
process inside the absorber and with high transport coefficients, but as soon as heat is
transferred between the cooling water and the solution the mass transfer process is
optimized, and the temperature profile of the solution becomes almost linear.
It was found that the heat and mass transfer increased when varying the length of
the absorber until it reached 14.25 m. After this value, these transfers remained almost
constant. Moreover, by reducing the cooling water inlet temperature, keeping the other
conditions constant, the heat transferred increases, with the cooling water distribution and
the solution concentration being linear.
Increasing the cooling water mass flow rate decreases the temperature and
concentration of the LiBr/H2O solution. When varying the material of the absorber using
copper, aluminum, and stainless steel, it was observed that the first two are better
materials to be used in the absorber tube due to higher thermal conductivities.
ACKNOWLEDGMENTS
The first author thanks the CAPES and PPGEM/UFPE. The third and fourth authors
thanks the CNPq for the Productivity Grant nº 313014/2022-1 and 3303417/2022-6.
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REFERENCES
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ISLAM MD.R, WIJEYSUNDERA NE, HO JC. Heat and mass transfer effectiveness and
correlations for counter-flow absorbers, International Journal Heat and Mass transfer,
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ISLAM MD.R, WIJEYSUNDERA NE, HO JC. Simplified models for coupled heat and
mass transfer in falling-film absorbers, International Journal Heat and Mass transfer,
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KIM, D. S., INFANTE FERREIRA, C. A. A Gibbs energy equation for LiBr aqueous
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NABIL, B. H., BECHIR, C.; SLIMANE, G. Global modeling of heat and mass transfers
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Olbricht, M., Luke, A. Experimental investigation of the heat and mass transfer in a tube
bundle absorber of an absorption chiller, Heat and Mass Transfer/Waerm, 2019, 55:
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ANEXOS
Nomenclature
Mass fraction of LiBr at the vapor-solution Convection heat transfer coefficient in
if; ℎ𝑎 ;
interface cooling water [W/(m.°K)]
Enthalpy of absorption in the liquid
p; Tube wall thickness [m] hab;
[J/kg]
Convective heat transfer coefficient in
s; Density of the LiBr/H2O solution [kg/m3] ℎ𝑖 ;
the LiBr/H2O solution [W/(m.°K)]
Partial enthalpy of water vapor
Kinematic viscosity of the LiBr/H2O
s; hpv; absorbed at the liquid-vapor interface
solution [m2/s]
[J/kg]
Enthalpy of the LiBr/H2O solution
s; Film thickness of LiBr/H2O solution [m] hs;
[J/Kg]
Enthalpy of water vapor at the
𝜇𝑎 Dynamic viscosity of cooling water [N.s/m2] h v;
solution-vapor interface [J/Kg]
Thermal conductivity of cooling water
𝑎; Constant in the equilibrium relationship 𝑘𝑎 ;
[W/m.K]
Thermal conductivity of the tube wall
𝑏; Coefficient in the equilibrium ratio [K-1] 𝑘𝑝 ;
[W/m.K]
Thermal conductivity of the LiBr/H2O
C; Enthalpy Constant [J/kg] 𝑘𝑠 ;
solution [W/m.K]
Mass transfer coefficient from the
𝐶𝑝 𝑎 ; Specific heat of cooling water [kJ/kg] Km; interface to the LiBr/H2O solution
[m/s]
𝐶𝑝 𝑠 ; Specific heat of the LiBr/H2O solution
L; Flat plate width [m]
[kJ/kg]
Heat capacity of the LiBr/H2O solution at
Cs; Ma; Mass flow of cooling water [kg/s]
constant LiBr mole fraction [J/(kg.K)]
Change in LiBr molar fraction in LiBr/H2O Mass flow rate of the LiBr/H2O
d s; Ms;
solution solution [kg/s]
Dimensionless Nusselt number for
dA; Absorption Area Differential [m2] Nua;
cooling water
Dimensionless Nusselt number for
dEc; Variation of the system's kinetic energy [W] Nus;
solution
dEp; Potential Energy Variation, [W] P; Absorber pressure [KPa]
Enthalpy variation of the LiBr/H2O solution
dhs; P0; Reference pressure [KPa]
[W/(m2.K)]
Variation in the mass absorption rate of water Prandtl's dimensionless number for
dmv; 𝑃𝑟𝑎 ;
vapor [kg/s] cooling water
Variation in the mass flow rate of the Prandtl's dimensionless number for the
dMs; 𝑃𝑟𝑠 ;
LiBr/H2O solution [kg/s] LiBr/H2O solution
Variation of heat transferred to the system
dQ r; Absorber tube radio [m]
[W]
Change in the rate of heat flow by
Dimensionless Reynolds number for
dQsa; conduction from the LiBr/H2O solution to 𝑅𝑒𝑎 ;
cooling water
the tube wall [W]
Dimensionless Reynolds number for
dTa; Change in cooling water temperature [K] 𝑅𝑒𝑠 ;
the solution
dTs; Change in solution temperature [K] Scs; Dimensionless Schmidt number
Variation of the internal energy of the system
dU Sh; Sherwood's dimensionless number
[W]
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