From nanometer aggregates to micrometer crystals: insight into the coarsening mechanism of calcite

Logan Nicholas Schultz*, Knud Dideriksen, Leonid Lakshtanov, Sepideh Sadat Hakim, Dirk Müter, F. Haußer, Klaus Bechgaard, Susan Louise Svane Stipp

*Corresponding author for this work
13 Citations (Scopus)

Abstract

Grain size increases when crystals respond to dynamic equilibrium in a saturated solution. The pathway to coarsening is generally thought to be driven by Ostwald ripening, that is, simultaneous dissolution and reprecipitation, but models to describe Ostwald ripening neglect solid-solid interactions and crystal shapes. Grain coarsening of calcite, CaCO3, is relevant for biomineralization and commercial products and is an important process in diagenesis of sediments to rock during geological time. We investigated coarsening of pure, synthetic calcite powder of sub-micrometer diameter crystals and aged it in saturated solutions at 23, 100, and 200 °C for up to 261 days. Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) surface area analysis showed rapid coarsening at 100 and 200 °C. Evidence of particle growth at 23 °C was not visible by SEM, but high resolution X-ray diffraction (XRD) data demonstrated steady growth of nanometer crystallites. The results can be described by theory where grains coarsen preferentially by aggregation at early times and high temperatures and by Ostwald ripening at later stages. Crystal form and dimension are influenced by the transition from one growth mechanism to the other. This has been poorly described by mean field coarsening models and offers predictive power to grain coarsening models.

Original languageEnglish
JournalCrystal Growth & Design
Volume14
Issue number2
Pages (from-to)552-558
Number of pages7
ISSN1528-7483
DOIs
Publication statusPublished - 2014

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