Abstract
Sulfate wastes are produced in large quantities and contain toxic heavy metals such as lead (Pb), posing environmental risks. Because of favorable solubility differences, these wastes can be repurposed for engineered carbon dioxide (CO2) sequestration. Understanding the fate and mobility of heavy metals during this process is important. This study focuses on Pb and the effect of zinc (Zn) on Pb in carbon mineralization. Synthesized gypsum was treated with a carbonate-rich solution at pH 11.5 to convert the sulfates to carbonates. Aqueous solutions and mineral solids were analyzed. Synchrotron-based micro-X-ray fluorescence and a novel application of Pb M3-edge X-ray absorption near-edge structure provided detailed insights into Pb distribution and mineral forms. Results showed significant reductions in aqueous Pb and Zn concentrations, indicating effective metal sequestration. Carbon mineralization transformed Pb from soluble anglesite (PbSO4) into insoluble cerussite (PbCO3) and hydrocerussite (Pb3(CO3)2(OH)2). Pb primarily precipitated onto calcium carbonate surfaces through surface-mediated precipitation reactions. While the presence of Zn modified crystallization dynamics, it did not impede Pb sequestration and potentially enhanced surface reactivity, facilitating greater Pb immobilization. These findings highlight carbon mineralization as a sustainable approach to immobilize toxic metals in sulfate wastes while advancing CO2 sequestration efforts.
Original language | English (US) |
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Pages (from-to) | 7366-7376 |
Number of pages | 11 |
Journal | Environmental Science and Technology |
Volume | 59 |
Issue number | 14 |
DOIs | |
State | Published - Apr 15 2025 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Chemistry
- Environmental Chemistry
Keywords
- beneficiary use
- calcite
- CCUS
- remediation
- solid waste
- trace element
- vaterite