Published December 17, 2024 | Version v1
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Lead Adsorption and Desorption at the Barite (001) Surface in the Presence of EDTA

  • 1. City University of New York
  • 2. University of Chicago
  • 3. Argonne National Laboratory

Description

Scaling minerals, such as barite, can cause detrimental consequences for oil/gas pipelines and water systems, but their formation can be inhibited by organic chelators such as ethylenediaminetetraacetic acid (EDTA). Here, we resolve how EDTA affects sorption and desorption of Pb at the barite (001) surface using a combination of X-ray scattering and microscopy measurements. In the presence of EDTA, Pb incorporated in the topmost part of the barite surface and adsorbed as inner-sphere complexes on the surface. In barite saturated solutions containing [Pb] ≥ 100 μM, overgrowth films grew along step edges. These films were exclusively monolayer thick, indicating that their growth was a self-limiting process. Approximately half of the Pb was removed after 14.5 h reaction with a Pb-free EDTA solution where most of the desorption occurred to adsorbed Pb rather than incorporated Pb. Dissolution proceeded primarily via step retreat and etch pit formation in EDTA, but in deionized water, the secondary phase was quickly removed within 3 min. Together these results suggest EDTA binds to both the surface and Pb in solution, which limits Pb sorption. However, EDTA binding to the surface also inhibits removal of the secondary phase that formed at higher Pb concentrations.

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dorfman-et-al-2024-lead-adsorption-and-desorption-at-the-barite-(001)-surface-in-the-presence-of-edta.pdf

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Additional details

Identifiers

DOI
10.1021/acsestwater.4c00836
Other
oai:uchicago.tind.io:14276

Funding

U.S. Department of Energy
DE-SC0024588
American Chemical Society
Petroleum Research Fund
National Science Foundation
EAR-1634415
U.S. Department of Energy
DE-SC0019108
U.S. Department of Energy
DE-AC02-06CH11357

UChicago Information

Division(s)
Physical Sciences Division
Center(s) or Institute(s)
Center for Advanced Radiation Sources, James Franck Institute