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International Journal of Mechanical & Mechatronics Engineering IJMME-IJENS Vol:18 No:05 33
180505-3737-IJMME-IJENS © October 2018 IJENS I J E N S
Improvement in Heat Transfer Inside a phase change
Energy System Maitham Jameel Zaidan and Mohammed H. Alhamdo
Al-Mustansiriya University, College of Engineering, Mechanical Engineering Department, Iraq
Abstract-- In this work, an experimental and numerical
investigation was designed for recover the waste heat from the
air conditioning system. The model includes a vertical thermal
glass capsule with diameter of 60 mm and length of 300 mm of
glass thickness 1.5 mm. The capsule containing paraffin wax as a
phase change material (PCM) with 9mm diameter copper tube
with U-shaped for passing water flow through it as a discharging
heat transfer fluid. The study focusses on the enhancement heat
transfer by adding Alumina nanoparticles (AL2O3) with volume
fractions (0.5%, 1%, 2% and 3%). The results indicate the
effects of AL2O3 decreases melting rate time a proximately
7,15,11,9% besides decreases solidification rate time
approximately 4,8,6,5% respectively as compared to pure
paraffin. Also, the effect of adding a pair of copper tubes inside
the paraffin wax was tested during melting and solidification
process.
Index Term-- Phase change material, paraffin wax, thermal
storage, thermal conductivity, nano particles
1 INTRODUCTION
The continuous growth in fuel prices, gas radiations and
the level of greenhouses are the main reasons for researchers
around the world to find alternative and renewable sources of
energy directly dependent on direct solar radiation sunlight as
well as the development of means to store this energy [1].
Flow around stationary cylinders that contains paraffin wax
draw attention many of researchers, the separation of the
boundary layer had a significant effect on the amount of the
heat transfer in additional the description of the streamline,
velocity and pressure profile was described by [2] . The heat
transfers contours from tubes and other bodies in cross flow
are determined by many parameters like stream velocity,
physical properties of fluid, thermal heat flux direction,
geometry of the bodies like smooth circular cylinders [3] [4],
corrugated cylinders.[5]
The technology of phase change materials (PCMs) are one of
these energy storage devices. This part will describe how
energy storage with phase change material technology may
play a role in tackling more of the storage problems within
energy systems [6].
Paraffin wax is a thermoplastic material that can be
reformed by heat. Paraffin is one of the components of the oil
take out through the refining process, coal and other organic
materials like bituminous shale, wood, fish tallow, lignite, etc.
The melting point of paraffin rises with increasing average
molecular weight and its range from 25°C to 68°C. However,
the applications of paraffin are limited because of it has low
thermal conductivity[7] .
According to the low thermal conductivity of the paraffin
wax, there are many passive techniques are used to enhance
thermal properties like adding the Nanoparticles to the hot
fluid [8][9], insert twisted tapes [10] [11], and continuous or
discrete ribs and other factors, [12] [13].
For many latent heat thermal energy storage systems, heat
transfer enhancement techniques are required. Several
procedures are suggested to enhance heat transfer in a latent
heat thermal energy storage system (LHTES), such as finned
tubes, fillers of metallic and matrix structures of metal, were
used to improve the thermal properties of the phase change
materials (PCMs). Enhancements followed with other
techniques are also including;
i. PCM inclosing dispersed high conductivity particles,
Lessing rings [14]
ii. Microencapsulated PCM [15].
iii. Active methods of agitators, vibrators, slurries and
scrapers.
iv. Extended surfaces such as fins and honeycombs [16].
v. PCM mixed with composite material [17] .
(Valan Arasua, et al., 2011) [18]studied the rate of heat
transfer enhancement of phase change materials of paraffin.
The results illustration that the enhancement in heat transfer
rate of paraffin wax is better for associated with the
nanomaterials.
(Kyad et al. 2016 ) [19] studied related previous methods for
enhancement the thermal conductivity of the used PCM,
mainly paraffin, to successfully charge and discharge latent
heat energy and appearances at the formulation of the phase
change problem. Also, experiences to improve the solid-liquid
phase change process were led to examine a technique of
improving the thermal conductivity of paraffin by
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180505-3737-IJMME-IJENS © October 2018 IJENS I J E N S
incorporating in it a 1% mass fraction of two additives
(Copper and Aluminum). It is found that useful heat gains
increased, and charging time was reduced by adding
aluminum Nano powder.
(Putra, Prawiro, and Amin 2016) [20] studies bees wax as a
(PCM) which has high thermal capacity, with the of studying
the thermo-physical performances and properties of bees wax
with CuO nano PCM. Adding nanoparticles of CuO improved
thermal conductivity of wax and its heat capacity will reduced.
The change in latent heat caused no important effects in the
performance of beeswax/CuO. Thermal conductivity
enhancement of the beeswax/CuO was reached by 0.53, 1.55,
1.91, 1.97, and 2.07 W/mK for 0.05, 0.1, 0.15, 0.2, and 0.25
wt% of nano-PCM, respectively
(Ali , et al 2013) [21] studied an experimental and numerical
different cases of enhancement thermal conductivity and the
rate of heat transfer of four pure paraffin, one of them
produced by an Iranian company (KCC Co.) ,the second
produced as a bee wax by (Haman Co., Germany) and the
others produced by (Al- Durra Refinery) of Iraqi oil company
(Grade A and Grade B). They found that the thermal
properties of the wax of Grade B are the best before and after
adding the additives. The copper network additives from 3%,
6% and 9% wt., increase the thermal conductivity of pure wax
Grade (B) by 105.14%, 257.47% and 274.76% respectively
and Grade (B) wax/copper network composite of 6% wt.,
decreased the charging and discharging times by 26.4% and
30.2% respectively.
The objective of this research is to manufacture a
Waste Heat Recovery System (WHRS) to reuse air
conditioning waste energy exiting from condenser. In
additional investigate the effect of different volume fractions
nanoparticles of AL2O3 suspended in the PCM to enhance
heat transfer performance. The experiential results will
compare with the results of ANSYS Fluent 17.2.
2 NUMERICAL SIMULATION
The physical model used in this work is a cylindrical
capsule with 0.06 m diameter, 0.3m long and thickness 1.5
mm. The capsule contains pure paraffin or paraffin spread
with 0.5%, 1% ,2% and 3% volume fraction of Al2O3
nanomaterials. The governing equations are as follows:
The continuity equation:
(1)
The equation of Momentum:
( ) ( )
(2)
The energy equation:
( ) (3)
Where: P is the static pressure, is the stress tensor, is
external body forces, ρ the gravitational body force, T is the
temperature, ρ is density, S is term of heat source, is the
velocity.
Boundary conditions 2.1
The boundary conditions are considered for the inlet air
constant temperature for the (HTF1) heat transfer fluid of 75C,
for the duct wall will set to be adiabatic because it was a well-
insulated. While for the inlet water; during discharging
process the second heat transferred fluid (HTF2) which was
water passing through the copper pipe with constant volume
flowrate and temperature as 0.01 l/s and 27 °C respectively.
Assumptions 2.2
There are some assumptions was produced in this case
like the PCM is Newtonian, incompressible and laminar, the
physical properties of paraffin wax are function of the
temperature, Transient three-dimensional models, the volume
difference resulting from the change in phase of wax is
ignored and no dissipation in power through the duct.
Generation of Mesh. 2.3
In the simulation of this work, ANSYS FLUENT 17.2
software produced to sole the Naiver- Stoke equations by
defaulting quadrilateral mesh element had been used because
of the simple geometry. To ensure high accuracy of
calculation a small grid size has been used, the model has a
mesh with range (300,000-500,000) nodes and (1,500,000-
2,000,000) elements. In this work the thermal properties of
PCMs, as viscosity and density are considered as function of
temperature variations using (Piecewise-Linear Definition)
method which determined by definite below correlations.
(
) (4)
ρ
(5)
Where A, B are constant coefficients, is the density of
PCM at the melting temperature , β is the thermal
expansion coefficient.[22]
The physical and thermal properties of the nanoPCM are
calculated from the next relations where the subscripts PCM
for paraffin wax and np for nanoparticles.
Density[23] :
Ф Ф (6)
Latent heat [24]:
Ф
(7)
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180505-3737-IJMME-IJENS © October 2018 IJENS I J E N S
Specific heat capacity [25]:
Ф Ф
(8)
Dynamic viscosity [25]:
Ф (9)
The active thermal conductivity is considered from the
correlation by Ref. [25]
( )Ф
( )Ф
Ф
√
( Ф)
Where ßk for AL2O3 = 8.4407 (100 Ф )-1.07304
ʆ
ʆ: correction factor, Ҡ
: is the Boltzmann constant = 1.381 10-
23 (J/K)
f (T.Ф) = (2.821710-2 Ф + 3.91710
-3)
+(-3.066910
-2
Ф-3.9112310-3
)
Where f (T.Ф) is obtained from the experimental data
3 EXPEREMANTAL WORK
In this work a well-insulated rectangular duct with a
single cylindrical capsule content paraffin wax as PCM inside
it. The duct having over-all length of (120cm) wit (32cm) of
square cross-sectional area. The PCM capsule locating at the
distance of (80cm) from the inlet region of the duct which
located at the end of the test system. Figure (1) shows the
physical symbol of the 3-D LHTES.
Fig. 3-1. Physical symbol of the numerical model.
The test rig was illustrated in Figure (2) to achieve the experimental tests.
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Fig. 2. Schematic of the test rig
Fig. 3. photograph of the test rig
The test section consists of two parts. The first part is a
square channel made of iron frame as shown in figure (3).
Two sides of test section are made from transparent plastic
materials (Perspex), with dimensions of 120 cm* 30 cm and 6
mm thickness. The second part is the PCM capsule under
investigation which is made from 6 cm diameter of Pyrex
glass with a length of 30 cm and a thickness of 1.5 mm. (U
shape) are inserted through wax inside capsules. The tubes
dimensions are 9 mm diameter and 35 cm length, as shown in
figure (4)
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Various types of PCM capsules have been investigated, this
include;
1- PCM capsule with one copper U tube and pure
paraffin wax, and then mixed with four different
volume ratios of nano AL2O3 (nPCM) as shown in
figure (5).
2- PCM capsule with two copper tube (U shape) and
optimum volume ratio of (nPCM) as shown in figure
(6) (7).
Fig. 5. Capsule with one copper U tube
Fig. 6. Capsule with two copper U tube
Fig. 7. Capsule with two copper U tube (solid work software
program 2017)
A 24,000 BTU / h air conditioner was used at three fan
speeds of the condenser to supply the test section with waste
hot air. The main purpose of water supply system is to
discharge the heat from paraffin wax in the test section by
passing water through the copper tube. To measure PCM, air
and water temperatures, 16 thermocouples with range of (-100
to 800) ℃ of k-type were fixed as shown below: (Fig. 8)
Fig. 3.Test section
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Fig. 8. Thermocouples location inside PCM capsule
Thermal conductivity apparatus. 3.1
Thermal conductivity can be measured for the pure wax based
on the ASTM standard (C518-04) titled "[Standard Test
Method for Steady State Thermal Transmission Properties by
Means of Heat Flow Apparatus]"[26] (Fig. 9), and according
to the method which described by [27]. Dynamic viscosity
where measured for different volume fractions of the
Nanoparticles.
Fig. 9. Thermal conductivity apparatus
The Calibration 3.2
Calibration was formed to set the values of the thermocouples
and the curve of the thermocouples reading calibration shown
in (Figure 10) and the error was 2.97%.
Fig. 10. Thermocouple Calibration Curve
Mixing of nanoPCM. 3.3
NanoPCM, with volume fraction 0.5%,1%,2% and 3% was
produced by using the ultrasonic device. The slow mixing of
AL2O3 nanoparticles inside paraffin wax is necessary for good
thermal properties of nanoPCM[20] .
4 RESULTS AND DISCUSSIONS
The thermal conductivity results with respect to the volume
fraction of the nanoparticles are shown in figure (11). It is
clear that pure PCM has lower heat transfer rate related to the
same amount of nanoPCM because the thermal conductivity
of pure PCM is lower than the nanoPCM. The results show the
thermal conductivity of the nanoPCM increased when the
volume fraction increased because of high thermal
conductivity of AL2O3 nano particles, that means the thermal
conductivity enhancement was directly proportional to the
volume fraction of the nanoPCM. Thermal conductivity
enhancement of the paraffin wax/AL2O3 was reached by 0.22,
0.23, 0.235 and 0.237 W/mK for 0.05, 0.1, 0.2, and 0.3 V% of
nano-PCM, respectively.
y = 0.9997x R² = 0.9977
0
10
20
30
40
50
60
70
80
0 10 20 30 40 50 60 70 80
Ther
mo
met
er t
emp
erat
ure
°C
Thermocouple temperature °C
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Fig. 11. Effect of nanoparticles on thermal conductivity of nanoPCM
The viscosity of paraffin is found to increase when the
volumetric ratio of AL2O3 nanoparticles increasing, as shown
in Figure (12) likewise, with increasing temperature, the
dynamic viscosity will decrease for the nanoPCM.
Fig. 12. Transient dynamic viscosity of paraffin wax mixed with various
concentration of nano Al2 O3
Figure (13) show the time of melting the wax with and
without nanoparticles. The enhancing of the thermal
conductivity decreases the melting time of nanoPCM.
However, it is clear that 1% nano particles is the best
concentration for enhancing the melting time of the PCM (i.e
1% the best concentration for increasing thermal conductivity
and decreasing melting time because when the volumetric
concentration increased larger than 1% lead to rise viscosity
and decrease the specific heat of nanoPCM.
The results show that addition of AL2O3 nanoparticles to a
paraffin wax as shown in (table1), decrease meting point and
enhance the other thermo-physical properties as shown in
table (2)
Table I The weight of AL2O3 nanoparticles on each volume fraction
Volume
fraction%
AL2O3
(g)
0
0
0.5
11.5
1
23
2
46
3
69
There are not important changes on rate of heat transfer in the
beginning of the melting in the four concentrations of
nanoparticles because the heat transfer by conduction only not
enough to make marked change in heat transfer, then when
paraffin begins to melt, the heat transfer turn to the convection
and the effect of viscosity is greatest because of the viscosity
of wax in liquid phase larger than in solid phase. Then for
higher AL2O3 nanoparticle concentration, the rate of heat
transfer will decrease because of increasing the viscosity
. Fig. 13. Melting processes of pure paraffin wax and wax/ Al2O3
nanoparticles
0.21
0.215
0.22
0.225
0.23
0.235
0.24
0.0% 1.0% 2.0% 3.0%
Ther
mal
co
nd
uct
ivit
y (w
/mk)
Volume fraction%
Maxwell eq.3.15[32]
Expermantal
0.002
0.007
0.012
25 40 55 70Dyn
amic
vis
cosi
ty n
s/m
2
Temperature ºC
Ф=0%AL2O3 nano particles
Ф=0.5%AL2O3 nano particles
Ф=1%AL2O3 nano particles
2025303540455055606570
0 30 60 90 120
Tem
per
atu
re (
°C)
Time (minute)
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Table II Properties of pure and nano paraffin under investigation
Ф= 3% Ф= 2% Ф= 1% Ф=
0.5%
Pure
paraffin Property
2808 2829 2850 2860 2871 Cp
(J/kg.K)
0.233 0.227 0.220 0.217 0.214 K
(W/m.K)
0.0136 0.0133 0.0130 0.0128 0.0127 µ
(kg/m.k)
62 62.4 62.5 63 63.4
Melting
point °C
Melting process of PCM 4.1
During melting process, for all the cases under investigation
the temperature of the upper plane (T7, T8 andT9) were
record higher temperature because of the different in densities
between hot and cold paraffin since the buoyancy force lift the
hot wax as shown in figure (14) (15). The thermocouples in
middle plane (T4, T5 and T6) were record temperatures less
than upper plane and higher than lower plane (T1, T2 and T3).
On the other hand, each thermocouple between the glass wall
and U tube (T1, T4 and T7) was record temperatures higher
than the others in the same plane because of its relative
neighboring to the wall which is exposed to the flow of hot air
during melting process of PCM. All thermocouples in the
center of capsule (T3, T5and T8) record temperature less than
others in the same plane because of relative remoteness from
the flow of hot air during melting process. Due to low thermal
conductivity of paraffin wax that make the upper plan store
more heating during charging process, so more time is needed
to make heat travel downwards. This difference in
temperatures of points in PCM was minimized by
enhancement the thermal conductivity of paraffin wax by
adding nano particles of (AL2O3 to enhance the rate of heat
transfer.
Fig. 14. Time of melting during charging process
Fig. 15. melting process in the PCM capsule
solidification process of PCM 4.2
The discharging process is achieved by passing a cold
water as a cold heat transfer fluid in the copper pipes and
stated directly after the melting process is completed. At initial
time, (approximately up to 10 minutes) the temperature of
PCM decreases sharply, because of large temperature
difference between paraffin wax and HTF2. After that the
temperature of paraffin wax will reduces slowly until reach to
constant value. It is observed that solidification starts around
60◦C. It can be seen, by adding AL2O3 nano particles of
(0.5,1,2 and 3%) to the pure paraffin wax, the solidification
time decrease by (4,8,6,5%) respectively, and by adding pair
of U-tube the solidification time decrease by 60% less than
when adding single U-tube because of doubled quantity of
high thermal conductivity copper U tube inside PCM. The
solidification occurs from the top of the capsule to the bottom
because the entry of cold water is from the top which absorbs
a high amount of heat from liquid PCM. this lead to drop in
temperature relatively fast in upper part of capsule. The other
common phenomenon in all cases is the solidification the of
paraffin wax that surrounding the copper pipes is faster than
the other paraffin in capsule due to the rapid loss of heat to the
water a cross copper pipe as shown in figure (16). This is one
of the main problems that prevent the utilization of all the heat
in the melting paraffin wax. Then, the temperature reaches
steady state very quickly, after complete solidification. It
necessity be noted that the whole required melting time is
leaser than the solidification time.
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5
minutes
10
minutes
15
minutes
20
minutes
25
minutes
Fig. 16. The process of solidification in PCM
5 Comparison between the numerical and experimental
results .
Practical experiments and theoretical simulations have
been compared as shown in figure (17). The results show
that there was an acceptable approximation between
experimental and theoretical results. The percent of
difference between the experimental and numerical data for
melting processes were about 10% increase in time period
of melting for numerical results. The difference between
both results (numerical and experimental) might be because
of some assumptions have been assumed in the ANSYS
FLUENT program software. This include thermal and
physical properties of the paraffin wax to simplify the
solution also the location of the thermocouples inside the
PCM may be changed because of the solidification or
melting of process.
Fig. 17. Comparison between the numerical and experimental results
6 NUMERICAL RESULTS
The results of the simulation in this work for the
melting and solidification of the PCM were performed using
ANSYS FLUENT 17.2 software program. Figures (18) to
(21) show the result of the temperature distribution inside
paraffin wax during charging and discharging process for
various water tube arrangements. At the beginning of the
melting process, the paraffin wax inside the capsule in the
solid state at a temperature of 300 k. The paraffin wax
begins to gain heat from hot heat transfer fluid (air) with
temperature of 342k. It is clearer from results that at the
beginning of this process the wax melts near the wall and
gradually continues to melt towards the center of the
capsule until the melting process is fully completed.
After melting process, the process of the discharging
(solidification) begins. This is done by using the second heat
transfer fluid (water) that enters to the copper pipes at a
temperature of 300 k. The results show that wax is gradually
starting to solidify, starting from the copper pipe wall
towards the wall of the capsule until the solidification
process is fully completed.
It is clear that the PCM temperature contours are non-
uniform during charging process due to the difference in
density and wax low thermal conductivity. In the beginning,
the conduction heat transfer is dominated in the system
(since the PCM in solid state) till the phase change of the
PCM occurred after melting; then both heat conduction and
convection are affected inside the system.
The conduction heat transfer occurs between the solid
surface of the PCM and the capsule wall. The melting
process early occurred near capsule wall and shaped a thin
layer of liquid PCM in a narrow melting area as a result of
heat transfer after about 30 mints. Due to the effect of free
convection, the liquid part of PCM is pushed to the top of
the capsule because of the buoyancy. The solid part of the
PCM is pressed down due to the different densities between
the liquid and solid of PCM. The melting time depends
largely on the number of copper pipes inside the PCM, since
the melting time decrease when the number of pipes
increase and vice versa, that is occur because the conduction
heat transfer depends on the contact area of the suffuses.
30
40
50
60
70
0 20 40 60 80
Tem
per
atu
re °
C
Time (minute)
EXP.
Num.
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30 min 60 min 90 min.
Plane A
Plane B
Plane C
Fig. 18. Temperature contours inside PCM during charging process through 1 U tube
B
C
A
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30 min 60 min 90 min.
Plane A
Plane B
Plane C
Fig. 19. Temperature contours inside PCM during charging process through 2 U tube
B
A
C
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5 min 15 min 25 min.
Plane A
Plane B
Plane C
Fig. 20. Temperature contours inside PCM during dischcharging process through 1 U tube
B
C
A
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A
B
C
5 min 15 min 25 min.
Plane A
Plane B
Plane C
Fig. 21. Temperature contours inside PCM during dischcharging process through 2 U tube
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7 CONCLUSIONS
1- In present work, the effect of volume fraction of
nanoparticles, of high thermal conductivity metal
were studied and discussed. The results in general
show a reduction in the melting and solidification
time of paraffin wax.
2- Diffusion of AL2O3 nanoparticles of AL2O3 in the
wax of paraffin enhances its low thermal
conductivity and therefore when the nanoparticles
had been added, the rate of thermal energy in
charging and discharging significantly enhancing.
3- Adding nanoparticles of AL2O3 to paraffin wax by
volume fraction 0.5%,1%,2% and 3% decreases
melting rate time approximately 7,15,11,9%
respectively compared with pure wax of paraffin.
4- Adding nanoparticles of AL2O3 to paraffin wax by
volume fraction 0.5%,1%,2% and 3% decreases
solidification rate time approximately,4,8,6,5%
respectively compared with pure wax of paraffin.
5- The period decreases for whole melting of the
paraffin wax as the thermal conductivity of
container material increases.
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