位阻效应
硫代硫酸盐
吸附
浸出(土壤学)
选择性
配体(生物化学)
选择性吸附
材料科学
无机化学
组合化学
化学
有机化学
催化作用
硫黄
生物化学
环境科学
受体
土壤科学
土壤水分
作者
Xinrong Li,Shuiliang Chen,Xianzhi Hu,Futing Zi
标识
DOI:10.1002/adfm.202307472
摘要
Abstract Designing suitable adsorbents is a key challenge in the recovery of Au(I) from thiosulfate gold‐leaching solutions as the ideal adsorbent not only possesses abundant active sites with high affinities and selectivities toward Au(I), but also demonstrates fast recovery of Au(I) at high purity and large capacity. Herein, guided by theoretical calculations, a water‐insoluble inclusion complex is synthesized using β‐cyclodextrin (β‐CD) and diphenylphosphine (DPP) as host and guest molecules, respectively, by a steric hindrance strategy for highly efficient and selective Au(I) recovery. The prepared β‐CD@DPP exhibits outstanding Au(I) adsorption performance, with a saturated loading capacity of 146.28 mg g −1 . The excellent adsorption performance of β‐CD@DPP for Au(I) is mainly attributed to the full exposure of the adsorption site and the weakly alkaline adsorption environment. Furthermore, β‐CD@DPP demonstrates outstanding selectivity for Au(I) in a Cu─NH 3 ─thiosulfate gold‐leaching solution, and the Au(I) recovery rate is higher than 99%. Synthesis of β‐CD@DPP primarily depends on the weak interactions between DPP and β‐CD. Mechanism of adsorption of Au(I) on β‐CD@DPP involves ligand exchange between PPh 2 − and [Au(S 2 O 3 ) 2 ] 3− . This study provides a new idea and material preparation method for highly efficient, selective, and large‐capacity recovery of Au(I) from thiosulfate leaching solution.
科研通智能强力驱动
Strongly Powered by AbleSci AI