Li Tingxian

Preparation and thermal performance of form-stable expanded graphite/stearic acid composite phase change materials with high thermal conductivity

Thermal energy storage plays an important role in improving the working reliability and utilization efficiency of renewable energy systems. Thermal energy storage includes sensible heat storage, latent heat storage using phase change material (PCM) and thermochemical heat storage. In comparison with sensible heat storage, latent heat storage has the distinct advantages of its high energy storage density and stable temperature during the energy storage and release processes. However, low thermal conductivity of PCM is the common drawback for various latent heat energy storage systems. The purpose of the research is to enhance the thermal conductivity of PCM by developing new form-stable composite phase change materials using expanded graphite matrix. Firstly, a preparation method “heating adsorption of liquid SA into expanded graphite (EG) matrix and compressing stable-shape composite” is employed to synthesis form- stable composite phase change material. Twenty samples with different EG contents and packed densities are prepared using stearic acid (SA) as phase change material and two kinds of EG with different dilatation as porous matrix. Secondly, the microstructures, thermal properties and thermal stabilities of different EG/SA samples are tested to analyze the influence of the dilatation of expanded graphite on the thermal performance of form-stable composite phase change materials. Moreover, EG/SA form-stable heat storage units with different EG contents and packed densities are fabricated to analyze the thermal storage/release performance through heating/cooling experiment. The microstructures of EG and EG/SA samples are observed using scanning electron microscopy (SEM) and the results show there exist obvious differences between two kinds of EG and SA distribution in the samples. The EG/SA samples with high dilatation EG are even more uniform because the high dilatation EG has larger pore size and pore volume. The data obtained from differential scanning calorimetry (DSC) show the addition of EG and compressing operation have negligible effect on the latent heat and slightly increase the phase transition temperature of pure SA. The form-stable EG/SA composite PCMs have lower supercooling degree than pure SA. LFA447 flash thermal diffusivity instrument is used to evaluate the effect of EG’s dilatation on the thermal conductivity of EG/SA samples. The results show that the use of high dilatation EG is more effective to improve the thermal conductivity of form-stable EG/SA composite PCMs when packed density is large. The radial thermal conductivity of form-stable 20 wt.%EG/SA phase change composite with packed density of 950u2005kgu2005m−3 is as high as 19.6u2005Wu2005m−1u2005K−1 when high dilatation EG is utilized. This figure is more than 110 times higher than that of pure SA. Finally, the thermal stability of EG/SA samples is conducted by repeating the charging and discharging processes of SA. These samples prepared by high dilatation EG have better thermal stability than the samples prepared by low dilatation EG. The EG with high dilatation can assure the uniform distribution of SA inside EG/SA sample and thus prevent the leakage of liquid SA during the phase change transformation process due to its dilated microstructure. The heating/cooling test results show that the heat storage/release time of EG/SA composite units is about 1/8–1/4 of that of pure SA unit, and this means the heat transfer can be significantly enhanced. It suggests that the form-stable EG/SA composite phase change materials prepared by high dilatation EG has good comprehensive performance due to its high thermal conductivity, good thermal stability and no leakage problem.