4.7 Article

Removal of rare-earth elements from aqueous solutions by microporous titanosilicate ETS-4

Journal

MICROPOROUS AND MESOPOROUS MATERIALS
Volume 357, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.micromeso.2023.112606

Keywords

Sorption; Response surface; REE; Recovery; Ion exchange

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The mining of Rare-Earth Elements (REE) has raised concerns due to its unsustainability and negative impacts on the environment, economy, and society. This study explored the use of microporous titanosilicate ETS-4 for the removal of a mixture of REE3+ from contaminated water. Factors such as pH, concentration, and sorbent amount were studied, and the results showed that increasing pH and higher sorbent amounts led to greater removal of REE3+. The study also revealed that ETS-4 has the potential to effectively remove high concentrations of REE3+ from aqueous solutions.
The mining of Rare-Earth Elements (REE) is an unsustainable practice that raises environmental, economic, and societal concerns. As a result, there is a need to develop suitable technologies for the removal of these elements from contaminated waters. Sorption is a clean and efficient method for decontaminating water, and microporous titanosilicates have shown promise for REE removal. However, the influence of solution parameters on this process remains poorly understood. In this study, the effect of pH (4-8), concentration (1-5 mu M), and sorbent amount (20-180 mg L-1) on the removal of a mixture of REE3+ (Y, La, Ce, Pr, Nd, Eu, Gd, Tb, Dy) from water by the microporous titanosilicate ETS-4 (Na9Ti5Si12O38(OH)center dot 12H(2)O) was assessed. A Box-Behnken design was used to investigate the experimental conditions, and the results were presented as three-dimensional response surfaces. The removal mechanism involves the ion exchange of Na+ by REE3+, with pH being the main variable in the process due to competition with H+. Increasing pH resulted in higher removal, with 100% removal achieved at ETS-4 amounts of 180 mg L-1 and REE concentrations of 1 mu M. Most REE3+ removal occurs within the first 15 min, with little difference between metals (except for Y, which exhibits lower removal). At ETS-4 amounts of 20 mg L-1, REE are highly concentrated in the sorbent, reaching 145 mg g(-1) (15% of the sorbent's mass, postsorption). These results demonstrate that even low amounts of ETS-4 have the potential to remove high concentrations of REE3+ from aqueous solutions with pH levels similar to those found in natural systems.

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