Heat transfer enhancement of high temperature thermal energy storage using metal foams and expanded graphite

Latent heat storage (LHS) can theoretically provide large heat storage density and significantly reduce the storage material volume by using the material’s fusion heat, Δh_m. Phase change materials (PCMs) commonly suffer from low thermal conductivities, being around 0.4 W m⁻¹ K⁻¹ for inorganic salts, which prolong the charging and discharging period. The problem of low thermal conductivity is a major issue that needs to be addressed for high temperature thermal energy storage systems. Since porous materials have high thermal conductivities and high surface areas, they can be used to form composites with PCMs to significantly enhance heat transfer. In this paper, the feasibility of using metal foams and expanded graphite to enhance the heat transfer capability of PCMs in high temperature thermal energy storage systems is investigated. The results show that heat transfer can be significantly enhanced by both metal foams and expanded graphite, thereby reducing the charging and discharging period. Furthermore, the overall performance of metal foams is superior to that of expanded graphite.     

Study on phase change temperature distributions of composite PCMs in thermal energy storage systems

A one‐dimensional (1D) physical model is developed for latent heat thermal energy storage (TES) systems using composite phase change materials (PCMs) with different phase change temperature (PCT) distributions. By theoretical investigation under the assumption of neglecting the sensible heat, the optimum linear PCT distributions which are corresponding to minimum phase change time are derived. To verify the theoretical results of the optimum linear PCT distributions, the finite difference method is adopted to simulate the cyclical freezing and melting processes of composite PCMs. The numerical results in which the sensible heat is taken into account show that: (1) the optimum linear PCT distributions obtained from the theoretical analyses seem to be the optimum ones of composite PCMs in practical latent heat TES systems; (2) the phase change time of composite PCMs with the optimum linear PCT distributions used in practical latent heat TES systems can be decreased by as much as 25–40% by properly selecting the segmented numbers of composite PCMs as compared with that of PCMs of a single PCT. Copyright © 1999 John Wiley & Sons, Ltd.     

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.     

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.     

Thermal behavior of paraffin-nano-Al2O3 stabilized by sodium stearoyl lactylate as a stable phase change material with high thermal conductivity

A new kind of nano composite phase change material (NCPCM) was prepared using sodium stearoyl lactylate (SSL) as a surfactant to improve the dispersion of the Al₂O₃ nano-particles (with 2.5, 5, 7.5, and 10 wt.%) in paraffin with a SSL/Al₂O₃ mass ratio of 1:3.5. To evaluate the efficiency of the prepared PCMs, the melting rate of them at a temperature range of 50–60 °C and the effective thermal conductivity values in the solid and liquid states at a temperature range of 25–75 °C were measured using the k-type thermocouple and the transient hot wire technique, respectively. The heat storage behavior of the samples was investigated and their melting temperature, latent heat, and thermal reliability were determined using differential scanning calorimetry (DSC). Results showed that effective thermal conductivity enhancement ratios for the sample containing 10.0 wt.% nano-Al₂O₃ were 31% and 13% in the solid and liquid states, respectively, which are higher than those reported in similar studies. In addition, melting rate increased by 27%. As expected, all the PCMs showed good thermal reliability after 120 melting/freezing cycles. Based on our results, it may be concluded that the prepared PCMs can be regarded as effective heat storage materials for application in energy storage systems.     

Galactitol hexa stearate and galactitol hexa palmitate as novel solid-liquid phase change materials for thermal energy storage

Galactitol has a melting point of 187.41 °C and a fusion enthalpy of 401.76 J g⁻¹. Its melting temperature is not suitable for many thermal energy storage applications although it has good latent heat storage capacity compared to the several traditional phase change materials (PCMs). The galactitol also has high supercooling degree as about 72 °C. These unfavorable properties limit the usage potential of galactitol in thermal energy storage applications. However, the phase change temperature and supercooling degree of galactitol can be reduced to a reasonable value and therefore its feasibility for energy storage systems can be increased. For this aim, in this study, galactitol hexa stearate (GHS) and galactitol hexa palmitate (GHP) were prepared as novel solid-liquid PCM by means of esterification reaction of the galactitol with palmitic acid and stearic acid. The GHP and GHS esters were characterized chemically using FT-IR and ¹H NMR techniques. By using DSC analysis method, the melting temperature and latent heat value of the PCMs were determined as 31.78 °C and 201.66 J g⁻¹ for GHP ester and 47.79 °C and 251.05 J g⁻¹ for GHS ester. Thermal cycling test showed that the prepared PCMs had good thermal reliability after thermal 1000 melting-freezing cycles. Thermogravimetric analysis (TGA) results revealed that the PCMs have good thermal stability over their working temperatures. In addition, thermal conductivity of the prepared PCMs was increased as about 26.3% for GHP and 53.3% for GHS by addition of 5 wt.% expanded graphite. Based on all results it can be concluded that the prepared GHP and GHS esters can be considered as promising solid-liquid PCMs for many energy storage applications such as solar energy storage, indoor temperature controlling in buildings, production of smart textile and insulation clothing due to their good energy storage properties.     

Heat transfer enhancement of fatty acids when used as PCMs in thermal energy storage

Phase change materials (PCM) used in latent heat storage systems usually have very low thermal conductivities. This is a major drawback in maintaining the required heat exchange rate between PCM and heat transfer fluid. This paper investigates the enhancement of the heat transfer between PCM and heat transfer fluid, using high thermal conductivity as additives like stainless steel pieces, copper pieces and graphite–PCM composite material. In the experiments, palmitic–lauric acid (80:20) (PL) and stearic–myristic acid (80:20) (SM) were used as PCMs. Test results show that heat transfer enhancement of copper pieces was better at 0.05 Ls^?1 flow rate compared to 0.025 Ls^?1. Using copper as an additive increased the heat transfer rate 1.7 times for melting and 3.8 times for freezing when flow rate was 0.050 Ls^?1. Decreasing the flow rate from 0.050 to 0.025 Ls^?1, increased the melting times 1.3 times and freezing times 1.8 times, decreasing heat transfer rates accordingly. The best result of heat transfer enhancement was observed for the PCM–graphite composite. However, changing the flow rate did not affect the heat transfer rate when graphite was used as additive. Copyright © 2007 John Wiley & Sons, Ltd.     

High Density Polyethylene/Paraffin Composites as Form-stable Phase Change Material for Thermal Energy Storage

Abstract

This article focuses on the preparation and thermo-physical properties of paraffin/high density polyethylene (HDPE) composites as form-stable solid-liquid phase change material (PCM) for thermal energy storage. In the paraffin/HDPE blend, the paraffin (P) dispersed into the HDPE serves as a latent heat storage material when the HDPE, as a supporting material, prevents the melted paraffin leakage thanks to its structural strength. Therefore, this type composite is form-stable and can be used as a PCM without encapsulation for thermal energy storage. In this study, two paraffins with melting temperatures of 48°C–50°C and 63°C–65°C were used. The mass percentages of paraffins in the composites could go high as 76% without any seepage of the paraffin in melted state. The dispersion of the paraffin into the network of the solid HDPE was investigated using scanning electronic microscope (SEM). The melting temperatures and latent heats of the form-stable P1/HDPE and P2/HDPE composite PCMs were determined as 44.32°C and 61.66°C, and 179.63 and 198.14 Jg^?1, by the technique of differential scanning calorimetry (DSC), respectively. Furthermore, the thermal conductivity of the composite PCMs were improved as about 33.3% for the P1/HDPE and 52.3% for the P2/HDPE by introducing the expanded and exfoliated graphite to the samples in the ratio of 3 wt%. The results reveal that the prepared form-stable composite PCMs have great potential for thermal energy storage applications in terms of their satisfactory thermal properties, improved thermal conductivity and cost-efficiency because of no encapsulation for enhancing heat transfer in paraffin.     

Laminar film condensation driven latent thermal energy storage in rectangular containers

This paper focuses on numerically analyzing the thermal transport phenomena in the transient conjugate problem of melting and laminar film condensation. The key focus is to identify an optimum container aspect ratio/shape and conditions for which the heat storage time and the storage capacity are minimum and maximum respectively. Since most solid–liquid phase change materials (PCMs) suffer from poor thermal conductivities, the major resistance to heat transfer comes from PCM. Hence, high thermal conductivity, low-cost metal foam is suggested for use along with PCM to minimize this resistance. The conjugate transient problem of film condensation driven solid–liquid phase change of PCM impregnated inside porous metal foam is numerically analyzed. An effective heat capacity formulation is employed for modeling the transient PCM phase change in porous foam and is solved using finite element method. It is coupled with laminar film condensation on the outside of the storage container. The model is then used for selecting the best aspect ratio for thermal energy storage (TES) containers that enables to store comparatively the maximum heat. The results of the developed model showed that the major resistance to heat transfer and hence efficient thermal energy storage depends strongly on the aspect ratio of the PCM storage containers.     

Development of pentadecane/diatomite and pentadecane/sepiolite nanocomposites fabricated by different compounding methods for thermal energy storage

Global warming is one of the most important consequences of excess energy consumption. Phase change materials (PCMs) have prominent advantages in thermal energy storage owing to their high latent heat capacities and small temperature variations during the phase change process. However, leakage is a major problem that limits the use of PCMs. Leakage may occur in encapsulated PCMs or in composites where the PCM is attached to the surface of a supporting material or within the pores of that material. In this study, pentadecane/diatomite and pentadecane/sepiolite nanocomposites were fabricated by using unmodified and microwave‐irradiated diatomite and sepiolite samples and by using different compounding processes, such as direct impregnation, vacuum impregnation, and ultrasonic‐assisted impregnation methods. The microstructures and the chemical and thermal properties of the composites were characterized by scanning electron microscopy, Fourier‐transform infrared spectroscopy, and differential scanning calorimetry. Subsequently, the thermal reliability and stability and the thermal conductivity of the PCM composites were also investigated. A melting temperature of 9.25°C and a latent heat capacity of 58.73 J/g were determined for the pentadecane/diatomite composite that was prepared with the direct impregnation method using a microwave‐treated diatomite sample. The pentadecane/sepiolite composite prepared in the melting temperature range 7.98°C to 8.53°C and latent heat capacity range 41.05 to 46.02 J/g. The results of the thermal analysis indicate that fabricated diatomite‐based or sepiolite‐based PCM composites have good potential as thermal energy storage materials.     

石墨泡沫/共晶盐复合相变材料制备

选择KNO3/NaNO3二元体系按照质量比4∶6制备共晶盐,对共晶盐进行了熔点及熔化潜热的测量;将石墨泡沫这一新型材料作为强化基体,共晶盐作为相变材料（PCM）,采用熔融浸渗法制备了适用于太阳能热发电系统储能装置的石墨泡沫/共晶盐复合相变材料。采用扫描电镜对复合相变材料表面的微观结构进行了表征,并对其熔点、潜热、等效导热系数等热物性参数进行了测试。结果表明：共晶盐与石墨泡沫复合效果比较理想;复合前后共晶盐的熔点和潜热几乎没有发生变化;复合相变材料的等效导热系数得到了显著提升,石墨泡沫对相变材料起到了导热强化作用,满足高温蓄热的要求。     

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).     

Preparation and characterization of nano‐enhanced myristic acid using metal oxide nanoparticles for thermal energy storage

Fatty acids have been broadly used as phase change materials (PCMs) for thermal energy storage. However, low thermal conductivity limits their performances. This paper investigates the influence of metal oxide nanoparticle addition on myristic acid (MA) as nano‐enhanced PCM (NEPCM). Stability, chemical, and thermal properties were considered. Four types of nanoaprticles, TiO₂, CuO, Al₂O₃, and ZnO, were dispersed in MA at 0.1, 0.5, 1, and 2 wt%. Stability and dispersion were checked by sediment photograph capturing and scanning electron microscopy/energy‐dispersive spectroscopy. The Fourier‐transformed infrared (FTIR) and X‐ray diffraction analysis confirmed no chemical interaction between the nanoparticles and MA. The results revealed a ratio of thermal conductivity of 1.50, 1.49, 1.45, and 1.37, respectively, for 2 wt% of ZnO, Al₂O₃, CuO, and TiO₂. The T‐history method confirmed this enhancement. The latent heat thermal energy storage (LHTES) properties of the nano‐enhanced MA were evaluated using differential scanning calorimetry. The latent heat capacities of nano‐enhanced MA samples have dropped between 9.64 and 5.01 % compared with pure MA, and phase change temperature range was not affected significantly. The NEPCM was subjected to 500 thermal cycling, it showed a good thermal reliability as LHTES properties remained unchanged, while FTIR analysis showed similar characteristics compared with uncycled samples, indicating a good chemical stability. Based on the results regarding with the LHTES properties, cycling thermal reliability, and higher thermal conductivity improvement, it can be achieved that the MA/Al₂O₃ (2.0 wt%) and MA/ZnO (2.0 wt%) composites could be better PCMs for solar TES applications.     

Phase change characteristics of ethylene glycol solution‐based nanofluids for subzero thermal energy storage

Nanofluids, particularly water‐based nanofluids, have been extensively studied as liquid–solid phase change materials (PCMs) for thermal energy storage (TES). In this study, nanofluids with aqueous ethylene glycol (EG) solution as the base fluid are proposed as a novel PCM for cold thermal energy storage. Nanofluids were prepared by dispersing 0.1–0.4 wt% TiO₂ nanoparticles into 12, 22, and 34 vol.% EG solutions. The dispersion stability of the nanofluids was evaluated by Turbiscan Lab. The liquid–solid phase change characteristics of the nanofluids were also investigated. Phase change temperature (PCT), nucleation temperature, and half freezing time (HFT) were investigated in freezing experiments. Subcooling degree and HFT reduction were then calculated. Latent heat of solidification was measured using differential scanning calorimetry. Thermal conductivity was determined using the hot disk thermal constant analyzer. Experimental results show that the nanoparticles decreased the PCT of 34 vol.% EG solution but minimally influenced the PCT of 12 and 22 vol.% EG solutions. For all nanofluids, the nanoparticles decreased the subcooling degree, HFT, and latent heat but increased the thermal conductivity of the EG solutions. The mechanism of the improvement of the phase change characteristics and decrease in latent heat by the nanoparticles was discussed. The nanoparticles simultaneously served as nucleating agent that induced crystal nucleation and as impurities that disturbed the growth of water crystals in EG solution‐based nanofluids. Copyright © 2016 John Wiley & Sons, Ltd.     

Thermal conductivity improvement of stearic acid using expanded graphite and carbon fiber for energy storage applications

The influence of expanded graphite (EG) and carbon fiber (CF) as heat diffusion promoters on thermal conductivity improvement of stearic acid (SA), as a phase change material (PCM), was evaluated. EG and CF in different mass fractions (2%, 4%, 7%, and 10%) were added to SA, and thermal conductivities of SA/EG and SA/CF composites were measured by using hot-wire method. An almost linear relationship between mass fractions of EG and CF additives, and thermal conductivity of SA was found. Thermal conductivity of SA (0.30 W/mK) increased by 266.6% (206.6%) by adding 10% mass fraction EG (CF). The improvement in thermal conductivity of SA was also experimentally tested by comparing melting time of the pure SA with that of SA/EG and SA/CF composites. The results indicated that the melting times of composite PCMs were reduced significantly with respect to that of pure SA. Furthermore, the latent heat capacities of the SA/EG and SA/CF (90/10 wt%) composite PCMs were determined by differential scanning calorimetry (DSC) technique and compared with that of pure SA. On the basis of all results, it was concluded that the use of EG and CF can be considered an effective method to improve thermal conductivity of SA without reducing much its latent heat storage capacity.     

The micro‐/nano‐PCMs for thermal energy storage systems: A state of art review

With advancement in technology—nanotechnology, various thermal energy storage (TES) materials have been invented and modified with promising thermal transport properties. Solid‐liquid phase change materials (PCMs) have been extensively used as TES materials for various energy applications due to their highly favourable thermal properties. The class of PCMs, organic phase change materials (OPCMs), has more potential and advantages over inorganic phase change materials (IPCMs), having high phase change enthalpy. However, OPCMs possess low thermal conductivity as well as density and suffer leakage during the melting phase. The encapsulation technologies (ie, micro and nano) of PCMs, with organic and inorganic materials, have a tendency to enhance the thermal conductivity, effective heat transfer, and leakage issues as TES materials. The encapsulation of PCMs involves several technologies to develop at both micro and nano levels, called micro‐encapsulated PCMs (micro‐PCM) and nano‐encapsulated PCMs (nano‐PCM), respectively. This study covers a wide range of preparation methods, thermal and morphological characteristics, stability, applications, and future perspective of micro‐/nano‐PCMs as TES materials. The potential applications, such as solar‐to‐thermal and electrical‐to‐thermal conversions, thermal management, building, textile, foam, medical industry of micro‐ and nano‐PCMs, are reviewed critically. Finally, this review paper highlights the emerging future research paths of micro‐/nano‐PCMs for thermal energy storage.     

Energy and exergy analysis of a latent heat storage system with phase change material for a solar collector

Analysis of energy and exergy has been performed for a latent heat storage system with phase change material (PCM) for a flat-plate solar collector. CaCl₂·6H₂O was used as PCM in thermal energy storage (TES) system. The designed collector combines in single unit solar energy collection and storage. PCMs are stored in a storage tank, which is located under the collector. A special heat transfer fluid was used to transfer heat from collector to PCM. Exergy analysis, which is based on the second law of thermodynamics, and energy analysis, which is based on the first law, were applied for evaluation of the system efficiency for charging period. The analyses were performed on 3 days in October. It was observed that the average net energy and exergy efficiencies are 45% and 2.2%, respectively.     

Solar thermal energy discharging from a multiple phase change materials storage tank

In this work we have studied numerically the charging and the discharging of solar thermal energy stored (TES) using latent heat from a storage unit contains PCMs. We have also studied the improvement of the heat transfer between fluid which is the water and the PCMs by adding the fins to our storage unit with various configurations, including in-line fins and staggered fins. Then, we studied the assembly of two PCMs in our storage unit. In addition, an experimental work has been validated. The ANSYSFLUENT 15 code was used to solve the formulation of the fusion/solidification processes, where three users define have been developed to describe the thermo-physical properties of the PCMs.     

Developing microencapsulated 12‐hydroxystearic acid (HSA) for phase change material use

Phase change materials (PCM) have an increasingly more important role as a thermal energy storage (TES) media. However, leakage problem of PCM causes limitation during their integration in TES systems. Therefore, the encapsulation of PCMs is attracting research interest to extend usage of PCMs in real TES applications in recent years. In this study, hydroxystearic acid (HSA) was encapsulated with polymethyl methacrylate (PMMA) and different PMMA comonomer shells via emulsion polymerization method for the first time in literature. HSA with high melting temperature range (74–78°C) can widen the scope of using PCMs, and the encapsulated form can make it more versatile. The chemical structures, morphologies, and thermophysical properties of capsules were determined by FT‐IR, SEM, DSC, TGA, and thermal infrared camera. Among the produced HSA capsule candidates, PMMA‐HEMA is the most promising with latent heat of 48.5 J/g with melting range of 47 to 85°C. SEM analysis indicated that the capsules have spherical shape with compact surface at nano‐micro (100–440 nm) size range; however, some capsules exhibited agglomeration.     

Synthesis and Characterization of Disodium Hydrogen Phosphate Dodecahydrate-Lauric-Palmitic Acid Used for Indoor Energy Storage Floor Units

Organic and inorganic phase change materials(PCMs) are considered potential materials for thermal energy storage(TES) with different phase change characteristics. In this study, a novel organic-inorganic composite phase change material(PCM) called disodium hydrogen phosphate dodecahydrate-lauric-palmitic acid(D-LA-PACM) was prepared. Expanded graphite(EG) was selected as the support material, and the novel organic-inorganic form-stable PCM called D-LA-PAPCM/EG was prepared using the vacuum adsorption method. Differential scanning calorimetry, Fourier transform infrared spectroscopy, X-ray diffraction, leakage testing, melting and solidification cycle testing, thermal conductivity testing, scanning electron microscopy observation of the micromorphology, and other characterization methods were used to study the microstructure and morphology, thermal physical parameters, thermal conductivity, stability of the PCMs, and the comprehensive material properties of D-LA-PAPCM under the composite action of EG. Results indicated that the melting and freezing temperatures and latent heats of D-LA-PAPCM/EG were measured to be 31.6℃ and 34.3℃ and 142.9 and 142.8 J/g, respectively. Although some of the lauric-palmitic acid(LA-PA) and disodium hydrogen phosphate dodecahydrate(DHPD) separated in the multiple porous structures of EG after 1000 cycles, they could still absorb and release latent heats independently, with D-LA-PAPCM/EG still exhibiting good thermal stability. The thermal conductivity of D-LA-PAPCM/EG was 1.361 W/(m·K). Therefore, the material and thermal properties of the prepared D-LA-PAPCM/EG indicate that it could be well used as a feasible material for energy-saving phase change floor units in indoor TES systems.