X-ray–driven reaction front dynamics at calcite-water interfaces

Author:

Laanait Nouamane12,Callagon Erika B. R.3,Zhang Zhan4,Sturchio Neil C.5,Lee Sang Soo1,Fenter Paul1

Affiliation:

1. Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, IL, USA.

2. Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, USA.

3. Department of Earth and Environmental Sciences, University of Illinois at Chicago, Chicago, IL, USA.

4. X-ray Science Division, Argonne National Laboratory, Argonne, IL, USA.

5. Department of Geological Sciences, University of Delaware, Newark, DE, USA.

Abstract

Driving dissolution with x-rays Carbonate minerals are important for Earth's carbon cycle. They precipitate directly from solution into diverse materials, depending on their physical or biological source. Whether carbonate minerals grow or dissolve is controlled by the thermodynamic drivers of the mineral/water interface. To control and observe the reactions, Lanaait et al. developed a synchrotron x-ray technique that images calcium carbonate surfaces in water and selectively tunes the solution saturation state (see the Perspective by Wolthers). The x-ray beam drives fast-moving reaction fronts far from equilibrium that are more limited by solution-ion transport than by surface processes. Science , this issue p. 1330 ; see also p. 1288

Funder

U.S. Department of Energy (DOE)

University of Delaware

Argonne National Laboratory (ANL)

University of Illinois at Chicago

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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