TY - JOUR
T1 - Porous potassium carbonate granules with enhanced diffusion kinetics for thermochemical heat storage
AU - Salehzadeh, Delaram
AU - Elahi, Behrooz
AU - ten Elshof, Johan E.
AU - Brem, Gerrit
AU - Mehrali, Mohammad
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/10/1
Y1 - 2024/10/1
N2 - The caking phenomenon poses a significant challenge in thermochemical heat storage systems, which arises from the agglomeration of powdered salt hydrates. This impedes the flow of gas molecules through the reactor bed and negatively impacts the reactions kinetics, leading to decreased overall efficiency of heat storage. To tackle this challenge, an innovative approach is proposed, involving the synthesis of porous potassium carbonate (K2CO3) granules using potassium bicarbonate (KHCO3) as a pore former in varying ratios of 10, 20, 40, and 50 wt%. It is essential to note that the maximum amount of KHCO3 for effective granulation is around 50 wt% of the total batch, as exceeding this limit prevents granule formation. This method results in the formation of porous K2CO3 granules that are 100% pure and free from any additives that could impact the energy density. In terms of diffusion kinetics, the granules with 40 wt% (K40) and 50 wt% (K50) of KHCO3 demonstrated significant improvements in effective diffusion coefficients in comparison with the K2CO3 granule without pore former. Regarding cyclic performance, K2CO3 granule without pore former showed slow kinetics and incomplete hydration even after 10 cycles. In contrast, the K40 and K50 granules demonstrated significantly faster hydration kinetics, with K40 achieving complete hydration by the 4th cycle and K50 reaching the highest water loading capacity of 1.5 molH2O/molK2CO3 from the first cycle. The K50 granule, with a hydrated state density of 1.74 g/cm3, achieved a volumetric energy density of 0.96 GJ/m3. Compared to other developed granules, K50 exhibited superior hydration kinetics, positioning it as a promising candidate for thermochemical heat storage applications. This study highlights the potential of modifying pore structure to improve the efficiency of thermochemical heat storage and demonstrates that the wet granulation technique can be effectively utilized for the mass production of salt hydrate granules.
AB - The caking phenomenon poses a significant challenge in thermochemical heat storage systems, which arises from the agglomeration of powdered salt hydrates. This impedes the flow of gas molecules through the reactor bed and negatively impacts the reactions kinetics, leading to decreased overall efficiency of heat storage. To tackle this challenge, an innovative approach is proposed, involving the synthesis of porous potassium carbonate (K2CO3) granules using potassium bicarbonate (KHCO3) as a pore former in varying ratios of 10, 20, 40, and 50 wt%. It is essential to note that the maximum amount of KHCO3 for effective granulation is around 50 wt% of the total batch, as exceeding this limit prevents granule formation. This method results in the formation of porous K2CO3 granules that are 100% pure and free from any additives that could impact the energy density. In terms of diffusion kinetics, the granules with 40 wt% (K40) and 50 wt% (K50) of KHCO3 demonstrated significant improvements in effective diffusion coefficients in comparison with the K2CO3 granule without pore former. Regarding cyclic performance, K2CO3 granule without pore former showed slow kinetics and incomplete hydration even after 10 cycles. In contrast, the K40 and K50 granules demonstrated significantly faster hydration kinetics, with K40 achieving complete hydration by the 4th cycle and K50 reaching the highest water loading capacity of 1.5 molH2O/molK2CO3 from the first cycle. The K50 granule, with a hydrated state density of 1.74 g/cm3, achieved a volumetric energy density of 0.96 GJ/m3. Compared to other developed granules, K50 exhibited superior hydration kinetics, positioning it as a promising candidate for thermochemical heat storage applications. This study highlights the potential of modifying pore structure to improve the efficiency of thermochemical heat storage and demonstrates that the wet granulation technique can be effectively utilized for the mass production of salt hydrate granules.
KW - UT-Hybrid-D
KW - Porous granules
KW - Potassium carbonate (KCO)
KW - Salt hydrates
KW - Thermochemical heat storage
KW - Hydration kinetics
UR - http://www.scopus.com/inward/record.url?scp=85201497438&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2024.154560
DO - 10.1016/j.cej.2024.154560
M3 - Article
AN - SCOPUS:85201497438
SN - 1385-8947
VL - 497
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 154560
ER -