Amorphous Calcium Carbonate Constructed from Nanoparticle Aggregates with Unprecedented Surface Area and Mesoporosity

材料科学 无定形固体 化学工程 介孔材料 纳米颗粒 比表面积 碳酸钙 多孔性 溶解 无定形磷酸钙 无定形碳酸钙 纳米技术 有机化学 复合材料 化学 催化作用 冶金 工程类
作者
Rui Sun,Peng Zhang,Éva G. Bajnóczi,Alexandra Neagu,Cheuk‐Wai Tai,Ingmar Persson,Maria Strømme,Ocean Cheung
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:10 (25): 21556-21564 被引量:58
标识
DOI:10.1021/acsami.8b03939
摘要

Amorphous calcium carbonate (ACC), with the highest reported specific surface area of all current forms of calcium carbonate (over 350 m2 g–1), was synthesized using a surfactant-free, one-pot method. Electron microscopy, helium pycnometry, and nitrogen sorption analysis revealed that this highly mesoporous ACC, with a pore volume of ∼0.86 cm3 g–1 and a pore-size distribution centered at 8–9 nm, is constructed from aggregated ACC nanoparticles with an estimated average diameter of 7.3 nm. The porous ACC remained amorphous and retained its high porosity for over 3 weeks under semi-air-tight storage conditions. Powder X-ray diffraction, large-angle X-ray scattering, infrared spectroscopy, and electron diffraction exposed that the porous ACC did not resemble any of the known CaCO3 structures. The atomic order of porous ACC diminished at interatomic distances over 8 Å. Porous ACC was evaluated as a potential drug carrier of poorly soluble substances in vitro. Itraconazole and celecoxib remained stable in their amorphous forms within the pores of the material. Drug release rates were significantly enhanced for both drugs (up to 65 times the dissolution rates for the crystalline forms), and supersaturation release of celecoxib was also demonstrated. Citric acid was used to enhance the stability of the ACC nanoparticles within the aggregates, which increased the surface area of the material to over 600 m2 g–1. This porous ACC has potential for use in various applications where surface area is important, including adsorption, catalysis, medication, and bone regeneration.
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