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Thermodynamics of Calcite Growth: Baseline for Understanding Biomineral Formation

Science
23 Oct 1998
Vol 282, Issue 5389
pp. 724-727

Abstract

The complexity of biomineralized structures suggests the potential of organic constituents for controlling energetic factors during crystal synthesis. Atomic force microscopy was used to investigate the thermodynamic controls on carbonate growth and to measure the dependence of step speed on step length and the dependence of critical step length on supersaturation in precisely controlled solutions. These data were used to test the classic Gibbs-Thomson relationship and provided the step edge free energies and free energy barriers to one-dimension nucleation for calcite. Addition of aspartic acid, a common component in biomineralizing systems, dramatically affected growth morphology and altered the magnitude of the surface energy.

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The most widely reported Ksp values range from 10−8.36 to 10−8.29 [see (20) and references therein]. Because steps on {101̅4} faces migrate at measurable rates when the ionic activity product (IAP) of our solution was equal to the lowest reported value, we determined Ksp from IAP measurements where step velocity equaled zero. This lower solubility is due to the lower pCO2 of our closed experimental system.
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We thank S. Potapenko for discussions. This work was performed under the auspices of the U.S. Department of Energy, Division of Geosciences and Engineering, by Georgia Institute of Technology (DE-FG02-98ER14843) and Lawrence Livermore National Laboratory under contract W-7405-Eng-48.

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Published In

Science
Volume 282 | Issue 5389
23 October 1998

Submission history

Received: 23 July 1998
Accepted: 21 September 1998
Published in print: 23 October 1998

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Authors

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H. Henry Teng
H. H. Teng and P. M. Dove, School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA. C. A. Orme and J. J. De Yoreo, Department of Chemistry and Materials Science, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
Patricia M. Dove*
H. H. Teng and P. M. Dove, School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA. C. A. Orme and J. J. De Yoreo, Department of Chemistry and Materials Science, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
Christine A. Orme
H. H. Teng and P. M. Dove, School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA. C. A. Orme and J. J. De Yoreo, Department of Chemistry and Materials Science, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.
James J. De Yoreo
H. H. Teng and P. M. Dove, School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA. C. A. Orme and J. J. De Yoreo, Department of Chemistry and Materials Science, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.

Notes

*
To whom correspondence should be addressed. E-mail: [email protected]

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