Abstract

In this study, salt hydrates were deposited on a porous carbon (PC) support to address the challenges associated with maintaining heat capacity and slow hydration kinetics in thermochemical heat storage (THS) systems. Mono-salt (MgSO4) or binary salt (MgSO4-MgCl2) composites on the PC were analyzed by thermogravimetry/differential scanning calorimetry (TG/DSC). The results show that binary salt composites exhibit faster hydration kinetics and higher water adsorption capacity than monosalt composites. The addition of MgCl2 overcomes the kinetic drawbacks caused by the hydrophobic nature of the support and the presence of salt aggregates. The PC_60binary composite achieves a water uptake of 0.75 g/g, exceeding the water uptake of PC_60MgSO4 (0.48 g/g). Furthermore, the heat released by the composites follows a similar trend to water sorption. PC_60MgSO4 produces 52 % (1356 J/g) of the heat released by pure MgSO4, while PC_60binary achieves 70 % (1840 J/g) of the heat released by pure mixed salts. These results suggest that the newly developed binary salt composites are promising for long-term heat storage applications. These experimental results highlight the improved performance of binary salt composites in terms of hydration kinetics, water adsorption and heat release. This study provides valuable pointers for the development of more efficient THS systems.

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