Thermochemical energy storage is considered as an auspicious method for the recycling of medium-temperature waste heat. The reaction couple Mg(OH)₂⁻MgO is intensely investigated for this purpose, suffering so far from limited cycle stability. To overcome this issue, Mg(OH)₂, MgCO₃, and MgC₂O₄·2H₂O were compared as precursor materials for MgO production. Depending on the precursor, the particle morphology of the resulting MgO changes, resulting in different hydration behavior and cycle stability. Agglomeration of the material during cyclization was identified as main reason for the decreased reactivity. Immersion of the spent material in liquid H₂O decomposes the agglomerates restoring the initial reactivity of the material, thus serving as a regeneration step.
Keywords: cycle stability; hydration reactivity; in-situ powder X-ray diffraction (PXRD); magnesium carbonate; magnesium hydroxide; magnesium oxalate; magnesium oxide; particle morphology; thermochemical energy storage; thermochemistry.