TY - JOUR
T1 - Citrate effects on amorphous calcium carbonate (ACC) structure, stability, and crystallization
AU - Tobler, Dominique J.
AU - Rodriguez-Blanco, Juan Diego
AU - Dideriksen, Knud
AU - Bovet, Nicolas
AU - Sand, Karina K.
AU - Stipp, Susan L.S.
N1 - Publisher Copyright:
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2015/5/27
Y1 - 2015/5/27
N2 - Understanding the role of citrate in the crystallization kinetics of amorphous calcium carbonate (ACC) is essential to explain the formation mechanisms, stabilities, surface properties, and morphologies of CaCO3 biominerals. It also contributes to deeper insight into fluid-mineral interactions, both in nature and for industrial processes. In this study, ACC formation and its crystallization are monitored in real time as a function of citrate (CIT) concentration in solution. Additionally, synchrotron radiation pair distribution function analyses combined with solid-state, spectroscopic, and microscopic techniques are used to determine the effect of CIT on ACC structure, composition, and size. Results show an increase in ACC lifetime coupled with an increase in CIT uptake by ACC and slight changes in ACC atomic structure with an increase in CIT concentration. ACC does not form at concentrations ≥ 75% CIT/Ca and vaterite is absent in all cases where CIT is present. These findings can be explained by CIT binding with Ca ions, thereby forming Ca-CIT complexes in solution and decreasing ACC and calcite saturation levels. The formation of CIT-bearing ACC with calcitic structure and the absence of vaterite formation suggest that these solution complexes form a calcite-type atomic arrangement while CIT probably also acts as a growth inhibitor.
AB - Understanding the role of citrate in the crystallization kinetics of amorphous calcium carbonate (ACC) is essential to explain the formation mechanisms, stabilities, surface properties, and morphologies of CaCO3 biominerals. It also contributes to deeper insight into fluid-mineral interactions, both in nature and for industrial processes. In this study, ACC formation and its crystallization are monitored in real time as a function of citrate (CIT) concentration in solution. Additionally, synchrotron radiation pair distribution function analyses combined with solid-state, spectroscopic, and microscopic techniques are used to determine the effect of CIT on ACC structure, composition, and size. Results show an increase in ACC lifetime coupled with an increase in CIT uptake by ACC and slight changes in ACC atomic structure with an increase in CIT concentration. ACC does not form at concentrations ≥ 75% CIT/Ca and vaterite is absent in all cases where CIT is present. These findings can be explained by CIT binding with Ca ions, thereby forming Ca-CIT complexes in solution and decreasing ACC and calcite saturation levels. The formation of CIT-bearing ACC with calcitic structure and the absence of vaterite formation suggest that these solution complexes form a calcite-type atomic arrangement while CIT probably also acts as a growth inhibitor.
KW - amorphous calcium carbonate
KW - biomineralization
KW - CaCO crystallization
KW - citric acid/citrate
KW - spherulitic growth
UR - http://www.scopus.com/inward/record.url?scp=85027918138&partnerID=8YFLogxK
U2 - 10.1002/adfm.201500400
DO - 10.1002/adfm.201500400
M3 - Article
AN - SCOPUS:85027918138
SN - 1616-301X
VL - 25
SP - 3081
EP - 3090
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 20
ER -