MgSO4-silica gel composites have a large potential for application in large-scale long-term energy storage systems, but the theoretical research on materials is not yet sufficiently thorough, and the reaction mechanism is still unclear, especially the lack of relevant experimental investigation and validation. Therefore, in order to better understand the nature and behavior of the desorption process, the reaction mechanism of monomer MgSO4·7H2O and MgSO4·7H2O-silica gel composites were investigated in this paper. The experimental results presented the desorption process of both the pure salt and the composites can be divided into six stages, and at 150 °C, the two can desorb 40.42 %–44.14 %, accounting for 79 %–86 % of the total desorption, so it is more appropriate to take 150 °C as the temperature of desorption in the energy storage system. The desorption mechanisms of pure salt and composite materials can be described by the same model in the same temperature range, and the desorption curve types and reaction mechanism models corresponding to different desorption temperatures were obtained, which were S-shape-A2 (110 °C and 120 °C), accelerated-R2 (130 °C), and decelerated-F1 (140 °C and 150 °C), respectively, which revealed the kinetics and control mechanisms of desorption process. The control mechanism, which was an important guideline for optimizing the heat and mass transfer process inside the salt particles. Compared with the pure salt, the activation energy and pre-exponential factor of the composites were lower, 48.55 kJ/mol (58.05 kJ/mol for the pure salt) and 3.31 × 104 s−1 (1.88 × 105 s−1 for the pure salt), respectively, indicating the number of active sites in the composites was higher and the reaction rate was faster; The lower the activation energy, the smaller the effect of temperature on the reaction rate constant. It can be seen the composite material is more advantageous in the process of practical application. After 60 cycles, the decay rate of adsorption/desorption performance of SM20 was only 5 %-8 %, indicating that the composite material had good cycling stability and can be used as a candidate material for large-scale long-term seasonal energy storage.
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