Investigates citric acid's effect on crystallization of amorphous calcium carbonate, highlighting its application in functional materials.
High Resolution Image Download MS PowerPoint Slide Amorphous CaCO 3 (ACC) has an intrinsically large specific surface area, rendering it a promising platform for developing various functional materials. However, its practical use is severely limited by an extremely short lifespan, which is typically only a few seconds, before its spontaneous recrystallization into vaterite or calcite. In this study, we investigate the use of citric acid to suppress the rapid crystallization of ACC in a mixed ethanol/ethylene glycol medium and to obtain reproducible high-surface-area ACC under controlled conditions. Experiments involving systematic variations in citric acid concentration (0.00–1.33% w/v) revealed that crystallization was completely inhibited at concentrations above 0.39% w/v, as confirmed by X-ray diffraction. Brunauer–Emmett–Teller analysis showed that ACC samples synthesized with 0.44–1.11% w/v citric acid achieved exceptionally high surface areas (600–700 m 2 /g). The observed suppression of crystallization is discussed in relation to previously reported interactions between citrate species and calcium carbonate phases, rather than being directly demonstrated at the molecular level. As a proof of concept, curcumin was loaded onto the prepared ACC samples, and enhanced dissolution behavior was observed, which plateaued above a specific surface area threshold. This finding highlights the importance of the surface-area-to-cargo ratio in future formulation strategies. The resulting stable high-surface-area ACC is a promising platform for the design of functional materials.
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Sakawaki et al. (2026) studied this question.
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