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Materials Today: Proceedings 46 (2021) 5639–5646

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Materials Today: Proceedings


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Recent progress and outlook of solar adsorption refrigeration systems


Manish Kumar Ojha a, Anoop Kumar Shukla a,⇑, Puneet Verma b, Ravindra Kannojiya a
a
Amity University, Noida, Uttar Pradesh, India
b
School of Chemistry, Physics and Mechanical Engineering, Queensland University of Technology, Brisbane 4001, Australia

a r t i c l e i n f o a b s t r a c t

Article history: Solar adsorption refrigeration systems are indispensable in the areas of cooling such as air conditioning,
Received 3 September 2020 ice making, food preservation, medicine and vaccine storage etc in remote areas. It is cheaper than other
Received in revised form 22 September devices and lack in noise and corrosion. It is completely an eco-friendly system which could be driven by
2020
low grade waste heat. Consumption of electricity is very less in this system as compared to other fields
Accepted 24 September 2020
Available online 26 October 2020
due to the elimination of compression process in adsorption refrigeration. Most of the adsorption system
delivers a COP between 0.1 and 0.2 and exceptions are also there. Because of the technical, economic and
environmental problems, researches are going on in these areas. Nowadays it is incorporated with vapour
Keywords:
Solar energy
compression system to make hybrid system in order to achieve a greater COP and efficiency. This paper
Adsorption presents the basic and advanced aspects of adsorption refrigeration cycle and its hybrid arrangements
Cooling with pre-existing system. This paper described the different types of conventional and novel adsorbent
Adsorbents – adsorbate working pairs and provides detailed review about the past and present state of art research
Adsorbates in this field.
Coefficient of performance Ó 2020 Elsevier Ltd. All rights reserved.
Selection and peer-review under responsibility of the scientific committee of the International Confer-
ence on Innovations in Clean Energy Technologies.

1. Introduction comparison between the absorption and adsorption refrigeration


systems, the later one can be powered by using large range of tem-
Nowadays the solar energy is widely used in different areas perature from 50 °C to 600 °C or even more. It doesn’t require liq-
such as power generation, carbon capture and storage, solar heat- uid pump or rectifier for the refrigerant, and free from corrosion,
ing, cooling and refrigeration [1-4]. The usage of solar power also it constitutes no vibration and less sensitive to the installation
becomes prominent in refrigeration field. The adsorption refriger- position [7].
ation started in 1970 s because of oil crisis, and then in 1990 s The working cycle of the adsorption consists of two sub cycles,
due to environmental hazards caused by chlorofluro carbons and i.e. one for the adsorbent and other for the adsorbate. The adsor-
hydrochlorofluro carbons as refrigerants. The adsorption refrigera- bent cycle comprises four processes, isosteric heating, isobaric des-
tion system is a good way to reduce the usage of CFC and HCFC by orption, isosteric cooling, isobaric adsorption whereas the
exploiting low grade energy such as solar heat, biogas etc as the adsorbate cycle consists of three processes, isobaric condensation,
driving energy for the system and also helps in avoiding larger isenthalpic expansion, and isobaric evaporation as shown in the
power usage by avoiding the compression process [5]. The mainte- Fig. 1.
nance cost for the adsorption refrigeration is very small as com- In the adsorption cycle, first the refrigerant gets cooled up and
pared to a vapour compression refrigeration or absorption get adsorbed on the adsorbent bed by losing its energy, then sec-
refrigeration system. Adsorption refrigeration system has several ondly the refrigerant is pre heated by giving heat to gain the
advantages over vapour compression in areas like power consump- threshold energy for the excitation of the refrigerant molecules,
tion, vibration, control etc. The various parameters such as cooling finally the refrigerant gain the energy for the excitation and get
water temperature, environmental temperature, and solar radia- desorbed from the adsorption bed. The rate of adsorption and des-
tion have high influence on adsorption refrigeration [6]. In a quick orption will change according to the working pairs used in the sys-
tem. Adsorption occurs due to the action of cohesive forces which
comprises of electrostatic forces, hydrogen bonding between the
⇑ Corresponding author. molecules which are agglomerated. It is basically a surface phe-
E-mail address: shukla.anoophbti@gmail.com (A.K. Shukla).

https://doi.org/10.1016/j.matpr.2020.09.593
2214-7853/Ó 2020 Elsevier Ltd. All rights reserved.
Selection and peer-review under responsibility of the scientific committee of the International Conference on Innovations in Clean Energy Technologies.
Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Fig. 2 shows the schematic diagram of adsorber where, the K


type thermocouples kept at different locations 0, 5, 10, 15, 20, 25
and 60 mm inside the adsorbent bed in order to know the temper-
ature variation around the screw bar and stainless-steel mesh. The
centre of the mesh is passed through the screw bar that makes it to
compress the ACF in adsorber. A nut is provided on the upper side
of the mesh to control the mesh position (Table 1).
Researchers have done many works to improve the cooling per-
formance in different systems, one such work was done by El-
Sharkawy etal. [7] used the pairs Activated Carbon Fibre – 20
(ACF-20) – ethanol and ACF 15 – ethanol to improve the cooling
performance which was driven by thermal energy. The tempera-
ture of evaporator is kept constant at 10 °C and the adsorber tem-
perature is varied from 11℃ to 60 °C by regulating the water bath
Fig. 1. Working cycle of the adsorption refrigeration [8]. and the same procedure is done at 15 °C of evaporator temperature
and finally found that the adsorption capacity of A20 is higher than
the A15. Therefore ACF-20 produces higher cooling rate as com-
nomenon happens between two surfaces. The process involves pared to the ACF-15. The further investigation on activated carbon
detachment of a substance from one surface to the other one by (maxsorb - III)-ethanol pair was carried out by using thermo gravi-
accumulation or concentration. The physical adsorption is exother- metric analyser (TGA) over an adsorption temperature range of 20–
mic, liberates heat during the process. 60 °C at an increment of 10 °C for solar powered adsorption cooling
In this paper a detailed study is done on the present state of art application [7]. Adsorption rate of ACF-ethanol pair was faster than
on adsorption refrigeration system to understand the fundamen- maxsorb-3 ethanol pair due to short diffusion particles of ACF as
tals of adsorption refrigeration system and research developments compared to granular shape of maxsorb-3 and observed a sudden
till now and to know the lagging and find the potential research surge of COP occurred when the increase of desorption tempera-
gap in this area. ture is below 80 °C. The study showed that 1.2 kg of ethanol can
be absorbed by 1 kg of maxsorb-3 and adsorption cooling cycle
2. Performance augmentation of various adsorption system of maxsorb-3 and ethanol can achieve a specific cooling effect as
high as 420 kJkg1. Dubinin-Asthakov (D-A) equation is extensively
Experiment on adsorption refrigeration system using ammonia- used on carbon-based adsorbents to approximate the equilibrium
water pair found that the refrigerator producing 1 tonne of ice uptake of gases and vapours.
requires 5 tonnes of carbon and 1.5 tonnes of ammonia [9]. It  n
A
was apparent that the mean carbon bed temperature increases W ¼ W0 exp½  ð1Þ
E
over time from the initial starting temperature of 50 °C up to quasi
steady state value of 200 °C. In another work, a non-regenerative Where, W is the equilibrium uptake of the working pair; W0 is
chiller was designed with two stage which uses silica gel and water the maximum adsorption capacity and E is the adsorption charac-
as an adsorbent and adsorbate pair [10]. Silica gel is taken in this teristic parameter of the working pair; the exponential parameter
experiment as it has lower regenerative temperature and water ‘n’ is a dimensionless parameter that provides the best fitting of ln
has larger latent heat of vaporization than the methanol. The total (W) versus adsorption potential (A) and is given by Eq. (2):
cycle time was 440 s and the result shows that the setup will able  
Ps
to utilize low temperature solar/waste heat between 40 and 75℃ A ¼ RTln ð2Þ
P
as driving heat source at coolant at 30℃, the COP of 0.36 was
observed with a driving heat source of 55℃ and at coolant temper- Where T is the adsorption temperature, Ps is the refrigerant sat-
ature of 30 °C and for stand by the cooling capacity is 3.2 kW. uration pressure and P is the equilibrium pressure.

Fig. 2. Schematic diagram of adsorber [6].

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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Table 1 and higher yield header pipe should be increase. The designed solar
Experimental Conditions for A-20 an A-15. collector can efficiently transfer heat reaching the evaporation
Adsorbent Evaporator temperature [oC] Adsorber temperature [oC] temperature of methanol (65 °C) in 25 min of exposure. Integration
ACF (A-20) 10 11–60 of artificial neural network found that adsorption refrigeration sys-
15 16–60 tem can be modelled with a high degree of accuracy. By using three
ACF (A-15) 10 11–60 criteria (root mean square error, correlation coefficient and coeffi-
cient of variance) performance was calculated and found that solar
COP is very much less than cycle coefficient of performance and
Numerical studies on continuous adsorption refrigeration sys- energy absorbed by the water in the absorber of solar concentrator
tem with activated carbon and methanol as working pair powered is only 20–35% during peak sun shining and heat is lost due to high
by Parabolic Trough Collector (PTC) was carried out and FORTRAN irreversibility. The cooling performance of zeolite adsorption sys-
and Tri-Diagonal Matrix Algorithm were used to find out the tem driven by low grade energy and adsorbent used was FAM
numerical solutions and simulate the results [5]. An amount of Z01 [15]. The experiment was conducted for a capacity of
274 g of activated carbon was used with an increase in bed thick- 10.5 kW. It was found that the zeolite system could be driven by
ness resulted in an increase in COP of cycle and optimal perfor- using low grade waste heat energy which could be as low as
mance was found in between 80 and 100 °C. Zhai etal. [11] made 55 °C. The COP of the system could be as high as 0.48 while the
a comparison between two systems i.e. with and without heat heating source is low grade waste heat of 55 °C. An experimental
storage with the working pair of silica gel – water and the heating investigation was done on two setups with increased number of
and cooling time cycle was found out to be 900 s for both the sys- alloy fins and enhanced heat and mass transfer with and without
tems. The system with heat storage showed more stability than the valve with activated carbon – methanol. In which polyethylene is
other due to the regulation of heat storage water tank. In the area used to avoid the heat loss at the backside of the finned tube.
of cooling, both systems went hand to hand and the system with The setup with valve showed a higher performance than the other
heat storage has higher solar collecting capacity and electrical which gave a cooling efficiency of 0.122 and produced 6.5 kg ice
COP. A four-bed adsorption system of jojoba seeds, palm seeds, per day [16].
coconut shell and charcoal activated carbon was proposed Hamdeh Fig. 3 shows the cross-sectional view of adsorbent bed collector.
and Mu’Taz [12] and they selected the activated carbon – methanol It has a finned tube which stores the adsorbent in several sections
pair as adsorbent and adsorbate. Due to the limited size of the to increase the heat transfer rate of the system. The transfer of
refrigeration unit, only 900 ml of methanol was used. The mini- absorbent is restricted to the inner tube by providing a fine mesh.
mum temperature obtained by the system was 9 ℃ and the COP Polyethylene is provided at the backside of the adsorbent bed to
was found out to between 0.18 and 0.2.The difference in perfor- minimize the heat loss.
mance between lab and practical condition can be improved by A comparison of expriment was carried out with the same
improving the refrigerant valve design and refrigerant liquid level working pair zeolite-methanol and two types of activated carbon
in evaporator and proposed silica gel-water adsorption chiller. was used, one of that is abstracted from avocado shell [14]. The
Study also reported that thermal performance increases by using methanol system works under intermittent cycle where there is
chilled water and lower heat rejection temperature [13]. Carlosri- no heat recovery. 100 g of each adsorbent adsorbed 6.3 ml, and
ous etal. [14] had performed experiment by using two concentric 25 ml of methanol respectively. Authors concluded that the
tube the external is vacuum evacuated and the inner tube filled adsorption capacity of activated carbon is very much higher than
with activated charcoal and covered with layer of black copper zeolite and gave a system performance of 0.21. An innovative four
oxide to absorb the solar radiation. It was found that 100 g of acti- bed, three stage adsorption cycle system was made by Abdul Fazal
vated carbon from coconut adsorbed 25 ml methanol and can pro- etal. This design was to improve the previous design, used silica
vide 3 °C temperature from 22 °C. To gain the lower temperature gel-water as the working pair. A maximum COP of 0.218 was

Fig. 3. Cross section diagram of adsorbent bed collector [14].

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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Fig. 4. Schematic diagram of laboratory prototype of adsorption cooling system [19].

observed which was higher than that of the previous one [17]. Use In another experiment metal chloride was used as the adsor-
of magnetic suspension balance adsorption measurement unit bent and water as the asorbate [20]. The metal chloride used was
showed the maximum adsorption capacity of H2 treated a composite of Zeolite 13X/CaCl2 which is good in making use of
Maxsorb-3/ethanol has maximum adsorption capacities of 1.2 solar waste heat. The experimental result tells that it could achieve
and 1.0 kg/kg respectively. In the same experimental setup another a cooling power of 371 W and a specific cooling power (SCP) of
thermodynamic analysis showed that H2 treated Maxsorb-3/ 106 W/kg. Fig. 4 represents the schematic diagram of laboratory
ethanol adsorption cycle can achieve a COP as high as 0.51 with prototype of adsorption cooling system. The above system consists
an evaporator temperature 5°C regeneration temperature of two phases. The first phase is the adsorption occurrence in
100 °C along with a coolant at 30 °C [18]. In 2015, Du et.al had per- adsorber A and desorption occurrence in adsorber B. In phase II
formed experiment and proposed detail about the design of solar adsorption would occur in adsorber B and desorption in adsorber
adsorption refrigeration system with CPC and study on the heat A. In the Fig. 4 the thinner line depicts the water pipeline for cool-
and mass transfer performance in which the system was based ing and heating applications of the adsorber beds whereas the
on composite parabolic reflector panel (CPC), working pair was thicker line represents the low-pressure pipeline for water vapour
activated carbon and methanol [19]. The experiment shows that or condensed water.
the parabolic trough could make the adsorption bed 100 °C with Activated carbon and HFC410a as adsorption pair achieved SCP
low intensity irradiation while the non-concentrated adsorption 0.2 kW/kg and cop 0.3 respectively at 350 K regeneration temper-
bed would need more than 900 W/m2 to achieve the same. When ature and 387 K evaporator temperature [21]. The cycle time has
the irradiation intensity was 600 and 400 W/m2, then temperature been recorded to be about 1000 sec. It also showed that increasing
rising for desorption temperature were 0.67 °C/min and 0.50 °C/ the evaporator temperature decrease the cycle time which lead to
min, COP were observed 0.166 and 0.143 respectively. COP will an increase in the SCP. In the same year Dusane and Ghuge [22]
increase with increase in heat and mass transfer. There was a surge performed experiment by using ANSYS software to analyses the
of desorption rate by 4.1% as the irradiation changes from 600 to temperature distribution over adsorption plate for the perfor-
400 W/m2 and finally the desorption rate reached 12.5%. In desorp- mance and analysis of solar adsorption system in tropical wet
tion processes the system pressure got changed in similar trend and dry climate zone of India. In summer we get good amount of
but the change of desorption rate was lagging the system pressure solar heat in morning but limited amount of cooling in night and
in both experiments. In an experimental study on single bed silica in winter the situation gets reversed, so the performance of system
gel –water adsorption refrigeration system, It was found that by depends on adsorption pair, processes and environment condi-
using hot water temperature 88℃ & cooling water temperature tions. Similarly analysis of two stage solar vapour adsorption
32℃ the COP is 0.27 for the predicted cooling temperature differ- refrigeration system found that at 4 kg evaporator load refrigera-
ence is 2.5 to 3 °C[12]. In the same year another study used Zeolite tion effect is 147.14 W when maximum solar COP is 0.096 [10].
–Water as a Adsorption pair and reported the COP of the system is Later on the same system was improvised by using activated car-
ranges from 0.32 to 0.6 at a maximum adsorption capacity of 0.3 kg bon and ethanol as working pair and found that the maximum
of adsorbate/0.85 kg of adsorbent. Author also proposed that the adsorption capacity of ethanol by activated carbon is 0.302 kg/kg
compression system can be replaced by adsorption system and by providing cooling temperature 25℃ and heating temperature
solar technology will be brought into the system to make it eco- 100℃, COP is 0.19 and cycle time is 2 h and 30 min (Table 2).
friendly.
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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Table 2
Review of adsorption refrigeration systems.

Source System Operating Cycle Working pair COP Remarks


Temp. (oC) time
[9] Ammonia water refrigerator 50–200 °C 180 Ammonia-water 0.31 A refrigerator producing 1 tonne of ices would
working on diurnal cycle sec need 5 tonnes of carbon and 1.5 tonnes of
ammonia
[23] Two stage non-regenerative 30–75 °C 440 Silica gel-water 0.36 Effectively worked at 55 °C with 30 °C of cooling
adsorption chiller driven by waste sec water
heat
[24] Adsorption refrigeration with two 11–60 °C NA ACF(A20)-ethanol, ACF(A15)- 10–20% A20 is better than A15 in all aspects
temperature constant water bath ethanol
and two water circulators
[25] Solar powered adsorption 20–80 °C 600 Maxsorb III-ethanol NA COP increases sharply after 80 °C of desorption
incorporated with Thermo sec temperature and can also absorb 1.2 kg of ethanol
Gravimetric Analyzer per kg of maxsorb III
[26] Continuous adsorption 20–250 °C NA Activated carbon-ammonia 0.43 The variation of adsorbent thickness affects the
refrigeration system with specific cooling power much greater than the COP
parabolic trough collector of the system
[27] Open cycle adsorption cooling 55–95 °C 900 Silica gel-water 0.34–0.35 In this experiment, the system with heat storage
system sec is more stable than the other because of the
regulating effect of heat storage water tank
[5] Solar adsorption refrigeration 9–103 °C NA Activated carbon-methanol 0.2 The lowest temperature was found out to be 9 °C
system with four beds whereas the ambient temperature was 26 °C
[15] Single stage zeolite-water 25–60 °C 300 FAM Z01-water 0.48 Zeolite adsorption could be done with low grade
adsorption system sec heat at 55 °C
[14] Double vacuumed glass Tube of N/A 25 min Methanol/Activated 0.21 It is possible to obtain up to 3 °C
boron-silicate harcoal100 g/25 ml
[28] Artificial Neural network were N/A N/A Activated carbon/R134a 0.334 SCP = 42.5(W/kg)
used for performance prediction
[29] Solar powered finned tube 25–80 °C NA Activated carbon-methanol 0.122 6.5 kg of ice is made per day
adsorption refrigeration system
[17] Innovative Four-Bed, Three-Stage 40–70 °C NA Silica gel-water 0.218 SCP and COP were significantly increased over
Adsorption Cycle whole range of heat source temperature
[30] Small scale sorption chiller N/A 12 min Water/Silica gel 0.5 By using chilled water at adsorber thermal
performance can be increase
[31] Solar adsorption refrigeration 4–65 °C NA Activated charcoal-methanol 0.21 100 g of activated charcoal adsorbed 25 ml of
system under intermittent cycle methanol, managed to obtain 4 °C
[18] Magnetic Suspension balance 30 °C N/A Maxsorb-III/Ethanol1 kg/1 kg 0.51 H2 treated Maxsorb-3/ethanol has the highest
adsorption measurement unit 70 °C adsorption capacities
[32] Solar adsorption refrigeration 20–125 °C NA Activated carbon-methanol 0.143– COP increased as the irradiation increases from
system with compound parabolic 0.166 400-600 W/m2
concentrator
[33] Single bed Silica Gel-Water 32 °C N/A Silica Gel/Water1 kg/0.3 kg 0.27 Selection of adsorption pair for low grade heat
adsorption 88 °C source affect much on system
[34] Two steel cylinders are used. 0 °C N/A Zeolite- Water0.8 kg/0.3 kg 0.32–0.6 Compression system can be replaced by
115 °C adsorption system and low-grade energy can be
integrated, Cycle is very long
[33] Glass tube having sorption bed, N/A N/A Low grade charcoal/Methanol N/A System performance highly depends on
also used ANSYS adsorption pairs and environment condition
[35] Single bed adsorption cooling Below 1000 Activated carbon/ 0.3 Increasing the evaporator temperature SCP and
cycle and adsorption bed has 80 °C sec HFC410a1 kg/0.35 kg COP increases
finned tube type heat exchanger
[36] Two stage solar vapour N/A N/A Activated carbon/Methanol Solar Temperature difference of evaporator during the
adsorption COP = 0.096 cooling process show a decline trend as the
evaporator load
[37] Two adsorption bed as thermal 25 °C 2h Activated carbon/ 0.19 Ethanol/Ac carbon is suitable pair for adsorption,
compressor 100 °C 30 min Ethanol1 kg/0.302 kg and it can be operated at low heat source

3. Adsorbents and adsorbates cise than the activated carbon – methanol system by reducing the
pipe diameters and compact heat exchangers. Silica gel is a viable
By the involvement of forces in the process, the adsorbents are option for the adsorption refrigeration made from sodium silicate
classified as physical, chemical or composite. The physical adsor- which is granular and has high porosity. Generally, the desorption
bents are most used for the adsorption refrigeration. Activated car- temperature is lower than 90℃ (could be as low as 50℃) and a
bon is frequently used in several experiments because of its high maximum of 120℃. This is because of the connection between
porosity and large surface area. Ammonia and methanol are the water and hydroxyl group of silica atom on its surface help in hold-
adsorbates which are often used with activated carbon. Activated ing the adsorption capability. Zeolite is a type of alumina silicate
carbon has the quality of large quantity adsorption and low crystal composed of alkali or alkali soil. Zeolite water has showed
adsorption heat. Low adsorption heat is responsible for COP of a better performance than silica gel – water due to its higher heat
the system because of the heat consumption of the system during of adsorption (3300–4200 kJ.kg1). It is very stable at higher tem-
desorption is majorly the adsorption heat. Similar effects are peratures makes them to put up a desorption temperature higher
observed on activated carbon and ammonia, but main difference than 200℃. It is not able to produce evaporative temperature
is the higher operating pressure. This makes the system more con- below 32°F and has low adsorption rate.

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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Chemical adsorption occurs due to the strong chemical bonds


between the adsorbent and adsorbate and the bond is responsible
for the complexation, coordination, hydrogenation and oxidation.
Metal chlorides and ammonia are frequently used as the working
pair, which exhibits the complexation force. The advantage of
metal chloride over physical adsorbent is the higher adsorption
rate but would adversely affect the system by salt formation and
require more energy for the desorption process. Properties of some
adsorbent and adsorbate combination is given in the Table 3.
Composite adsorbents are used to improve heat and mass trans-
fer of chemical adsorbent, increase adsorption rate of physical
adsorbent. These are complex compounds made from metal chlo-
rides and expanded graphite, activated carbon fibre, zeolite or sil- Fig. 5. The ethanol uptake at Ps/P = 0.9 (Tads = 25oC) [37].

ica gel. It is flexible in nature i.e. the adsorption characteristics


could be changed by changing the structure of pore of silica gel
and by changing proportions of silica gel and chlorides or by alter-
ing types of salts.
Fig. 5 depicts the ethanol uptake of various adsorbents and
Fig. 6 shows the stability time/1000 in minutes. It is evident from
these figures that the maximum uptake and stability is achieved by
maxsorb which is a derivative of activated carbon. The marxsorb
could achieve the uptake of nearly 1.2 kg of ethanol per kg of max-
sorb and the stability time is noted to be 0.5. No other pairs could
achieve the same result, so this strengthens the statement that the
maxsorb-ethanol pair is the best [7].
The Fig. 7 shows specific cooling energy of different working
pair at various regeneration temperature (oC). It can be observed
from Fig. 7 that the ethanol-maxsorb combination provides the
highest specific cooling energy as compared to the other working
pairs. As the regeneration temperature increases the specific cool- Fig. 6. Uptake of several carbon adsorbents vs stability time/1000 [min].

ing energy of maxsorb-ethanol pair increases significantly. The


best result is that the pair could achieve a specific cooling energy of high reactivity. In some experiments ethanol of 99.9% purity
around 400 kJ/kgads at a regeneration temperature of 120 °C [37]. has been used with activated carbon (maxsorb-III) [7].

3.1. Work done by using activated carbon and its derivatives – 3.2. Work done by using activated carbon and its derivatives –
Methanol/Ethanol Ammonia

Majority of the work in solar adsorption has been done by using Numerical studies were done on the systems using this working
activated carbon and its derivatives like Maxsorb-III, A-15, A-20 etc pair. A higher COP is observed in the experiment of 0.43 [5]. The
with methanol. Due to the excellent porosity and surface area, the system is equipped with PTC (Parabolic Trough Solar Collector).
usage of activated carbon is maximised in this field. The adsorbate It is not advisable to use ammonia as adsorbate because it is haz-
frequently used was methanol in most of the cases. El- ardous to human health. Any leakage of ammonia could poison
Sharkawyetal. [7] aimed to improve the cooling performance of the food materials stored, if the system is designed for refrigeration
the system by using A-20, A-15 and methanol in his system. Sim- purpose.
ilar works are done by several authors on different systems
[7,12,14,16,19]. Climatic conditions during the performance in 3.3. Work done by using Ammonia-water
most of these experiments were almost the same. The solar collec-
tors were placed at an angle between 35 and 45°. The COP is Experiments using ammonia-water are comparatively less than
observed between 0.096 and 0.21 in case of activated carbon and that of activated carbon-methanol pair. As ammonia is a toxic gas,
methanol. Certain systems used ethanol in place of methanol for it is not used frequently in experiments. Citroph etal. [9] used
the experiments gave a better COP than the previous systems men- ammonia-water for a refrigeration process running on diurnal
tioned above. A maximum COP of 0.51 was observed by utilising cycle. This pair is not appreciated due to the toxicity of ammonia.
maxsorb-III and ethanol in the system [18]. The investigator had
used magnetic suspension particle system in which hydrogen trea- 3.4. Work done by using silica gel-water
ted adsorbent is used. According to the working pairs used, acti-
vated carbon with ethanol is better than that of methanol, but This is also a promising pair for the refrigeration purposes. In
there is a little difficulty of using ethanol in the system because case of COP, a good range of 0.2–0.5 has been shown in the exper-

Table 3
Properties of some adsorbent and adsorbate combination.

Adsorbent Adsorbate Maximum adsorption capacity (kg/kg) Adsorption temperature (℃) Pressure (bar) ODP GWP
Activated carbon Methanol 0.259 30 0.0523 0 2.8
Silica gel Water 0.116 30 0.09587 0 NA
Zeolite Water 0.236 30 0.09587 0 NA
Activated carbon Ethanol 1.2 30 0.09675 0 NA

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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

Fig. 7. Comparison of different specific cooling energy for low temperature working pair.

iments [10,11,15]. The regeneration temperature of silica gel is 4.4. Activated carbon and hydrogen
lower as compared to activated carbon which is an advantage for
the former, and the latent heat of vaporization of water is high Huang et al. [34] investigated the performance of hydrogen on
as compared to methanol and ethanol. There is a high advantage super activated carbon prepared by using potassium hydroxide
for silica gel-water and activated carbon-methanol pairs over the under N2 or CO2.The hydrogen capacity of activated carbon was
others because of the capability to be driven by relative low heat totally relied on micro pore volume. Usage of this combination
or by near ambient temperatures so that waste heat below was not appreciated because of the presence of acidic group that
100 °C could be recovered, which is highly desirable property. suppresses the storage of hydrogen on activated carbon due to
steric hindrance effect. In order to minimize the effect, a catalyst
can be utilized.
4. New working pairs
4.5. Activated carbon (Maxsorb-III) and n-butane
4.1. Activated carbon and diethyl ether
Saha et al. [39] used maxsorb-III and n-butane (C4H10) foe the
Ghouti et al. [38] used activated carbon and diethyl ether as the
experiment to find out the adsorption isotherm of the adsorbate
working pair. The chemical formula for diethyl ether is (C2H5)2O. In
on pitch based adsorbent at different temperatures and pressures
their experiment, the adsorption bed consists of multi tubular
are measured. The adsorption capacity was found out to be
arrangement in which activated carbon was incorporated in
0.8 kg of n-butane per kg of maxsorb-III with an adsorption tem-
meshed tubes engulfed by a cylinder. The experiment was con-
perature of 35 °C. The cycle time was noted to be 1400 s.
ducted at 26 °C, 35 °C, 50 °C of adsorber temperature. It was found
that the time taken to achieve the equilibrium temperature
between the working pairs reduces as the temperature increases. 4.6. Activated carbon and CO2
The best result was obtained at 50 °C of adsorber temperature.
Shen etal. [40] used activated carbon in beads form with carbon
dioxide as working pair for the experimental study of its adsorp-
4.2. Activated carbon (Maxsorb-III) and R134a tion properties. The equilibrium of adsorption process was noted
at different temperature and pressure ranges. The best result was
Shmroukh etal. [29] opted maxsorb-III and R134a for carrying 0.0844 g of CO2 on 1 g of activated carbon on bead form at
out the experiment between the temperatures ranging from 100 kPa and 303 K. The isosteric heat was found out to be
20 °C to 60 °C. R134a is the refrigerant generally used in VCRS. 23.17 kJ/mol.
The experiment was observed under different temperature ranges
25, 32, 40, 52 and 60 °C. It was found that 1 kg of maxsorb-III could
adsorb 1.6 kg of R134a and the cycle time for the experiment was 5. Conclusion
1200 s. Authors also used activated carbon and R134a for the
experiment. The experimental temperature ranges vary from 25 Adsorption refrigeration has many advantages over vapour
to 50 °C. Result says that the best outcome was observed at 25 °C compression and vapour absorption systems. It can be used for a
that 1 kg of activated carbon could adsorb 0.8352 kg of R134a. wide range of application such as ice making, refrigeration, air con-
ditioning and can also use as a cold storage for preserving food
materials, vaccines etc. Most of the adsorption refrigeration sys-
4.3. Activated carbon (Maxsorb-III) and R507A tems deliver a COP in range between 0.1 and 0.3. Adsorption refrig-
eration system has a COP of 0.48 by using a two-stage adsorption
Shmroukh etal. [29] opted maxsorb-III and R507A for the exper- chiller with zeolite-water as the working pair in combination with
iment. Four different temperatures were used for the conduction of a driving heat source of 55 °C and heat sink temperature at 30 °C. It
experiment. Out of that, at 20 °C, it was observed that an adsorp- is reported from the recent literatures that the COP and SCP of the
tion rate of maxsorb-III is as high as 1.3 kg per kg and the cycle adsorption refrigeration systems would increase by the increase of
time was 1100 s. adsorption and desorption temperature. Nowadays activated car-
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Manish Kumar Ojha, Anoop Kumar Shukla, P. Verma et al. Materials Today: Proceedings 46 (2021) 5639–5646

bon is used as adsorbents frequently over other kind of adsorbents [16] X.u. Ji, M. Li, J. Fan, P. Zhang, B. Luo, L. Wang, Structure optimization and
performance experiments of a solar-powered finned-tube adsorption
due to its large surface area and high porosity. This distinguishes
refrigeration system, Appl. Energy 113 (2014) 1293–1300.
activated carbon from other adsorbents such as silica gel, zeolite, [17] A.F.M.M. Rahman, Y. Ueda, A. Akisawa, T. Miyazaki, B.B. Saha, Design and
metal chlorides. Activated carbon – methanol is used mainly in performance of an innovative four-bed, three-stage adsorption cycle, Energies
experimental studies because it achieved sub-zero temperature 6 (2013) 1365–1384.
[18] K. Uddin, I.I. El-Sharkawy, T. Miyazaki, B.B. Saha, S. Koyama, H.-S. Kil, J.
and hence it is used in freezing applications. In order to achieve Miyawaki, S.-H. Yoon, Adsorption characteristics of ethanol onto functional
a continuous cooling effect a minimum of two absorbers are activated carbons with controlled oxygen content, Appl. Therm. Eng. 72 (2)
required in the adsorption refrigeration systems. (2014) 211–218.
[19] W.P. Du, M. Li, Y.F. Wang, J.H. He, J.X. He, Design of solar adsorption
refrigeration system with CPC and study on the heat and mass transfer
CRediT authorship contribution statement performance, E&ES 93 (2017) 012005.
[20] C.Y. Tso, K.C. Chan, C.Y.H. Chao, C.L. Wu, Experimental performance analysis on
an adsorption cooling system using zeolite 13X/CaCl2 adsorbent with various
Manish Kumar Ojha: Conceptualization, Data curation, Writing operation sequences, Int. J. Heat Mass Transf. 85 (2015) 343–355.
- original draft. Anoop Kumar Shukla: Supervision, Review and [21] A. Askalany, K. Habib, M. Ghazy, M.K. Assadi, Adsorption cooling system
employing activated carbon/Hfc410a adsorption pair, (2006).
editing. Puneet Verma: Review and editing. Ravindra Kannojiya:
[22] B.M. Dusane, N.C. Ghuge, Performance evaluation of solar adsorption system
Data curation. with/without wing using methanol-charcoal, Int. J. 2 (2017).
[23] B.B. Saha, K.C.A. Alam, A. Akisawa, T. Kashiwagi, K.C. Ng, H.T. Chua, Two-stage
Declaration of Competing Interest non-regenerative silica gel-water adsorption refrigeration cycle, Am. Soc.
Mech. Eng. Adv. Energy Syst. Div. Publ. AES. 40 (2000) 65–69.
[24] M.A. Alghoul, M.Y. Sulaiman, B.Z. Azmi, M.A. Wahab, Advances on multi-
The authors declare that they have no known competing finan- purpose solar adsorption systems for domestic refrigeration and water
cial interests or personal relationships that could have appeared heating, Appl. Therm. Eng. 27 (5-6) (2007) 813–822.
[25] M. Ghazy, A.A. Askalany, B.B. Saha, Maxsorb III/HFC404a as an adsorption pair
to influence the work reported in this paper. for renewable energy driven systems, Int. J. Refrig. 120 (2020) 12–21.
[26] P. Hu, J.-J. Yao, Z.-S. Chen, Analysis for composite zeolite/foam aluminum–
Reference water mass recovery adsorption refrigeration system driven by engine exhaust
heat, Energy Convers. Manage. 50 (2) (2009) 255–261.
[27] JingYi Wu, S. Li, YanFei Hu, Study on cyclic characteristics of the solar-powered
[1] N. Khandelwal, M. Sharma, O. Singh, A.K. Shukla, Recent developments in
adsorption cooling system, Sci. China Ser. E-Technol. Sci. 52 (6) (2009) 1551–
integrated solar combined cycle power plants, J. Therm. Sci. 29 (2) (2020) 298–
1562.
322.
[28] V. Baiju, C. Muraleedharan, Performance prediction of solar adsorption
[2] A. Kumar Shukla, Z. Ahmad, M. Sharma, G. Dwivedi, T. Nath Verma, S. Jain, P.
refrigeration system by ann, ISRN Thermodyn. 2012 (2012) 1–8.
Verma, A. Zare, Advances of carbon capture and storage in coal-based power
[29] A.N. Shmroukh, A.H.H. Ali, A.K. Abel-Rahman, Experimental study on
generating units in an Indian context, Energies 13 (2020) 4124.
adsorption capacity of activated carbon pairs with different refrigerants,
[3] A.K. Shukla, A. Sharma, M. Sharma, G. Nandan, Thermodynamic investigation
World Acad. Sci. Eng. Technol. Int. J. Chem. Mol. Nucl. Mater. Metall. Eng. 7
of solar energy-based triple combined power cycle, Energy Sourc. Part
(2013) 496–512.
Recovery Util. Environ. Eff. 41 (2019) 1161–1179.
[30] Z. Lu, R. Wang, Z. Xia, L. Gong, Experimental investigation adsorption chillers
[4] M. Sharma, A.K. Shukla, A. Singh, S. Johri, H.P. Singh, Parametric analysis of
using micro-porous silica gel–water and compound adsorbent-methanol,
solar energy conversion system using parabolic concentrator and thermopile,
Energy Convers. Manage. 65 (2013) 430–437.
Int. J. Ambient Energy 41 (12) (2020) 1409–1414.
[31] M.S. Fernandes, G.J.V.N. Brites, J.J. Costa, A.R. Gaspar, V.A.F. Costa, Review and
[5] A.E. Fadar, A. Mimet, M. Pérez-García, Modelling and performance study of a
future trends of solar adsorption refrigeration systems, Renew. Sustain. Energy
continuous adsorption refrigeration system driven by parabolic trough solar
Rev. 39 (2014) 102–123.
collector, Sol. Energy 83 (6) (2009) 850–861.
[32] M. Umair, A. Akisawa, Y. Ueda, Simulation study of continuous solar
[6] K. Sumathy, K.H. Yeung, L.i. Yong, Technology development in the solar
adsorption refrigeration system driven by compound parabolic concentrator,
adsorption refrigeration systems, Prog. Energy Combust. Sci. 29 (4) (2003)
Open Renew. Energy J. 7 (1) (2014) 1–12.
301–327.
[33] B.M. Dusane, N.C. Ghuge, A Review On Solar Adsorption Refrigeration System,
[7] I.I. El-Sharkawy, B.B. Saha, S. Koyama, J. He, K.C. Ng, C. Yap, Experimental
(n.d.).
investigation on activated carbon–ethanol pair for solar powered adsorption
[34] C.-C. Huang, H.-M. Chen, C.-H. Chen, Hydrogen adsorption on modified
cooling applications, Int. J. Refrig. 31 (8) (2008) 1407–1413.
activated carbon, Int. J. Hydrogen Energy 35 (7) (2010) 2777–2780.
[8] A. Sharafianardakani, M. Bahrami, A quasi steady state model for adsorption
[35] A. Sharafian, S.M. Nemati Mehr, P.C. Thimmaiah, W. Huttema, M. Bahrami,
cooling systems: Automotive applications, in: Energy Sustain. Am. Soc. Mech.
Effects of adsorbent mass and number of adsorber beds on the performance of
Eng., 2012: pp. 1263–1272.
a waste heat-driven adsorption cooling system for vehicle air conditioning
[9] R.E. Critoph, Rapid cycling solar/biomass powered adsorption refrigeration
applications, Energy 112 (2016) 481–493.
system, Renew. Energy 16 (1-4) (1999) 673–678.
[36] A.B. Puthumana, P. Paulose, R. Raveendran, D.P. Shouri, Analysis of two stage
[10] B.B. Saha, A. Akisawa, T. Kashiwagi, Solar/waste heat driven two-stage
solar vapour adsorption refrigeration system, Int. J. Mech. Eng. Technol. 8
adsorption chiller: the prototype, Renew. Energy 23 (1) (2001) 93–101.
(2017).
[11] X.Q. Zhai, R.Z. Wang, Experimental investigation and performance analysis on
[37] I.M. Astina, R. Sokha, P.S. Darmanto, Study on adsorption refrigeration system
a solar adsorption cooling system with/without heat storage, Appl. Energy 87
using activated carbon–ethanol as working pair, Int. J. Therm. Environ. Eng. 15
(3) (2010) 824–835.
(2017) 143–150.
[12] N.H. Abu Hamdeh, M.A. Al-Muhtaseb, Optimization of solar adsorption
[38] M.A. Al-Ghouti, I. Yousef, R. Ahmad, A.M. Ghrair, A.A. Al-Maaitah,
refrigeration system using experimental and statistical techniques, Energy
Characterization of diethyl ether adsorption on activated carbon using a
Convers. Manage. 51 (8) (2010) 1610–1615.
novel adsorption refrigerator, Chem. Eng. J. 162 (1) (2010) 234–241.
[13] E.-J. Bakker, R. de Boer, S. Smeding, N. Sijpheer, M. van der Pal, Development of
[39] B.B. Saha, A. Chakraborty, S. Koyama, S.-H. Yoon, I. Mochida, M. Kumja, C. Yap,
an innovative 2.5 kW silicagel-water adsorption chiller, (2011).
K.C. Ng, Isotherms and thermodynamics for the adsorption of n -butane on
[14] C. Rius-Alonso, L.O. de Lachica, E. Cardenas-Anaya, M. Marin-Becerril, J.
pitch based activated carbon, Int. J. Heat Mass Transf. 51 (7-8) (2008) 1582–
Poblado-Barrales, X. Rebollo-Arana, Y. Gonzalez-Quezada, SOLAR ADSORPTION
1589.
REFRIGERATION USING METHANOL/ACTIVATED CHARCOAL, in: INTED2012
[40] C.Z. Shen, C.A. Grande, P. Li, J.G. Yu, A.E. Rodrigues, Adsorption equilibria and
Proc., IATED, 2012: pp. 4571–4578.
kinetics of CO {sub 2} and N {sub 2} on activated carbon beads, (2010).
[15] A. Myat, N.g. Kim Choon, K. Thu, Y.-D. Kim, Experimental investigation on the
optimal performance of Zeolite–water adsorption chiller, Appl. Energy 102
(2013) 582–590.

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