Cellulose-based solid-solid phase change materials synthesized in ionic liquid

A series of cellulose graft poly(ethylene glycol) (cellulose-graft-PEG) copolymers as phase change materials (PCMs) were synthesized in ionic liquid by using 4, 4-diphenylmethane diisocyanate as coupling reagent. FTIR and ¹H NMR characterized the structure of the copolymers. Differential scanning calorimetry (DSC) indicated that the copolymers showed phase transitions with large thermal storage density, and the phase change temperature is in the range of 40-60 °C. The transition temperature and enthalpy can be tailored by changing the molecular weight and the content of poly(ethylene glycol) (PEG) side chains. The copolymers are solid-solid PCMs with good thermal stability. Expanded graphite (EG) with 2, 5 and 10 wt% was added to the PCMs to improve the thermal conductivity. It was found that the thermal conductivity enhanced significantly with increasing EG content. The cellulose-graft-PEG/EG composite PCMs have potential applications in thermal energy storage and temperature control.     

Synthesis and thermal properties of poly(styrene-co-ally alcohol)-graft-stearic acid copolymers as novel solid–solid PCMs for thermal energy storage

A series of poly(styrene-co-allyalcohol)-graft-stearic acid copolymers were synthesized as novel polymeric solid–solid phase change materials (SSPCMs). The graft copolymerization reactions between poly(styrene-co-allyalcohol) and stearoyl chloride were verified by Fourier transform infrared (FT-IR) and Proton Nuclear Magnetic Resonance (¹H NMR) spectroscopy techniques. The crystal morphology of the SSPCMs was investigated using polarized optical microscopy (POM) technique. Thermal energy storage properties of the synthesized SSPCMs were measured using differential scanning calorimetry (DSC) analysis. The POM results showed that the crystalline phase of the copolymers transformed to amorphous phase above their phase transition temperatures. Thermal energy storage properties of the synthesized SSPCMs were investigated by differential scanning calorimetry (DSC) and found that they had typical solid–solid phase transition temperatures in the range of 27–30 °C and high latent heat enthalpy between 34 and 74 J/g. Especially, the copolymer with the mole ratio of 1/1 (poly(styrene-co-allyalcohol)/stearoyl chloride) is the most attractive one due to the highest latent heat storage capacity among them. The results of DSC and FT-IR analysis indicated that the synthesized SSPCMs had good thermal reliability and chemical stability after 5000 thermal cycles. Thermogravimetric (TG) analysis results suggested that the synthesized SSPCMs had high thermal resistance. In addition, thermal conductivity measurements signified that the synthesized PCMs had higher thermal conductivity compared to that of poly(styrene-co-allyalcohol). The synthesized copolymers as novel SSPCMs have considerable potential for thermal energy storage applications such as solar space heating and cooling in buildings and greenhouses.     

Thermal properties and characterization of palmitic acid/nano silicon dioxide/graphene nanoplatelet for thermal energy storage

Palmitic acid (PA), nano silicon dioxide (nano SiO₂), and graphene nanoplatelets (GNPs) were fabricated to composite phase change materials (PCMs) for thermal energy storage. PA acted as PCM, nano SiO₂ was used as supporting material. GNP as thermal conductivity promoter was added to modify composite PCM. Nano SiO₂ has good adsorption property and can adsorb liquid PCM to prevent leakage. Leakage measurement indicated that PA maximum content in composite PCM is 70 wt%. Chemical and crystal structures, and microstructure of composite PCM were tested by Fourier transformation infrared spectroscope, X-ray diffractometer and scanning electronic microscope, which showed that the raw materials are well mixed by physical action. Differential scanning calorimeter result presented that composite PCM possess phase change temperature at about 60°C and latent heat of 128.42 kJ/kg. Thermogravimetric analyzer and thermal cycle experiment showed that composite PCM have outstanding thermal stability and durability. Thermal conductivity apparatus measurement results indicated that thermal conductivity of composite PCM with 5 wt% GNP is 1.65 times that of composite PCM without GNP. Therefore, this composite PCM are potential materials for thermal energy storage.     

Fatty acid/poly(methyl methacrylate) (PMMA) blends as form-stable phase change materials for latent heat thermal energy storage

Fatty acids such as stearic acid (SA), palmitic acid (PA), myristic acid (MA), and lauric acid (LA) are promising phase change materials (PCMs) for latent heat thermal energy storage (LHTES) applications, but high cost is the most drawback which limits the utility area of them in thermal energy storage. The use of fatty acids as form-stable PCM will increase their feasibilities in practical LHTES applications due to reduced cost of the energy storage system. In this regard, a series of fatty acid/poly(methyl methacrylate) (PMMA) blends, SA/PMMA, PA/PMMA, MA/PMMA, and LA/PMMA were prepared as new kinds of form-stable PCMs by encapsulation of fatty acids into PMMA which acts as supporting material. The blends were prepared at different mass fractions of fatty acids (50, 60, 70, 80, and 90% w/w) to reach maximum encapsulation ratio. All blends were subjected to leakage test by heating the blends over the melting temperature of the PCM. The blends that do not allow leakage of melted PCM were identified as form-stable PCMs. The form-stable fatty acid/PMMA (80/20 wt.%) blends were characterized using optic microscopy (OM), viscosimetry, and Fourier transform infrared (FT-IR) spectroscopy methods, and the results showed that the PMMA was compatible with the fatty acids. In addition, thermal characteristics such as melting and freezing temperatures and latent heats of the form-stable PCMs were measured by using differential scanning calorimetry (DSC) technique and indicated that they had good thermal properties. On the basis of all results, it was concluded that form-stable fatty acid/PMMA blends had important potential for some practical LHTES applications such as under floor space heating of buildings and passive solar space heating of buildings by using wallboard, plasterboard or floor impregnated with a form-stable PCM due to their satisfying thermal properties, easily preparing in desired dimensions, direct usability without needing an add encapsulation and eliminating the thermal resistance caused by shell and thus reducing cost of LHTES system.     

Experimental and numerical investigation of the melting process and heat transfer characteristics of multiple phase change materials

The melting and heat transfer characteristics of multiple phase change materials (PCMs) are investigated both experimentally and numerically. Multiple PCMs, which consist of three PCMs with different melting points, are filled into a rectangle-shaped cavity to serve as heat storage unit. One side of the cavity is set as heating wall. The melting rate of multiple PCMs was recorded experimentally and compared with that of single PCM for different heating temperatures. A two-dimensional mathematical model to describe the phase change heat transfer was developed and verified experimentally. The properties of multiple PCMs, including the effect of the melting point difference (combined type), thermal conductivity, and latent heat, on the heat transfer performance of the PCM were analyzed numerically. The results show that, the melting time decreases before it increases, with an increasing melting point difference for the multiple PCMs. In addition, the melting point decreases with increasing distance from the heating wall. Most of these types of multiple PCMs melt faster than the single PCM, and the multiple PCMs, with the melting point arranged as 322 K/313 K/304 K, has the shortest melting time in this study. The melting rate of the multiple PCMs, 322 K/313 K/304 K, accelerates faster than for the single PCM as the thermal conductivity, latent heat, and heating wall temperature increase. Finally, generalized results are obtained using a dimensionless analysis for both single and multiple PCMs.     

High latent heat storage and high thermal conductive phase change materials using exfoliated graphite nanoplatelets

Using exfoliated graphite nanoplatelets (xGnP), paraffin/xGnP composite phase change materials (PCMs) were prepared by the stirring of xGnP in liquid paraffin for high electric conductivity, thermal conductivity and latent heat storage. xGnP of 1, 2, 3, 5 and 7 wt% was added to pure paraffin at 75 °C. Scanning electron microscopy (SEM) morphology showed uniform dispersion of xGnP in the paraffin wax. Good dispersion of xGnP in paraffin/xGnP composite PCMs led to high electric conductivity. The percolation threshold of paraffin/xGnP composite PCMs was between 1 and 2 wt% in resistivity measurement. The thermal conductivity of paraffin/xGnP composite PCMs was increased as xGnP loading contents. Also, reproducibility of paraffin/xGnP composite PCMs as continuous PCMs was manifested in results of electric and thermal conductivity. Paraffin/xGnP composite PCMs showed two peaks in the heating curve by differential scanning calorimeter (DSC) measurement. The first phase change peak at around 35 °C is lower and corresponds to the solid-solid phase transition of the paraffin, and the second peak is high at around 55 °C, corresponding to the solid-liquid phase change. The latent heat of paraffin/xGnP composite PCMs did not decrease as loading xGnP contents to paraffin. xGnP can be considered as an effective heat-diffusion promoter to improve thermal conductivity of PCMs without reducing its latent heat storage capacity in paraffin wax.     

Thermal characterization of phase change materials based on linear low-density polyethylene,paraffin wax and expanded graphite

Thermal characterization of Phase Change Materials (PCMs) based on linear low-density polyethylene (LLDPE), paraffin wax (W) and expanded graphite (EG) is reported in this paper. Investigated PCMs showed high potential for application in energy storage systems.The latent heat, L_m, sensible heat Q_sens, and the ability of the prepared PCMs to store and release thermal energy were investigated using specific home-made equipment based on the transient guarded hot plane method (TGHPT). The sensible heat of PCM containing 40 wt.% of paraffin wax was investigated in the temperature range 25–35 °C, they exhibited a drop in Q_sens from 31 to 24 J/g depending on the concentration of EG. A similar decrease in sensible heat with increased loading of EG was observed for PCMs containing 50 wt.% of EG.The storage and release of thermal energy during phase change which is associated with the latent heat of the materials were investigated within the temperature range 20–50 °C. PCMs containing 40 wt.% of paraffin wax exhibited latent heat of 36 J/g, whereas the latent heat of PCMs containing 50 wt.% of paraffin wax was 49 J/g. The addition of EG decreased the time needed to melt and solidify PCMs due to increase in thermal conductivity of PCMs with increase in EG content. This behavior was confirmed by the thermal conductivity measurements, where thermal conductivity increased from 0.252 for sample without EG to 1.329 W/m × °C for PCM containing 15 wt.% of EG.The reproducibility of storage and release of thermal energy by PCMs was demonstrated by subjecting them to repeated heating and cooling cycles (over 150 cycles).     

High-chain fatty acid esters of myristyl alcohol with odd carbon number: Novel organic phase change materials for thermal energy storage—2

A series of high-chain fatty acid esters of 1-tetradecanol (myristyl alcohol) were synthesized via esterification of 1-tridecanoic, 1-pentadecanoic, 1-heptadecanoic and 1-nonadecanoic acids under vacuum and in the absence of catalyst. The esterification reactions were controlled by FT-IR spectroscopy. Differential scanning calorimeter (DSC) and thermo-gravimetric analyzer (TGA) were intensively used to determine the thermal properties of the presented novel organic phase change materials (PCM). The thermal properties were given in terms of phase change temperature, enthalpy, specific heat (C_p) and thermal decomposition temperature with related statistical calculations. The thermal reliability of the synthesized PCMs, which is an important property for utilization, was determined via measuring the change in thermal properties after 1000 thermal cycles. The DSC analyses indicated that the melting points of the novel organic PCMs were between 40 and 50 °C with phase change enthalpy above 200 kJ/kg. The results showed that these thermal storage materials were favorable for low temperature heat transfer applications with superior thermal properties and reliability among the known PCMs.     

Thermal Energy Storage Performance of Fatty Acids as a Phase Change Material

Thermal energy storage performance of fatty acids and a eutectic mixture as phase change materials (PCMs) has been investigated experimentally. The selected PCMs for this study were palmitic acid, myristic acid, stearic acid, and a mixture of stearic and myristic acids in eutectic combination ratio of 65.7 wt% myristic acid and 34.3 wt% stearic acid. The PCMs have a melting temperature range of 50.0°C to 61.20°C and a latent heat range of 162.0 J/g to 204.5 J/g. The inlet temperature and the mass flow rate of heat transfer fluid (HTF) were selected as experimental parameters to test the thermal energy storage performance of the PCMs. The transition times, temperature range, propagation of the solid-liquid interface, as well as heat flow rate characteristics of the employed cylindrical tube storage system were studied at varied experimental parameters. The experimental results show that the melting front moves to inward in the radial directions as well as in the axial directions from the top toward to the bottom of the PCM tube. It was observed that the convection heat transfer in the liquid phase plays an important role in the melting process. The changes in the studied HTF parameters have more effect on the melting processes than the solidification processes of the PCMs. The average heat storage efficiency calculated from data for all the PCMs is 51.5%, meaning that 48.5% of the heat actually was lost somewhere.     

Application of a ground source heat pump system with PCM‐embedded radiant wall heating for buildings

This paper deals with the utilization of a renewable energy‐based integrated system with the latent heat storage option for building thermal management systems. Both energy and exergy‐based assessments of the current combined system are conducted. For this purpose, phase change material (PCM)‐embedded radiant wall heating system using solar heating and ground source heat pump (GSHP) is studied thermodynamically. Heat is essentially stored within the PCMs as used in the panels to increase the effectiveness. The stored heat is released when the solar energy is not available. In the thermal energy storage analyses, four different PCMs are considered. The present results show that the overall first ‐ law (energy) and second ‐ law (exergy) efficiencies of the PCM‐free radiant heating system are much lower than the case with the PCM‐embedded radiant heating system. Therefore, it is confirmed that the energy efficiency increases from 62% to 87% while the exergy efficiency rises from 14% to 56% with the option where SP26E PCM is employed accordingly.     

Influences of expanded graphite on structural morphology and thermal performance of composite phase change materials consisting of fatty acid eutectics and electrospun PA6 nanofibrous mats

In the present work, three fatty acid eutectics of capric acid (CA)–lauric acid (LA), capric acid–palmitic acid (PA), and capric acid–stearic acid (SA) were prepared through melt-blending followed by ultrasonication and were investigated as model phase change materials (PCMs); for comparison, the individual fatty acid of CA was also studied. The DSC measurements indicated that the phase transition temperatures of fatty acid eutectics were lower than those of individual fatty acid of CA. Thereafter, the polyamide 6 (PA6) nanofibers and PA6/EG composite nanofibers with 10 wt.% expanded graphite (EG) were prepared by electrospinning; and then composite PCMs with fatty acid eutectics absorbed in and/or supported by the overlaid mats of electrospun nanofibers (e.g., PA6 and PA6/EG) were explored for storage and retrieval of thermal energy. Influences of the EG on structural morphologies, thermal energy storage properties and thermal energy storage/retrieval rates of composite PCMs were respectively characterized by scanning electron microscopy (SEM), differential scanning calorimeter (DSC) and measurement of melting/freezing times. The results indicated that the additions of EG caused the interfaces between fatty acid eutectics and PA6 nanofibrous mats to become more illegible; increased the absorption capacity of fatty acid eutectics within nanofibrous mats. The enthalpies of melting and crystallization of composite PCMs with EG were higher than those of the corresponding composite PCMs without EG, whereas there were no appreciable changes on the phase transition temperatures. The EG improved thermal energy storage/retrieval rates of composite PCMs were also confirmed by comparing the melting/freezing times of CA/PA6/EG and CA–SA/PA6/EG with those of CA/PA6 and CA–SA/PA6, respectively. The results from the SEM observation showed that composite PCMs had no or little variations in shape and surface morphology after heating/cooling processes.     

Thermal conductivity and latent heat thermal energy storage characteristics of paraffin/expanded graphite composite as phase change material

This study aimed determination of proper amount of paraffin (n-docosane) absorbed into expanded graphite (EG) to obtain form-stable composite as phase change material (PCM), examination of the influence of EG addition on the thermal conductivity using transient hot-wire method and investigation of latent heat thermal energy storage (LHTES) characteristics of paraffin such as melting time, melting temperature and latent heat capacity using differential scanning calorimetry (DSC) technique. The paraffin/EG composites with the mass fraction of 2%, 4%, 7%, and 10% EG were prepared by absorbing liquid paraffin into the EG. The composite PCM with mass fraction of 10% EG was considered as form-stable allowing no leakage of melted paraffin during the solid–liquid phase change due to capillary and surface tension forces of EG. Thermal conductivity of the pure paraffin and the composite PCMs including 2, 4, 7 and 10 wt% EG were measured as 0.22, 0.40, 0.52, 0.68 and 0.82 W/m K, respectively. Melting time test showed that the increasing thermal conductivity of paraffin noticeably decreased its melting time. Furthermore, DSC analysis indicated that changes in the melting temperatures of the composite PCMs were not considerable, and their latent heat capacities were approximately equivalent to the values calculated based on the mass ratios of the paraffin in the composites. It was concluded that the composite PCM with the mass fraction of 10% EG was the most promising one for LHTES applications due to its form-stable property, direct usability without a need of extra storage container, high thermal conductivity, good melting temperature and satisfying latent heat storage capacity.     

Study on the efficiency of effective thermal conductivities on melting characteristics of latent heat storage capsules

Improvement of the thermal conductivity of a phase change materials (PCM) is one effective technique to reduce phase change time in latent heat storage technology. Thermal conductivity is improved by saturating porous metals with phase change materials. The influence of effective thermal conductivity on melting time is studied by analyzing melting characteristics of a heat storage circular capsule in which porous metal saturated with PCM is inserted. Numerical and approximate analyses were made under conditions where there are uniform or non-uniform heat transfer coefficients around the cylindrical surface. Four PCMs (H₂O, octadecane, Li₂CO₃, NaCl) and three metals (copper, aluminum and carbon steel) were selected as specific materials. Porosities of the metals were restricted to be larger than 0.9 in order to keep high capacity of latent heat storage. Results show that considerable reduction in melting time was obtained, especially for low conductivity PCMs and for high heat transfer coefficient. Melting time obtained by approximate analysis agrees well with numerical analysis. A trial estimation of optimum porosity is made balancing the desirable conditions of high latent heat capacity and reduction of melting time. Optimum porosity decreases with increase in heat transfer coefficient.     

Micro-encapsulated paraffin/high-density polyethylene/wood flour composite as form-stable phase change material for thermal energy storage

Six novel polymer-based form-stable composite phase change materials (PCMs), which comprise micro-encapsulated paraffin (MEP) as latent heat storage medium and high-density polyethylene (HDPE)/wood flour compound as supporting material, were prepared by blending and compression molding method for potential latent heat thermal energy storage (LHTES) applications. Micro-mist graphite (MMG) was added to improve thermal conductivities. The scanning electron microscope (SEM) images revealed that the form-stable PCMs have homogeneous constitution and most of MEP particles in them were undamaged. Both the shell of MEP and the matrix prevent molten paraffin from leakage. Therefore, the composite PCMs are described as form-stable PCMs. The differential scanning calorimeter (DSC) results showed that the melting and freezing temperatures as well as latent heats of the prepared form-stable PCMs are suitable for potential LHTES applications. Thermal cycling test indicated the form-stable PCMs have good thermal stability although it was subjected to 100 melt–freeze cycles. The thermal conductivity of the form-stable PCM was increased by 17.7% by adding 8.8 wt% MMG. The results of mechanical property test indicated that the addition of MMG has no negative influence on the mechanical properties of form-stable composite PCMs. Taking one with another, these novel form-stable PCMs have the potential for LHTES applications in terms of their proper phase change temperatures, improved thermal conductivities, outstanding leak tightness of molten paraffin and good mechanical properties.     

Heat pipe with PCM for electronic cooling

This article experimentally investigates the thermal performances of a heat pipe with phase change material for electronic cooling. The adiabatic section of heat pipe is covered by a storage container with phase change material (PCM), which can store and release thermal energy depending upon the heating powers of evaporator and fan speeds of condenser. Experimental investigations are conducted to obtain the system temperature distributions from the charge, discharge and simultaneous charge/discharge performance tests. The parameters in this study include three kinds of PCMs, different filling PCM volumes, fan speeds, and heating powers in the PCM cooling module. The cooling module with tricosane as PCM can save 46% of the fan power consumption compared with the traditional heat pipe.     

Structure and thermal properties of expanded graphite/paraffin composite phase change material

Different contents of expanded graphite (EG) composite phase change material (PCM) were prepared by the melt mixing method, taking paraffin as the PCM and EG as the supporting material. Phase compositions of EG, paraffin, and EG/paraffin composite were investigated using X-ray diffraction (XRD). Microstructures of EG and EG/paraffin composite PCMs with different EG contents were observed by a scanning electron microscope (SEM). Thermal properties, such as phase-transition temperature and latent heat of the materials, were determined by differential scanning calorimetry (DSC). Mass loss and thermal properties after 100 heating cycles were measured. The results show that physical absorption exists between paraffin and EG. EG is beneficial for the PCM composite to reduce leakage of paraffin, decrease the phase change temperature and latent heat, and strengthen the thermal stability. The solid–liquid phase change latent heat of materials is larger than that of the solid–solid one. The heating cycle has little effect on the phase-transition temperature and latent heat.     

Preparation of pentadecane/poly(melamine‐urea‐formaldehyde) microcapsules for thermal energy storage applications

Phase change materials (PCMs) with suitable melting ranges for thermal energy storage applications are alkanes, paraffins, fatty acids, eutectic mixtures, and inorganic PCMs. Paraffinic hydrocarbons and fatty acids with low solubility in water are usually the preferred candidates. Pentadecane, which is an alkane hydrocarbon with the chemical formula C₁₅H₃₂, was used as PCM in this study. The pentadecane was microencapsulated with a poly(melamine‐urea‐formaldehyde (MUF)) shell for thermal energy storage. Pentadecane/poly(MUF) microcapsules were prepared by in situ polymerization method. The morphological analysis of pentadecane microcapsules was analyzed with scanning electron microscopy (SEM). Thermal properties of microcapsulated pentadecane were determined by differential scanning calorimetry (DSC). The results demonstrated that pentadecane/PUF microcapsules were prepared successfully, and they offer proper phase transition temperature range (8.7°C and 8.1°C) and heat enthalpy values (84.5 and ?88.2 kJ/kg) for thermal energy storage applications. According to the results, it was determined that pentadecane/poly(MUF) microcapsules have good potential for thermal energy storage applications.     

Microencapsulated phase change slurries for thermal energy storage in a residential solar energy system

Phase change materials (PCMs) are attractive for use in thermal energy storage applications and thermal regulation/control due to their high-energy storage density over a small temperature range. The direct use of phase change materials for energy storage and/or heat transfer applications has been limited due to the low thermal conductivity of the PCM particularly when solidifying on the heat transfer surface. A Phase change slurry (PCS) consists of small micro-encapsulated PCM particles suspended in a carrier fluid which enhances the heat transfer to the PCM. The PCS can serve not only as the thermal storage media but also as the heat transfer fluid, and hence may have many potentially important applications including in the field of heating, ventilation and air-conditioning (HVAC), refrigeration, solar energy and heat exchangers. A test system to examine PCS performance in residential thermal energy storage applications has been developed to both observe and characterise the thermal processes that occur in a thermal store with a helical coil heat exchanger. These test results will be used to improve the system design and identify limitations when used for intermittent application.     

Review on heat transfer analysis in thermal energy storage using latent heat storage systems and phase change materials

Thermal energy storage (TES) is a technology that stocks thermal energy by heating or cooling a storage medium so that the stored energy can be used later for heating and cooling applications and for power generation. TES has recently attracted increasing interest to thermal applications such as space and water heating, waste heat utilisation, cooling, and air conditioning. Phase change materials (PCMs) used for the storage of thermal energy as latent heat are special types of advanced materials that substantially contribute to the efficient use and conservation of waste heat and solar energy. This paper provides a comprehensive review on the development of latent heat storage (LHS) systems focused on heat transfer and enhancement techniques employed in PCMs to effectively charge and discharge latent heat energy, and the formulation of the phase change problem. The main categories of PCMs are classified and briefly described, and heat transfer enhancement technologies, namely dispersion of low‐density materials, use of porous materials, metal matrices and encapsulation, incorporation of extended surfaces and fins, utilisation of heat pipes, cascaded storage, and direct heat transfer techniques, are also discussed in detail. Additionally, a two‐dimensional heat transfer simulation model of an LHS system is developed using the control volume technique to solve the phase change problem. Furthermore, a three‐dimensional numerical simulation model of an LHS is built to investigate the quasi‐steady state and transient heat transfer in PCMs. Finally, several future research directions are provided.     

Phase change and heat transfer characteristics of a eutectic mixture of palmitic and stearic acids as PCM in a latent heat storage system

The phase change and heat transfer characteristics of a eutectic mixture of palmitic and stearic acids as phase change material (PCM) during the melting and solidification processes were determined experimentally in a vertical two concentric pipes energy storage system. This study deals with three important subjects. First is determination of the eutectic composition ratio of the palmitic acid (PA) and stearic acid (SA) binary system and measurement of its thermophysical properties by differential scanning calorimetry (DSC). Second is establishment of the phase transition characteristics of the mixture, such as the total melting and solidification temperatures and times, the heat transfer modes in the melted and solidified PCM and the effect of Reynolds and Stefan numbers as initial heat transfer fluid (HTF) conditions on the phase transition behaviors. Third is calculation of the heat transfer coefficients between the outside wall of the HTF pipe and the PCM, the heat recovery rates and heat fractions during the phase change processes of the mixture and also discussion of the effect of the inlet HTF parameters on these characteristics. The DSC results showed that the PA–SA binary system in the mixture ratio of 64.2:35.8 wt% forms a eutectic, which melts at 52.3 °C and has a latent heat of 181.7 J g⁻¹, and thus, these properties make it a suitable PCM for passive solar space heating and domestic water heating applications with respect to climate conditions. The experimental results also indicated that the eutectic mixture of PA–SA encapsulated in the annulus of concentric double pipes has good phase change and heat transfer characteristics during the melting and solidification processes, and it is an attractive candidate as a potential PCM for heat storage in latent heat thermal energy storage systems.