Journal
MINERALS ENGINEERING
Volume 206, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.mineng.2023.108504
Keywords
Platinum; Calixarene; Selective complexation; Theoretical calculation; Solvent extraction
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In this study, the extraction performance and complexation mechanism of p-di-ethyl-amino-methylthiacalix[4]arene (L) towards Pt(IV) were investigated. The results indicated that L had excellent complexation ability towards Pt(IV) and could selectively extract it from a solution containing multiple competing ions.
In the present study, the extraction performance and complexation mechanism of p-di-ethyl-amino-methylthiacalix[4]arene (L) toward Pt(IV) in a hydrochloric acid system were investigated. The effects of various parameters including solution pH, L to Pt(IV) mole ratio, Cl- concentration, acidity and reaction time on the complexation process of L with Pt(IV) were systematically investigated. The experimental results indicated that L has excellent complexation ability toward Pt(IV) that about 90 % of Pt(IV) could be extracted within 2 min under the optimal conditions. Moreover, L could selectively extract Pt(IV) from the HCl system containing multiple competing ions such as Ce(III), Zr(IV), La(III), Fe(III), Ni(II), Mg(II), and Al(III). The complexation mechanism between L and Pt(IV) was further clarified by slope analysis, scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDS), and proton nuclear magnetic resonance (1H NMR) titrations. Theoretical analysis of thermodynamics, complexation structure and intermolecular interactions between L and Pt(IV) during the solvent extraction process were performed through density functional theory (DFT) calculations. The results showed that the protonation of L occurs first to form the complex of L & sdot;2HCl, which further reacts with PtCl62- forming the complex of L & sdot;2H+& sdot;PtCl62- through anion-exchange, achieving the efficient and selective extraction of platinum.
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