Growth behaviour of silica/carbonate nanocrystalline composites of calcite and aragonite
The precipitation of barium and strontium carbonate in alkaline silica gels or silica solutions produces nanocrystalline self-assembled composite materials displaying biomimetic shapes and textures. We have crystallized concomitantly in time and space two anhydrous polymorphs of calcium carbonate, u...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2017 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/211460 |
| Acceso en línea: | http://hdl.handle.net/10261/211460 |
| Access Level: | acceso abierto |
| Palabra clave: | Silica Carbonate Calcite Crystal |
| Sumario: | The precipitation of barium and strontium carbonate in alkaline silica gels or silica solutions produces nanocrystalline self-assembled composite materials displaying biomimetic shapes and textures. We have crystallized concomitantly in time and space two anhydrous polymorphs of calcium carbonate, under similar conditions at different temperatures. The orthorhombic phase aragonite produces nanocrystalline aggregates exhibiting non-crystallographic morphologies and complex textures characteristic of silica biomorphs. Conversely, the simultaneously forming trigonal phase, calcite, yields rhombohedral crystals that experience fibrous growth and that maintain memory of the point symmetry group of the crystalline structure. Experiments performed at different temperatures (room temperature, 45, 60 and 80 °C) revealed that the higher the temperature the higher the aragonite/calcite precipitation ratio, but the crystallization of calcite was never fully inhibited. We have studied the growth mechanism, the growth texture and the morphogenesis for both cases. We have found that the dramatic difference between the crystallization behaviours of the two mineral phases is due to the difference in the growth mechanism at the nanoscale. |
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