Crystallization kinetics of amorphous calcium carbonate in confinement

Jack Cavanaugh, Michael L. Whittaker, Derk Joester*

*Corresponding author for this work

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Phase transformations of carbonates are relevant to a wide range of biological, environmental, and industrial processes. Over the past decade, it emerged that crystallization pathways in these systems can be quite complex. Metastable intermediates such as amorphous calcium carbonate (ACC) were found to greatly impact composition, structure, and properties of more stable phases. However, it has been challenging to create predictive models. Rapid transformation of ACC in bulk has been one obstacle in the determination of nucleation rates. Herein, it is reported that confinement in microfluidic droplets allows separating in time the precipitation of ACC and subsequent nucleation and growth of crystalline CaCO3. An upper limit of 1.2 cm-3 s-1 was determined for the steady-state crystal nucleation rate in the presence of ACC at ambient conditions. This rate has implications for the formation of calcium carbonate in biomineralization, bio-inspired syntheses, and carbon sequestration.

Original languageEnglish (US)
Pages (from-to)5039-5043
Number of pages5
JournalChemical Science
Volume10
Issue number19
DOIs
StatePublished - Jan 1 2019

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Crystallization kinetics
Calcium Carbonate
Nucleation
Biomineralization
Carbonates
Biosynthesis
Crystallization
Microfluidics
Carbon
Phase transitions
Crystalline materials
Crystals
Chemical analysis

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Cavanaugh, Jack ; Whittaker, Michael L. ; Joester, Derk. / Crystallization kinetics of amorphous calcium carbonate in confinement. In: Chemical Science. 2019 ; Vol. 10, No. 19. pp. 5039-5043.
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Crystallization kinetics of amorphous calcium carbonate in confinement. / Cavanaugh, Jack; Whittaker, Michael L.; Joester, Derk.

In: Chemical Science, Vol. 10, No. 19, 01.01.2019, p. 5039-5043.

Research output: Contribution to journalArticle

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