The multiple eutectic nitrates with a low melting point are widely used in the field of solar thermal utilization due to their good thermophysical properties. The addition of nanoparticles can improve the heat transfer and heat storage performance of nitrate. This article explored the effect of MgO nanoparticles on the thermal properties of ternary eutectic nitrates. As a result of the decomposition reaction of the Mg(OH)₂ precursor at high temperature, MgO nanoparticles were synthesized in situ in the LiNO₃–NaNO₃–KNO₃ ternary eutectic nitrate system. XRD and Raman results showed that MgO nanoparticles were successfully synthesized in situ in the ternary nitrate system. SEM and EDS results showed no obvious agglomeration. The specific heat capacity of the modified salt is significantly increased. When the content of MgO nanoparticles is 2 wt %, the specific heat of the modified salt in the solid phase and the specific heat in the liquid phase increased by 51.54% and 44.50%, respectively. The heat transfer performance of the modified salt is also significantly improved. When the content of MgO nanoparticles is 5 wt %, the thermal diffusion coefficient of the modified salt is increased by 39.3%. This study also discussed the enhancement mechanism of the specific heat capacity of the molten salt by the nanoparticles mainly due to the higher specific surface energy of MgO and the semi-solid layer that formed between the MgO nanoparticles and the molten salt.

Using thermal storage materials with excellent thermal properties in the energy utilization system enables efficient use of renewable energy sources. Organic phase change materials (PCMs) have the advantages of high heat storage density, no corrosion, and low cost, but low thermal conductivity and insufficient heat transfer capacity have always been the bottlenecks in their application. In this paper, melamine foam@ reduction graphene oxide (MF@rGO) and carbon foam@ reduction graphene oxide (CF@rGO) composite foams with double carbon networks were prepared by self-assembly method and further employed in 1-octadecinal (OD) PCMs. The microstructure, chemical composition, phase change behavior, thermal conductivity, and photothermal conversion performance of MF@rGO/OD and CF@rGO/OD were studied in detail using SEM, FTIR, Raman DSC, and LFA. The melting and solidification enthalpies of CF@rGO/OD composite PCMs were 208.3 J/g and 191.4 J/g, respectively, its thermal conductivity increased to 1.54 W/m·K, which is 6.42 times that of pure OD. The porous structure and high thermal conductivity of the double carbon network substantially enhance the efficiency of energy storage and release in composite PCMs. CF@rGO/OD composite PCMs have excellent heat storage performance and heat transfer capacity, and a wide range of application prospects in the fields of low-temperature solar heat storage, precision instrument temperature control, and intelligent buildings.

The effect of gallium on the oxide film structure and overall oxidation resistance of low melting point Sn–Bi–Zn alloys was investigated under air atmosphere using thermogravimetric analyses. The liquid alloys studied had a Ga content of 1–7 wt.%. The results showed that the growth rates of the surface scale formed on the Sn–Bi–Zn–Ga alloys conformed to the parabolic law. The oxidation resistance of Sn–Bi–Zn alloys was improved by Ga addition and the activation energies increased from 12.05 kJ∙mol⁻¹ to 22.20 kJ∙mol⁻¹. The structure and elemental distribution of the oxide film surface and cross-section were found to become more complicated and denser with Ga addition. Further, the results of X-ray photoelectron spectroscopy and X-ray diffraction show that Ga elements accumulate on the surface of the liquid metal to form oxides, which significantly slowed the oxidation of the surface of the liquid alloy.

Multiform NiO nanowalls with a high specific surface area were constructed in situ on carbon foam (CF) to construct NiO@CF/OD composite phase change materials (CPCMs). The synthesis mechanism, microstructures, thermal management capability, and photothermal conversion of NiO@CF/OD CPCMs were systematically studied. Additionally, the collaborative enhancement effects of CF and multiform NiO nanowalls on the thermal properties of OD PCMs were also investigated. NiO@CF not only maintains the porous 3D network structure of CF, but also effectively prevents the aggregation of NiO nanosheets. The chemical structures of NiO@CF/OD CPCMs were analyzed using XRD and FTIR spectroscopy. When combined with CF and NiO nanosheets, OD has high compatibility with NiO@CF. The thermal conductivity of NiO@CF/OD-L CPCMs was 1.12 W/m·K, which is 366.7% higher than that of OD. The improvement in thermal conductivity of CPCMs was theoretically analyzed according to the Debye model. NiO@CF/OD-L CPCMs have a photothermal conversion efficiency up to 77.6%. This article provided a theoretical basis for the optimal design and performance prediction of thermal storage materials and systems.

Solid–liquid phase-change materials (PCMs) have attracted considerable attention in heat energy storage due to their appropriate phase-transition temperatures and high thermal storage density. The primary issues that need to be addressed in the wide application of traditional PCMs are easy leakage during solid–liquid phase transitions, low thermal conductivity, and poor energy conversion function. The heat transfer properties of PCMs can be improved by compounding with carbon materials. Carbon nanotubes (CNTs) are widely used in PCMs for heat storage because of their high thermal conductivity, strong electrical conductivity, and high chemical stability. This study investigates the thermal properties of 1-octadecanol (OD) modified with different diameters and amounts of CNTs using the melt blending method and the ultrasonic dispersion method. The aim is to enhance thermal conductivity while minimizing latent heat loss. The physical phase, microstructure, phase-change temperature, phase-transition enthalpy, thermal stability, and thermal conductivity of the OD/CNTs CPCMs were systematically studied using XRD, FTIR, SEM, DSC, and Hot Disk. Moreover, the heat charging and releasing performance of the OD/CNTs CPCMs was investigated through heat charging and releasing experiments, and the relationship among the composition–structure–performance of the CPCMs was established.

The specific heat capacity plays a crucial role in influencing the heat transfer efficiency of materials. Considering the relatively low specific heat capacity of metals, this study focuses on investigating the impact of second-phase nano Ni particles on the microstructure and thermophysical properties of the alloy matrix. The alloys’ phase compositions and microstructures were examined using X-ray diffraction phase analysis (XRD), electron probe micromorphology analysis (EPMA), and X-ray fluorescence spectroscopy (XRF). Furthermore, the thermophysical properties of the alloys were comprehensively analyzed through the employment of a differential scanning calorimeter (DSC) and the laser flash method (LFA). The addition of second-phase nanoparticles significantly increased the specific heat capacity of the alloy in the liquid state; however, the phenomenon of nanoparticle agglomeration diminishes this improvement. The analysis of the specific heat enhancement mechanism indicates that ordered states are formed between the second-phase solid nanoparticles and the melted metal in the liquid state. With the increase in temperature, the destruction of these ordered states requires additional heat, resulting in the increase of specific heat capacity.