Here we report a scalable and template-free production strategy in the synthesis of a mesoporous calcium carbonate, which undergoes self-assembled nanostructure formation through a temperature-induced aggregation and polymorphic transformation of the colloids. The specific surface area and pore size distribution of resulting mesoporous calcium carbonate are clearly different depending on the aging temperature. The specific surface area and average pore size for aging temperature of 293 K are 207.3±9.8 m 2 /g and 8.8±0.6 nm, respectively, and 65.1±10.1 m 2 /g and 19.9±2.6 nm at 473 K. Additionally, we apply the mesoporous calcium carbonate powder to formaldehyde vapor adsorbent. We measure the adsorbed amount of gaseous formaldehyde and find that the vaterite-rich powder has larger adsorption per unit area than the calcite-rich one.
We report a synthesis strategy for pure hydroxyapatite (HAp) using an amorphous calcium carbonate (ACC) colloid as the starting source. Room-temperature phosphorylation and subsequent calcination produce pure HAp via intermediate amorphous calcium phosphate (ACP). The pre-calcined sample undergoes a competitive transformation from ACC to ACP and crystalline calcium carbonate. The water content, ACC concentration, Ca/P molar ratio, and pH during the phosphorylation reaction play crucial roles in the final phase of the crystalline phosphate compound. Pure HAp is formed after ACP is transformed from ACC at a low concentration (1 wt%) of ACC colloid (1.71 < Ca/P < 1.88), whereas Ca/P = 1.51 leads to pure β-tricalcium phosphate. The ACP phases are precursors for calcium phosphate compounds and may determine the final crystalline phase.
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