Abstract
The effects of pH and Mg on the crystallization of amorphous calcium carbonate (ACC) to vaterite and/or calcite were studied using a combination of in situ time resolved synchrotron-based techniques and electron microscopy. The experiments showed that Mg increased the stability of ACC and favoured the formation of calcite over vaterite. A neutral (∼7) starting pH during mixing promoted the transformation of ACC into calcite via a dissolution/ reprecipitation mechanism. Conversely, when ACC formed in a solution that started with a high initial pH (∼11.5), the transformation to calcite occurred via metastable vaterite, which formed via a spherulitic growth mechanism. In a second stage this vaterite transformed to calcite via a surface-controlled dissolution and recrystallization mechanism. These crystallization pathways can be explained as a consequence of the pH-dependent composition, local structure, stability and dissolution rates of ACC. © 2011 Elsevier B.V. All rights reserved.
Original language | English |
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Pages (from-to) | S477-S479 |
Journal | Journal of Alloys and Compounds |
Volume | 536 |
Issue number | 1 |
DOIs | |
Publication status | Published - 25 Sept 2012 |
Keywords
- Amorphous materials
- Crystal growth
- Nanostructured materials
- Synchrotron radiation