Issue 8, 2024

One-pot in situ construction of amido and hydroxyl co-modified layered double hydroxides for selective scandium adsorption

Abstract

Selective recovery of scandium has always been a research challenge and hotspot. Adsorption recovery is an effective method for selective separation and has aroused wide interest due to its environmental protection, energy saving, and high-efficiency recovery of low-concentration Sc3+. In this work, 3-amidopropyltriethoxysilane (KH550) was successfully introduced onto layered double hydroxides (LDHs) using a one-pot in situ hydrothermal method. Compared to traditional methods, the novel one-step in situ strategy leads to more groups being loaded onto the LDHs. The material has a high adsorption capacity and selectivity for scandium. The optimized KH550-LDHs (4K-LDHs) prepared with the optimal modified volume of 4 mL showed a high saturated adsorption capacity of 22.73 mg g−1 and good scandium adsorption stability. This adsorbent not only selectively extracts Sc3+ from mixed rare earth ion systems but also effectively recovers Sc3+ from the Ca2+, Co2+, Mn2+, Zn2+ and Al3+ coexisting ion solutions. The synergy between amido and hydroxyl groups provides abundant active sites for selective adsorption. The research showed that the modified material was fitted with pseudo-second-order kinetics and the Langmuir model. This work provides a one-pot in situ construction strategy for preparing amido and hydroxyl co-modified layered double hydroxides for selective scandium adsorption.

Graphical abstract: One-pot in situ construction of amido and hydroxyl co-modified layered double hydroxides for selective scandium adsorption

Supplementary files

Article information

Article type
Paper
Submitted
09 Sep 2023
Accepted
17 Jan 2024
First published
19 Jan 2024

New J. Chem., 2024,48, 3525-3532

One-pot in situ construction of amido and hydroxyl co-modified layered double hydroxides for selective scandium adsorption

S. Huang, C. Yuan, J. Li, L. Zhang, H. Zhao, W. Zhao and X. Zhang, New J. Chem., 2024, 48, 3525 DOI: 10.1039/D3NJ04232D

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