Replacement of calcite (CaCO3) by Cerussite (PbCO3)

Ke Yuan, Sang Soo Lee, Vincent De Andrade, Neil C. Sturchio, Paul Fenter

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

The mobility of toxic elements, such as lead (Pb) can be attenuated by adsorption, incorporation, and precipitation on carbonate minerals in subsurface environments. Here, we report a study of the bulk transformation of single-crystal calcite (CaCO3) into polycrystalline cerussite (PbCO3) through reaction with acidic Pb-bearing solutions. This reaction began with the growth of a cerussite shell on top of calcite surfaces followed by the replacement of the remaining calcite core. The external shape of the original calcite was preserved by a balance between calcite dissolution and cerussite growth controlled by adjusting the Pb2+ concentration and pH. The relation between the rounded calcite core and the surrounding lath-shaped cerussite aggregates was imaged by transmission X-ray microscopy, which revealed preferentially elongated cerussite crystals parallel to the surface and edge directions of calcite. The replacement reaction involved concurrent development of ∼100 nm wide pores parallel to calcite c-glide or (120) planes, which may have provided permeability for chemical exchange during the reaction. X-ray reflectivity measurements showed no clear epitaxial relation of cerussite to the calcite (104) surface. These results demonstrate Pb sequestration through mineral replacement reactions and the critical role of nanoporosity (3% by volume) on the solid phase transformation through a dissolution−recrystallization mechanism.

Original languageEnglish
Pages (from-to)12984-12991
Number of pages8
JournalEnvironmental Science and Technology
Volume50
Issue number23
DOIs
StatePublished - Dec 6 2016
Externally publishedYes

Funding

The authors thank Dr. Magali S. Ferrandon for help with XRD measurements and Rachel E. Koritala and Jie Wang for help with SEM. This work is supported by the Geosciences Research Program, Office of Basic Energy Sciences, U.S. Department of Energy (DOE), under Contract No. DE-AC02-06CH11357. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. Use of the Center for Nanoscale Materials, an Office of Science user facility, was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357.

FundersFunder number
DOE Office of Science
Geosciences Research Program
Office of Basic Energy Sciences
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Argonne National LaboratoryDE-AC02-06CH11357

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