Abstract

The phase change behavior of organic and inorganic phase change materials, namely paraffin wax, microcrystalline wax, Na 2SO 4·10H 2O and CaCl 2·6H 2O, with melting temperatures close to room temperature, was evaluated by differential scanning calorimetry. The melting and solidification temperatures, supercooling, heat of fusion and thermal cycling stability of these materials, with and without additives, were determined. Paraffin wax, with or without α-Al 2O 3 or BN particles, are potentially good thermal interface materials, because of the negative supercooling (down to −7°C), large heat of fusion (up to 142 J/g) and excellent thermal cycling stability. Microcrystalline wax is not suitable, due to its unclear endothermic and exothermic peaks and wide melting temperature range. The addition of 20–60 wt.% α-Al 2O 3 to paraffin wax decreases the melting temperature by 7°C. Beyond 60 wt.% α-Al 2O 3, the melting temperature of paraffin wax increases toward the value without α-Al 2O 3. The heat of fusion of paraffin wax attains a minimum at 20 wt.% α-Al 2O 3. The addition of BN has little effect on the phase change behavior of paraffin wax. The inorganic materials Na 2SO 4·10H 2O and CaCl 2·6H 2O, with and without nucleating additives, are not suitable for use as thermal interface materials, due to the incongruent melting and decomposition behavior, large supercooling (8°C or more) and thermal cycling instability.

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