Latent Heat Values Research Articles

Enhancing solar flat plate collector efficiency with advanced phase change materials and expanded boron nitride

ABSTRACT Thermal energy storage, particularly through Phase Change Materials (PCMs), is gaining significant attention for its ability to enhance storage capacity and thermal conductivity. PCMs help alleviate the strain on renewable energy sources and stabilize load fluctuations. This study integrates a novel combination of LiNO3-NaSO4·10H2O-NaCl with boron nitride into Flat Plate Collectors (FPCs) to boost system performance. This Composite Phase Change Material (CPCM) increases latent heat value by up to 245.80 kJ, enhancing thermal decomposition and absorption rates while reducing heat losses. Boron nitride improves thermal conductivity by 25%, from 1.378 W/m·K to 5.543 W/m·K, increasing the CPCM's charging rate. The specific heat capacity rises from 4.2 J/g·°C to 5 J/g·°C at a maximum temperature of 90°C. As a result, the collector's efficiency improves by 15%, achieving an overall system efficiency of 88%. Water serves as the heat transfer fluid, and simulations are conducted using Python in Anaconda Jupyter Notebook.

The Impact of Binary Salt Blends’ Composition on Their Thermophysical Properties for Innovative Heat Storage Materials

Heat storage is an emerging field of research, and, therefore, new materials with enhanced properties are being developed. Examples of phase change materials that provide high heat storage are inorganic salts and salt mixtures. They are commonly used for industrial applications due to their high operational temperature and latent heat. These parameters can be modified by combining different types of salts. This paper presents the experimental study of the impact of the composition of binary salts on their thermophysical properties. Unlike the literature data, this article provides a detailed analysis of the phase change process in both directions: solid–liquid and liquid–solid. The results indicate that the highest latent heat was observed for a 70% NaNO3 content in the NaNO3–KNO3 mixture. Therefore, when this salt is used for heat storage, the most favorable choice is a 70:30 ratio, which provides the highest heat storage density and the lowest phase transition temperature. In the case of the NaNO3–NaNO2 mixture, the highest value of latent heat occurs for a ratio of 80:20, resulting in phase transition temperatures of 267.0 °C for the solid–liquid transition, and 253.5 °C for the liquid–solid transition. For heat storage applications, it is recommended to use pure NaNO2 salt instead of the NaNO3–NaNO2 mixture.

Novel nano-Y2O3/myristic acid nanocomposite PCM for cooling performances of electronic device with various fin designs

Effective thermal management is critical for enhancing the longevity and operational efficiency of electronic devices. This research introduces a novel cooling approach by incorporating Yttrium Oxide (Y2O3) nanoparticles into Phase Change Materials (PCMs) to improve thermal management in electronic devices. This study focuses on developing nanocomposite PCMs with Y2O3 nanoparticles embedded in a myristic acid (MA) matrix through melting and physical mixing. Nanoparticles were added to MA at various mass fractions: 0.5 %, 1 %, 1.5 %, and 2 %. Structural and morphological analyses were conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field emission scanning electron microscopy combined with energy dispersive X-ray spectroscopy (FE-SEM-EDX). Thermophysical properties were characterized using differential scanning calorimetry (DSC) and thermal conductivity measurements with the KD2-Pro device. The inclusion of Y2O3 nanoparticles significantly enhanced the thermal conductivity of the PCM, reaching up to 0.229 W/m·K in the solid phase and 0.177 W/m·K in the liquid phase, representing improvements of 43.125 % and 18 %, respectively, over the base PCM. The highest average specific heat capacity (Cp) values in the solid and liquid phases were 1.98 J/g·°C and 2.69 J/g·°C, respectively, for the 2 % nanoparticle-additive sample. DSC analysis indicated slight shifts in phase transition temperatures and a noticeable reduction in latent heat values, from 215 J/g to 202 J/g for solidification and from 209 J/g to 201 J/g for melting. Computational analysis using ANSYS-FLUENT software validated the enhanced thermal dissipation properties of the nanocomposite PCM. Additionally, an examination of fin configurations within the PCM containers revealed that rectangular fins provided superior cooling efficacy compared to trapezoidal ones. This study demonstrates that the development of nano- Y2O3 enhanced MA nanocomposite PCMs presents a promising avenue for applications in electronic device thermal management and thermal energy storage.

Supramolecular porous phase change materials for encapsulation of nitrate with amino-expanded graphite by cucurbit[7]uril

The demand for oil and natural gas energy is increasing dramatically, and the extraction of conventional oil and gas reservoirs is in a stage of exhaustion. In order to stabilize the functionalized properties of oil-based drilling fluids (OBDF) during the extraction of oil and gas reservoirs in ultra-deep wells, the present experiments were carried out on the material (EG-NIT/CB[7]) obtained by encapsulating nitrate (NIT) in expanded graphite (EG) with porous structure through the supramolecular self-assembly property of cucurbit[7]uril (CB[7]). The structural properties were analyzed using various analytical tools and the results showed that our material synthesis was successful. And the effect of mass fraction of EG, CB[7] on the heat transfer and storage of EG-NIT and EG-NIT/CB[7] materials was investigated. The increase in mass fraction of EG can increase the thermal conductivity of EG-NIT up to 7.4 times and the introduction of CB[7] further improves the thermal conductivity of EG-NIT/CB[7] by up to 1.38 W/m·k. The latent heat value of EG-NIT/CB[7] decreased by only 4.7% after 200 cycles. Meanwhile, under the condition of 150 °C, adding EG-NIT/CB[7] to drilling fluids can reduce the temperature of drilling fluids by 2.8 °C. And it improves the stability of drilling fluids, the viscosity almost does not change, and it can also play a certain role in inhibiting the leakage of drilling fluids. Therefore, the EG-NIT/CB[7] developed by us can be practically applied in ultra-deep drilling projects.

Experimental Study on the Effect of Additives for Phase Change Hysteresis Performance

Phase change energy storage materials are the core of phase change energy storage technology. Phase change hysteresis can cause phase change materials not to store and release thermal energy as expected, and most studies have not focused on this. A low-temperature eutectic phase change material CaCl2·6H2O–MgCl2·6H2Omaterial prepared was investigated, and some influencing factors of the phase change hysteresis phenomenon and its regular characteristics were aspired to be obtained. The melting-solidification curves were obtained using a step-cooling test bench, and the latent heat values and heat absorption and exothermic curves of materials with different proportions were measured by a differential scanning calorimeter. The experimental results show that the temperature difference of the phase change hysteresis tended to increase gradually with the increase of the mass fraction of the nucleating agent, and the hysteresis temperature difference increases from the initial 3.9 °C–15.02 °C when SrCl2·6H2O was added by 2.4%. The temperature difference of the phase change hysteresis increased gradually with the increase of the mass fraction of the thickener. This paper provides a new idea for optimizing the properties of phase change energy storage materials and provides a possibility for realizing the parametric control of phase change hysteresis factors.

A Novel Concept of Nano-Enhanced Phase Change Material.

In the actual context of growing concerns over sustainability and energy efficiency, Phase Change Materials (PCMs) have gained attention as promising solutions for enhancing energy storage and release efficiency. On another hand, materials based on graphene oxide (GO) have proven antibacterial activity, biocompatibility, efficiency in microbial growth inhibition, and pollutant removal. Integrating nanoparticles into PCMs and creating Nano-Enhanced Phase Change Materials (NEPCMs) have opened new horizons for optimizing the performance of these systems and sustainable development. The key objective of this work is to gain insight into NECPMs, which are used in solar wall systems to enhance solar energy storage. Paraffin RT31 was mixed with Cu nanoparticles, graphene oxide (GO), and Cu-decorated GO (Cu@GO) at loading ratios ranging from 1% to 4% (w/w nanoparticles with respect to RT31). The compositions were characterized through Differential Scanning Calorimetry (DSC) and rheology tests. The decoration of the carbon-based nanoparticles was performed using the ultrasonication procedure, and the decoration efficiency was confirmed through X-ray Photoelectron Spectroscopy (XPS). The rheologic measurements were performed to correlate the flow behavior of the NEPCM with their composition at various temperatures. The study methodically investigated these composites' latent heat values, phase change peak temperatures, and solidification phase change temperatures. Compared to pure paraffin, the solidification of the formulations obtained using Cu@GO exhibits the largest increase in latent heat, with a 12.07% growth at a concentration of 2%. Additionally, at a 4% concentration of NEPCM, the largest increase in thermal conductivity was attained, namely 12.5%.

Review of organic and inorganic waste-based phase change composites in latent thermal energy storage: Thermal properties and applications

Systematization and analysis of standalone waste materials that can serve as phase change materials (PCMs), and composites consisting of commercially available PCMs combined with organic and inorganic waste materials is presented. Within the conducted review research, obtained thermal properties of so far investigated waste-derived PCMs were presented, assessing, among other, their latent heat storage capacity, thermal conductivity, and thermal and cyclic stability. Refined coconut oil and Allanblackia oil exhibited exceptional thermal and cyclic stability along with high values of latent heat, amounting 105 kJ kg−1 and 81 kJ kg−1, respectively. In some cases incorporation of waste materials significantly improved thermal properties, e.g. the addition of carbonized waste tire rubber to dodecyl alcohol increased its thermal conductivity to 0.431 W m−1K−1, representing an increase by a factor of 2.3. This enhancement led to a 17.2 % reduction in heating times and a 20 % reduction in cooling times compared to using pure PCM. Besides providing extensive data on thermophysical properties of phase change composites, the study provides a comprehensive overview of their applications, economic feasibility, and environmental implications. This extensive review shows the potential of waste-derived PCMs to contribute to a circular economy by repurposing waste materials for sustainable energy solutions and reducing environmental impacts. The findings indicate that while valorising wastes or by-products as latent thermal energy storage materials is feasible, more research efforts are required towards potential commercialization.

Silica-based aerogels encapsulate organic/inorganic composite phase change materials for building thermal management

Phase change energy storage materials are widely used in thermal management because they reduce energy consumption and effectively address issues such as energy supply and demand mismatches. However, challenges such as leakage in solid-liquid phase change materials (PCMs), flammability in organic solid-liquid PCMs, and supercooling and phase separation in inorganic solid-liquid PCMs still need to be resolved for their practical applications. In this study, we used methyl palmitate, dodecahydrate disodium hydrogen phosphate, and decahydrate sodium carbonate as the main PCMs, sodium carboxymethyl cellulose as an emulsifier and thickener, and silica aerogel as the encapsulating material to successfully prepare a novel shape-stabilized organic/inorganic composite PCM (CPCM). The prepared CPCM exhibits excellent shape stability and flame retardancy without supercooling or phase separation issues. In addition, the prepared CPCM has a high latent heat value (174.1 J/g) and a suitable phase transition temperature (22.9 °C), and its thermal performance remains basically unchanged after 100 heating/cooling cycles. Furthermore, this CPCM also demonstrates exceptional performance in building thermal management. This study provides a new solution to the problems of flammability, supercooling, phase separation and easy leakage of CPCM currently used in the field of building thermal management.

Development of a novel Al-Si microcapsules with heat-resistant, high latent heat, and efficient solar heat absorption

Aluminum-silicon (Al-Si) alloys are prominent in high-temperature thermal storage due to their high thermal storage density, thermal conductivity, and low cost. Despite their potential, the corrosivity and chemical activity from their liquid phase leakage limit broader applications. The hydrothermal method, often used for encapsulating Al-Si into microencapsulated phase change materials (MEPCMs), consumes the core material, reducing latent heat values. Additionally, the inability to modify the shell material fails to meet multifunctional demands. Addressing solar thermal application needs, we developed a novel heat-resistant, high-latent-heat Al-Si MEPCMs using a “double-layer coating, sacrificial inner layer” approach. This method, originally proposed by our research group and first extended to the microencapsulation of high-temperature phase change materials (PCM), uses Al-12Si as the core, PMMA as the sacrificial layer, and SiO2 as the outer shell.The MEPCMs demonstrated an encapsulation efficiency of 90.7 % and a latent heat value of 454.9 J/g. By adjusting the core–shell ratio, the size of the internal void was optimized to enhance thermal performance and cyclic stability, with MEPCM-S3 maintaining 98.6 % of its latent heat (439.5 J/g) after 10 thermal shocks and 300 thermal cycles. Furthermore, surface loading of carbon black (CB) enhanced the spectral absorption rate to 87.72 % in the 200–2500 nm range, marking an 11 % increase. These modifiable, high-latent heat, and cycle-resistant Al-Si MEPCMs hold broad prospects for applications in high-temperature thermal storage and as next-generation efficient solar energy storage media.

HEAT BUDGET OF THE BARENTS SEA SURFACE IN WINTER

Variability of the total heat balance (HB) of the Barents Sea during the cold period of the year has been studied. The cold period is that of cooling of the sea surface when the heat flux is permanently oriented towards the atmosphere. The contribution of two major components of the HB, i. e. sensible and latent heat fluxes, to the observed increase of the total winter heat transfer at the sea-atmosphere interface has been estimated. Data on short-wave and long-wave radiation fluxes, and sensible and latent heat values were obtained from the atmos-pheric reanalysis of the European Center for Medium-term Weather Forecasting ERA5. HB of the sea surface was calculated as a sum of short-wave and long-wave radiation fluxes and those of sensible and latent heat. The total HB, as well as the total flux of sensible and latent heat for the cold period were calculated by summing up the corresponding values between the start and end dates of the cooling season. Calculations demonstrated an increase in the sum of HB over the cold season for the northern part of the Barents Sea (up to 2000 MJ/m2 over 40 years), and a decrease in the southern part of the sea (up to 1000 MJ/m2 over 40 years). In the northern part of the sea, the contribution of sensible and latent heat fluxes decreases to 0,3-0,4. The observed trend of sum of HB over the cold season and its turbulent components could with high probability be explained by increasing difference between air temperature and sea surface temperature.

Flame-retardant and phase-changing microcapsules incorporating black phosphorus for efficient solar energy storage

A novel phase change microcapsule has been developed and synthesized for solar energy storage systems. The fabrication process involved the in-situ polymerization of phase change microcapsules, wherein cellulose nanocrystals (CNCs) were employed as Pickering emulsifiers and nano-fillers to enhance the properties of the melamine formaldehyde resin (MF) shells. These enhancements included improved emulsifying ability, mechanical strength, and sustainability. Subsequently, black phosphorus (BP), a two-dimensional material with high solar absorption intensity and a wide frequency range, was covalently modified by MF to enhance the photothermal capacity of the microcapsules and reduce the thermal resistance between the photothermal material and the phase change material (PCM), this functionalized BP was referred to as MF@BP. The phase change microcapsules without and with MF@BP exhibit high latent heat values of 210.79 J g−1 and 207.92 J g−1, respectively. Furthermore, the PCM core content was measured at 88.9% and 88.5%, and the encapsulation rates are 99.0% and 98.8%, respectively. The PCM microcapsules with MF@BP demonstrated excellent photothermal characteristics with an efficiency of 92.04%. Additionally, the PCM microcapsules exhibit stability below 200 °C and retain 99.4% of their latent heat even after 100 cycles of heating and cooling. Furthermore, the PCM microcapsules display self-extinguishing properties due to the flame retardancy of the MF shell, and the incorporation of black phosphorus further enhanced the flame retardancy. Overall, these PCM microcapsules exhibit significant potential for utilization in solar energy systems.

Thermal Behavior of Composite Material Based on Phase Change Material/Plaster as Thermal Energy Storage in Multilayer Wall: Experimental Study.

This study aims to explore the effects of augmenting the mass proportion of a composite comprising paraffin and beeswax (PBPCM) within plaster, which influences the thermal insulation of a dual wall. This work is primarily based on the thermal properties of the composite material PBPCM/plaster with varying percentages of PBPCM. Various essential parameters, such as density, thermal conductivity, specific heat capacity, thermal diffusivity, and latent heat, were assessed and juxtaposed with those of conventional plaster for the PBPCM/plaster composite material. The evaluation of this composite material was executed through an experimental device on a laboratory scale. The obtained results show that the increase in the mass fraction of PBPCM in the plaster decreased the thermal conductivity of plaster more than 3 times, whereas this increase of the PBPCM fraction in plaster enhances heat retention, specifically in specific heat capacity under constant conditions. Nevertheless, in a dynamic state, thermal effusivity has the lowest value for 50% PBPCM. The recommendation is to utilize 50% PBPCM, as it yields an optimal thermal effusivity, and significant values of specific heat capacity and latent heat have been noted for this percentage of PBPCM, measuring 1263.77 kJ/kg K and 18.9 kJ, respectively. Additionally, an increase in the PBPCM percentage narrows the temperature range suitable for effective thermal energy storage.

Stabilizing a low temperature phase change material based on Glaubers salt

The aim of this research is to enhance the performance of Glauber's salt (sodium sulfate decahydrate, SSD) as a phase change material (PCM) for thermal energy storage applications, as well as for shipping of temperature-sensitive materials. The study investigates the effects of modifying SSD with potassium chloride (KCl) and ammonium chloride (NH4Cl) to achieve lower phase transition temperatures of between +6 °C and + 13 °C. Sodium polyacrylate (PAAS) is employed as a thickening agent to prevent phase separation, and borax is used as a nucleating agent to suppress supercooling. Various ratios of KCl:NH4Cl are tested, and the impact of PAAS concentration on phase segregation is explored. The results show that a 2 wt% concentration of PAAS effectively prevents phase separation. Samples with a KCl:NH4Cl ratio of 1:1.83 exhibit stable phase transition behavior and maintain latent heat values within the range of 130–140 J/g after 30 thermal cycles. Maintaining a total KCl and NH4Cl proportion of 10 wt% is crucial to achieve the desired lower melting temperature. The study highlights the significance of thermal cycling in improving the stability of the PCM. The optimized SSD-based eutectic PCM formulations hold promise for applications in the cold chain industry.

Enhancing thermal performance of energy storage concrete through MPCM integration: An experimental study

Phase change materials melt and solidify at different temperature ranges called Phase change hysteresis. This phenomenon should be understood and evaluated in order to adequately design energy storage concretes for applications. Although many studies have analyzed the phase change process in pure - phase change materials such as paraffin. However, there is not enough information about the Phase change hysteresis of energy storage concrete. In order to realistically reproduce the working condition of concrete. This study explores phase change hysteresis in energy storage concrete slabs, focusing on the impact of microcapsule concentration and temperature change rate on thermal efficiency. Experiments were conducted to analyze the thermophysical properties, particularly observing the variations in specific heat capacity and phase transition temperatures. Results showed that increasing the microcapsule concentration enhances the specific heat capacity and latent heat of phase change, while faster temperature changes intensify hysteresis effects. Compared with the results of previous studies. Phase change hysteresis is more significant due to the pore and complex structure of energy storage concrete that impedes heat transfer. The experimental latent heat values were approximately 75 % of theoretical predictions, likely due to microcapsule damage and microstructural impacts on heat transfer. The study's findings are crucial for optimizing the thermal performance of energy storage concrete.

Preparation and properties of gel-type low-temperature phase change materials

In the context of the dual‑carbon target, there is a high emphasis on the energy efficiency of traditional mechanical cold storage systems with significant power consumption. Additionally, the implementation of time-of-use electricity pricing has played a crucial role in driving the rapid advancement of energy storage technology. The application of energy storage technology in cold storage can significantly reduce the energy consumption of the refrigeration system, save operating costs by shifting peak demand to valleys, and reduce start and stop frequencies. Therefore, studying phase-change materials with high latent heat, low cost, and good performance for cold storage is of great practical application in cold storage. The paper developed four types of gel-type phase-change cold storage materials with high latent heat, low cost, and good cycle stability. These materials mainly consist of NH4Cl, KCl, and deionized water. The phase transition temperature ranges from −18 to −21 °C, the latent heat of phase change is approximately 260 to 289 J/g, and the thermal conductivity ranges from 0.58 to 0.60 W/(m·K), which can meet the cooling demand of cold storage facilities. Furthermore, by comparing the phase transition temperature, latent heat value of phase change, and cyclic stability, a gel-type PCM with good comprehensive properties was selected for corrosion and corrosion inhibition studies with five common metal samples in welded and non-welded forms. The results showed that material B2 had slight corrosion on 1060 aluminum, 6061 aluminum, and 304 stainless steels, but no obvious corrosion phenomenon was found on 316 stainless steels. The corrosion rate of the material on red copper was the highest, and the corrosion was too strong. In addition, the corrosion of welded parts is more serious than that of non-welded parts, and the welding points are more susceptible to corrosion. Adding the corrosion inhibitor BTA to material B2 can reduce the corrosion rate of red copper by more than 94 %.

Development of CaCl2·6H2O-mannitol/SiO2 shape-stabilized composite phase change material for the radiant cooling panel system

Radiant cooling panel systems are now popular solution for low carbon buildings, so has received great attention of researchers. Current development, however, is that radiant cooling panel systems have low cooling efficiency and cause high pressure on national energy supply during peak energy consumption periods. This study, therefore, has developed a novel composite phase change material (CPCM) coupled with a typical radiant cooling panel system, providing longer indoor comfort duration and less temperature fluctuation, while also alleviating the pressure on national energy supply during peak energy consumption. In this study, eutectic hydration salt of CaCl2·6H2O and mannitol have been combined with SiO2 to prepare a shape-stabilized CPCM. It has been placed in a test room to justify the impact of the new material. Experimental results have demonstrated some major properties of this material, namely, a melting point of 20.7 °C, a high latent heat value of 119.8 J/g, and a supercooling degree of 1.3 °C, as well as good stability and thermal reliability. Therefore, it can be used as a good solution for radiant cooling panel systems. Comparing the results with another test room with ordinary radiant cooling panels, the room with the new CPCM panel showed less indoor temperature fluctuation and 73 % longer indoor comfort duration. This work provides further development of using hydrated salts and CPCMs with different phase change temperatures in radiant cooling panel systems.

Graphene oxide modified sodium alginate/polyethylene glycol phase change material hydrogel scaffold composite with photothermal temperature control for potential bone tissue regeneration

The challenge of precisely regulating temperature during the photo-thermal bone promotion remains unresolved. Phase change material (PCM), capable of undergoing a phase transition at a specific temperature, offers a solution by photothermal temperature regulation through the storage and release of heat. This study incorporated biocompatible polyethylene glycol (PEG) with specific phase transition points as PCM. A phase change hydrogel scaffold was then synthesized through semi-crosslinking PEG with calcium-ion-chelated sodium alginate (SA) acting as the structural framework. Additionally, the newly developed graphene oxide (GO) modified composite scaffolds (GO-PHSC), featuring 0.5 wt% GO, not only demonstrated outstanding photothermal conversion efficiency and an optimal phase change temperature (42.2 °C) but also exhibited desirable values for latent enthalpy (100 J/g) and latent heat recovered (LHR) (93.3%). Moreover, the form-stability test demonstrated the PCM scaffolds' exceptional resistance to leakage and maintenance of shape stability even at elevated temperatures (70 °C). Beyond achieving passive temperature control in photothermal therapy, experimental findings highlighted that the phase change hydrogel, incorporating calcium ions and GO, met various requirements such as physicochemical properties, microstructure, mechanics, mineralization, biocompatibility, and cell affinity. These collective attributes suggest that GO-PHSC emerges as a promising scaffold composite candidate for temperature-controlled photothermal therapy in bone regeneration.

Investigation on the effect of physical parameters of PCMs on the exothermic properties of energy storage units of bilayer tubes

Based on the structure of bilayer tube energy storage unit (ESU), the study investigates the effects of physical parameters and arrangement combinations of phase change materials (PCMs) on the heat storage and exothermic performance of the ESU. The control variable method is used to focus on a single physical parameter of the phase change material to analyze its influence on the heat storage and exothermic performance. Use of experimental and numerical modelling, we firstly analyze the influence of the thermal conductivity of PCMs on the thermal storage and discharge performance, and then study the influence of the latent heat value of PCMs on the thermal storage and discharge performance, and compare and analyze its thermal performance parameters with those of traditional ESUs. Studies have shown that the thermal conductivity of the bilayer ESU can be minimized by up to 26.9% and the heat release time can be increased by up to 23.8% compared with the conventional ESU. The latent heat value of the bilayer ESU can be minimized by up to 28.1% and the heat release time can be increased by up to 35.3% as opposed to the conventional ESU. Obviously, the selection of PCMs must be considered for each parameter, and the selection of PCMs with appropriate parameters plays a crucial role for different energy storage conditions.

An intrinsic antistatic polyethylene glycol‐based solid–solid phase change material for thermal energy storage and thermal management

AbstractPolyethylene glycol (PEG) is an important and popular phase change material (PCM), but is not a good antistatic material, which would cause the accumulation of static electricity and electrostatic discharge when used for the thermal energy storage and thermal management of electrical devices. Herein, we prepared a PEG‐based solid–solid PCM (SSPCM) with good antistatic property by introducing an ionic liquid onto the macromolecular chains. This SSPCM is in solid state even at 90°C, avoiding the leakage issue of pure PEG. Its latent heat values in the melting and solidifying processes are 56.2 and 30.6 J g−1, respectively. Additionally, this SSPCM has good thermal stability and thermal reliability for thermal storage and thermal management according to thermogravimetric and thermal cycling tests. The volume‐ and surface resistivity of the SSPCM at ambient temperature are 108.87 Ω m and 108.92 Ω, respectively, showing good antistatic performance.

Study on the dynamic thermal response of phase change material integrated wall under indoor-outdoor dual thermal disturbances

The study mainly explored the dynamic thermal response of phase change material integrated wall (PCMW) under indoor-outdoor dual thermal disturbances (IODTD). A dual wave thermal disturbance dynamic boundary condition was proposed for PCMW based on the outdoor meteorological data and typical solar energy building analytical models of Lhasa, Yinchuan and Xi'an in China. The influence of different construction modes on the thermal performance of PCMW was numerically investigated by the sensible heat capacity method under IODTD. Then determined the crucial thermophysical parameters of PCM and analyzed the variation characteristics of temperature and heat flux fields of PCMW. The heat transfer frequency responses of different walls to outdoor thermal disturbances were calculated by the harmonic response method. The results indicated that the optimal location of PCM was on the interior side of the wall, and the critical values of phase change temperature and latent heat were 16 °C and 120 kJ/kg, respectively. It presented the maximum temperature and heat flux were 10 % and 36.2 % greater than ordinary walls (OW). Compared with OW, the attenuation and delay time of PCMW on outdoor sol-air temperature wave performed significantly, which plotted a higher decrement factor and longer time lag under external disturbances of different orders.