氧烷
矿化(土壤科学)
硫酸盐
环境化学
碳纤维
金属
固碳
同步加速器
化学
环境科学
矿物学
材料科学
光谱学
二氧化碳
氮气
物理
有机化学
量子力学
复合数
核物理学
复合材料
作者
Jun Hu,Lauren N. Pincus,Dominik Wierzbicki,Yonghua Du,Catherine A. Peters
标识
DOI:10.1021/acs.est.5c01640
摘要
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.
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