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American Mineralogist

Journal of Earth and Planetary Materials

Ed. by Baker, Don / Xu, Hongwu / Swainson, Ian

IMPACT FACTOR 2018: 2.631

CiteScore 2018: 2.55

SCImago Journal Rank (SJR) 2018: 1.355
Source Normalized Impact per Paper (SNIP) 2018: 1.103

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Volume 100, Issue 5-6


A route for the direct crystallization of dolomite

Juan Diego Rodriguez-Blanco
  • School of Earth and Environment, University of Leeds, Leeds LS2 9JT, U.K.
  • Nano Science Center, Department of Chemistry, University of Copenhagen, 2100 Copenhagen, Denmark
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/ Samuel Shaw
  • School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
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/ Liane G. Benning
  • Corresponding author
  • School of Earth and Environment, University of Leeds, Leeds LS2 9JT, U.K.
  • GFZ German Research Centre for Geosciences, Telegrafenberg, D-14473 Potsdam, Germany
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Published Online: 2015-05-12 | DOI: https://doi.org/10.2138/am-2015-4963


The direct crystallization of dolomite from an aqueous solution at temperatures between 60-220 °C was followed in situ through time-resolved synchrotron-based energy-dispersive X‑ray diffraction combined with offline high-resolution imaging, X‑ray diffraction, and infrared spectroscopy. Crystalline CaMg(CO3)2 phases form through a three-stage process. In the first stage, a nanoparticulate magnesium-deficient, amorphous calcium carbonate (Mg-ACC) with a nominal formula of Ca0.606Mg0.394CO3·1.37H2O forms. After a temperature-dependent induction time, during stage 2 the Mg-ACC partially dehydrates and orders prior to its rapid (<5 min) crystallization to non-stoichiometric proto-dolomite. This occurs via the dissolution of Mg-ACC, followed by the secondary nucleation of proto-dolomite from solution. The proto-dolomite crystallization proceeds via spherulitic growth that follows a growth front nucleation mechanism with a de-nuovo and continuous formation of nanocrystalline proto-dolomite subunits that form spherical aggregates. In stage three of the reaction, the proto-dolomite transforms to highly crystalline and stoichiometric dolomite on a much longer timescale (hours to days), via an Ostwald-ripening mechanism. Such a three-stage crystallization can explain microbially induced proto-dolomites observed in modern hypersaline settings and may also be the route by which the Cryogenian cap dolomite deposits of the Neoproterozoic formed.

Keywords: Dolomite; proto-dolomite; spherulitic growth; amorphous calcium carbonate

About the article

Received: 2014-03-07

Accepted: 2014-10-29

Published Online: 2015-05-12

Published in Print: 2015-05-01

Citation Information: American Mineralogist, Volume 100, Issue 5-6, Pages 1172–1181, ISSN (Online) 1945-3027, ISSN (Print) 0003-004X, DOI: https://doi.org/10.2138/am-2015-4963.

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© 2015 by Walter de Gruyter Berlin/Boston. This work is licensed under the MSA License. (view license)

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