Binding mechanisms of Y and HREE sorption on birnessite: New insights into the formation and sustainable development of regolith-hosted REE deposits

Abstract Regolith-hosted rare earth element (REE) deposits are the world’s primary source of heavy REEs (HREEs) critical to the global clean-energy transition. Previous studies suggested that REEs in regolith-hosted deposits are largely inherited from their parent granites. However, several HREE-dominated deposits occur in the weathering crusts of light REE (LREE)-enriched granites, where the mechanisms of REE fractionation remain poorly understood. Also, the conventional mining method of regolith-hosted REE deposits has limited efficiencies in REE recovery while causing enormous environmental contamination. Herein, we have investigated the distribution and speciation of Y and REEs in three representative regolith-hosted REE deposits (i.e., Gucheng and Shangyou, HREE-dominated; Renju, LREE-dominated) as well as Y-sorbed birnessite from batch experiments. Our results show that birnessite in all three deposits is a minor constituent but contains anomalously high concentrations of REEs and contributes to 25.3, 23.4, and 26.5% of the HREE contents of mineralized saprolites. Measured Y K-edge X–ray absorption spectroscopic data suggest that Y3+ (representing HREE3+) is adsorbed on birnessite as YO8 complexes in all three deposits but via different linkages: i.e., the bidentate corner-sharing mode in the HREE-dominated deposits but a mixture of both bidentate corner-sharing and edge-sharing modes in the LREE-dominated deposit. These binding mechanisms are also observed in Y-sorbed birnessite prepared at different ionic strengths. Therefore, different binding mechanisms of Y and HREE sorption on birnessite together with its preferential adsorption of HREE not only are responsible for the formation of HREE-dominated deposits from LREE-enriched granites but have important implications for the sustainable development of regolith-hosted REE deposits.

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Journal
American Mineralogist
Published
2024-10-18
DOI
https://doi.org/10.2138/am-2024-9451
Citations
2
Primary Topic
Geochemistry and Elemental Analysis
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article
Field-Weighted Citation Impact
0.69
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Binding mechanisms of Y and HREE sorption on birnessite: New insights into the formation and sustainable development of regolith-hosted REE deposits

Hui Zheng, Ning Chen, Reza Deevsalar, Yuzhou Feng et al.
2 citations
American Mineralogist
Geochemistry and Elemental Analysis
0.69
article

Binding mechanisms of Y and HREE sorption on birnessite: New insights into the formation and sustainable development of regolith-hosted REE deposits

Hui Zheng, Ning Chen, Reza Deevsalar, Yuzhou Feng, Kenan Cao, Bing Xiao, Ayetullah Tunc, Yu-Xiang Zhu, Mohsen Shakouri, Leo Ka Long Cheung, Renfei Feng, Hong‐Yuan Chen, Yuanming Pan, Qunfeng Xiao
article en
2 citations

Abstract

Abstract Regolith-hosted rare earth element (REE) deposits are the world’s primary source of heavy REEs (HREEs) critical to the global clean-energy transition. Previous studies suggested that REEs in regolith-hosted deposits are largely inherited from their parent granites. However, several HREE-dominated deposits occur in the weathering crusts of light REE (LREE)-enriched granites, where the mechanisms of REE fractionation remain poorly understood. Also, the conventional mining method of regolith-hosted REE deposits has limited efficiencies in REE recovery while causing enormous environmental contamination. Herein, we have investigated the distribution and speciation of Y and REEs in three representative regolith-hosted REE deposits (i.e., Gucheng and Shangyou, HREE-dominated; Renju, LREE-dominated) as well as Y-sorbed birnessite from batch experiments. Our results show that birnessite in all three deposits is a minor constituent but contains anomalously high concentrations of REEs and contributes to 25.3, 23.4, and 26.5% of the HREE contents of mineralized saprolites. Measured Y K-edge X–ray absorption spectroscopic data suggest that Y3+ (representing HREE3+) is adsorbed on birnessite as YO8 complexes in all three deposits but via different linkages: i.e., the bidentate corner-sharing mode in the HREE-dominated deposits but a mixture of both bidentate corner-sharing and edge-sharing modes in the LREE-dominated deposit. These binding mechanisms are also observed in Y-sorbed birnessite prepared at different ionic strengths. Therefore, different binding mechanisms of Y and HREE sorption on birnessite together with its preferential adsorption of HREE not only are responsible for the formation of HREE-dominated deposits from LREE-enriched granites but have important implications for the sustainable development of regolith-hosted REE deposits.

American MineralogistVol. 110(6)
Chinese Academy of Sciences (CN), Guangzhou Institute of Geochemistry (CN), University of Saskatchewan (CA), ORCID (US), University of Chinese Academy of Sciences (CN), Canadian Light Source (Canada) (CA)
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Openalex Percentile: Top 28%
Geochemistry and Elemental Analysis
0.69
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