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International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1631
Erythritol based Nano-PCM for Solar Thermal Energy Storage
R Manickam1, P.Kalidoss2, Dr.S.Suresh3, Dr.S.Venkatachalapathy4
1Dept. of Mechanical Engineering & Saranathan College of Engineering, TN, India
2Research Scholar, Dept. of Mechanical Engineering & NIT Trichy, TN, India
3Associate Professor, Dept. of Mechanical Engineering & NIT Trichy, TN, India
4Associate Professor, Dept. of Mechanical Engineering & NIT Trichy, TN, India
---------------------------------------------------------------------***----------------------------------------------------------------------
Abstract - Phase Change Material (PCM) plays an
important role as a thermal energy storage device by utilizing
its high storage density and latent heat property. The thermo-
physical policies of Erythritol, (a sugar alcohol), was
investigated as a potential material for developing
increasingly meaty solar thermal energystoragesystemsthan
those currently available. This latent heat storage medium
could be utilized for commercial and industrial applications
using solar thermal energy storage in the temperature range
of 100–150°C. The objective of this investigation was to
determine via experimentation, if TiO2andCNTnanoparticles
sparse in pure Erythritol for mixtures of 1, and 3%(by weight)
improved the thermal performance of Erythritol for solar
thermal energy systems. Nanoparticles only physically
interacted with Erythritol, and not chemically, plane without
25 thermal cycles. Without cycling, Nano-Erythritol studied
here suffered a lower subtract in heat of fusion than pure
Erythritol, which makes Nano-Erythritol increasinglysuitable
for solar thermal storage applications at 100–150°C.
Key Words: Phase change material (PCM), Nanoparticles,
Thermal cycling, Heat of fusion, Melting temperature, solar
thermal energy storage.
1. INTRODUCTION
Recently, a lot of materials are unchanginglyselectedasPCM
for thermal storage system including Water and Barium
hydroxide, but these thermal storage systems are limited in
heat storage density, safety and phase transpiration
temperature. Organic PCMs such as sugar alcohols can
potentially underpass the gap between peak heat demand
and supply by storing energy in the form of latent heat due
to their availability and suitable melting and freezing
temperature ranges. AL2O3 nanoparticles used paraffin to
disperse sodium stearoyl lactylate as a surfactant and found
composite relaxing temperature of 2.5, 5.0, 7.5, and 10.0 wt
percentage nano AL2O3 is 1.20, 1.50, 1.35, 1.65 C higher
then unadulterated paraffin and 4.13 kJ/kg, 5.41 kJ/kg ,
14.86 kJ/kg and 22 kJ/kg. (M.Nourani.[1]). Reported a make
good in the heat limit of nano titania value erythritol by40%
in strong stage and 14% in liquid (or gas) stage when an
value semester of 0.2 vol% of nano-titania was put to
use.(L.Zhichao[2]). The objective of this investigation wasto
determine via experimentation, if Al2O3 and CuO
nanoparticles sparse in pure MI for mixtures of 1, 2 and 3%
(by weight) improved the thermal performance of MI for
solar thermal energy systems. Without thermal cyclingMI-A
is increasingly suited for thermal energy storage than MI-C.
(D.K. Singh [3]). The thermal conductivity of the PCMs was
found to increase by 407.8 percent witha massof10percent
unalleviated one of the short stat threads. The loss of
enthalpies, however, is 11.3% for variegated parts or
materials made of 10% short stat threads. With their low
space between parts and good thermal conductivity of CNT
offer ramified unused quality as mixed substances.(ZhangQ
[4]). A review of the integration of PCM into solar collectors
and water storage tanks was presented. They discussed the
techniques used to modernize the characteristics of PCM
heat transfer, such as the use of highly conductive additives
and fins. (Abokersh MH [5]).Studied eicosane / graphene
Nano platelets (GNPs) and found that the midpoint latent
heat of join by heating 1, 2, 5 and 10 wt. percent of
variegated parts or materials is lower than that of well-
spoken eicosane by 0.5, 1.7, 5.4 and 16.0 percent separately
and points of variegated parts or materials are slowly
removed scrutinizingly independentlyofsubtracting weight,
quantity of GNPs. (X. Fang [6]). It gave quiet thought to the
palmitic corrosive TiO2 1 as a Nano- upgraded natural stage
transpiration material and found that the traction in liquid
temperature 2 was variegated from the observationrange of
0.26 and 2 C 3 and the rest of the mixing heat somewhere in
the range of 2 percent and 15.5 percent and no heatfromthe
mixture of palmitic corrosive was reduced by 17.88 percent
without 1500 liquefied. (R.K. Sharma [7]). Sparse Al2O3
nanoparticles with paraffin, a mass portion of 5 and 10 wt.
percent and a ripen of 7 and 13 percent in fusion heat.
Whereas the thermal conductivity has been improved for 5
and 10 wt. percent Al2O3 nanoparticles was 2 and 6 percent
separately. (C.J. Ho [8]). Revealed a thermal conductivity
upgrade of 48% and 60% for paraffin containing 10 wt %
and 20 wt % of iron nanoparticles separately. In writing a
few reviews show that there is no uncontrived relationship
between the mass semester of nanoparticles and the
resurgence of warm conductivity. (N. Sahan [9]).
Studied the constrained melting of wax inside a spherical
sheathing was found that the waviness and excessive
melting of the marrow of the PCM was shown to be
underestimated by the experimental observation due to the
support structure to hold the sphere. (N.A.M. Amin [10])
Recently, lots of sustentation has been paid to the minutiae
of new PCMs for TES applications at intermediate
temperature (100-200 °C). Hence, the use of sugar alcohols
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1632
(SA) as a TES material has received a lot of consideration.
Erythritol has gotten the most sustentation among all SA. It
is characterized by relatively large melting enthalpy of 340
J/g. (Kakiuchi H [11]) reported that the low thermal
conductivity of the PCMs can be profoundly enhanced by
embedding PCM within a metal matrix structure. (Ettouney
Hisham [12]). Prepared CNTs grafted with octanol and
oleylamine to successfully increase CNT dispersibility in
palmitic acid. However, less research is carried out on the
undercooling and thermal cycling stability of PCMs, in
particular the composites of erythritol / CNT. (Wang J [13]).
Erythritol has been selected as candidate material: it is a
PCM for recovery unused heat at temperatures at virtually
relatively upper enthalpy
transpiration in the transition solid-liquidorviceversa (330
J/g). (S. N. Gunasekara [14]). Studied grapheme Nano
platelets (GNPs) and found that stereotype latent heat of
fusion of the 1, 2, 5 and 10 wt. % composite is lower than
that of pure eicosane by 0.5, 1.7, 5.4 and 16.0% and melting
points of composites was shown nearly self-sustaining of
loading of GNPs. (X. Fang [15]
Till stage no study has been reported on the label of
nanoparticle impregnated erythritol. Hence, the aim of this
study is to evaluate and typify the latent heat storage
potential of erythritol with and without Nano-additives for
meaty solar latent heat storage applications in the
temperature range of 100–150°C.Thermal cyclingtestshave
been performed on pure Erythritol with TiO2 and CNT
nanoparticles (particle size 30–50 nm) with mass fractions
of 1 and 3 wt.%. The measurementswereperformedover 25
charging-discharging cycles using differential scanning
calorimetric (DSC), thermo gravimetric wringer equipment
(TGA), Fourier transform infra-red (FT-IR) spectroscopy to
observe thermos-physical properties, mass change, latent
heat of energy, molecularimmigrationandfunctional groups
and the distribution of nanoparticles in Erythritol
2. METHODOLOGY
Commercially misogynist pure Erythritol, chemical formula
C4H10O4, was obtained from (SpectrochemPvt.Ltd.,Mumbai,
India) with a mass density of 1.45 g/cm3, molecular weight
of 122.12, melting range between 116°C to 120°C was
employed. Titanium Oxide (TiO2) and Carbon Nano tubes
nanoparticles (particle size 30–50 nm) were procured from
Alfa Aesar, USA
Fig-1 Experimental setup
For thermal cycling process, an experimental set up
consisting of constant temperature hot plate heater (Fig. 1),
was used. During charging 30 g of the PCM (Erythritol mixed
with nanoparticles) was heated using a hot plate from 30°C
to 150°C in a silver beaker. The molten PCM was cooled
normally from 150°C to room condition (30°C) by passive
cooling. Calibrated J-type thermocouples used to measure
and record the temperature of PCM. The physical state of
PCM during melting and solidification was confirmed
visually. The temperatures were recorded at 30 s intervals
during melting and solidification.
3. NANO-ERYTHRITOL
TiO2 and CNT nanoparticles were uniformlymixedat1and3
wt% to Erythritol by using a low energy ball mill which was
rotated for 1 h at 250 rpm for uniform mixing using three
stainless steel balls providing centrifugal force. Melting
temperature, time taken for melting and the variation of
melting point over 25 charging and discharging cycles were
recorded, no major change observed for melting points
during thermal cycling. The time taken for melting and
freezing was about 12 min, for each Nano-Erythritol
suspension studied. Fig. 2 and 3 shows Nano-Erythritol
before and after 25 thermal cycles.
Fig-2 Before thermal cycling (BTC)
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1633
Fig-3 After thermal cycling (ATC)
Sample of pure Erythritol, Erythritol-TiO2 and Erythritol-
CNT weighing 20 mg were taken before beginning of the
thermal cycling and at the end of 25th cycle for DSC and FT-
IR tests. PerkinElmer DSC equipment (DSC 6000) was used
for these tests. The test were carried out in N2 atmosphere in
the temperature range of 30°C–150°C with a heating rate of
10°C/min. PerkinElmer TGA equipment (TGA 4000) was
used for TGA tests. Material decomposition was
characterized by the mass loss measured with a high-
precision balance. A PerkinElmerFT-IR spectrometer(FT-IR
spectrum two) with wavelength range from 8300 to350cm-
1 was employed for analyzing the chemical compatibility
between pure MI and nanoparticlesoverwavenumberrange
of 4000–500 cm-1 in steps of 4 cm-1.
4. RESULT AND DISCUSSION
DSC equipment was used to measure the energy of nano-
pcm samples at 1% and 3% of before and after thermal
cycling. Table 1 shows the heat of fusion for pure erythritol,
before thermal cycling, was measured to be 285.5 kJ/kg and
for Pcm-Nano it was measuredtobe294.9kJ/kg,363.3kJ/kg
respectively for 1 and 3 wt. %. This amounts to be decrease
of 33.6 kJ/kg and increase of 34.8 kJ/kg respectively for 1
and 3 wt. %. When compared pure Erythritol with Nano-
Erythritol significant rise of 10.7%inthe heatoffusionin the
case of 3 wt. %. Heat of fusion of pure erythritol after 25
cycles was measured to be 264.3 kJ/kg which was 4.2 kJ/kg
less as compared to pure erythritol. After 25 charging and
discharging cycles, heat of fusion for 1 and 3 wt.% was
measured to be 290.4 kJ/kg, 321.1 kJ/kg respectively which
have 1.6% and 11.17% lesser heat of fusion when compared
to before thermal cycling.
Table-1: phase changing property before and after
thermal cycling
Pcm-
Nano
(wt. %)
Phase change peak
temperature (°C)
Latent heat (kJ/kg)
Melting Melting
(25
cycles)
Melting Melting
(25
cycles)
0.0 119.5 118.9 285.5 264.3
1.0 122.1 121.9 294.9 290.4
3.0 123.8 121.7 363.3 323.1
Chart-1 DSC curve for 1% of before thermal cycling
Chart-2 DSC curve for 1% after thermal cycling
Chart-3 DSC curve for 3% before thermal cycling
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1634
Chart-4 DSC curve for 3% after thermal cycling
Melting point of pure erythritol was measured to be 119.5°C
and for Nan-Pcm with 1 and 3 wt. % it was found to increase
by 2.6°C and 4.3°C respectively, when compared to pure
erythritol. After thermal cycling by 25 times, the melting of
pure erythritol was found to decrease by 0.6°C and similarly
for 1 and 3 wt. %, the melting point decreased by 0.2°C and
2.1°C respectively. Furthermore, reductioninmeltingpoints
of 3 wt. % was lesser compare to 1 wt. % solution after 25
thermal cycles (see Chart 1, 2, 3 and 4). From the view point
of thermal storage media, 3 wt. % is more desirable as
compared to 1 wt. % due to a lower reduction in the heat of
fusion on addition of nanoparticles.
FTIR equipment was used to measure the transmission
spectra of erythritol- TiO2 and CNT mixtures,seechart5,6,7
and 8. Functional groups present in the samples aredetailed
in Table 2. There was an indication ofreactionwithnitrogen,
and some halogens during thermal cycling. Same functional
groups are observed on addition of Nano particles (TiO2 and
CNT). Major functional groups are strong OH (usually
stretching vibration) and CH3, CH2 and CH (2 or 3 bands)
with wavenumbers are 3252 cm-1 and 2974 cm-1 in nano-
pcm (BTC 1%) which has infra-red Transmission of 82.48%
and 88.20% respectively.
ATC 1%, BTC 3% and ATC 3% showedtransmission83.17%,
83.76% and 84.51% respectively for 3219 cm-1, 3176 cm-1
and 3245 cm-1 respectively. After the 25th cycle a slight
decrease in transmission in the functional group region
(4000–1500 cm-1) for all samples can be seen in chart 6&8,
though this fluctuation was less compared to those without
cycling, as shown in chart 7 and 8 and in Table 1. It indicates
that pure erythritol and TiO2 with CNT nanoparticles were
chemically stable even after 25 cycles of melting and
solidification. It can be inferred that erythritol and
nanoparticles only interacted thermo-physically and no
chemical interaction took place.
Chart-5 FTIR measured transmission spectra BTC 1%
Chart-6 FTIR measured transmission spectra ATC 1%
Chart-7 FTIR measured transmission spectra BTC 1%
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1635
Chart-8 FTIR measured transmission spectra ATC 3%
Table-2: Functional group present in the sample before
and after thermal cycling.
Wavenumber
(cm-1)
Functional group
3252 Strong O-H, stretching vibration
2974 CH3,CH2 and CH
1259 C-N amine stretching
1078 C-F (Strong)
618 C-Br (strong)
Thermo-Gravimetric Analysis describes themasslossonthe
sample of 1%, 3% wt. before and after thermal cycling is
shown in chart 8-12.
Chart-9 TGA curve for BTC 1%
Chart-10 TGA curve for ATC 1%
Chart-11 TGA curve for BTC 3%
Chart-12 TGA curve for ATC 3%
BTC and ATC 1% has been mass loss are 0.4% and 0.5%. 3%
wg of BTC and ATC mass loss are 0.11% and 0.6%. The
higher mass loss is ATC 3% and lower mass loss is ATC 3%.
The samples are stable with in the application temperature
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1636
range from 300-1500C. If adding the more amount of Nano
particles to minimize the mass loss.
5. CONCLUSION
Thermal and chemical properties of erythritol with nano
particles are TiO2 and CNT with 1, 3 wt. have been
experimentally studiedusingDSC,TGAandFTIR.DSCresults
describe if adding large amount ofnanoparticles,toincrease
the latent heat of fusion and melting points.1wt.showedthe
increase the 0.80C and 2.10C increase of 3wt. due to charging
and discharging cycles.Erythritol-nano1wt.and3wt.ofafter
thermal cycling have been excellentlychemical stabilityover
temperature range from300-1500CusingFTIR.Also1wt.and
3wt. of before thermal cycling have been good thermal
stability. TGA results showed the BTC and ATC 1wt. % have
been 0.4% and 0.5%. Also showed BTC and ATC of 3wt. %
are 0.11% and 0.6% with temperature range from 300-
1500C. In view of results,Erythritol basednano-pcmcouldbe
prescribed as a potential material for solar thermal
application at 300-1500C.
REFERENCES
[1] M. Nourani, N. Hamdami, J. Keramat, A. Moheb, M.
Shahedi, Thermal behavior of paraffin-nano-Al2O3
stabilized by sodium stearoyl lactylate as a
stablephase change material with high thermal
conductivity, Renew. Energy 88(2016) 474–482
(Apr 30).
[2] L. Zhichao, Z. Qiang, W. Gaohui, Preparation and
enhanced heat capacity of nano-titania doped
erythritol as phase change material,Int.J.HeatMass
Transfer. 80 (2015) 653–659 (Jan 31).
[3] D.K. Singh , S. Suresh , H. Singh , B.A.J. Rose , S.
Tassou , N. Anantharaman. Myo-inositol based
nano-PCM for solar thermal energystorage.Applied
Thermal Engineering 110 (2017) 564–572
[4] Zhang Q, Luo Z, Guo Q, Wu G. Preparation and
thermal properties of shortcarbonfibers/erythritol
phase change materials. Energy Convers Manage
2017;136:220–8
[5] Abokersh MH, Osman M, El-Baz O, El-Morsi M,
Sharaf O. Review of the phase change material
(PCM) usage for solar domestic water heating
systems (SDWHS). Int J Energy Res 2018;
42:329e57.
[6] X. Fang, L.W. Fan, Q. Ding, X. Wang, X.L. Yao, J.F.Hou,
Z.T. Yu, G.H. Cheng, Y.C. Hu, K.F. Cen, Increased
thermal conductivity of eicosane-based composite
phase change materials in the presenceofgraphene
nanoplatelets, Energy Fuels 27 (7) (2013) 4041–
4047 (Jun 13)
[7] R.K. Sharma, P. Ganesan, V.V. Tyagi, H.S. Metselaar,
S.C. Sandaran, Thermal properties and heat storage
analysis of palmitic acid-TiO2 composite as
nanoenhanced organic phase change material
(NEOPCM), Appl. Therm.Eng.99(2016)1254–1262
(Apr 25).
[8] C.J. Ho, J.Y. Gao, Preparation and thermophysical
properties of nanoparticle-inparaffin emulsion as
phase change material, Int. Commun. Heat Mass
Transfer 36 (2009) 467–470 (May 31).
[9] N. Sahan, M. Fois, H. Paksoy, Improving thermal
conductivity phase change materials-A study of
paraffin nanomagnetite composites, Solar Energy
Mater. Solar Cells 137 (2015) 61–67.
[10] N.A.M. Amin, F. Bruno, M. Belusko,Effectivethermal
conductivity for melting in PCM encapsulated in a
sphere, Appl. Energy 122 (2014) 280–287.
[11] Kakiuchi H, Yamazaki M, Yabe M, et al. A Study of
Erythritol as Phase Change Material[J]
[12] Ettouney Hisham, El-Dessouky Hisham, Al-Ali
Amani. Heat transfer during phase change of
paraffin wax stored in spherical shells. J Solar Eng
2005;127(3):357–65.
[13] Wang J, Xie H, Xin Z, Li Y. Increasing the thermal
conductivity of palmitic acid by the addition of
carbon nanotubes. Carbon 2010;48:3979–86
[14] S. N. Gunasekara, R. Pan, J. N. Chiu, V.Martin,Polyols
as phase change materials for surplus thermal
energy storage, Applied Energy 162 (2016), 1439-
1452
[15] X. Fang, L.W. Fan, Q. Ding, X. Wang, X.L. Yao, J.F.
Hou, Z.T. Yu, G.H. Cheng, Y.C. Hu, K.F. Cen, Increased
thermal conductivity of eicosane-based composite
phase change materials in the presenceofgraphene
nanoplatelets, Energy Fuels 27 (7) (2013) 4041–
4047 (Jun 13).

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IRJET- Erythritol based Nano-Pcm for Solar Thermal Energy Storage

  • 1. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1631 Erythritol based Nano-PCM for Solar Thermal Energy Storage R Manickam1, P.Kalidoss2, Dr.S.Suresh3, Dr.S.Venkatachalapathy4 1Dept. of Mechanical Engineering & Saranathan College of Engineering, TN, India 2Research Scholar, Dept. of Mechanical Engineering & NIT Trichy, TN, India 3Associate Professor, Dept. of Mechanical Engineering & NIT Trichy, TN, India 4Associate Professor, Dept. of Mechanical Engineering & NIT Trichy, TN, India ---------------------------------------------------------------------***---------------------------------------------------------------------- Abstract - Phase Change Material (PCM) plays an important role as a thermal energy storage device by utilizing its high storage density and latent heat property. The thermo- physical policies of Erythritol, (a sugar alcohol), was investigated as a potential material for developing increasingly meaty solar thermal energystoragesystemsthan those currently available. This latent heat storage medium could be utilized for commercial and industrial applications using solar thermal energy storage in the temperature range of 100–150°C. The objective of this investigation was to determine via experimentation, if TiO2andCNTnanoparticles sparse in pure Erythritol for mixtures of 1, and 3%(by weight) improved the thermal performance of Erythritol for solar thermal energy systems. Nanoparticles only physically interacted with Erythritol, and not chemically, plane without 25 thermal cycles. Without cycling, Nano-Erythritol studied here suffered a lower subtract in heat of fusion than pure Erythritol, which makes Nano-Erythritol increasinglysuitable for solar thermal storage applications at 100–150°C. Key Words: Phase change material (PCM), Nanoparticles, Thermal cycling, Heat of fusion, Melting temperature, solar thermal energy storage. 1. INTRODUCTION Recently, a lot of materials are unchanginglyselectedasPCM for thermal storage system including Water and Barium hydroxide, but these thermal storage systems are limited in heat storage density, safety and phase transpiration temperature. Organic PCMs such as sugar alcohols can potentially underpass the gap between peak heat demand and supply by storing energy in the form of latent heat due to their availability and suitable melting and freezing temperature ranges. AL2O3 nanoparticles used paraffin to disperse sodium stearoyl lactylate as a surfactant and found composite relaxing temperature of 2.5, 5.0, 7.5, and 10.0 wt percentage nano AL2O3 is 1.20, 1.50, 1.35, 1.65 C higher then unadulterated paraffin and 4.13 kJ/kg, 5.41 kJ/kg , 14.86 kJ/kg and 22 kJ/kg. (M.Nourani.[1]). Reported a make good in the heat limit of nano titania value erythritol by40% in strong stage and 14% in liquid (or gas) stage when an value semester of 0.2 vol% of nano-titania was put to use.(L.Zhichao[2]). The objective of this investigation wasto determine via experimentation, if Al2O3 and CuO nanoparticles sparse in pure MI for mixtures of 1, 2 and 3% (by weight) improved the thermal performance of MI for solar thermal energy systems. Without thermal cyclingMI-A is increasingly suited for thermal energy storage than MI-C. (D.K. Singh [3]). The thermal conductivity of the PCMs was found to increase by 407.8 percent witha massof10percent unalleviated one of the short stat threads. The loss of enthalpies, however, is 11.3% for variegated parts or materials made of 10% short stat threads. With their low space between parts and good thermal conductivity of CNT offer ramified unused quality as mixed substances.(ZhangQ [4]). A review of the integration of PCM into solar collectors and water storage tanks was presented. They discussed the techniques used to modernize the characteristics of PCM heat transfer, such as the use of highly conductive additives and fins. (Abokersh MH [5]).Studied eicosane / graphene Nano platelets (GNPs) and found that the midpoint latent heat of join by heating 1, 2, 5 and 10 wt. percent of variegated parts or materials is lower than that of well- spoken eicosane by 0.5, 1.7, 5.4 and 16.0 percent separately and points of variegated parts or materials are slowly removed scrutinizingly independentlyofsubtracting weight, quantity of GNPs. (X. Fang [6]). It gave quiet thought to the palmitic corrosive TiO2 1 as a Nano- upgraded natural stage transpiration material and found that the traction in liquid temperature 2 was variegated from the observationrange of 0.26 and 2 C 3 and the rest of the mixing heat somewhere in the range of 2 percent and 15.5 percent and no heatfromthe mixture of palmitic corrosive was reduced by 17.88 percent without 1500 liquefied. (R.K. Sharma [7]). Sparse Al2O3 nanoparticles with paraffin, a mass portion of 5 and 10 wt. percent and a ripen of 7 and 13 percent in fusion heat. Whereas the thermal conductivity has been improved for 5 and 10 wt. percent Al2O3 nanoparticles was 2 and 6 percent separately. (C.J. Ho [8]). Revealed a thermal conductivity upgrade of 48% and 60% for paraffin containing 10 wt % and 20 wt % of iron nanoparticles separately. In writing a few reviews show that there is no uncontrived relationship between the mass semester of nanoparticles and the resurgence of warm conductivity. (N. Sahan [9]). Studied the constrained melting of wax inside a spherical sheathing was found that the waviness and excessive melting of the marrow of the PCM was shown to be underestimated by the experimental observation due to the support structure to hold the sphere. (N.A.M. Amin [10]) Recently, lots of sustentation has been paid to the minutiae of new PCMs for TES applications at intermediate temperature (100-200 °C). Hence, the use of sugar alcohols
  • 2. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1632 (SA) as a TES material has received a lot of consideration. Erythritol has gotten the most sustentation among all SA. It is characterized by relatively large melting enthalpy of 340 J/g. (Kakiuchi H [11]) reported that the low thermal conductivity of the PCMs can be profoundly enhanced by embedding PCM within a metal matrix structure. (Ettouney Hisham [12]). Prepared CNTs grafted with octanol and oleylamine to successfully increase CNT dispersibility in palmitic acid. However, less research is carried out on the undercooling and thermal cycling stability of PCMs, in particular the composites of erythritol / CNT. (Wang J [13]). Erythritol has been selected as candidate material: it is a PCM for recovery unused heat at temperatures at virtually relatively upper enthalpy transpiration in the transition solid-liquidorviceversa (330 J/g). (S. N. Gunasekara [14]). Studied grapheme Nano platelets (GNPs) and found that stereotype latent heat of fusion of the 1, 2, 5 and 10 wt. % composite is lower than that of pure eicosane by 0.5, 1.7, 5.4 and 16.0% and melting points of composites was shown nearly self-sustaining of loading of GNPs. (X. Fang [15] Till stage no study has been reported on the label of nanoparticle impregnated erythritol. Hence, the aim of this study is to evaluate and typify the latent heat storage potential of erythritol with and without Nano-additives for meaty solar latent heat storage applications in the temperature range of 100–150°C.Thermal cyclingtestshave been performed on pure Erythritol with TiO2 and CNT nanoparticles (particle size 30–50 nm) with mass fractions of 1 and 3 wt.%. The measurementswereperformedover 25 charging-discharging cycles using differential scanning calorimetric (DSC), thermo gravimetric wringer equipment (TGA), Fourier transform infra-red (FT-IR) spectroscopy to observe thermos-physical properties, mass change, latent heat of energy, molecularimmigrationandfunctional groups and the distribution of nanoparticles in Erythritol 2. METHODOLOGY Commercially misogynist pure Erythritol, chemical formula C4H10O4, was obtained from (SpectrochemPvt.Ltd.,Mumbai, India) with a mass density of 1.45 g/cm3, molecular weight of 122.12, melting range between 116°C to 120°C was employed. Titanium Oxide (TiO2) and Carbon Nano tubes nanoparticles (particle size 30–50 nm) were procured from Alfa Aesar, USA Fig-1 Experimental setup For thermal cycling process, an experimental set up consisting of constant temperature hot plate heater (Fig. 1), was used. During charging 30 g of the PCM (Erythritol mixed with nanoparticles) was heated using a hot plate from 30°C to 150°C in a silver beaker. The molten PCM was cooled normally from 150°C to room condition (30°C) by passive cooling. Calibrated J-type thermocouples used to measure and record the temperature of PCM. The physical state of PCM during melting and solidification was confirmed visually. The temperatures were recorded at 30 s intervals during melting and solidification. 3. NANO-ERYTHRITOL TiO2 and CNT nanoparticles were uniformlymixedat1and3 wt% to Erythritol by using a low energy ball mill which was rotated for 1 h at 250 rpm for uniform mixing using three stainless steel balls providing centrifugal force. Melting temperature, time taken for melting and the variation of melting point over 25 charging and discharging cycles were recorded, no major change observed for melting points during thermal cycling. The time taken for melting and freezing was about 12 min, for each Nano-Erythritol suspension studied. Fig. 2 and 3 shows Nano-Erythritol before and after 25 thermal cycles. Fig-2 Before thermal cycling (BTC)
  • 3. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1633 Fig-3 After thermal cycling (ATC) Sample of pure Erythritol, Erythritol-TiO2 and Erythritol- CNT weighing 20 mg were taken before beginning of the thermal cycling and at the end of 25th cycle for DSC and FT- IR tests. PerkinElmer DSC equipment (DSC 6000) was used for these tests. The test were carried out in N2 atmosphere in the temperature range of 30°C–150°C with a heating rate of 10°C/min. PerkinElmer TGA equipment (TGA 4000) was used for TGA tests. Material decomposition was characterized by the mass loss measured with a high- precision balance. A PerkinElmerFT-IR spectrometer(FT-IR spectrum two) with wavelength range from 8300 to350cm- 1 was employed for analyzing the chemical compatibility between pure MI and nanoparticlesoverwavenumberrange of 4000–500 cm-1 in steps of 4 cm-1. 4. RESULT AND DISCUSSION DSC equipment was used to measure the energy of nano- pcm samples at 1% and 3% of before and after thermal cycling. Table 1 shows the heat of fusion for pure erythritol, before thermal cycling, was measured to be 285.5 kJ/kg and for Pcm-Nano it was measuredtobe294.9kJ/kg,363.3kJ/kg respectively for 1 and 3 wt. %. This amounts to be decrease of 33.6 kJ/kg and increase of 34.8 kJ/kg respectively for 1 and 3 wt. %. When compared pure Erythritol with Nano- Erythritol significant rise of 10.7%inthe heatoffusionin the case of 3 wt. %. Heat of fusion of pure erythritol after 25 cycles was measured to be 264.3 kJ/kg which was 4.2 kJ/kg less as compared to pure erythritol. After 25 charging and discharging cycles, heat of fusion for 1 and 3 wt.% was measured to be 290.4 kJ/kg, 321.1 kJ/kg respectively which have 1.6% and 11.17% lesser heat of fusion when compared to before thermal cycling. Table-1: phase changing property before and after thermal cycling Pcm- Nano (wt. %) Phase change peak temperature (°C) Latent heat (kJ/kg) Melting Melting (25 cycles) Melting Melting (25 cycles) 0.0 119.5 118.9 285.5 264.3 1.0 122.1 121.9 294.9 290.4 3.0 123.8 121.7 363.3 323.1 Chart-1 DSC curve for 1% of before thermal cycling Chart-2 DSC curve for 1% after thermal cycling Chart-3 DSC curve for 3% before thermal cycling
  • 4. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1634 Chart-4 DSC curve for 3% after thermal cycling Melting point of pure erythritol was measured to be 119.5°C and for Nan-Pcm with 1 and 3 wt. % it was found to increase by 2.6°C and 4.3°C respectively, when compared to pure erythritol. After thermal cycling by 25 times, the melting of pure erythritol was found to decrease by 0.6°C and similarly for 1 and 3 wt. %, the melting point decreased by 0.2°C and 2.1°C respectively. Furthermore, reductioninmeltingpoints of 3 wt. % was lesser compare to 1 wt. % solution after 25 thermal cycles (see Chart 1, 2, 3 and 4). From the view point of thermal storage media, 3 wt. % is more desirable as compared to 1 wt. % due to a lower reduction in the heat of fusion on addition of nanoparticles. FTIR equipment was used to measure the transmission spectra of erythritol- TiO2 and CNT mixtures,seechart5,6,7 and 8. Functional groups present in the samples aredetailed in Table 2. There was an indication ofreactionwithnitrogen, and some halogens during thermal cycling. Same functional groups are observed on addition of Nano particles (TiO2 and CNT). Major functional groups are strong OH (usually stretching vibration) and CH3, CH2 and CH (2 or 3 bands) with wavenumbers are 3252 cm-1 and 2974 cm-1 in nano- pcm (BTC 1%) which has infra-red Transmission of 82.48% and 88.20% respectively. ATC 1%, BTC 3% and ATC 3% showedtransmission83.17%, 83.76% and 84.51% respectively for 3219 cm-1, 3176 cm-1 and 3245 cm-1 respectively. After the 25th cycle a slight decrease in transmission in the functional group region (4000–1500 cm-1) for all samples can be seen in chart 6&8, though this fluctuation was less compared to those without cycling, as shown in chart 7 and 8 and in Table 1. It indicates that pure erythritol and TiO2 with CNT nanoparticles were chemically stable even after 25 cycles of melting and solidification. It can be inferred that erythritol and nanoparticles only interacted thermo-physically and no chemical interaction took place. Chart-5 FTIR measured transmission spectra BTC 1% Chart-6 FTIR measured transmission spectra ATC 1% Chart-7 FTIR measured transmission spectra BTC 1%
  • 5. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1635 Chart-8 FTIR measured transmission spectra ATC 3% Table-2: Functional group present in the sample before and after thermal cycling. Wavenumber (cm-1) Functional group 3252 Strong O-H, stretching vibration 2974 CH3,CH2 and CH 1259 C-N amine stretching 1078 C-F (Strong) 618 C-Br (strong) Thermo-Gravimetric Analysis describes themasslossonthe sample of 1%, 3% wt. before and after thermal cycling is shown in chart 8-12. Chart-9 TGA curve for BTC 1% Chart-10 TGA curve for ATC 1% Chart-11 TGA curve for BTC 3% Chart-12 TGA curve for ATC 3% BTC and ATC 1% has been mass loss are 0.4% and 0.5%. 3% wg of BTC and ATC mass loss are 0.11% and 0.6%. The higher mass loss is ATC 3% and lower mass loss is ATC 3%. The samples are stable with in the application temperature
  • 6. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 04 | Apr 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1636 range from 300-1500C. If adding the more amount of Nano particles to minimize the mass loss. 5. CONCLUSION Thermal and chemical properties of erythritol with nano particles are TiO2 and CNT with 1, 3 wt. have been experimentally studiedusingDSC,TGAandFTIR.DSCresults describe if adding large amount ofnanoparticles,toincrease the latent heat of fusion and melting points.1wt.showedthe increase the 0.80C and 2.10C increase of 3wt. due to charging and discharging cycles.Erythritol-nano1wt.and3wt.ofafter thermal cycling have been excellentlychemical stabilityover temperature range from300-1500CusingFTIR.Also1wt.and 3wt. of before thermal cycling have been good thermal stability. TGA results showed the BTC and ATC 1wt. % have been 0.4% and 0.5%. Also showed BTC and ATC of 3wt. % are 0.11% and 0.6% with temperature range from 300- 1500C. In view of results,Erythritol basednano-pcmcouldbe prescribed as a potential material for solar thermal application at 300-1500C. REFERENCES [1] M. Nourani, N. Hamdami, J. Keramat, A. Moheb, M. Shahedi, Thermal behavior of paraffin-nano-Al2O3 stabilized by sodium stearoyl lactylate as a stablephase change material with high thermal conductivity, Renew. Energy 88(2016) 474–482 (Apr 30). [2] L. Zhichao, Z. Qiang, W. Gaohui, Preparation and enhanced heat capacity of nano-titania doped erythritol as phase change material,Int.J.HeatMass Transfer. 80 (2015) 653–659 (Jan 31). [3] D.K. Singh , S. Suresh , H. Singh , B.A.J. Rose , S. Tassou , N. Anantharaman. Myo-inositol based nano-PCM for solar thermal energystorage.Applied Thermal Engineering 110 (2017) 564–572 [4] Zhang Q, Luo Z, Guo Q, Wu G. Preparation and thermal properties of shortcarbonfibers/erythritol phase change materials. Energy Convers Manage 2017;136:220–8 [5] Abokersh MH, Osman M, El-Baz O, El-Morsi M, Sharaf O. Review of the phase change material (PCM) usage for solar domestic water heating systems (SDWHS). Int J Energy Res 2018; 42:329e57. [6] X. Fang, L.W. Fan, Q. Ding, X. Wang, X.L. Yao, J.F.Hou, Z.T. Yu, G.H. Cheng, Y.C. Hu, K.F. Cen, Increased thermal conductivity of eicosane-based composite phase change materials in the presenceofgraphene nanoplatelets, Energy Fuels 27 (7) (2013) 4041– 4047 (Jun 13) [7] R.K. Sharma, P. Ganesan, V.V. Tyagi, H.S. Metselaar, S.C. Sandaran, Thermal properties and heat storage analysis of palmitic acid-TiO2 composite as nanoenhanced organic phase change material (NEOPCM), Appl. Therm.Eng.99(2016)1254–1262 (Apr 25). [8] C.J. Ho, J.Y. Gao, Preparation and thermophysical properties of nanoparticle-inparaffin emulsion as phase change material, Int. Commun. Heat Mass Transfer 36 (2009) 467–470 (May 31). [9] N. Sahan, M. Fois, H. Paksoy, Improving thermal conductivity phase change materials-A study of paraffin nanomagnetite composites, Solar Energy Mater. Solar Cells 137 (2015) 61–67. [10] N.A.M. Amin, F. Bruno, M. Belusko,Effectivethermal conductivity for melting in PCM encapsulated in a sphere, Appl. Energy 122 (2014) 280–287. [11] Kakiuchi H, Yamazaki M, Yabe M, et al. A Study of Erythritol as Phase Change Material[J] [12] Ettouney Hisham, El-Dessouky Hisham, Al-Ali Amani. Heat transfer during phase change of paraffin wax stored in spherical shells. J Solar Eng 2005;127(3):357–65. [13] Wang J, Xie H, Xin Z, Li Y. Increasing the thermal conductivity of palmitic acid by the addition of carbon nanotubes. Carbon 2010;48:3979–86 [14] S. N. Gunasekara, R. Pan, J. N. Chiu, V.Martin,Polyols as phase change materials for surplus thermal energy storage, Applied Energy 162 (2016), 1439- 1452 [15] X. Fang, L.W. Fan, Q. Ding, X. Wang, X.L. Yao, J.F. Hou, Z.T. Yu, G.H. Cheng, Y.C. Hu, K.F. Cen, Increased thermal conductivity of eicosane-based composite phase change materials in the presenceofgraphene nanoplatelets, Energy Fuels 27 (7) (2013) 4041– 4047 (Jun 13).