Selective adsorption of Pd(II) over interfering metal ions (Co(II), Ni(II), Pt(IV)) from acidic aqueous phase by metal-organic frameworks

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Vol. 345; pp. 337 - 344
• Main Authors: Lin, Shuo, Bediako, John Kwame, Cho, Chul-Woong, Song, Myung-Hee, Zhao, Yufeng, Kim, Jeong-Ae, Choi, Jong-Won, Yun, Yeoung-Sang
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.08.2018
• Subjects: Metal-organic frameworks; PdCl42; PtCl62; Selective adsorption; Metal-organic frameworks; Selective adsorption; PdCl42; PtCl62
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2018.03.173

[Display omitted] •This is the earliest report of selective MOFs (UiO-66-NH2) for an ionic target (PdCl42−).•The protonated amino groups show high affinity for PdCl42−.•The convenient diffusion of the PdCl42− through the apertures of the UiO-66-NH2 are found. Metal-organic frameworks (MOFs) have successfully employed as a class of adsorbents for selective separation of CO2 and some organics from gas and liquid phases; however, little attention has been paid to MOFs applications for selective adsorption of ionic targets from aqueous solutions. Besides, selective separation of precious metals is of great importance from the standpoint of realizing a new sustainable development concept of “urban mining”. While, separation of precious metals is challenging, as they are often present in acidic solutions with many interfering metal ions. Herein, Zr(IV)-cluster-based MOFs were synthesized in this study for the selective adsorption of Pd(II), as a model precious metal ion, from acidic aqueous solutions containing Co(II), Ni(II), Pd(II), and Pt(IV). Among the various Zr-MOFs synthesized (i.e. UiO-66, UiO-66-NH2 and UiO-66-NHCOCH3), UiO-66-NH2 showed the highest Pd(II) selectivity, with the Pd(II) uptake in the mixture-metals solution being around 181 times higher than that of Pt(IV). The Pd(II) selectivity of UiO-66-NH2 was attributed to higher binding affinity of the protonated amino groups (–NH3+) for PdCl42− and more convenient diffusion of the PdCl42− through the apertures (pores) of the UiO-66-NH2 – which have the appropriate inner sizes befitting PdCl42− penetration – than for Pt(IV) ions (PtCl62−).