Experimental and Numerical Investigation of the Dehydration of Ca(OH)2 at Low Steam Pressures

Abstract

The CaO/Ca(OH)2 system can be the basis for cost-efficient long-term energy storage, as the chemically stored energy is not affected by heat losses, and the raw material is cheap and abundantly available. While the hydration (thermal discharge) has already been addressed by several studies, for the dehydration (thermal charge) at low partial steam pressures, there is a lack of numerical studies validated at different conditions and operation modes. However, the operation at low steam pressures is important, as it decreases the dehydration temperature, which can enable the use of waste heat. Even if higher charging temperatures are available, for example by incorporating electrical energy, the reaction rate can be increased by lowering the steam pressure. At low pressures and temperatures, the limiting steps in a reactor might change compared to previous studies. In particular, the reaction kinetics might become limiting due to a decreased reaction rate at lower temperatures, or the reduced steam density at low pressures could result in high velocities, causing a gas transport limitation. Therefore, we conducted new measurements with a thermogravimetric analyzer only for the specific steam partial pressure range between 0.8 and 5.5 kPa. Based on these measurements, we derived a new mathematical fit for the reaction rate for the temperature range between 375 and 440 °C. Additionally, we performed experiments in an indirectly heated fixed bed reactor with two different operation modes in a pressure range between 2.8 and 4.8 kPa and set up a numerical model. The numerical results show that the model appropriately describes the reactor behavior and is validated within the measurement uncertainty. Moreover, our study revealed an important impact of the operation condition itself: the permeability of the reactive bulk is significantly increased if the dehydration is initiated by a rapid pressure reduction compared to an isobaric dehydration by a temperature increase. We conclude that the pressure reduction leads to structural changes in the bulk, such as channeling, which enhances the gas transport. This finding could reduce the complexity of future reactor designs. Finally, the presented model can assist the design of thermochemical reactors in the validated pressure and temperature range.